Telomere shortening has been causally linked to cellular senescence in different species, and in humans, telomere shortening has been associated with aging and poorer survival. In addition, prior genetic studies suggest that telomere length is heritable. We hypothesize that telomere shortening is associated with aging, and it is variable and heritable in the Old Order Amish (OOA). The primary objectives of this research proposal are three-fold: (1) to examine whether shorter telomere lengths (TLs) are positively associated with aging at a population level; (2) to characterize genetic epidemiology of TLs and, (3) to identify genetic markers associated or linked to TLs. Telomere lengths will be measured using a newly developed and validated quantitative-PCR method. Information on TL measurements and age-related phenotypes will be obtained from 1,300 individuals in ongoing studies in the OOA. These subjects, who are participants in other studies, have been or will be extensively characterized with regards to traits related to cardiovascular diseases, metabolic syndrome, osteoporosis, and inflammation. Furthermore, data from a 5-cM genome-scan are already available in 1,000 study participants, which allow us to conduct a genome-wide linkage study searching for loci related to TL. No additional funding will be required for phenotypic characterization of age-related traits or genotyping for genome-wise scan in this proposed study. This proposed study will hopefully provide Insight into the association between telomere length and aging in humans and help in evaluating whether telomere length can be used as a biological marker of aging. Any positive findings will encourage further investigation into the biological relationship between TLs and aging. Unraveling the genetic pathways involved in the regulation of telomere length will have important and farreaching implications in understanding many aspects of human health and diseases. Such knowledge may also aid in the development of regenerative medicine, cultured tissue transplantation, and stem cell therapeutics.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG023692-04
Application #
7238648
Study Section
Special Emphasis Panel (ZRG1-ASG (01))
Program Officer
Rossi, Winifred K
Project Start
2004-05-01
Project End
2009-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
4
Fiscal Year
2007
Total Cost
$295,900
Indirect Cost
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Bendjilali, Nasrine; Hsueh, Wen-Chi; He, Qimei et al. (2014) Who are the Okinawans? Ancestry, genome diversity, and implications for the genetic study of human longevity from a geographically isolated population. J Gerontol A Biol Sci Med Sci 69:1474-84
Oelsner, E C; Pottinger, T D; Burkart, K M et al. (2013) Adhesion molecules, endothelin-1 and lung function in seven population-based cohorts. Biomarkers 18:196-203
Virtanen, Jyrki K; Siscovick, David S; Lemaitre, Rozenn N et al. (2013) Circulating omega-3 polyunsaturated fatty acids and subclinical brain abnormalities on MRI in older adults: the Cardiovascular Health Study. J Am Heart Assoc 2:e000305
Njajou, O T; Cawthon, R M; Blackburn, E H et al. (2012) Shorter telomeres are associated with obesity and weight gain in the elderly. Int J Obes (Lond) 36:1176-9
Evans, Daniel S; Kapahi, Pankaj; Hsueh, Wen-Chi et al. (2011) TOR signaling never gets old: aging, longevity and TORC1 activity. Ageing Res Rev 10:225-37
Swarbrick, Michael M; Evans, Daniel S; Valle, Maria I et al. (2011) Replication and extension of association between common genetic variants in SIM1 and human adiposity. Obesity (Silver Spring) 19:2394-2403
Njajou, Omer T; Blackburn, Elizabeth H; Pawlikowska, Ludmila et al. (2010) A common variant in the telomerase RNA component is associated with short telomere length. PLoS One 5:e13048
Njajou, Omer T; Hsueh, Wen-Chi; Blackburn, Elizabeth H et al. (2009) Association between telomere length, specific causes of death, and years of healthy life in health, aging, and body composition, a population-based cohort study. J Gerontol A Biol Sci Med Sci 64:860-4
Njajou, Omer T; Kanaya, Alka M; Holvoet, Paul et al. (2009) Association between oxidized LDL, obesity and type 2 diabetes in a population-based cohort, the Health, Aging and Body Composition Study. Diabetes Metab Res Rev 25:733-9
Hsueh, Wen-Chi; Silver, Kristi D; Pollin, Toni I et al. (2007) A genome-wide linkage scan of insulin level derived traits: the Amish Family Diabetes Study. Diabetes 56:2643-8

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