Lin Henry, Mares Julie A, LaMonte Michael J, Brady William E, Sahli Michelle W, Klein Ronald, Klein Barbara E K, Nie Jing, Millen Amy E
a Department of Epidemiology and Environmental Health , University at Buffalo, The State University of New York , Buffalo , NY , USA.
b Department of Ophthalmology and Visual Sciences , University of Wisconsin-Madison , Madison , WI , USA.
Ophthalmic Epidemiol. 2017 Oct;24(5):311-322. doi: 10.1080/09286586.2017.1290259. Epub 2017 Mar 23.
To examine the association between xanthophyll intake and prevalent early age-related macular degeneration (AMD) using data from the Atherosclerosis Risk in Communities Study (n = 10,295). Potential effect modification by genetic polymorphisms and biomarkers of high-density lipoprotein (HDL) metabolism was explored.
Xanthophyll intake was assessed at visit 1 (1987-1989) using food frequency questionnaires. Prevalent early AMD was assessed at visit 3 (1993-1995) via retinal photographs. Logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI) for AMD by quintiles of xanthophyll intake, adjusted for age, sex, race, field center, and pack-years of smoking. To evaluate effect modification, the association between tertiles (T) of xanthophyll intake and AMD was stratified by complement factor H (CFH) rs1061170 and age-related maculopathy susceptibility 2 (ARMS2) rs10490924 genotypes, as well as by median cutpoints of HDL biomarkers.
Xanthophyll intake was not associated with AMD in the overall sample, Caucasians (n = 8257), or African-Americans (n = 2038). Exploratory analyses observed that the association between xanthophyll intake and AMD varied statistically significantly by CFH rs1061170 genotype among Caucasians (p for interaction = 0.045) but not African Americans. No interactions were observed between xanthophyll intake and ARMS2 rs10490924. Moreover, higher xanthophyll intake was associated with decreased odds of AMD among participants with lower HDL (OR = 0.79, 95% CI 0.57-1.09) but not higher HDL (p for interaction = 0.048).
Xanthophyll intake was not associated with early AMD. Further studies to investigate this association by genetic susceptibility or variations in HDL metabolism are needed.
利用社区动脉粥样硬化风险研究(n = 10295)的数据,研究叶黄素摄入量与早期年龄相关性黄斑变性(AMD)患病率之间的关联。探讨了遗传多态性和高密度脂蛋白(HDL)代谢生物标志物的潜在效应修饰作用。
在第1次随访(1987 - 1989年)时使用食物频率问卷评估叶黄素摄入量。在第3次随访(1993 - 1995年)时通过视网膜照片评估早期AMD的患病率。采用逻辑回归按叶黄素摄入量五分位数估计AMD的比值比(OR)和95%置信区间(CI),并对年龄、性别、种族、研究中心和吸烟包年数进行校正。为评估效应修饰作用,按补体因子H(CFH)rs1061170和年龄相关性黄斑病变易感性2(ARMS2)rs10490924基因型以及HDL生物标志物的中位数切点,对叶黄素摄入量三分位数(T)与AMD之间的关联进行分层分析。
在总体样本、白种人(n = 8257)或非裔美国人(n = 2038)中,叶黄素摄入量与AMD均无关联。探索性分析发现,在白种人中,叶黄素摄入量与AMD之间的关联因CFH rs1061170基因型存在显著统计学差异(交互作用p = 0.045),而非裔美国人中未观察到这种差异。在叶黄素摄入量与ARMS2 rs10490924之间未观察到交互作用。此外,在HDL水平较低的参与者中,较高的叶黄素摄入量与AMD几率降低相关(OR = 0.79,95% CI 0.57 - 1.09),而在HDL水平较高的参与者中则无此关联(交互作用p = 0.048)。
叶黄素摄入量与早期AMD无关联。需要进一步研究通过遗传易感性或HDL代谢变化来探究这种关联。