Genetic predisposition to obesity and risk of subclinical atherosclerosis.
Genetic predisposition to obesity and risk of subclinical atherosclerosis.
复制标题
DOI:
10.1016/j.gene.2014.07.059
复制
发表时间:
2014-10
期刊:
影响因子:
3.5
通讯作者:
Juan Shi;Jie Hong;L. Qi;B. Cui;W. Gu;Yifei Zhang;Li-juan Li-Li-juan-Li-2107984010;Lin Miao;Rui Wang;Weiqing Wang;G. Ning
中科院分区:
文献类型:
--
作者:
Juan Shi;Jie Hong;L. Qi;B. Cui;W. Gu;Yifei Zhang;Li-juan Li-Li-juan-Li-2107984010;Lin Miao;Rui Wang;Weiqing Wang;G. Ning
Obesity has been associated with increased common carotid artery (CCA) intima–media thickness (IMT), a measure of subclinical atherosclerosis. We assessed the association between genetic predisposition to obesity and CCA IMT. The study included 428 young Chinese adults with CCA IMT measured using a high-resolution B-mode tomographic ultrasound system. We created a genetic risk score (GRS) by summing the risk alleles of 6 obesity-associated genetic variants confirmed in our previous analyses. The GRS was significantly associated with greater CCA IMT (p < 0.001) after adjustment for age and gender. Per 2 alleles of the GRS was related to 0.023 mm increment in IMT. The association was attenuated by one half with additional adjustment for obesity status, but remained significant (p = 0.009). In addition, we found that blood pressure significantly modified the association between the GRS and CCA IMT (p for interaction = 0.001). The associations between the GRS and CCA IMT were stronger in participants with systolic blood pressure (SBP) ≥ 120 mm Hg and/or diastolic blood pressure (DBP) ≥ 80 mm Hg (per 2 allele increment of the GRS relating to 0.028 mm greater CCA IMT, p for trend < 0.001) than those with SBP < 120 mm Hg and DBP < 80 mm Hg (per 2 allele increment of the GRS relating to 0.001 smaller CCA IMT, p for trend = 0.930). Our data provides suggestive evidence supporting the potential causal relation between obesity and development of subclinical atherosclerosis. Elevated blood pressure might amplify the adverse effect of obesity on cardiovascular risk.