Article Text

Download PDFPDF
Genetic and clinical findings in a Chinese cohort with Leber congenital amaurosis and early onset severe retinal dystrophy
  1. Ke Xu,
  2. Yue Xie,
  3. Tengyang Sun,
  4. Xiaohui Zhang,
  5. Chunjie Chen,
  6. Yang Li
  1. Beijing Ophthalmology & Visual Sciences Key Laboratory, Beijing Tongren Eye Center, Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing, China
  1. Correspondence to Dr Yang Li, Beijing Institute Ophthalmology, Beijing Tongren Hospital, Beijing, China; yanglibio{at}aliyun.com

Abstract

Background Leber congenital amaurosis (LCA) and early onset severe retinal dystrophy (EOSRD) are clinically and genetically heterogeneous inherited retinal disorders that cause severe visual impairment in children. The objective of this study was to describe the mutation profile and phenotypic characteristics in Chinese patients with LCA or EOSRD.

Methods Retrospective consecutive case series (2010–2017) study was performed in 148 probands (91 with LCA and 57 with EOSRD). All patients underwent ophthalmic evaluation. Mutations were revealed using targeted next-generation sequencing, followed by Sanger DNA-sequencing and real-time quantitative PCR analysis.

Results We identified two diseasing-causing mutations in 88 unrelated patients, heterozygous autosomal dominant mutations in 11 probands and X-linked hemizygous mutations in 11 patients, for an overall mutation detection rate of 74.3% (110/148). We detected 158 different disease-causing mutations involving 14 LCA genes, 16 retinitis pigmentosa or cone-rod dystrophy genes and 3 syndromic retinal dystrophy genes. Of these 158 mutations, 98 were novel. The most common mutation was p.Q141X of AIPL1, with a gene-specific allele frequency of 60%. The first five most frequently mutated genes were AIPL1 (11.0%), RPGRIP1 (8.8%) and CEP290, GUCY2D and RPE65 (each 7.7%) in the patients with LCA and RPGR (12.3%), CRB1 (10.5%), RPE65 (10.5%), RDH12 (7.0%) and RP2 (5.3%) in the patients with EOSRD.

Conclusions Our results revealed that the mutation spectrum of patients with LCA differs from that of the patients with EOSRD and established the configuration of the mutation frequencies for each LCA gene in Chinese patients, thereby providing essential information for future genetic counselling and gene therapy.

  • Leber congenital amaurosis (LCA)
  • early-onset severe retinal dystrophy (EOSRD)
  • next generation sequencing
  • mutation spectrum
View Full Text

Statistics from Altmetric.com

Footnotes

  • Contributors KX participated in study design, data collection and analysis, and manuscript preparation. YX and TS participated in data collection and analysis. XZ participated in data analysis. CC contributed in colecting clinical data of patients. YL participated in study design and revised the manuscript critically for important intellectual content. All authors approved the final version.

  • Funding This study was supported by the National Key R&D Program of China,2016YFC0905200 and the High-level Talents training plan of the health system of Beijing (No 2013-2-021).

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement All data relevant to the study are included in the article or uploaded as supplementary information.

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.