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Director's Statement

FY2008 NIH Budget Hearing – House Appropriations Subcommittee on Labor, Health and Human Services, Education and Related Agencies on March 6, 2007

Richard J. Hodes, M.D., Director
National Institute on Aging
March 6, 2007


Mr. Chairman and Members of the Committee:

I am pleased to present the Fiscal Year (FY) 2008 President's budget request for the National Institute on Aging (NIA). The FY 2008 request provides $1,047,148,000 for the NIA.

I would like to thank you for this opportunity to provide testimony for today's hearing. I am Richard J. Hodes, M.D., Director of the National Institute on Aging. The NIA leads a broad scientific effort to understand the nature of aging and to extend the healthy, active years of life. I am pleased to share with you examples of recent progress in aging research.

The face of aging in the United States is changing dramatically – and rapidly, according to a recent U.S. Census Bureau report commissioned by the NIA. Today, older Americans are very different from their predecessors, living longer, having lower rates of disability, achieving higher levels of education, and less often living in poverty. The baby boomers, the first of whom celebrated their 60th birthdays in 2006, promise to further redefine what it means to grow older in America.

The NIA provides leadership in aging research, training, health information dissemination, and other programs relevant to aging and older people. The Institute's robust research portfolio covers all aspects of aging, from the basic cellular and molecular changes that occur as we age, to the prevention and treatment of common age-related conditions, to the behavioral and social aspects of growing older, including the demographic and economic implications of an aging society. In addition, the NIA is the lead Federal agency for research related to the critically important effort to prevent and treat Alzheimer's disease. Finally, our education and outreach programs provide vital information to older people across the Nation on a wide variety of topics, including living with chronic conditions, maintaining optimal health, and caregiving.


While it is true that our senior and elderly citizens are aging far better today than in previous decades, the specter of Alzheimer's disease (AD), one of the most devastating neurodegenerative diseases, is a source of enormous concern as we and our loved ones age. Approximately 4.5 million Americans are currently battling AD, with annual costs for the disease estimated to exceed $100 billion.1 Moreover, the rapid aging of the American population threatens to increase this burden significantly in the coming decades. By 2050, the number of Americans with AD could rise to some 13.2 million, an almost three-fold increase.2

The NIA supports an extensive research program with the goal of facilitating early diagnosis of AD and developing more effective preventive strategies and therapeutic interventions. Moving forward in each of these areas requires the translation of findings from the laboratory through preclinical testing and into full-scale clinical trials. Recent advances have been made on several fronts.

Neuroimaging. The discovery of compounds such as Pittsburgh Compound B and, more recently, FDDNP that enable the visualization of AD's characteristic amyloid plaques and neurofibrillary tangles in the living brain – an impossibility until several years ago – will not only enable scientists to diagnose AD earlier, but may also help researchers and clinicians develop new treatments and monitor their effectiveness, as well as reduce the time and cost of clinical trials. Research in this area has been intense and productive, with the Alzheimer's Disease Neuroimaging Initiative (ADNI) continuing to be a major venue for facilitating neuroimaging research relevant to AD.

Genetics. Discovery of risk factor genes will help illuminate the underlying disease processes of AD, open up novel areas of research, and identify new targets for drug therapy. Until late 2006, only one risk factor gene for late-onset AD, the more common form of the disease, had been identified. Researchers have now determined that variations in a gene known as SORL1 may be an additional factor in the development of late onset AD. This discovery provides a completely new genetic clue about the late onset forms of AD. Further research is needed to determine the role of SORL1 in AD pathogenesis.

Research is continuing in this important area through the AD Genetics Initiative, which to date has recruited nearly 1,000 families to establish a data base for studies of familial inheritance of AD. In addition, the NIA has established a national genetics data repository to facilitate access by qualified investigators to genotypic data for the study of the genetics of late-onset AD. Investigators have already begun submitting data to this repository and requesting additional data for genetic studies.

Pre-Clinical and Translational Research. NIA plans to speed drug discovery and movement of promising new treatments and prevention strategies into clinical trials. The launch of a major new translational research effort to expand the range of novel compounds to be tested for their effect in preventing or slowing progression of cognitive decline, mild cognitive impairment, and AD, and to more quickly move research from the laboratory to clinical trials in humans, will further support our efforts in this regard.

Clinical Research. The NIA is currently supporting approximately 25 AD-related clinical trials. NIA plans to use the knowledge gained through basic and mechanistic studies to select the most promising imaging and biological markers, as well as improved clinical and neuropsychological evaluation methods, to design and perform less expensive, shorter, and more efficient drug trials. Recent progress in understanding the basic genetic and molecular processes of AD has provided new mechanism-based approaches to designing interventions. In addition, NIA-supported researchers are studying simple lifestyle changes that may confer protective benefits on cognition. For example, in one recent study, increased vegetable consumption was found to reduce risk of cognitive decline in women. In another, certain mental exercises were found to help older individuals maintain their cognitive abilities; the benefits may last as long as five years.


Preservation of cognition in specific domains can be of particular importance to the safety and independence of aging adults. For example, NIA-supported researchers have provided the underlying research for and developed the Useful Field of View (UFOV) test to help predict the degree to which a person may safely perform activities such as driving. The measure is now a major component of assessments tested and about to be adopted by three state Departments of Motor Vehicles for use in screening older drivers. NIA-supported research will also provide the foundation for development of training to help older adults improve their visual attention and speed of processing based on UFOV testing, and for the translation of this training as part of driving safety programs for older adults.

In addition to testing ways to maintain cognitive function, NIA-supported investigators are actively seeking ways to maintain physical function into older age. For example, several studies suggest that physical exercise may prevent physical disability, including impaired mobility, in healthy and frail older adults. To develop definitive evidence regarding the effectiveness of such interventions, NIA and grantee researchers have designed the LIFE (Lifestyle Interventions and Independence in Elders) study, a clinical trial testing the effects of a physical activity program vs. a health education program among older Americans in preventing major disability. A successful pilot study (LIFE-P) completed in 2005 showed both feasibility and positive preliminary data, permitting design and consideration of this large-scale clinical trial.

A large body of research in animal models indicates that substantially reducing caloric intake while maintaining optimal nutrition results in significant increase in life span. The NIA-supported Comprehensive Assessment of Long-Term Effects of Reducing Intake of Energy (CALERIE) will help to determine if these beneficial effects extend to humans. Results from pilot studies demonstrated that overweight people who cut their calories by 25 percent for six months have reduced fasting insulin levels and core body temperature, two markers that have been associated with increased longevity in animal models and that may be similarly associated with human longevity. A two-year study will begin in early January 2007 to determine whether healthy non-obese men and women ages 25-45 who reduce their caloric intake by 25 percent maintain these metabolic changes, and will measure other long-term effects of sustaining lowered caloric intake on factors related to aging changes and risks for age-related diseases.

Because an intensive regimen of restricted food intake may prove difficult for many people to follow over the long term, and may in fact have adverse consequences in some circumstances, investigators are also searching for compounds that mimic the effects of caloric restriction on the body. One compound currently under study is resveratrol, an activator of a family of enzymes called sirtuins, whose cell-protective activities are themselves the subject of intensive scientific inquiry. In a recent study, overweight, aged male mice given a high-fat diet supplemented with resveratrol had better health and survival than aged overweight mice who did not receive the compound. Resveratrol's safety and effectiveness to address aging and age- or obesity-related conditions in humans have not been demonstrated, and further research is needed on the short- and long-term effects of resveratrol supplementation in animals and humans.

The NIA Intervention Testing Program supports the testing of compounds with the potential to extend the lifespan and delay disease and dysfunction in a mouse model. Plans are to renew this promising initiative in FY 2007 for funding in FY 2008. In addition, NIA is continuing to search for genes and biological pathways that influence longevity and aging through the Longevity Associated Gene initiative, which to date has identified over one hundred new longevity-associated genes, along with many conserved biological processes and pathways that regulate longevity in a host of divergent species, including humans.

New research findings may one day translate into better ways to support the aging immune system. A new initiative on “Membrane Associated Signaling Defects in Immune Cells with Aging” seeks to shed light on the cellular processes that may lead to impaired immune function in older people. This research may ultimately lead to the development of interventions to bolster the immune system and reduce vulnerability to disease and disability in older people.

Thank you for the opportunity to provide my testimony to this Subcommittee and to describe these examples of research targeted at improving the health and quality of life of aging and older adults. I would be happy to answer any questions you may have.

Data from the Alzheimer's Association. See also Ernst, RL; Hay, JW. “The U.S. Economic and Social Costs of Alzheimer's Disease Revisited.” American Journal of Public Health 1994; 84(8): 1261 – 1264. This study cites figures based on 1991 data, which were updated in the journal's press release to 1994 figures. (Return to text)

Hebert, LE et al. “Alzheimer Disease in the U.S. Population: Prevalence Estimates Using the 2000 Census.” Archives of Neurology August 2003; 60 (8): 1119 – 1122. (Return to text)

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