Genetic admixture, adipocytokines, and adiposity in black Americans: The health, aging, and body composition study

被引:22
|
作者
Fyr, Christina L. Wassel
Kanaya, Alka M.
Cummings, Steve R.
Reich, David
Hsueh, Wen-Chi
Reiner, Alexander P.
Harris, Tamara B.
Moffett, Susan
Li, Rongling
Ding, Jingzhong
Miljkovic-Gacic, Iva
Ziv, Elad
机构
[1] Univ Minnesota, Dept Epidemiol, Minneapolis, MN 55454 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Calif Pacific Med Ctr, San Francisco, CA USA
[4] Harvard Univ, Boston, MA 02115 USA
[5] Univ Washington, Seattle, WA 98195 USA
[6] NIH, Bethesda, MD 20892 USA
[7] Univ Pittsburgh, Pittsburgh, PA USA
[8] Univ Tennessee, Memphis, TN USA
[9] Wake Forest Univ, Winston Salem, NC 27109 USA
关键词
D O I
10.1007/s00439-007-0353-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Adipocytokines are a subset of cytokines produced by adipose tissue and are associated with risk of type II diabetes and atherosclerosis. Levels of adipocytokines differ between Black and White Americans, even after adjustment for differences in adiposity, diseases associated with adipocytokines including type 2 diabetes and cardiovascular disease, and general socioeconomic status indicators such as income. We used a series of ancestry informative markers to estimate genetic ancestry in a population-based study of older Black Americans, and examined the association between genetic ancestry and adipocytokines and soluble receptors to help determine which of these may be most amenable to admixture mapping. We typed 35 ancestry informative markers in 1,241 self-reported Black Americans with available DNA from the Health, Aging, and Body Composition (Health ABC) study with available DNA and used a maximum likelihood approach to estimate percent European ancestry. We used linear regression models to determine the association between these adipocytokines and percent ancestry, and staged models to examine whether adiposity or other measures affected the associations of genetic ancestry and adipocytokines. Mean European ancestry was 22.3 +/- 15.9%. In multivariate adjusted models, the strongest associations observed were between higher European ancestry and interleukin-6 soluble receptor (IL-6 SR), C-reactive protein (CRP), and adiponectin levels, with interleukin-2 soluble receptor (IL-2 SR) and soluble tumor necrosis factor receptor II (TNF-alpha SR II) also showing more modest but significant associations. The association with adiponectin became stronger after adjustment for adiposity. These novel findings suggest that admixture mapping may identify genetic factors influencing the levels of IL-6 SR, CRP, IL-2 SR, and adiponectin.
引用
收藏
页码:615 / 624
页数:10
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