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补体因子H基因型、鱼类摄入量和炎症标志物对队列中年龄相关性黄斑变性长期风险的联合影响。

Combined effects of complement factor H genotypes, fish consumption, and inflammatory markers on long-term risk for age-related macular degeneration in a cohort.

作者信息

Wang Jie Jin, Rochtchina Elena, Smith Wayne, Klein Ronald, Klein Barbara E K, Joshi Tripti, Sivakumaran Theru A, Iyengar Sudha, Mitchell Paul

机构信息

Vision Research, Department of Ophthalmology and the Westmead Millennium Institute, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Am J Epidemiol. 2009 Mar 1;169(5):633-41. doi: 10.1093/aje/kwn358. Epub 2008 Dec 13.

Abstract

At baseline in 1992-1994, the authors assessed the combined effects of complement factor H (CFH) genotypes with smoking, fish consumption, and inflammatory markers on the risk of age-related macular degeneration (AMD) in 3,654 persons aged > or =49 years. They reexamined 75% of the survivors after 5 and 10 years, confirming incident AMD by side-by-side photographic grading. Of the 2,452 persons followed in the Blue Mountains Eye Study, 1,881 were genotyped (rs1061170), with CC, CT, and TT identified in 13.6%, 46.7%, and 39.7%, respectively. AMD risk increased with each additional C allele (early AMD: age- and sex-adjusted relative risk (RR) = 1.6, 95% confidence interval (CI): 1.2, 1.9; late AMD: RR = 2.3, 95% CI: 1.5, 3.6). Late AMD risk among current smokers with the CC/CT genotypes (RR = 10.7, 95% CI: 3.4, 33.9) was 5-fold that for genotypically similar nonsmokers (RR = 2.2, 95% CI: 0.9, 5.5) versus current nonsmokers with TT genotypes. Weekly compared with less than weekly consumption of fish was associated with reduced late AMD risk in participants with the CC genotype (RR = 0.15, 95% CI: 0.03, 0.8) but not the CT (RR = 0.7, 95% CI: 0.3, 2.0) or TT (RR = 1.3, 95% CI: 0.2, 7.2) genotypes. This study documents joint contributions from genetic and systemic factors in determining the progression of AMD.

摘要

在1992年至1994年的基线期,作者评估了补体因子H(CFH)基因型与吸烟、鱼类消费以及炎症标志物对3654名年龄≥49岁人群年龄相关性黄斑变性(AMD)风险的综合影响。5年和10年后,他们对75%的幸存者进行了复查,通过并排照片分级确认了AMD发病情况。在蓝山眼研究中随访的2452人里,1881人进行了基因分型(rs1061170),分别鉴定出CC、CT和TT基因型的比例为13.6%、46.7%和39.7%。每增加一个C等位基因,AMD风险就会增加(早期AMD:年龄和性别调整后的相对风险(RR)=1.6,95%置信区间(CI):1.2,1.9;晚期AMD:RR = 2.3,95% CI:1.5,3.6)。CC/CT基因型的当前吸烟者中晚期AMD风险(RR = 10.7,95% CI:3.4,33.9)是基因型相似的非吸烟者(RR = 2.2,95% CI:0.9,5.5)相对于TT基因型当前非吸烟者的5倍。与每周食用鱼类少于一次相比,每周食用鱼类与CC基因型参与者晚期AMD风险降低相关(RR = 0.15,95% CI:0.03,0.8),但与CT基因型(RR = 0.7,95% CI:0.3,2.0)或TT基因型(RR = 1.3,95% CI:0.2,7.2)无关。本研究记录了遗传和全身因素在决定AMD进展中的共同作用。

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