首页> 外文期刊>BMC Medical Genetics >Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
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Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin

机译:在沙特原产地骨髓闭合和伪萃取青光眼骨质发信号通路中ACVR1和RS1043784中ACVR1和RS1043784中的多态性分析

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Glaucoma is a polygenic neurodegenerative disease and the second most common cause of blindness in Saudi Arabia. To test the hypothesis that genetic variants in the genes involved in the bone morphogenic protein (BMP) signaling pathway may be associated with glaucoma, we investigated the association between 3′ untranslated region variants, rs12997 in ACVR1 and rs1043784 in BMP6, and primary angle-closure glaucoma (PACG) and pseudoexfoliation glaucoma (PXG). In a case-control study, TaqMan? real-time PCR-based genotyping was done in 444 subjects consisting of 250 controls, 101 PACG and 95 PXG cases, and tested for genetic association with glaucoma-types and other clinical phenotypes. Rs12997[G] allele in ACVR1 exhibited significant 2-fold increased risk of PACG (p?=?0.005) in women but not in men. Similarly, genotype analysis also showed that subjects carrying rs12997[G/G] genotype were at ?2-fold risk of PACG that remained significant after adjustment for age, sex, and Bonferroni correction in the recessive model. Furthermore, this effect was also significant in women only. In PXG, the rs12997[G/G] genotype showed a significant trend towards increased risk of the disease (OR?=?2.04, 95% CI?=?0.99–4.18, p?=?0.049) but did not survive the Bonferroni correction. Regression analysis showed that rs12997[G/G] genotype was a significant predictor of PACG independent of age, sex, and rs1043784 genotypes. Likewise, age and rs12997[G/G] genotype showed significant effect on PXG outcome. The rs12997[A/G] genotype showed significant association with cup/disc ratio as compared to wild-type (p?=?0.005) in PXG. Genotype and allele frequencies of rs1043784 in BMP6 did not show any significant association either with PACG or PXG. Our results suggest that the polymorphism rs12997 in the ACVR1 gene involved in the BMP signaling pathway is significantly associated with PACG and PXG in a Saudi cohort. This is the first study to associate this variant/gene with PACG and PXG. However, further studies would be needed to replicate these findings in a large population-based cohort.
机译:青光眼是一种多基因神经退行性疾病和沙特阿拉伯失明的第二个最常见的原因。为了测试涉及骨形态发生蛋白(BMP)信号传导途径的基因中的遗传变异可能与青光眼相关,我们在BMP6中调查了3'未翻译区域变体,RS12997的关联,BMP6和rs1043784。闭合青光眼(PACG)和伪炼金糖(PXG)。在一个案例控制研究中,塔克曼?基于PCR的基因分型在444个受试者中进行,由250个对照,101帕格和95例PXG病例组成,并测试与青光眼类型和其他临床表型的遗传关联。 ACVR1中的RS12997 [G]等位基因在女性中表现出显着的2倍以下的PACG(p?= 0.005)的风险。类似地,基因型分析还显示,携带RS12997 [G / g]基因型的受试者在隐性模型中调整后仍然显着的PACG患者,其风险仍然显着。此外,这种效果仅在女性中也显着。在PXG中,RS12997 [G / G]基因型显示出疾病的风险增加的显着趋势(或?=?2.04,95%CI?=?0.99-4.18,P?=?0.049),但没有生存Bonferroni更正。回归分析表明,RS12997 [G / g]基因型是PACG的显着预测因子,与年龄,性别和Rs1043784基因型无关。同样,年龄和RS12997 [G / g]基因型对PXG结果显示出显着影响。与PXG中的野生型(P?= 0.005)相比,RS12997 [A / G]基因型与杯/盘比率显着结合。 BMP6中Rs1043784的基因型和等位基因频率未显示PACG或PXG的任何重要关联。我们的结果表明,BMP信号通路中涉及的ACVR1基因中的多态性RS12997与沙特队队列中的PACG和PXG显着相关。这是第一项与PACG和PXG相关联的该变体/基因的研究。然而,需要进一步的研究以在大型人口的队列中复制这些发现。

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