Postel Eric A, Agarwal Anita, Caldwell Jennifer, Gallins Paul, Toth Cynthia, Schmidt Silke, Scott William K, Hauser Michael A, Haines Jonathan L, Pericak-Vance Margaret A
Duke University Eye Center, Durham, North Carolina, USA.
Ophthalmology. 2006 Sep;113(9):1504-7. doi: 10.1016/j.ophtha.2006.02.049. Epub 2006 Jul 7.
To determine if the complement factor H gene (CFH) determines risk for development of geographic atrophy (GA).
Retrospective case-control study.
The independent case-control data set contained 647 age-related macular degeneration (AMD) cases (grades 3, 4, or 5) and 163 controls (grades 1 or 2).
To determine if CFH had any effect on determining risk for development of GA in an independent case-control data set of 647 AMD cases and 163 controls, the rs1061170 single-nucleotide polymorphism was tested for association, separating grades and analyzing them independently against the controls. Odds ratios were calculated using standard logistic regression models.
The outcome variable was AMD affection status, and genotypes were coded according to a log-additive model.
There were 407 grade 5, 107 grade 4, 133 grade 3, 35 grade 2, and 128 grade 1 individuals. There was significant association with AMD when comparing grades 3, 4, and 5 versus the controls. The highest odds ratio was obtained when analyzing the grade-4 cases versus the grade-1 controls (OR = 3.217, P<0.0001).
Our results indicate that CFH increases the risk of developing GA (grade 4) as well as neovascular (grade 5) and milder (grade 3) disease. Although neovascular disease is responsible for the majority of severe vision loss with AMD, GA is also a significant cause of vision loss, and without effective treatment. Therefore, an attempt to clarify its pathogenesis is of the utmost importance.
确定补体因子H基因(CFH)是否决定地图样萎缩(GA)的发生风险。
回顾性病例对照研究。
独立的病例对照数据集包含647例年龄相关性黄斑变性(AMD)患者(3级、4级或5级)和163名对照者(1级或2级)。
为了确定CFH在一个包含647例AMD患者和163名对照者的独立病例对照数据集中对GA发生风险的决定作用,对rs1061170单核苷酸多态性进行关联测试,将分级分开并与对照者独立分析。使用标准逻辑回归模型计算比值比。
结局变量为AMD患病状态,基因型根据对数加性模型编码。
有407例5级、107例4级、133例3级、35例2级和128例1级个体。将3级、4级和5级与对照者比较时,与AMD存在显著关联。分析4级病例与1级对照者时获得最高比值比(OR = 3.217,P<0.0001)。
我们的结果表明,CFH增加了发生GA(4级)以及新生血管性(5级)和较轻(3级)疾病的风险。虽然新生血管性疾病是导致AMD严重视力丧失的主要原因,但GA也是视力丧失的重要原因,且缺乏有效治疗方法。因此,阐明其发病机制的尝试至关重要。