| Literature DB >> 24951543 |
Jiemin Liao1, Xinyi Su1, Peng Chen2, Xu Wang2, Liang Xu3, Xiang Li4, Lennard Thean5, Clement Tan5, Ava G Tan6, Wan-Ting Tay7, Gyungah Jun8, Yingfeng Zheng7, Merwyn Chew7, Ya Xing Wang3, Queenie S Tan7, Veluchamy A Barathi9, Barbara E Klein10, Seang-Mei Saw11, Eranga N Vithana1, E-Shyong Tai12, Sudha K Iyengar13, Paul Mitchell6, Chiea-Chuen Khor14, Tin Aung1, Jie Jin Wang15, Jost B Jonas16, Yik-Ying Teo17, Tien Yin Wong18, Ching-Yu Cheng19.
Abstract
Age-related cataract is a leading cause of blindness worldwide, especially in developing countries where access to cataract surgery remains limited. Previous linkage and candidate gene studies suggested genetic influences on age-related nuclear cataract but few genetic markers have been identified thus far. We conducted genome-wide association studies on 4569 Asians (including 2369 Malays and 2200 Indians), and replicated our analysis in 2481 Chinese from two independent cohorts (1768 Chinese in Singapore and 803 Chinese in Beijing). We confirmed two genome-wide significant loci for nuclear cataract in the combined meta-analysis of four cohorts (n = 7140). The first locus was at chromosome 3q25.31 in KCNAB1 (rs7615568, fixed-effect Pmeta = 2.30 × 10(-8); random-effect Pmeta = 1.08 × 10(-8)). The second locus was at chromosome 21 in the proximity of CRYAA (rs11911275, fixed-effect Pmeta = 2.77 × 10(-8); random-effect Pmeta = 1.98 × 10(-9)), a major protein component of eye lens. The findings were further supported by up-regulation and down-regulation of KCNAB1 and CRYAA in human lens capsule, respectively, as the severity of nuclear cataract increases. The results offer additional insights into the pathogenesis of nuclear cataract in Asians.Entities:
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Year: 2014 PMID: 24951543 DOI: 10.1093/hmg/ddu315
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150