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Genetic and environmental risk factors for age-related macular degeneration in persons 90 years and older

机译:90岁及以上年龄相关性黄斑变性的遗传和环境危险因素

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Purpose. We studied associations of genetic polymorphisms in age-related maculopathy susceptibility 2 (ARMS2) and complement factor H (CFH) in nonagenarians with age-related macular degeneration (AMD). Methods. This case-control study comprised 2737 persons (1204 controls, 1433 AMD cases), including 166 nonagenarians (52 controls, 114 AMD cases). Single nucleotide polymorphisms (SNPs) in the genes ARMS2 and CFH were determined. Risk scores were computed by multiple logistic regression analysis, including genetic and environmental risk factors (smoking, hypertension, body mass index, diabetes) for different age groups (70, 70-79, 80-89, ≥90 years [nonagenarians]). Results. In nonagenarians, ARMS2 showed the weakest associations with AMD (odds ratio [OR] = 1.52, P = 0.127) compared to the other groups (OR, 70 years = 2.23, P = 1.03 × 10-13; OR, 70-79 years = 2.70, P = 1.00 × 10-13; OR, 80-89 years = 3.11, P = 6.56 × 10-8). For CFH, ORs for AMD increased with age (70 years OR = 1.96, P = 1.80 × 10-11; 70-79 years OR = 1.89, P = 4.48 × 10-13; 80-89 years OR = 2.71, P = 1.28 × 10-7), but decreased again in the nonagenarians (OR = 2.21, P = 0.005). Compared to the group 70 years, reduced minor allele frequencies (MAFs) for AMD patients were observed in the nonagenarians (CFH 0.54 vs. 0.43, P = 0.009; ARMS2 0.44 vs. 0.29, P = 2.97 × 10-5), while the MAFs in controls were not significantly different. The genetic risk score revealed the lowest discriminative power in the nonagenarians with an area-under-curve (AUC) of 0.658 for receiver-operating characteristics (AUC 80-89 years = 0.768, 70-79 years = 0.704, 70 years = 0.682), while no significant difference was seen for the environmental risk score (AUC 70 years = 0.579, 70-79 years = 0.567, 80-89 years = 0.600, 90 years = 0.608). Conclusions. Risk alleles in CFH and ARMS2 have a significantly smaller effect on AMD development in nonagenarians, while environmental factors retain a similar effect.
机译:目的。我们研究了与年龄相关性黄斑变性(AMD)的非agenarians中与年龄相关的黄斑病变易感性2(ARMS2)和补体因子H(CFH)的遗传多态性的关联。方法。这项病例对照研究包括2737人(1204名对照,1433例AMD病例),包括166名非流产者(52名对照,114例AMD病例)。确定了基因ARMS2和CFH中的单核苷酸多态性(SNP)。通过多重逻辑回归分析计算风险评分,包括不同年龄组(<70岁,70-79岁,80-89岁,≥90岁[非流产]的遗传和环境风险因素(吸烟,高血压,体重指数,糖尿病)) 。结果。与其他组(OR,70岁= 2.23,P = 1.03×10-13; OR,70-79岁)相比,在非agenararians中,ARMS2与AMD的关联最弱(优势比[OR] = 1.52,P = 0.127)。 = 2.70,P = 1.00×10-13;或80-89年= 3.11,P = 6.56×10-8)。对于CFH,AMD的OR随年龄而增加(<70岁OR = 1.96,P = 1.80×10-11; 70-79岁OR = 1.89,P = 4.48×10-13; 80-89岁OR = 2.71,P = 1.28×10-7),但在非流产者中再次下降(OR = 2.21,P = 0.005)。与<70岁年龄组相比,非肺动脉狭窄的AMD患者的次要等位基因频率(MAF)降低(CFH 0.54 vs. 0.43,P = 0.009; ARMS2 0.44 vs. 0.29,P = 2.97×10-5),而对照组中的MAF没有显着差异。遗传风险评分显示,在非高加纳人中,对于接收者的操作特征,其曲线下面积(AUC)为0.658(AUC 80-89年= 0.768,70-79年= 0.704,<70年= 0.682 ),但环境风险评分无明显差异(AUC <70年= 0.579,70-79年= 0.567,80-89年= 0.600,> 90年= 0.608)。结论。 CFH和ARMS2中的风险等位基因对非高加纳人中AMD的发育影响要小得多,而环境因素则保持相似的作用。

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