Gangnon Ronald E, Lee Kristine E, Klein Barbara E K, Iyengar Sudha K, Sivakumaran Theru A, Klein Ronald
Department of Biostatistics, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
Arch Ophthalmol. 2012 Sep;130(9):1169-76. doi: 10.1001/archophthalmol.2012.693.
To investigate the effect of age, sex, and the Y402H variant in the complement factor H (CFH) gene on the incidence, progression, and regression of age-related macular degeneration (AMD) as well as the effect of these factors and AMD on mortality, using multistate models.
Analyses included 4379 persons aged 43 to 84 years at the time of the census. The status of AMD on a 5-level severity scale was graded from retinal photographs taken at up to 5 study visits between 1988 and 2010. Multistate models in continuous time were used to model the effects of age, sex, and CFH genotype on the incidence, progression, and regression of AMD and mortality.
The CFH Y402H genotype CC was associated, relative to genotype TT (reported as hazard ratio; 95% CI), with increased incidence of AMD (no to minimally severe early AMD, 1.98; 1.57-2.49), progression of AMD (minimally severe early to moderately severe early AMD, 1.73; 1.29-2.33; moderately severe early to severe early AMD, 1.30; 0.86-1.94; and severe early to late AMD, 1.72; 1.01-2.91) but not with regression of AMD or mortality. Late AMD was associated with increased mortality (1.37; 1.15-1.62) relative to no AMD, but earlier stages of AMD were not.
Using the multistate models, we show that the Y402H risk variant is associated with lifetime incidence of early AMD and progression of early to late AMD and that late AMD is associated with mortality risk.
采用多状态模型研究年龄、性别以及补体因子H(CFH)基因中的Y402H变异对年龄相关性黄斑变性(AMD)的发病率、进展和消退的影响,以及这些因素和AMD对死亡率的影响。
分析纳入了普查时年龄在43至84岁之间的4379人。根据1988年至2010年间最多5次研究访视时拍摄的视网膜照片,将AMD的严重程度分为5级。使用连续时间多状态模型来模拟年龄、性别和CFH基因型对AMD发病率、进展、消退及死亡率的影响。
相对于基因型TT(报告为风险比;95%可信区间),CFH Y402H基因型CC与AMD发病率增加相关(从无到轻度早期AMD,1.98;1.57 - 2.49),AMD进展相关(从轻度早期到中度早期AMD,1.73;1.29 - 2.33;从中度早期到重度早期AMD,1.30;0.86 - 1.94;从重度早期到晚期AMD,1.72;1.01 - 2.91),但与AMD消退或死亡率无关。相对于无AMD,晚期AMD与死亡率增加相关(1.37;1.15 - 1.62),但早期AMD阶段则不然。
通过多状态模型,我们表明Y402H风险变异与早期AMD的终生发病率以及早期到晚期AMD的进展相关,且晚期AMD与死亡风险相关。