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中国先天性晶状体异位患者中双等位基因 ADAMTSL4 变异:对基因型-表型关系的影响。

Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships.

机构信息

Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China.

NHC Key Laboratory of Myopia (Fudan University); Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.

出版信息

Hum Mutat. 2022 Dec;43(12):2141-2152. doi: 10.1002/humu.24483. Epub 2022 Oct 17.

Abstract

ADAMTSL4 variants are one of the common causes of congenital ectopia lentis (EL), reported ocular comorbidities of which include iris anomalies, cataract, and glaucoma. However, a genotype-phenotype correlation has not been established. Potentially pathogenic ADAMTSL4 variants were screened from a Chinese cohort of congenital EL using panel-based next-generation sequencing followed by multiple bioinformatics analyses. The genotype-phenotype correlation was assessed via a systematic review of ADAMTSL4 variants within our data and those from the literature. A total of 12 variants of ADAMTSL4, including seven frameshift variants, one nonsense variant, two splicing variants, and two missense variants, were found in nine probands. Combing genetic and clinical information from 72 probands in the literature revealed 37 ADAMTSL4 variants known to cause EL, and the ethnic difference was prominent. The lens was inclined to dislocate inferior temporally (22, 27.16%), while the pupil was always located oppositely (9, 81.82%). Several anterior segments anomalies were identified, including ectopia pupillae (15, 18.52%), persistent pupillary membrane (9, 11.10%), poor pupil dilation (4, 30.8%), cataract (13, 24.10%), and glaucoma (8, 13.33%). Genotype-phenotype analysis revealed that truncation variants had higher risks of combined iris anomalies, including either ectopia pupillae or a persistent pupillary membrane (p =  0.007). The data from this study not only extend our knowledge of the ADAMTSL4 variant spectrum but also suggest that deleterious variants of ADAMTSL4 might be associated with severe ocular phenotypes.

摘要

ADAMTSL4 变异是先天性晶状体异位 (EL) 的常见原因之一,已报道其眼部合并症包括虹膜异常、白内障和青光眼。然而,尚未建立基因型-表型相关性。使用基于面板的下一代测序对先天性 EL 的中国队列进行筛选,然后进行多次生物信息学分析,以筛选潜在的致病性 ADAMTSL4 变异。通过对我们数据中 ADAMTSL4 变异和文献中 ADAMTSL4 变异的系统综述,评估基因型-表型相关性。在九个先证者中发现了 12 种 ADAMTSL4 变异,包括 7 种移码变异、1 种无义变异、2 种剪接变异和 2 种错义变异。结合文献中 72 个先证者的遗传和临床信息,发现了 37 种已知引起 EL 的 ADAMTSL4 变异,且种族差异明显。晶状体倾向于颞下脱位(22,27.16%),而瞳孔总是位于对侧(9,81.82%)。确定了几种前节异常,包括瞳孔异位(15,18.52%)、永存瞳孔膜(9,11.10%)、瞳孔扩张不良(4,30.8%)、白内障(13,24.10%)和青光眼(8,13.33%)。基因型-表型分析表明,截断变异与联合虹膜异常的风险更高,包括瞳孔异位或永存瞳孔膜(p=0.007)。本研究的数据不仅扩展了我们对 ADAMTSL4 变异谱的认识,还表明 ADAMTSL4 的有害变异可能与严重的眼部表型相关。

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