Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA.
Hum Mol Genet. 2011 Dec 1;20(23):4707-13. doi: 10.1093/hmg/ddr382. Epub 2011 Aug 26.
Primary open-angle glaucoma (POAG) is a genetically complex common disease characterized by progressive optic nerve degeneration that results in irreversible blindness. Recently, a genome-wide association study (GWAS) for POAG in an Icelandic population identified significant associations with single nucleotide polymorphisms (SNPs) between the CAV1 and CAV2 genes on chromosome 7q31. In this study, we confirm that the identified SNPs are associated with POAG in our Caucasian US population and that specific haplotypes located in the CAV1/CAV2 intergenic region are associated with the disease. We also present data suggesting that associations with several CAV1/CAV2 SNPs are significant mostly in women.
原发性开角型青光眼(POAG)是一种遗传复杂的常见疾病,其特征为进行性视神经退行性病变,导致不可逆转的失明。最近,冰岛人群的一项针对 POAG 的全基因组关联研究(GWAS)发现,7q31 染色体上的 CAV1 和 CAV2 基因之间的单核苷酸多态性(SNP)与疾病显著相关。在这项研究中,我们证实了在我们的白种人美国人群中,所鉴定的 SNP 与 POAG 相关,并且位于 CAV1/CAV2 基因间区的特定单倍型与该疾病相关。我们还提供的数据表明,与几个 CAV1/CAV2 SNP 的关联在女性中更为显著。