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Susceptibility to advanced age-related macular degeneration and alleles of complement factor H, complement factor B, complement component 2, complement component 3, and age-related maculopathy susceptibility 2 genes in a Mexican population

机译:墨西哥人群中与年龄相关的高级黄斑变性和补体因子H,补体因子B,补体成分2,补体成分3和年龄相关性黄斑病变易感性2基因的易感性

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Purpose: To investigate the association of age-related macular degeneration (AMD)–high risk alleles of the complement factor H (CFH), complement factor B (CFB), complement component 2 (C2), complement component 3 (C3), and age-related maculopathy susceptibility 2 (ARMS2) genes in a Mexican population for the first time. Methods: Genotyping was performed for the Y402H variant of CFH, for the L9H, R32Q, and K565E variants of CFB, the E318D variant of C2, the A69S variant of ARMS2, and the R102G variant of C3 in 159 Mexican mestizo patients at advanced stages of AMD, i.e., CARMS (Clinical Age-Related Maculopathy Staging System) grade 4 or 5. The frequency of these variants was also investigated in a group of 152 control subjects without AMD. Genomic DNA was extracted from blood leukocytes, and genotyping was performed using PCR followed by direct sequencing. Allele-specific restriction enzyme digestion was used to detect the R102G polymorphism in C3. Results: There were significant differences in the allelic distribution between the two groups for CFH Y402H (p=1×10?5), ARMS A69S (p=4×10?7), and CFB R32Q (p=0.01). The odds ratios (95% confidence interval) obtained for the risk alleles of these three variants were 3.8 (2.4–5.9), 3.04 (2.2–4.3), and 2.5 (1.1–5.7), respectively. Haplotype analysis including the two most significantly associated alleles (CFH Y402H and ARMS A69S) indicated that the C-T combination conferred an odds ratio (95% confidence interval) of 6.9 (3.2–14.8). The exposed attributable risk for this particular haplotype was 85.5%. Conclusions: This is the first case-control investigation of AMD–high risk alleles in a Latino population. Our results support that CFH, ARMS2, and CFB AMD-risk alleles are consistently associated with the disease, even in ethnic groups with a complex admixture of ancestral populations such as Mexican mestizos.
机译:目的:研究年龄相关性黄斑变性(AMD)–补体因子H(CFH),补体因子B(CFB),补体成分2(C2),补体成分3(C3)和墨西哥人群中首次出现与年龄有关的黄斑病易感性2(ARMS2)基因。方法:在159名墨西哥中期患者中,对CFH的Y402H变异体,CFB的L9H,R32Q和K565E变异体,C2的E318D变异体,ARMS2的A69S变异体和C3的R102G变异体进行了基因分型等级为AMD的CARMS(临床年龄相关性黄斑病变分期系统)等级为4或5。还在152名无AMD的对照组中研究了这些变异的频率。从血液白细胞中提取基因组DNA,并使用PCR进行基因分型,然后直接测序。等位基因特异性限制酶消化用于检测C3中的R102G多态性。结果:CFH Y402H(p = 1×10?5),ARMS A69S(p = 4×10?7)和CFB R32Q(p = 0.01)在两组之间的等位基因分布存在显着差异。这三个变异的风险等位基因获得的比值比(95%置信区间)分别为3.8(2.4-5.9),3.04(2.2-4.3)和2.5(1.1-5.7)。包含两个最相关的等位基因(CFH Y402H和ARMS A69S)的单倍型分析表明,C-T组合的比值比(95%置信区间)为6.9(3.2-14.8)。该特定单倍型的暴露归因风险为85.5%。结论:这是拉丁美洲人人群中AMD高危等位基因的首次病例对照研究。我们的结果支持CFH,ARMS2和CFB AMD风险等位基因始终与疾病相关,即使在祖传人口复杂混合的族裔群体(例如墨西哥混血儿)中也是如此。

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