Department of Ophthalmology, College of Medicine, King Saud University, P.O. Box 245, Riyadh, 11411, Saudi Arabia.
Glaucoma Research Chair in Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
BMC Med Genet. 2020 Jul 8;21(1):145. doi: 10.1186/s12881-020-01076-0.
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.
青光眼是一种多基因神经退行性疾病,也是沙特阿拉伯第二大致盲原因。为了验证骨形态发生蛋白(BMP)信号通路相关基因中的遗传变异是否与青光眼相关的假说,我们研究了 3'非翻译区变异 rs12997 在 ACVR1 中的作用和 rs1043784 在 BMP6 中的作用与原发性闭角型青光眼(PACG)和假性剥脱性青光眼(PXG)之间的关联。
在一项病例对照研究中,我们对 444 名受试者进行了 TaqMan®实时 PCR 基因分型,其中包括 250 名对照、101 名 PACG 和 95 名 PXG 病例,并对青光眼类型和其他临床表型进行了遗传关联测试。
ACVR1 中的 rs12997[G]等位基因在女性中表现出 PACG 风险增加 2 倍(p=0.005),但在男性中没有。同样,基因型分析还表明,携带 rs12997[G/G]基因型的受试者患 PACG 的风险增加了 2 倍以上,在隐性模型中,经年龄、性别和 Bonferroni 校正后,这种关联仍然显著。此外,这种影响在女性中也很显著。在 PXG 中,rs12997[G/G]基因型显示出疾病风险增加的显著趋势(OR=2.04,95%CI=0.99-4.18,p=0.049),但未通过 Bonferroni 校正。回归分析表明,rs12997[G/G]基因型是独立于年龄、性别和 rs1043784 基因型的 PACG 的重要预测因子。同样,年龄和 rs12997[G/G]基因型对 PXG 结果有显著影响。与野生型相比,rs12997[A/G]基因型与杯/盘比显著相关(p=0.005)。BMP6 中的 rs1043784 基因型和等位基因频率与 PACG 或 PXG 均无显著关联。
我们的研究结果表明,BMP 信号通路中涉及的 ACVR1 基因的多态性 rs12997 与沙特队列中的 PACG 和 PXG 显著相关。这是第一项将该变体/基因与 PACG 和 PXG 相关联的研究。然而,还需要进一步的研究来在大型基于人群的队列中复制这些发现。