In FY 2009, the NIA currently estimates support of 1,522 RPGs, including 350 new and competing projects. Support levels for other funding mechanisms include 74 research centers for $86 million; 257 other research grants, including 230 research career awards, for a total of $34.51 million; 600 full-time training positions for $24.14 million, and a total of $71.6 million for R&D contracts.
On February 17, 2009, the President signed into law H.R. 1, the American Recovery and Reinvestment Act of 2009 (ARRA). The ARRA was enacted to: (1) preserve and create jobs and promote economic recovery, (2) assist those most impacted by the recession, (3) provide investments to increase economic efficiency by spurring technological advances in science and health, (4) invest in transportation, environmental protection, and other infrastructure that will provide long-term economic benefits, and (5) stabilize State and local government budgets, in order to minimize and avoid reductions in essential services and counterproductive state and local tax increases. Included in the ARRA bill is $7.4 billion for NIH which is available until September 30, 2010. The NIA portion of the economic stimulus is $273.3 million.
On July 24, the House Appropriations Committee passed H.R. 3293, the FY 2010 Labor, Health and Human Services, and Education bill. The bill provides NIH with a total program level of $31.26 billion, which is $500 million over the FY 2010 President’s Budget, and 3.1 percent higher than the FY 2009 Enacted level. For NIA, the House Mark is $1.12 billion, which is 3.6 percent higher than the FY 2009 Enacted level of $1.08 billion.
On July 30, the Full Senate Appropriations Committee approved by a voice vote the FY 2010 Labor, Health and Human Services, and Education bill. The bill provides NIH with a total program level of $30.76 billion, the same level as the FY 2010 President’s Budget. For NIA, the Senate Mark is $1.1 billion, which is 1.7 percent higher than the FY 2009 Enacted level of $1.08 billion.
Preliminary work on the budget for FY 2011 has begun using the FY 2010 President’s Budget request as the base. After intermediate stages of review, the President’s Budget request for FY 2011 will be presented to Congress in February 2010, at which time it will become available to the public.
A table showing the NIA FY 2008, 2009 and 2010 funding levels by budget mechanism is included below. Please note that this table does not include ARRA funds or ARRA-solicited applications and the FY 2009 column does not reflect the proposed NIA reprogramming.
(Dollars in thousands)
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H.R. 3293, the FY 2010 Labor, HHS, Education Appropriations – On July 24, 2009, the House passed H.R. 3293 by a roll call vote of 264 to 153. The $730.5 billion FY 2010 spending bill provides $160.7 billion in discretionary spending, $11 billion more than in 2009 and $1.8 billion more than President Obama requested. The NIH Funding level in the bill remained unchanged at the full conference level and provides a 3.1 percent overall increase from FY 2009 Enacted level– a total of $31.258 billion.
On July 28, the Senate subcommittee approved its $163.1 billion discretionary spending draft, which is approximately $300 million more than the House-passed bill. Floor action on the Senate measure was not expected before the Senate recess on Aug 7.
H.R. 2987, the Cure and Understanding Through Research for Alzheimer’s Disease (La Cura Act) of 2009 – On June 19, Congresswoman Linda Sanchez (D-CA) introduced H.R. 2987 in the House. The measure proposes to amend the Public Health Service Act to ensure sufficient resources and increase efforts for research at the National Institutes of Health relating to Alzheimer's disease, to authorize an education and outreach program to promote public awareness and risk reduction with respect to Alzheimer's disease (with particular emphasis on education and outreach in Hispanic populations) and for other purposes. The measure is pending action by the House Committee on Energy and Commerce.
H.R. 3286/S. 1492 – On July 22, Representative Markey (D-MA) and Senator Barbara Mikulski (D- MD) introduced the Alzheimer’s Breakthrough Act of 2009. H.R. 3286/S. 1492 would increase the authorization level for Alzheimer’s disease (AD) research, and require the Director of NIA to make supporting AD research a priority for the Institute. In addition, the legislation would require an expansion of clinical research on AD with a focus on (1) early diagnosis and detection, (2) the relationship of vascular disease and AD, and (3) expediting the translation of research findings into effective treatments and prevention strategies. The bill would require the Secretary, HHS, within three years of enactment of the legislation and every three years thereafter, to convene a summit on AD for the purpose of providing a detailed overview of current research activities at NIH, as well as to discuss and solicit input to potential areas of collaboration related to research, prevention, and treatment of AD between NIH and other Federal agencies.
H.R. 3170, the FY 2010 Financial Services and General Government Appropriations Act. – On July 16, the House passed H.R. 3170 by a vote of 219-208. This legislation contains many government-wide provisions applicable to NIH. Of note, it continues the A-76 prohibition regarding competitive sourcing and contains a new provision that would require each department or agency to develop an inventory of service contracts. Regarding the annual cost-of-living allowance for Federal employees, H.R. 3170 does not contain a pay raise provision since the House agrees with the Administrations’ request of two percent.
S. 1110, the Medicare Payment Advisory Commission (MedPAC) Reform Act of 2009 – On May 20, Senator Harry Reid (D-NV) introduced S. 1110. Of interest to NIH, provisions would authorize the Commission to advise the Secretary, through the Agency for Healthcare Research and Quality (AHRQ) and NIH, on priorities for health services research. In addition, it would authorize the Commission to have access to all raw data and research conducted or funded by the Federal government, including data and research produced by NIH, the Centers for Medicare & Medicaid Services (CMS), and AHRQ. Finally, NIH and AHRQ would be required, not less than twice a year, to submit a report to the Commission containing information on any research conducted which has relevance for the determinations and recommendations being considered by the Commission. S. 1110 was referred to the Senate Committee on Finance.
S. 1142, the Informed Health Care Decision Making Act of 2009 – On May 21, Senator Jack Reed (D-RI), introduced S. 1142. The bill would require the disclosure of comparative clinical effectiveness information in labeling and advertisements (if no such information exists, then such a disclosure must be made). In order to carry out this new mandate, the Secretary, acting through the U.S. Food and Drug Administration (FDA), would be required to establish methodological standards for the sources of evidence appropriate for inclusion of comparative clinical effectiveness information in labeling and advertisements.
Comparative clinical effectiveness in this legislation is defined as “the clinical outcomes, effectiveness, safety, and clinical appropriateness of a drug or device in comparison to 1 or more drugs or devices, respectively, approved to prevent, diagnose, or treat the same health condition for the same patient demographic subpopulation.” S. 1142 was referred to the Senate Committee on Health, Education, Labor, and Pensions.
Comparative Effectiveness Research (CER) NIH Committees and LegislationDr. Richard Hodes, NIA Director, and Dr. Elizabeth Nabel, National Heart, Lung and Blood Institute (NHLBI) Director, serve as co-chairs for the NIH CER Coordinating Committee. Dr. Richard Suzman, NIA Division of Behavioral and Social Research, is a member of the NIH Agency for Healthcare Research and Quality Workgroup (AHRQ) Dr. Marie Bernard, NIA Deputy Director, is representing Dr. Richard Suzman on the Trans-NIH Comparative Effectiveness Portfolio Workgroup.
Several legislative measures have been proposed to amend the CER provisions passed in the American Recovery and Reinvestment Act of 2009 (ARRA). CER provisions have been proposed and may be included in the final Health Reform bills.
H.R. 3200 – On July 17, the House Committee on Ways and Means approved, by a vote of 23-18, H.R. 3200, America’s Affordable Health Choices Act of 2009. Of the over 40 amendments offered, only the 794-page manager’s amendment was adopted. Provisions establishing a center for comparative effectiveness research remain in this version. An amendment offered by Wally Herger (R-CA) to prohibit CMS from using federally-funded clinical comparative effectiveness research data to make coverage decisions was rejected by a vote of 15-26.
H.R. 2520/S. 1099 – On May 20, Representative Ryan (R-WI) and Senator Tom Coburn (R-OK) introduced H.R. 2520 and S. 1099, respectively, the Patients’ Choice Act. Of interest to NIH is section 904, which would terminate the Federal Coordinating Council for Comparative Effectiveness Research established by the American Recovery and Reinvestment Act (P.L. 111-16). The legislation would also establish an interagency coordinating committee to develop a national strategic plan for disease prevention. The NIH Director would be a member of this committee. H.R. 2520 was jointly referred to the House Committees on Energy and Commerce and Ways and Means. S. 1099 was referred to the Senate Committee on Finance.
Small Business Innovation Research (SBIR) and Small Business Technology Research (STTR) Legislation:
On July 23, the Senate passed S. 1390, the National Defense Authorization Act for Fiscal Year 2010. Included in this authorization bill, as an amendment, was the full text of the Senate-passed bill S. 1233, the SBIR/STTR Reauthorization Act of 2009. This latter measure includes the increase of the SBIR set-aside from 2.5 to 3.5 percent and the increase of the STTR from 0.3 to 0.6, which would bring the total for the program to 4.1 percent. The House passed its version of the National Defense Authorization Act in June. Conferees have been named and the measure was ready for conference to begin on August 5.
S. 1513 – On July 24, the Senate passed S. 1513, a bill to provide for an additional temporary extension of programs under the Small Business Act and the Small Business Investment Act of 1958. The bill would extend the current extension from July 31 to September 30, 2009. The bill was debated in the House on July 28, and passed under suspension by voice vote on July 29.
NIA Congressional Briefings:
On July 21, at the request of Representative Lucille Roybal-Allard (D-CA), Dr. Richard Hodes, Dr. Richard Suzman, Dr. Sid Stahl, and Dr. Tamara Jones, met with Mrs. Roybal-Allard and her staff to provide an update on the NIA Roybal Centers for Translational Research in the Behavioral and Social Sciences of Aging.
Dr. Jaron Lockett joined the NIA as the new Intramural Scientific Recruiter and Associate Training Director for the National Institute on Aging (NIA). Dr. Lockett received his Ph.D. at Detroit's Wayne State University in Cellular and Molecular Pathobiology after graduating with an undergraduate degree in biology from Bowie State University. He did postdoctoral work in the Laboratory of Neurosciences under Dr. Stuart Maudsley and in the Laboratory of Immunology under Dr. Ashani Weeraratna.
Dr. Josephine Egan accepted the appointment as the new Chief, Laboratory of Clinical Investigation (LCI), NIA. Dr. Egan has served as Acting Chief since the departure of Dr. Darrell Abernethy in 2007.
Ms. Barbara Torrey joined BSR on August 10, 2009, as a special volunteer. Ms. Torrey is a Visiting Scholar at the Population Reference Bureau in Washington, DC, and was Executive Director of Behavioral and Social Sciences at the National Research Council until 2002. Before joining the National Research Council, Ms. Torrey had directed the Center for International Research at the US Census Bureau, was the Deputy Assistant Secretary for Income Security Policy at the Department of Health and Human Services and a fiscal economist at the Office of Management and Budget. She did both her undergraduate and graduate work at Stanford University in development economics. Subsequently, she did much of her research on the interactions of population change and economics. She has lived and worked in Japan, South East Asia, and East Africa. She has published a number of articles on both domestic and international topics and is a member of the Population Association of America (PAA) and a fellow of the American Association for the Advancement of Science (AAAS). Ms. Torrey will assist BSR with the development of initiatives in economics.
Dr. Miroslaw Mackiewicz joined the Division of Neuroscience as a Health Scientist Administrator to develop and manage the Integrative Neurobiology and Sleep/Biological Rhythms Sections in the Neurobiology of Aging Branch. Dr. Mackiewicz earned his Ph.D. in Medical Sciences from the Institute of Oncology at the National Cancer Institute in Warsaw, Poland. He completed his postdoctoral training at the Wistar Institute of Anatomy and Biology where he conducted cancer-related research including mapping of genetic rearrangements in human carcinomas. He then moved to the Center for Sleep and Respiratory Neurobiology at the University of Pennsylvania School of Medicine as a postdoctoral fellow where he studied sleep and the impact of sleep and age on energy stores in the CNS. Prior to joining NIA, Dr. Mackiewicz was a Research Assistant Professor of Medicine at the University of Pennsylvania School of Medicine and was Director of the Molecular Biology, Behavioral Assessment, and Biomarker Core Laboratories at the Center for Sleep and Respiratory Neurobiology. His research focused on the molecular mechanisms regulating sleep and wakefulness, employing techniques of molecular biology, biochemistry, genetics and genomics. He is an active member of the Sleep Research Society where he served on the Presidential Task Force on Genetics and Sleep.
Dr. Lorenzo Refolo joined the Division of Neuroscience as the program director for the area of the molecular and cellular etiology of Alzheimer’s disease. He received a Ph.D. in Molecular Genetics from the Department of Microbiology and Molecular Genetics at the New Jersey State University of Medicine and Dentistry and subsequently trained as a post-doctoral fellow at Mt. Sinai Medical Center in New York, investigating the molecular and cell biology of the Alzheimer's Amyloid Precursor Protein. After concluding his post-doctoral training, Dr. Refolo held faculty positions at the Mayo Clinic Jacksonville and New York University’s Nathan Kline Institute for Psychiatric Research. Following his academic career, Dr. Refolo served as the Scientific Director at the Institute for the Study of Aging. From 2005 until the present, he was a program director in the Neurodegeneration Cluster at the National Institute of Neurological Disorders and Stroke (NINDS) where his major responsibility was management of grants on ALS and Alzheimer's and Parkinson's diseases.
Departures:
Dr. Shari Ling, Staff Clinician, Clinical Research Branch (CRB), departed NIA to accept a position at the Center for Medicare and Medicaid Services (CMS). She will continue to work with the CRB as a special volunteer.
Dr. Samer Najjar, Staff Clinician, Laboratory of Cardiovascular Science (LCS), left NIA to accept a position at the Washington Hospital Center. He will continue to work with the Clinical Research Branch as a special volunteer.
I. Past Meetings
Harmonization of Longitudinal Aging Surveys – February 9-14, 2009 This BSR-supported exploratory meeting brought together a group of experts, including the principal investigators from the Health and Retirement Survey (HRS), comparable international studies, and teams developing such studies, to a meeting to support harmonization of surveys and the development of a cross-national research agenda on health and health systems. The meeting was held in New Delhi, India. (For more information, contact Drs. Richard Suzman or John Phillips, BSR, Ph: 301-496-3136.)
Clinical Trials on Vitamin D Supplementation in Older Individuals – March 2-3, 2009Following recommendations by the Clinical Trials Advisory Panel, DGCG organized and sponsored an exploratory workshop to review issues on the effects of vitamin D supplementation on clinical and/or functional outcomes in older persons to better inform a decision about the need for and types of clinical trials in the topic area. The workshop was held on March 2-3, 2009 in Bethesda, MD. Participants reviewed the strength of current evidence regarding the effects of vitamin D supplementation on numerous clinical and functional outcomes in the elderly and discussed design features for possible future clinical trials, including target population, effect size and dose/blood level response relationships with outcomes such as physical function and falls. The workshop proceedings were reviewed by the Clinical Trials Advisory Panel at its meeting on May 12 when the Panel made final recommendations to DGCG as to whether to proceed with any initiative on the topic. (For more information, contact Dr. Sergei Romashkan, DGCG, Ph: 301-435-3047.)
NIA-Alzheimer’s Association Meeting on Alzheimer’s Disease Prevalence – March 19-20, 2009The Division of Neuroscience (DN), in conjunction with Division of Behavioral and Social Research (BSR) and the Alzheimer’s Association, held an advisory workshop on the prevalence of Alzheimer’s disease (AD) on March 19-20, 2009, in Washington, DC. The goals of the meeting were: (1) to review the major projects that have produced national prevalence figures and to review other recent research efforts focusing on diagnostic approaches that may shed some light on why national prevalence figures for AD differ; (2) to review data trends on the prevalence of dementia and AD; and (3) to consider the utility of using computer and web-based technology to facilitate case ascertainment in population-based studies of Mild Cognitive Impairment (MCI)/Cognitive Impairment no Dementia(CIND)/AD/dementia. An executive summary of the workshop presentations, discussions, and potential future research directions and challenges will be submitted for publication. A draft of this executive summary will be available for consideration at September Council. (For further information, contact: Dr. Dallas Anderson, DN, Ph: 301-496-9350; andersda@nia.nih.gov .)
Integrating the GWAS (Genome-Wide Association Study) into the Health and Retirement Survey (HRS) - April 16-17, 2009This BSR-supported exploratory meeting, held in Bethesda, MD, had a goal of identifying the best phenotypes for focus and statistical and analytic issues that may arise in conducting a genome-wide scan on the Heath and Retirement Study (HRS). Participants included HRS researchers and scientists in the fields of behavioral and social phenotypes, statistical genetics, and population genetics. (For more information, contact Dr. Erica Spotts, DBSR, Ph: 301-496-3138.)
An Advisory Workshop to Develop Consensus Criteria for Defining Normal Aging in Rodent Models - April 20-22, 2009 Recent scientific advances in aging and age-associated diseases serve as key drivers to learn more about aging phenotypes in rodents and humans. The NIA-supported workshop on biosignatures of aging, held in May 2008, identified the need for developing consensus criteria on normal aging phenotypes. It was agreed that better defined aging phenotypes would strengthen many future NIA-supported studies on normal aging and age-associated diseases. The objective of the April 2009 workshop was to develop consensus criteria for normal aging phenotypes that would include physiological, cellular, and molecular aspects of normal aging. They can be applied to studies in rodent models to: 1) develop and validate biomarker/bio-signature panels, 2) test the influence of genetic background, 3) test potential interventions to promote health aging, and 4) study gene-environment interactions.
Invited participants represented various disciplines including geriatrics, immune, musculoskeletal, and cardiovascular systems, and metabolism. Geriatricians considered aspects of human aging and its potential connections to the study of rodent aging biology. Experts who work with invertebrate model organisms were also invited. A future journal article is anticipated. (For more information, contact: Dr. Mahadev Murthy, DAB, 301-496-6402.)
Harnessing Neuroplasticity for Human Applications - April 21-22, 2009The NIA participated in the organization of an exploratory workshop on Harnessing Neuroplasticity for Human Applications by the NIH Blueprint for Neuroscience Research. The workshop built on previous Blueprint activities to focus on plasticity at the circuit level or “circuit retraining,” which includes alterations in central nervous system (brain and/or spinal cord) structure and function that support enduring changes in behavior. These alterations may involve qualitative and/or quantitative changes at the cellular or synaptic level that alter, restore, adapt, activate, or form novel circuitry to affect function and behavior. To identify research opportunities for promoting circuit retraining to improve functional outcomes, 30 invited participants with expertise in basic and/or clinical research areas, such as neuroimaging, animal models, clinical trials, deep brain and non-invasive brain stimulation, neurofeedback, virtual reality, pharmacology, therapeutic exercise, and learning-based behavioral interventions, worked as a group to develop background papers and presented at the workshop in one of the four relevant aspects of (1) adult trauma and stroke, (2) mental and addictive disorders, (3) neurodegeneration and aging, and (4) pediatric and developmental disorders. A consensus report (or reports) from the workshop will be developed and published to guide future research priorities in neuroplasticity-based therapeutic intervention and assessment strategies, technological advances and tools for promoting and understanding circuit-level changes, resource issues and barriers, and collaborative opportunities. (For more information, contact Dr. Wen G. Chen, DN, Ph: 301-496-9350; chenw@nia.nih.gov.)
II. Future Meetings
Social, Emotional, and Socioeconomic Behaviors in Aging – May 21, 2009This BSR-supported exploratory meeting will highlight cutting edge research in domains of psychology of aging that rely on interdisciplinary and multilevel approaches to understanding the social, behavioral, psychological, and biological factors that contribute to positive aging outcomes. This meeting, to be held in Berkeley, California, one day prior to the Annual Convention of the Association for Psychological Science in San Francisco, will explore the potential for advancing integrative psychological research on topics such as self-regulation, social communication and understanding, social stress, well-being, trust, cooperation, and social status. (For more information, contact Dr. Lis Nielsen, BSR, Ph: 301-402-4156.)
The Role of the Cytoskeleton in Cellular Aging – May 22, 2009The primary goal for this exploratory workshop is to assemble a group of experts in cytoskeletal biology with experts in aging research to identify novel approaches, roadblocks, challenges, and opportunities in determining if and how the cytoskeleton changes with age. It is anticipated that the expert panel will provide NIA with specific recommendations on the best approach to advance the science in this underserved area of research. The workshop will be held in Rockville, MD. (For more information, contact Dr. Jose Velázquez, DAB, 301-496-6402.)
NIH Pain Consortium Symposium: Advances in Pain Research – May 26, 2009 The NIA will co-sponsor and participate in organizing the 4th Annual Symposium on Advances in Pain Research by the NIH Pain Consortium. This year the symposium will feature 10-12 presentations from NIH grantees to highlight cutting-edge research accomplishments in areas of genes and genetic studies to understand risk factors for chronic pain, assess treatment responses and abuse potentials, and develop pain research tools and animal models. These are issues of public health significance. Approximately 20 posters from NIH-funded young investigators will be presented and, at the end of the symposium, there will be an open session for participants to provide feedback on pain research opportunities. (For more information, contact Dr. Wen G. Chen, DN, Ph: 301-496-9350; chenw@nia.nih.gov.)
Workshop: Non-Pharmacological Treatments for Back Pain – May 27, 2009 Chronic pain and its associated morbidity and disability are major health problems around the world. In spite of huge expenditures on care (e.g., annual US expenditures for back pain alone are estimated at $50B to $100B annually), available treatment options and approaches are less than fully satisfactory. Although studies suggest that complementary and alternative medicine (CAM) therapies – spinal manipulation, massage, and acupuncture – are the three most utilized interventions for back pain, the evidence base for such interventions is limited. Thus, there is a compelling need for effectiveness research on non-pharmacological interventions for back pain, including CAM interventions, especially as they are administered and utilized in real-world settings and across a broad range of outcome measures meaningful to patients and their health care providers. The NIA is participating in a trans-NIH Steering Committee, led by the National Center for Complementary and Alternative Medicine (NCCAM), to organize a one-day workshop, in the form of roundtable discussions among a panel of experts, to identify and explore a range of important and timely clinical research questions related to non-pharmacological interventions to treat back pain. The outcome of this workshop will help inform future research directions for the NIH and the biomedical scientific community. (For more information, contact Dr. Wen G. Chen, DN, Ph: 301-496-9350; chenw@nia.nih.gov, and Dr. Basil A. Eldadah, DGCG, Ph: 301-496-6761; eldadahb@nia.nih.gov.)
Workshop on Results from the 2004 National Long-Term Care Survey –May 28-29, 2009The purpose of this BSR-supported exploratory meeting is to present new research taking advantage of the 2004 (and final) wave of the National Long-term Care Survey (NLTCS) to further our understanding of disability and the aging life course. Scholars have been invited based upon submitted abstracts, and other interested researchers and policymakers have been invited to participate as well. The meeting will be held in Bethesda, Maryland, and has been planned in coordination with the National Archive of Computerized Data on Aging. (For more information, contact Georgeanne Patmios, BSR, Ph: 301-496-3138.)
Electronic Technologies to Address the Study of Independent Living – Spring 2009This BSR-supported meeting will explore how a technology platform identical or similar to that used by TRIL (Technology Research for Independent Living) and CLARITY (Centre for Sensor Web Technologies) might address a broad range of social, behavioral, and health-related questions. TRIL is a joint program between Irish universities and Intel, aimed at developing technologies to enable elderly persons to live at home. CLARITY is a group of academics and industry partners established as a Science Foundation of Ireland Centre for Science Engineering and Technology. (For more information, contact Georgeanne Patmios or Dr. Jonathan King, BSR, Ph: 301-496-3136.)
Workshop on Changes in Central Regulation of Bone in Aging – June 9, 2009 The primary goal for this exploratory workshop is to assemble a group of experts in neuro and endocrine regulation of bone biology with experts in aging research, to identify novel approaches, roadblocks, challenges and opportunities in further developing the emerging area of aging and neuroendocrine regulation of bone. It is anticipated that the expert panel will provide NIA with specific recommendations on the best approaches to advance the science in this emerging area. The workshop will be held in Bethesda, MD. (For more information, contact Dr. John Williams, DAB, 301-496-6402.)
Conference to Develop Revised Diagnostic Criteria for MCI and Dementia - June 15, 2009The Division of Neuroscience (DN) will convene an advisory workshop on June 15, 2009 in Bethesda, MD to examine the current state of knowledge on early diagnosis of MCI and dementia and methods to differentiate Alzheimer’s disease from other dementing illnesses. Approximately 20 experts in the field will be invited to participate in a roundtable discussion to examine the evidence and make recommendations as to the timing and organization of an advisory conference on revising the criteria for AD diagnosis. Discussion topics will include clinical methods, neuropsychological testing, and the use of imaging and fluid biomarkers in the differential diagnosis of MCI, AD and other dementias of the aging. (For further information, contact: Dr. Creighton Phelps, DN, Ph: 301-496-9350; phelpsc@nia.nih.gov.)
Genetics and Behavioral and Social Interventions – June 23-24, 2009This BSR-supported exploratory meeting will be convened to discuss use of genetic information to better understand and plan behavioral and social interventions. Background papers commissioned during FY08 will be presented. (For more information, contact Dr. Erica Spotts, BSR, Ph: 301-496-3138.)
Systems Biology Approaches to Understanding Aging - July 27-31, 2009Launching an integrated, systems approach to understanding the biology of aging and longevity was one of the central recommendations of the Biology of Aging Summit held in September 2008. This proved to be a central theme of many of the individual working groups at the Summit. Dr. Geoffrey West of the Santa Fe Institute and Dr. Michal Jazwinski of Tulane University approached DAB staff (Anna McCormick and Jose Velazquez) about co-sponsoring this exploratory workshop on “Systems Biology Approaches to Understanding Aging.” Drs. West, Jazwinski, McCormick, and Velazquez are the primary scientific organizers of the proposed workshop planned for July 27-31, 2009, in Santa Fe, NM. Mark Collins of the Glenn Foundation and Stephanie Lederman of AFAR were active participants at the Biology of Aging Summit and offered to co-sponsor this workshop.
The major goals are to gather experts in many areas of aging biology and systems biology to discuss research opportunities related to understanding the biology of aging and to explore rational plans to develop a systematic and integrated systems biology approach to understanding aging biology. Several NIA staff members will be invited to participate in this workshop because of wide-spread interest in this scientific discipline and approach to further aging research. (For more information, contact Dr. Anna McCormick, DAB, 301-496-6402.)
Priorities for Social and Behavioral Research on the Elderly in Disasters – July 2009This BSR-supported exploratory meeting, organized by the National Academies of Science (NAS), under the auspices of the Committee on Population and the Disasters Roundtable, will be convened to review research on the elderly, both in community and institutionalized, in natural and man-made disasters, to discuss priorities for behavioral and social science research. Relevant Program Announcements issued in 2006 will expire in 2009. This meeting will include researchers and staff from funding and planning agencies to take stock of relevant research (both NIH-funded and other) and discuss priorities for research and translation in the future. (For more information, contact Dr. John Haaga, BSR, Ph: 301-496-3131.)
Alternative Animal Models for Aging Research - July/August, 2009 Over the years, the aging research community has extensively leveraged many invertebrate, yeast and vertebrate models (rodents, birds, non-human primates, etc.) for studies in aging and age-associated diseases. Despite the extensive use of these models for aging research, there are still significant scientific gaps, which can be addressed with the use of alternative and often underutilized animal models in aging research. Within this context, aquatic species (zebra fish, freshwater turtle, annual fish, Japanese medaka, etc.) have received very limited attention from the aging research community and grant support from NIA. These models may prove to be valuable for studies involving physiology, genetics, anatomy and pathology.
In addition, short-lived common marmosets (Callithrix jacchus) appear to be useful primate models for aging studies relative to other primate models currently in use. They are small (350-400 grams) South American primates and capable of producing twins or triplets every 5.5 months. However, the marmoset model needs further development for defined phenotypes such as physical, metabolic, physiological, immunological, cognitive and psychosocial functions. Furthermore, genomic tools may have to be further developed for exploiting this model in aging research. The overall objective of this NIA-supported exploratory workshop is to assemble experts who work with these models and have them evaluate their usefulness for aging research. (For more information, contact Dr. Mahadev Murthy, DAB, 301-496-6402.)
TBI and the Risk of Dementia - August 2009Head trauma, a frequent occurrence in the United States and other industrialized nations, is the leading cause of brain injury. Centers for Disease Control estimates suggest that at least 1.4 million people sustain a traumatic brain injury (TBI) per year in the United States, and the costs of TBI in the US are estimated to be $48 billion dollars annually. The societal burden caused by TBI may actually be much greater, as there is growing evidence that TBI is a risk factor for Alzheimer’s disease (AD) and other neurodegenerative disorders. However, the exact nature of the relationship between head trauma and AD is still unclear and needs further study. The Division of Neuroscience (DN) is organizing a multidisciplinary exploratory workshop, in August 2009 in Bethesda, MD, bringing together expert clinicians, epidemiologists, geneticists and basic research scientists from the TBI and AD fields, as well as from other relevant fields, who will critically appraise the current state of knowledge on TBI and risk of AD and outline possibilities for further research. (For further information, contact: Dr. Laurie Ryan, DN, Ph: 301-496-9350; ryanl@mail.nih.gov.)
Work, Health and Retirement: Developing a Whitehall in Washington – August 2009This BSR-supported exploratory meeting will bring together experts from the research community and the federal government to discuss research opportunities on federal workforce retirement and health. A planning teleconference will be held in May to develop the agenda for the meeting. (For more information, contact Dr. John Phillips, BSR, Ph: 301-496-3138.)
Models Systems to Study the Epigenetics of Aging and Longevity – September 2009Understanding the role of epigenetics in tissue-specific aging and organismal longevity was identified as one of the top research priorities for DAB at the Biology of Aging Summit held in September 2008. This year NIA joined the RoadMap “Epigenetics of Health and Human Disease” RFA and several investigators have sent letters of intent regarding aging-related projects, which is very encouraging. One limitation of this RoadMap RFA is the almost exclusive focus on studying epigenetics in humans and human cell models.
With respect to understanding the role of epigenetics in aging and longevity, Summit participants highlighted the opportunity and added value to be gained from parallel studies in well-studied models systems including Drosophila, C. elegans and mice. The major goal of the planned workshop on “Model Systems to Explore the Epigenetics of Aging” is to discuss the advantages and disadvantages of these three model systems and to try to develop a coordinated and cooperative approach to studying this evolving field of research on aging. Several experts in epigenetics, genetics, biology and physiology will be invited to the planned three-day discussion-focused workshop to develop a plan for studying the epigenetics of aging and longevity. Several NIA staff will also be invited to attend due to broad NIA-based interest in epigenetics. This exploratory workshop is planned for September, 2009. (For more information, contact Dr. Anna McCormick, DAB, 301-496-6402.)
Financial Innovation and Retirement Security: From Ideas to Implementations – Sept 2009This BSR-supported exploratory workshop will address the challenge of how to design financial products to enhance the financial security of older Americans. The nature of the risks that are faced in later life remains poorly understood. The meeting will focus on three topics: (1) Managing Longevity Risk, (2) Managing Health Costs and other Expenditure Risks, and (3) Framing and Decision-Making. (For more information, contact Dr. John Phillips, BSR, Ph: 301-496-3138.)
NIH Pain Consortium Symposium: Advances in Pain Research – May 26, 2009 The NIA co-sponsored and participated in the organization of the 4th Annual Symposium on Advances in Pain Research by the NIH Pain Consortium in Bethesda, MD. This year the symposium featured twelve presentations from NIH grantees that highlighted cutting-edge research accomplishments in areas of genes and genetic studies to understand risk factors for chronic pain, assess treatment responses and abuse potentials, and develop pain research tools and animal models. Dr. Roger Fillingim from the University of Florida presented his work on genetic contributions to ethnic differences in chronic pain, which is currently funded by NIA. In addition, seventeen posters from NIH-funded new investigators were presented, and at the end of the symposium there was an open session for participants to provide feedback on pain research opportunities. (For more information, contact Dr. Wen G. Chen, DN, Ph: 301-496-9350, chenw@nia.nih.gov.)
Workshop on Results from the 2004 National Long-Term Care Survey – May 28-29, 2009The purpose of this NIA/BSR-supported exploratory meeting held in Bethesda, MD, was to present new research taking advantage of the 2004 (and final) wave of the National Long-term Care Survey (NLTCS) to further our understanding of disability and the aging life course. Scholars were invited based upon submitted abstracts, and other interested researchers and policymakers were invited to participate as well. (For more information, contact Ms. Georgeanne Patmios, BSR, Ph: 301-496-3138.)The Science of Behavior Change Roadmap Development meeting - June 15-16, 2009This meeting featured more than 60 invited experts and an equal number of NIH extramural staff from seventeen participating ICs. The meeting charge was to identify areas within the science of behavior change that were especially important or ripe for further development by NIH, either through the Roadmap process or some other trans-NIH effort. The meeting report was expected to be released in late summer. Dr. Richard Suzman, Director of NIA’s Division of Behavioral and Social Research (BSR) is the co-chair of this effort with Dr. Patricia Grady, the Director of the National Institute of Nursing Research (NINR). Dr. Jonathan King, of NIA/BSR, is the coordinator of this ongoing Roadmap effort. (For more information, contact Dr. Jonathan King, BSR, Ph: 301-594-5942.)
NIA staffed, exhibited, and/or disseminated materials at the following meetings and conferences:
NIA coordinated a meeting with the Geronotological Society of America (July 23).
(For more information about NIA’s exhibits, contact Ms. Vicky Cahan, Communications Director, OCPL, Ph: 301-496-1752. For more information about meetings with professional organizations or associations, contact Dr. Tamara Jones, Legislative Officer, Ph: 301-451-8835.)
(For more information about NIA’s awards, contact Ms. Vicky Cahan, Communications Director, OCPL, Ph: 301-496-1752.)
A new Census Bureau Report, An Aging World: 2008, commissioned by NIA/BSR and published July 21, 2009, examines nine international population trends identified in 2007 by the NIA and the US Department of State. An Aging World: 2008 contains detailed information on life expectancy, health, disability, gender balance, marital status, living arrangements, education and literacy, labor force participation and retirement, and pensions among older people around the world. The number of people worldwide age 65 and older is estimated at 506 million as of midyear 2008; by 2040, that number will hit 1.3 billion. Thus, in just over 30 years, the proportion of older people will double from 7 percent to 14 percent of the total world population. This new report examines the demographic and socioeconomic trends accompanying this unprecedented rate of increase in the average age of the world’s population. (See NIA news release at: http://www.nia.nih.gov/NewsAndEvents/PressReleases/20090720global.htm.) (For more information, contact Dr. Richard Suzman, BSR, Ph: 301-496-3131.)
The following new NIA publications were completed:
The following publications were updated and/or reprinted:
(For more information about NIA’s publications, contact Ms. Vicky Cahan, Communications Director, OCPL, Ph: 301-496-1752.)
The following news releases were distributed to audiences in print and on the internet:
(For more information about NIA’s press activities, contact Ms. Vicky Cahan, Communications Director, OCPL, Ph: 301-496-1752.)
E-mail Alert Launched
NIHSeniorHealth
Excerpts from the NIH GUIDE - April 13, 2009 – August 21, 2009Includes Notices and Initiatives: Requests for Applications (RFAs) and Program Announcements (PAs), published since the May 2009 Council presentation of the Director’s Status Report (DSR) to the National Advisory Council on Aging (NACA).
Also check our NIA website for “Funding Opportunities” at http://www.nia.nih.gov/GrantsAndTraining/FundingOpportunities/CurrentFundingOpportunities.htm
(Shown here are selected Notices and Initiatives relevant to NIA/National Institutes of Health/DHHS).
TABLE OF CONTENTS
AnnouncementNumber
IssuingOrganization
ReleaseDate
Opening Date(SF424 Only)
ExpirationDate
ActivityCode(s)
Title
RFA-AG-10-006
NIA
08/19/2009
10/09/2009
11/10/2009
R01
Effects of Gene-Social Environment Interplay on Health and Behavior in Later Life (R01)
Purpose – This initiative invites R01 applications for the development of multidisciplinary collaborations among existing longitudinal twin and family studies, with a focus on social and behavioral factors associated with aging outcomes. This FOA is intended to lay the foundation for future studies of the role of gene-environment interplay in accounting for links between social experiences and physical health, functionality, and psychological well-being in midlife and older age.
Scientific/Research Contact:Erica L. Spotts, Ph.D. Division of Behavioral and Social Research National Institute on Aging7201 Wisconsin Avenue, Suite 533Bethesda, MD 20892-9201 Telephone: (301) 451-4503 Fax: 301-402-0051Email: spottse@mail.nih.gov
RFA-AG-10-008
10/02/2009
11/03/2009
Healthy Aging through Behavioral Economic Analyses of Situations (R01)
Purpose – This initiative invites applications that propose to translate basic findings from Behavioral Economics into behavior change interventions targeting health behaviors associated with chronic health conditions of mid-life and older age. Applications will propose small pilot clinical trials or demonstration projects based on collaborations between individuals with expertise in behavioral economics and psychologists or clinicians with expertise in aging or implementing behavioral interventions.
Scientific/Research Contact:Dr. Jonathan W. King Division of Behavioral and Social ResearchNational Institute on Aging 7201 Wisconsin Ave., Room 533 Bethesda, MD 20892-9205 Telephone: (301) 402-4156 Fax: (301) 402-0051 Email: kingjo@nia.nih.gov
RFA-AG-10-005
07/29/2009
n/a
10/01/2009
U01
Limited Competition: The National Institute on Aging Multicenter Study on Exceptional Survival in Families: The Long Life Family Study (LLFS) (U01)
Purpose – The purpose of this FOA is to determine the degree and patterns of familial transmission and aggregation of exceptional longevity and healthy survival to advanced age as characterized by a variety of phenotypic measures, with a further goal of also understanding potential genetic factors that contribute to exceptional survival.
Scientific/Research Contact:Ms. Winifred K. RossiDeputy Director, Division of Geriatrics and Clinical Gerontology National Institute on Aging7201 Wisconsin Ave., Room 3C307Bethesda, MD 20892-9205Telephone: (301) 496-3836 FAX: (301) 402-1784Email: winnie_rossi@nih.gov
RFA-AG-10-004
07/17/2009
09/30/2009
10/31/2009
Awards to Support Research on the Biology of Aging in Invertebrates (R01)
Purpose – This FOA invites research applications that focus on the identification and characterization of new invertebrate models for investigating the biology of aging and the genetics behind this process. Applications focusing on models that are currently in extensive use in the aging field will be considered non-responsive to this FOA.
Scientific/Research Contact:Mahadev Murthy, Ph.D., M.B.A.Program DirectorDivision of Aging Biology (DAB)National Institute on Aging7201 Wisconsin Ave., Room 2C231Bethesda, MD 20892-9205Tel: (301) 496-6402Fax: (301) 402-5997E-Mail: mmurthy@mail.nih.gov
RFA-OD-09-006
NIH
10/23/2009
K12
Building Interdisciplinary Research Careers in Women’s Health (K12)
Purpose – This initiative invites institutional career development award applications for Building Interdisciplinary Research Careers in Women's Health (BIRCWH) Career Development Programs, hereafter termed "Programs." Programs will support mentored research career development of junior faculty members, known as BIRCWH Scholars, who have recently completed clinical training or postdoctoral fellowships, and who will be engaged in interdisciplinary basic, translational, behavioral, clinical, and/or health services research relevant to women's health or sex/gender factors.
Scientific/Research Contact:Robin Barr, Ph.D. Division of Extramural Activities National Institute on AgingRoom 2C2187201 Wisconsin Avenue, Room 2C218Bethesda, MD 20892-9205 (use Bethesda, MD 20814 for express mailing)Telephone: (301) 496-9322Fax: (301) 402-2945Email: BarrR@nia.nih.gov
RFA-OD-09-008
06/02/2009
08/01/2009
09/02/2009
RC3
Recovery Act Limited Competition: Biomedical Research, Development, and Growth to Spur the Acceleration of New Technologies (BRDG-SPAN) Pilot Program (RC3)
Purpose – This initiative is supported by funds provided to the NIH under the American Recovery & Reinvestment Act of 2009. The purpose of this pilot program is to address the funding gap between promising research and development (R&D) and transitioning to the market -- often called the “Valley of Death -- by contributing to the critical funding needed by applicants to pursue the next appropriate milestone(s) toward ultimate commercialization; i.e., to carry out later stage research activities necessary to that end.
Scientific/Research Contact:
RFA-OD-09-009
R43
Recovery Act Limited Competition: Small Business Catalyst Awards for Accelerating Innovative Research (R43)
Purpose – This initiative invites grant applications from small business concerns that propose to accelerate innovation through high risk, high reward research and development (R&D) that has commercial potential and is relevant to the mission of the NIH. The Small Business Catalyst Award is further expected to support entrepreneurs of exceptional creativity, drawn from scientific and technological environments beyond NIH, who propose pioneering and possibly transformative approaches to addressing major biomedical or behavioral challenges with the potential for downstream commercial development.
Scientific/Research Contact:Dr. Michael-David A.R.R. KernsNational Institute on Aging, NIHGateway Building, Suite 2C2187201 Wisconsin Ave., MSC 9205Bethesda, MD 20892-9205Phone: 301-496-9322Fax: 301-402-2945Email: mk417e@nih.gov
RFA-OD-09-007
04/20/2009
08/24/2009
09/25/2009
R15
Recovery Act Limited Competition: Academic Research Enhancement Award (R15)
Purpose – The purpose of the Academic Research Enhancement Award (AREA) program is to stimulate research in educational institutions that provide baccalaureate or advanced degrees for a significant number of the Nation's research scientists, but that have not been major recipients of NIH support. These AREA grants create opportunities for scientists and institutions otherwise unlikely to participate extensively in NIH programs, to contribute to the Nation's biomedical and behavioral research effort. AREA grants are intended to support small-scale health-related research projects proposed by faculty members of eligible, domestic institutions.
RFA-MH-10-020
NIMH
07/15/2009
11/25/2009
U54
The Human Connectome Project (U54)
Purpose – The overall purpose of this five year Human Connectome Project (HCP) is to develop and share knowledge about the structural and functional connectivity of the human brain. Under this initiative, “connectivity” is defined at the level showing structural and/or functional linkages from one major subdivision (cortical areas or subcortical nuclei) of the brain to others. It is recognized that many current technologies are best suited to collect data from cerebral cortex, though, to the extent that it is possible, subcortical connectomic data are also of great interest to the Project.
Scientific/Research Contact:Bradley Wise, Ph.D.National Institute on AgingNIH, DHHSGateway Building, Suite 3507201 Wisconsin Avenue, MSC 9205Bethesda, MD 20892Tel: 301-496-9350
PAR-09-233
09/28/2010
R24
Network Infrastructure Support for Emerging Behavioral and Social Research Areas in Aging (R24)
Purpose – The purpose of this FOA is to provide infrastructure support in specific emerging interdisciplinary areas of behavioral and social research in aging using the NIH Resource-Related Research Project (R24) mechanism. The infrastructure support will facilitate research networks through meetings, conferences, small scale pilots, training, and dissemination to encourage growth and development in specified emerging areas and resources.
Scientific/Research Contact:Lis Nielsen, Ph.D. Division of Behavioral and Social Research National Institute on Aging 7201 Wisconsin Ave., #533Bethesda, MD 20892-9205 Telephone: (301) 402-4156 Fax: (301) 402-0051 Email: nielsenli@nia.nih.gov
PA-09-216
07/06/2009
09/05/2009
09/08/2012
Mechanisms Underlying the Links between Psychosocial Stress, Aging, the Brain and the Body (R01)
Purpose – The purpose of this FOA is to encourage aging-relevant research elucidating the underlying mechanisms and processes that link psychosocial stressors to health outcomes in older individuals. Multidisciplinary and interdisciplinary research at multiple levels of analysis in animal models and in humans, integrating neuroscience and biological processes with behavioral and psychosocial approaches is strongly encouraged. Longitudinal research capturing processes of cumulative exposure to psychosocial stressors and dysregulation, and research exploring resilience and vulnerability risk factors underlying individual variability in stress-linked diseases in aging also are particularly encouraged.
Scientific/Research Contact:Suzana S. Petanceska, Ph.D.Division of NeuroscienceNational Institute on AgingGateway Building, Suite 3507201 Wisconsin Avenue, MSC 9205Bethesda, MD 20892-9205Telephone: (301) 496-9350FAX: (301) 496-1494Email: petanceskas@mail.nih.gov
PA-09-217
The Role of Apolipoprotein E, Lipoprotein Receptors and CNS Lipid Homeostasis in Brain Aging and Alzheimers Disease (R01)
Purpose – This initiative encourages multidisciplinary and interdisciplinary research to elucidate how Apolipoprotein E, lipoprotein receptors and CNS lipid homeostasis influence brain aging and the transition to neurodegeneration in Alzheimer’s disease (AD). The ultimate goal is to gain an in depth understanding of the mechanisms by which the Apolipoprotein E e4 allele confers increased AD risk for the purpose of advancing the overall search for efficacious AD treatments and Apolipoprotein E e4-directed therapeutics in particular.
PA-09-190,
06/03/2009
Bioenergetics, Fatigability, and Activity Limitations in Aging (R01)
PA-09-191, and PA-09-192
09/16/2009
R21 and R03
Bioenergetics, Fatigability, and Activity Limitations in Aging (R21) (R03)
Purpose – These FOAs encourage applications that propose to 1) elucidate specific alterations in bioenergetics related to increased fatigability and activity limitations; 2) develop and evaluate improved measures of fatigability related to bioenergetics; 3) evaluate interventions for increased fatigability and activity limitations that target alterations in bioenergetics and lead to improved quality of life.
Scientific/Research Contact:Basil Eldadah, MD, PhDDivision of Geriatrics and Clinical GerontologyNational Institute on Aging7201 Wisconsin Avenue, 3C-307Bethesda, MD 20892-9205Phone: (301) 496-6761Fax: (301) 402-1784Email: eldadahb@nia.nih.gov
PA-09-193,
05/28/2009
09/06/2012
Mechanisms, Measurement, and Management of Pain in Aging: from Molecular to Clinical (R01)
PA-09-194, and PA-09-195
Mechanisms, Measurement, and Management of Pain in Aging: from Molecular to Clinical (R21) (R03)
Purpose – These FOAs encourage proposals to study the mechanisms and processes by which aging and/or age-related diseases and conditions affect the experience of pain, and to evaluate existing or new pain assessment methods and management approaches, especially in older adults. Human and animal model studies are appropriate for this FOA.
Scientific/Research Contact:Wen G. Chen, Ph.D. Division of NeuroscienceNational Institute on Aging7201 Wisconsin Ave., Suite 350 Bethesda, MD 20892 Telephone: (301) 496-9350 FAX: (301) 496-1494Email: chenw@nia.nih.gov
PA-09-165 and
04/17/2009
05/05/2009
05/08/2012
Renal Function and Chronic Kidney Disease in Aging (R01)
PA-09-166
R21
Renal Function and Chronic Kidney Disease in Aging (R21)
Purpose – These FOA s invites research applications in both animal models and in humans, addressing the etiology, pathophysiology, risk factors, consequences, prevention, or treatment of CKD in older patients. Applications should focus on the 1) biology and pathophysiology of CKD in animal models; 2) etiology and pathophysiology of CKD in the elderly; 3) epidemiology and risk factors for the development of CKD with advancing age; and/or 4) diagnosis, medical management and clinical outcomes of CKD in this population.
Scientific/Research Contact: Susan G. Nayfield, M.D., M.Sc.Chief, Geriatrics BranchDivision of Geriatrics and Clinical GerontologyNational Institute on Aging7201 Wisconsin Avenue, Suite 3C-307Bethesda, MD 20892-9205 Phone: (301) 496-6761Fax: (301) 402-1784E-mail: nayfiels@mail.nih.gov
PA-09-207
06/12/2009
07/08/2009
F30
Ruth L. Kirschstein National Research Service Awards for Individual Predoctoral MD/PhD and Other Dual Doctoral Degree Fellows (F30)
Purpose – The purpose of the Ruth L. Kirschstein National Research Service Awards (Kirschstein-NRSA) is to provide support to individuals for combined MD/PhD and other dual doctoral degree training (e.g. DO/PhD, DDS/PhD, AuD/PhD). The participating Institutes award this Kirschstein-NRSA individual fellowship (F30) to qualified applicants with the potential to become productive, independent, highly trained physician-scientists and other clinician-scientists, including patient-oriented researchers in their scientific mission areas.
PA-09-208
F31
Ruth L. Kirschstein National Research Service Awards for Individual Predoctoral Fellows (F31)
Purpose – The purpose of this individual predoctoral research training fellowship is to provide support for promising doctoral candidates who will be performing dissertation research and training in scientific health-related fields relevant to the missions of the participating NIH Institutes and Centers (ICs) during the tenure of the award.
PA-09-209
07/13/2009
Ruth L. Kirschstein National Research Service Awards for Individual Predoctoral Fellowships (F31) to Promote Diversity in Health-Related Research
Purpose – The purpose of this individual predoctoral research training fellowship is to improve the diversity of the health-related research workforce by supporting the training of predoctoral students from groups that have been shown to be underrepresented. Such candidates include individuals from underrepresented racial and ethnic groups, individuals with disabilities, and individuals from disadvantaged backgrounds. Detailed eligibility criteria are described in the full announcement.
PA-09-210
F32
Ruth L. Kirschstein National Research Service Awards (NRSA) for Individual Postdoctoral Fellows (F32)
Purpose – The purpose of this individual postdoctoral research training fellowship is to provide support to promising Fellowship Applicants with the potential to become productive, independent investigators in scientific health-related research fields relevant to the missions of participating NIH Institutes and Centers.
PA-09-211
F33
Ruth L. Kirschstein National Research Service Awards (NRSA) for Individual Senior Fellows (F33)
Purpose – The National Institutes of Health (NIH) awards individual senior level research training fellowships to experienced scientists who wish to make major changes in the direction of their research careers or who wish to broaden their scientific background by acquiring new research capabilities as independent investigators in research fields relevant to the missions of participating NIH Institutes and Centers.
Scientific/Research Contact:Chyren Hunter, Ph.D.Division of Extramural ActivitiesGateway Building, Room 2C2187201 Wisconsin Avenue, MSC 9205Bethesda, MD 20892-9205Use Bethesda MD 20814 for express mailingOffice phone: 301-496-9322E-mail: Hunterc@nia.nih.gov
PA-09-186
05/15/2009
05/16/2009
R34
NIH Clinical Trial Planning Grant Program (R34)
Purpose – This initiative invites applications under the NIH Clinical Trial Planning Grant Program, the purpose of which is to provide support for the development of a Phase III clinical trial. This includes the establishment of the research team, the development of tools for data management and oversight of the research, the definition of recruitment strategies, and the finalization of the protocol and other essential elements of the study included in a manual of operations/procedures. The Clinical Trial Planning Grant is not designed for the collection of preliminary data or the conduct of pilot studies to support the rationale for a clinical trial.
PA-09-163
04/16/2009
R03
NIH Small Research Grant Program (Parent R03)
Purpose – This initiative supports small research projects that can be carried out in a short period of time with limited resources. Investigator-initiated research, also known as unsolicited research, is research funded as a result of an investigator submitting a research grant application to NIH in an investigator’s area of interest and competency. The R03 grant mechanism supports different types of projects including pilot and feasibility studies; secondary analysis of existing data; small, self-contained research projects; development of research methodology; and development of new research technology.
PA-09-164
NIH Exploratory/Developmental Research Grant Program (Parent R21)
Purpose – The Exploratory/Developmental Grant (R21) mechanism is intended to encourage exploratory and developmental research projects by providing support for the early and conceptual stages of these projects. These studies may involve considerable risk but may lead to a breakthrough in a particular area, or to the development of novel techniques, agents, methodologies, models, or applications that could have a major impact on a field of biomedical, behavioral, or clinical research.
PAR-09-219
NIGMS
08/17/2009
Exploratory Innovations in Biomedical Computational Science and Technology (R21)
Purpose – The NIH is interested in promoting research and developments in biomedical informatics and computational biology that will support rapid progress in areas of scientific opportunity in biomedical research. As defined here, biomedical informatics and computational biology includes database design, graphical interfaces, querying approaches, data retrieval, data visualization and manipulation, data integration through the development of integrated analytical tools, and tools for electronic collaboration, as well as computational and mathematical research including the development of structural, functional, integrative, and analytical computational models and simulations.
Scientific/Research Contact:José M. Velázquez, Ph.D.Director, Cell Biology Program Division of Aging BiologyNational Institute on Aging7201 Wisconsin Ave, Suite 2C231Bethesda, MD 20892Tel : 301-496-6428Fax: 301-402-0010
PA-09-255
NIDDK
08/14/2009
Erythropoiesis: Components and Mechanisms (R01)
Purpose – This initiative encourages investigator-initiated R01 applications that propose hypothesis-driven research using erythroid cells. The aim of this program is to support research efforts towards a complete description of the molecular and cellular components of erythropoiesis and how these components contribute to erythropoiesis. and cytokine determinants in the erythroid lineages so that new therapeutics may be developed to measure and combat anemia.
PAR-09-251
NINDS
08/13/2009
Optimization of Small Molecule Probes for the Nervous System (R21)
Purpose – The purpose of this funding opportunity is to facilitate the development of small molecule probes that will add a pharmacological dimension to basic neuroscience work, and enable proof-of-principle studies linking nervous system therapeutic targets, mechanisms or phenotypes to disease onset or progression.
PAR-09-218
08/05/2009
Innovations in Biomedical Computational Science and Technology (R01)
Purpose – This announcement covers broad-based research in biomedical informatics and computational biology, and is coordinated by the NIH Biomedical Information Science and Technology Initiative (BISTI) committee. Through this and related opportunities, Institutes and Centers of the NIH offer support for: fundamental research in biomedical informatics and computational biology; development of new computational tools and technologies; and applications of computational technologies to a particular domain area(s) in biomedical research. See www.bisti.nih.gov for more information.
Scientific/Research Contact:José M. Velázquez, Ph.D.Director, Cell Biology Program Division of Aging BiologyNational Institute on Aging7201 Wisconsin Ave, Suite 2C231Bethesda, MD 20892Tel : 301-496-6428Fax: 301-402-0010Email: jvelazqu@mail.nih.gov
PAR-09-220
11/05/2009
R43, R44
Innovations in Biomedical Computational Science and Technology Initiative (SBIR [R43/R44])
PAR-09-221
R41, R42
Innovations in Biomedical Computational Science and Technology Initiative (STTR [R41/R42])
Purpose – These two funding opportunity announcements (FOAs) solicit Small Business Innovation Research (SBIR) grant applications and Small Business Technology Transfer (STTR) grant applications from small business concerns (SBCs) that propose innovative research in biomedical informatics and computational biology to promote the progress of biomedical research.
PAR-09-224
NCI
07/09/2009
07/06/2012
Improving Diet and Physical Activity Assessment (R01)
PAR-09-225
07/17/2012
Improving Diet and Physical Activity Assessment (R21)
Purpose – These initiatives seek innovative research to enhance the quality of measurements of dietary intake and physical activity. Applications submitted under this FOA may include development of: novel assessment approaches; better methods to evaluate instruments; assessment tools for culturally diverse populations or various age groups, including older adults; improved technology or applications of existing technology; statistical methods to assess or correct for measurement errors or biases, methods to investigate the multidimensionality of diet and physical activity behavior through pattern analysis; or integrated measurement of diet and physical activity along with the environmental context of such behaviors.
Scientific/Research Contact:Chhanda Dutta, Ph.D.Geriatrics and Clinical Gerontology ProgramNational Institute on Aging (NIA)7201 Wisconsin Avenue, Suite 3E-327, MSC 9205Bethesda, MD 20892-9205Telephone: (301) 435-3048Fax: (301) 402-1784Email: duttac@mail.nih.gov
NOT-AG-09-007
08/21/2009
NIA Intervention Testing Program Solicits Proposals for Compounds to Test for Anti-Aging Activity in Mice
NOT-OD-09-135
Amendment to the Instructions for Ruth L. Kirschstein National Research Service Award (NRSA) Institutional Research Training Grant Applications and Other Research Training and Research Education Grant Applications Using Form PHS 398 Fillable Data Tables
NOT-OD-09-137
Small Business Innovation Research (SBIR) Program Contract Solicitation (PHS 2010-1) Now Available
NOT-OD-09-138
Recovery Act of 2009: FederalReporting.gov Opens for Registration
NOT-OD-09-134
08/12/2009
Reminder: Investigators Should Update their eRA Commons Profiles to Include Degree and Residency Completion Dates
NOT-OD-09-136
Clarification on the Use of an NIHMSID to Indicate Compliance with the NIH Public Access Policy
NOT-OD-09-128
08/06/2009
Reminder of NIH Requirements for Submission of Financial, Administrative, and Scientific Closeout Reports in a Timely and Accurate Fashion
NOT-OD-09-133
Clarification of Eligibility for Participation in RFA-OD-09-009, Recovery Act Limited Competition: Small Business Catalyst Awards for Accelerating Innovative Research (SBIR [R43])
NOT-OD-09-129
07/31/2009
Recovery Act of 2009: Information on Quarterly Reporting Requirements for NIH Award Recipients
NOT-OD-09-131
Corrections to the Instructions in SF424 (R&R) Individual Fellowship Application Guide for NIH and AHRQ
NOT-OD-09-127
07/23/2009
NIH Enhances Process of Notice of Award (NoA) Email Notifications
NOT-OD-09-125
07/22/2009
Extension of Receipt Date for RFA-OD-09-006 (BIRCWH):Building Interdisciplinary Research Careers in Women's Health (K12)
NOT-OD-09-126
Important Registration Reminders for Businesses Submitting in Response to New Recovery Act Funding Opportunity Announcements
NOT-OD-09-122
NIH Offers SBIR Niche Assessment Program to Phase I Awardees
NOT-OD-09-123
Status of Applications and Awards under the New NIH Guidelines for Human Stem Cell Research
NOT-OD-09-121
07/10/2009
NIH Opens xTrain to All Institutions Registered with the eRA Commons
NOT-OD-09-101
Notice of Availability of Vitamin D Standard Reference Material
NOT-OD-09-120
Recovery Act of 2009: Revised NIH Award Terms Available
NOT-OD-09-116
NIH Guidelines for Human Stem Cell Research
NOT-OD-09-117
Amendment: Ruth L. Kirschstein National Research Service Awards for Individual Predoctoral Fellowships (F31) to Promote Diversity in Health-Related Research (PA-09-209)
NOT-OD-09-113
06/25/2009
Announcing a Delay in Transition to Electronic Submission of Applications for Institutional Training and Institutional Career Development Programs
NOT-OD-09-114
Extension of Modified Application Submission, Referral and Review for Appointed NIH Advisory Group Members
NOT-OD-09-107
06/18/2009
NIH Extramural Loan Repayment Programs (LRP)
NOT-OD-09-108
Extramural Loan Repayment Program for Clinical Researchers (LRP-CR): Program Specific Information
NOT-OD-09-110
Extramural Loan Repayment Program for Health Disparities Research (LRP-HDR): Program Specific Information
NOT-OD-09-112
Extramural Clinical Research Loan Repayment Program for Individuals from Disadvantaged Backgrounds (LRP-IDB): Program Specific Information
NOT-OD-09-106
Announcing New Business Processes and Confirming the Transition of Individual National Research Service Award (NRSA) Fellowship (F) Applications to Electronic Submission
NOT-OD-09-105
06/05/2009
Notice of Correction to Grant Application Appendix Materials in Small Research Grant (R03) FOAs
NOT-OD-09-100
Reminder and Clarification of NIH Policies on Similar, Identical, or Essentially Identical Applications, Submission of Applications Following RFA Review, and Submission of Applications with a Changed Activity Code
NOT-OD-09-093
05/08/2009
Revision of PA-08-190: Research Supplements to Promote Diversity in Health-Related Research
NOT-OD-09-094
Revision of PA-08-191: Research Supplements to Promote Re-Entry into Biomedical and Behavioral Research Careers
NOT-OD-09-099
NIH Requests Comments on Proposed Amendment of Regulations on the Responsibility of Applicants for Promoting Objectivity in Research for which Public Health Service Funding is Sought and Responsible Prospective Contractors
NOT-OD-09-088
05/04/2009
Announcing a new business process for submitting revised abstracts, specific aims, and/or public health relevance statements when changing the scope of proposed research projects
NOT-OD-09-092
05/01/2009
Delays in Grant Application Submission Due to Closure of Institutions because of 2009 H1N1 Flu Concerns
NOT-OD-09-087
04/24/2009
Error-Correction Window Extended for All Electronic Applications with Submission Deadlines through May 1, 2009
NOT-OD-09-085
Implementation of Executive Order on Removing Barriers to Responsible Scientific Research Involving Human Stem Cells
RFA-RM-09-010
NIH/Roadmap
08/18/2009
09/20/2009
10/21/2009
DP1
2010 NIH Directors Pioneer Award Program (DP1)
RFA-RM-09-008
07/16/2009
09/15/2009
Development of New Technologies Needed for Studying the Human Microbiome (R01)
RFA-RM-09-009
Development of New Technologies Needed for Studying the Human Microbiome (R21)
RFA-RM-09-007
05/27/2009
P41
Pilot-Scale Libraries (PSL) for High-Throughput Screening (P41)
NOT-RM-09-014
Notice of Intent to Publish a Request for Applications (RFA) for the 2010 NIH Directors Pioneer Award Program (DP1)
NOT-RM-09-015
Notice of Intent to Publish a Request for Applications (RFA) for the 2010 NIH Directors New Innovator Award Program (DP2)
NOT-RM-09-013
05/07/2009
Notice of Correction to Award Information for PAR-08-024 Assay Development for High Throughput Molecular Screening
NOT-RM-09-012
Notice of Change to Application Instructions for the 2009 NIH Directors New Innovator Award (DP2)
NOT-RM-09-011
04/27/2009
Notice of Opportunity for Fast Track Entry of Assay Projects for High Throughput Screening into the NIH Roadmap Molecular Libraries Probe Production Centers Network
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