Springelkamp Henriët, Iglesias Adriana I, Cuellar-Partida Gabriel, Amin Najaf, Burdon Kathryn P, van Leeuwen Elisabeth M, Gharahkhani Puya, Mishra Aniket, van der Lee Sven J, Hewitt Alex W, Rivadeneira Fernando, Viswanathan Ananth C, Wolfs Roger C W, Martin Nicholas G, Ramdas Wishal D, van Koolwijk Leonieke M, Pennell Craig E, Vingerling Johannes R, Mountain Jenny E, Uitterlinden André G, Hofman Albert, Mitchell Paul, Lemij Hans G, Wang Jie Jin, Klaver Caroline C W, Mackey David A, Craig Jamie E, van Duijn Cornelia M, MacGregor Stuart
Department of Ophthalmology, Department of Epidemiology and.
Department of Epidemiology and.
Hum Mol Genet. 2015 May 1;24(9):2689-99. doi: 10.1093/hmg/ddv027. Epub 2015 Jan 30.
Primary open-angle glaucoma (POAG) is a blinding disease. Two important risk factors for this disease are a positive family history and elevated intraocular pressure (IOP), which is also highly heritable. Genes found to date associated with IOP and POAG are ABCA1, CAV1/CAV2, GAS7 and TMCO1. However, these genes explain only a small part of the heritability of IOP and POAG. We performed a genome-wide association study of IOP in the population-based Rotterdam Study I and Rotterdam Study II using single nucleotide polymorphisms (SNPs) imputed to 1000 Genomes. In this discovery cohort (n = 8105), we identified a new locus associated with IOP. The most significantly associated SNP was rs58073046 (β = 0.44, P-value = 1.87 × 10(-8), minor allele frequency = 0.12), within the gene ARHGEF12. Independent replication in five population-based studies (n = 7471) resulted in an effect size in the same direction that was significantly associated (β = 0.16, P-value = 0.04). The SNP was also significantly associated with POAG in two independent case-control studies [n = 1225 cases and n = 4117 controls; odds ratio (OR) = 1.53, P-value = 1.99 × 10(-8)], especially with high-tension glaucoma (OR = 1.66, P-value = 2.81 × 10(-9); for normal-tension glaucoma OR = 1.29, P-value = 4.23 × 10(-2)). ARHGEF12 plays an important role in the RhoA/RhoA kinase pathway, which has been implicated in IOP regulation. Furthermore, it binds to ABCA1 and links the ABCA1, CAV1/CAV2 and GAS7 pathway to Mendelian POAG genes (MYOC, OPTN, WDR36). In conclusion, this study identified a novel association between IOP and ARHGEF12.
原发性开角型青光眼(POAG)是一种致盲性疾病。该疾病的两个重要风险因素是家族史阳性和眼压(IOP)升高,而眼压也具有高度遗传性。迄今为止发现的与眼压和POAG相关的基因有ABCA1、CAV1/CAV2、GAS7和TMCO1。然而,这些基因仅解释了眼压和POAG遗传性的一小部分。我们在基于人群的鹿特丹研究I和鹿特丹研究II中,使用推算至千人基因组的单核苷酸多态性(SNP)对眼压进行了全基因组关联研究。在这个发现队列(n = 8105)中,我们鉴定出一个与眼压相关的新位点。最显著相关的SNP是rs58073046(β = 0.44,P值 = 1.87 × 10⁻⁸,次要等位基因频率 = 0.12),位于ARHGEF12基因内。在五项基于人群的研究(n = 7471)中进行独立重复验证,结果显示效应大小方向相同且具有显著相关性(β = 0.16,P值 = 0.04)。该SNP在两项独立的病例对照研究中也与POAG显著相关[n = 1225例病例和n = 4117例对照;比值比(OR) = 1.53, P值 = 1.�9 × 10⁻⁸],尤其与高眼压性青光眼相关(OR = 1.66, P值 = 2.81 × 10⁻⁹;正常眼压性青光眼的OR = 1.29, P值 = 4.23 × 10⁻²)。ARHGEF12在RhoA/RhoA激酶途径中起重要作用,该途径与眼压调节有关。此外,它与ABCA1结合,并将ABCA1、CAV1/CAV2和GAS7途径与孟德尔POAG基因(MYOC、OPTN、WDR36)联系起来。总之,本研究确定了眼压与ARHGEF12之间的一种新关联。