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1 International Longevity Center-USA, New York.
2 The Ellison Medical Foundation, Bethesda, Maryland.
3 Biology of Aging Program, National Institute on Aging, Bethesda, Maryland.
4 Metagenics, Inc., Gig Harbor, Washington.
5 National Center for Toxicology Research, Jefferson, Arkansas.
6 Texas College of Osteopathic Medicine, Fort Worth.
7 The Institute for the Study of Aging, New York.
8 Kronos Longevity Research Institute, Phoenix, Arizona.
9 Canyon Ranch Health Resort, Tucson, Arizona.
10 Canyon Ranch in the Berkshires, Lenox, Massachusetts.
11 Desert Life Medical Plaza, Tucson, Arizona.
12 Penn State University, College of Health and Human Development, University Park, Pennsylvania.
13 The University of Texas, San Antonio.
14 The University of Texas, Health Science Center, San Antonio.
15 Department of Physiology/Pharmacology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
16 University of Wisconsin, Madison.
17 University of Washington, Seattle.
Address correspondence to Robert N. Butler, International Longevity Center-USA, 60 E. 86th St., New York, NY 10028. E-mail: robertb{at}ilcusa.org
Leading biologists and clinicians interested in aging convened to discuss biomarkers of aging. The goals were to come to a consensus, construct an agenda for future research, and make appropriate recommendations to policy makers and the public-at-large. While there was not total agreement on all issues, they addressed a number of questions, among them whether biomarkers can be identified and used to measure the physiological age of any individual within a population, given emerging information about aging and new technological advances. The hurdles to establishing informative biomarkers include the biological variation between individuals that makes generalizations difficult; the overlapping of aging and disease processes; uncertainty regarding benign versus pathogenic age-related changes; the point at which a process begins to do damage to the organism, and, if so, when does it occur; and when to distinguish critical damage from noncritical damage. Finally, and significantly, it is difficult to obtain funding for this research.
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S. Melov and A. Hubbard Microarrays as a Tool to Investigate the Biology of Aging: A Retrospective and a Look to the Future Sci. Aging Knowl. Environ., October 20, 2004; 2004(42): re7 - re7. [Abstract] [Full Text] [PDF] |
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