Heritability and correlates of intercellular adhesion molecule-1 in the Framingham Offspring Study.
Heritability and correlates of intercellular adhesion molecule-1 in the Framingham Offspring Study.
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Framingham 后代研究中细胞间粘附分子 1 的遗传力和相关性。
DOI:
10.1016/j.jacc.2004.03.048
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发表时间:
2004
影响因子:
24
通讯作者:
Benjamin,EmeliaJ
中科院分区:
文献类型:
--
作者:
KeaneyJr,JohnF;Massaro,JosephM;Larson,MartinG;Vasan,RamachandranS;Wilson,PeterWF;Lipinska,Izabella;Corey,Diane;Sutherland,Patrice;Vita,JosephA;Benjamin,EmeliaJ
ObjectivesWe sought to determine the clinical factors and heritability associated with inflammation measured as circulating levels of soluble-intercellular adhesion molecule-1 (sICAM-1) in a community-based cohort.BackgroundSeveral prospective studies indicate that circulating sICAM-1 is predictive of future cardiovascular events. However, in some studies this predictive value is lost after multivariable adjustment for traditional cardiovascular disease (CVD) risk factors. We addressed the heritability of sICAM-1 and its relation to CVD risk factors in a community-based cohort.MethodsWe examined 3,295 subjects from the Framingham Heart Study and measured sICAM-1 levels. We then used linear and stepwise multivariable regression to determine predictors or sICAM-1 levels.ResultsIn age- and gender-adjusted regression models, increased sICAM-1 levels were positively associated with age, total/high-density lipoprotein cholesterol, systolic blood pressure, body mass index (BMI), blood glucose, diabetes, smoking, and prevalent CVD. In stepwise multivariable regression models, sICAM-1 levels remained associated with age, female gender, total/high-density lipoprotein cholesterol ratio, BMI, blood glucose, smoking, and prevalent CVD. The residual heritability of sICAM-1 was 24%.ConclusionsIn addition to prevalent CVD, established CVD risk factors and non-traditional ones such as BMI were associated with systemic inflammation as determined by sICAM-1 levels. There also is significant heritability of sICAM-1, which suggests a genetic component to systemic inflammation.
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影响因子:
37.8
作者:
Wilson, PWF;D'Agostino, RB;Kannel, WB
通讯作者:
Kannel, WB
影响因子:
8.7
作者:
Nageh, MF;Sandberg, ET;Beaudet, AL
通讯作者:
Beaudet, AL
影响因子:
37.8
作者:
Shih-Jen Hwang;C. Ballantyne;A. Sharrett;L. Smith;C. Davis;A. Gotto;E. Boerwinkle
通讯作者:
Shih-Jen Hwang;C. Ballantyne;A. Sharrett;L. Smith;C. Davis;A. Gotto;E. Boerwinkle
影响因子:
56.9
作者:
HOTAMISLIGIL, GS;SHARGILL, NS;SPIEGELMAN, BM
通讯作者:
SPIEGELMAN, BM
影响因子:
9.8
作者:
Almasy, L;Blangero, J
通讯作者:
Blangero, J