Oncotarget

Research Papers:

Family-based whole exome sequencing of atopic dermatitis complicated with cataracts

Wenxin Luo, Wangdong Xu, Lin Xia, Dan Xie, Lin Wang, Zaipei Guo, Yue Cheng, Yi Liu and Weimin Li _

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Oncotarget. 2017; 8:59446-59454. https://doi.org/10.18632/oncotarget.19739

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Abstract

Wenxin Luo1,*, Wangdong Xu2,*, Lin Xia3, Dan Xie3, Lin Wang4, Zaipei Guo5, Yue Cheng1, Yi Liu2 and Weimin Li1

1Department of Respiratory and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China

2Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China

3State Key Laboratory of Biotherapy and Collaborative Innovation Center for Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China

4Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China

5Department of Dermatology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, PR China

*Wenxin Luo and Wangdong Xu contributed equally to this work, and should be considered as the co-first author

Correspondence to:

Weimin Li, email: weimin003@163.com

Keywords: atopic dermatitis, cataracts, mutation

Received: November 07, 2016     Accepted: June 02, 2017     Published: July 31, 2017

ABSTRACT

Background: Atopic dermatitis (AD) is a common skin disorder with elevated prevalence. Cataract induced by AD rarely occurs in adolescent and young adult patients, which is also called atopic cataract. Using whole exome sequencing, we aimed to explore genetic alterations among AD and atopic cataract.

Result: We recruited a 19 year-old Chinese male with AD accompanied with cataracts, his father with AD and his mother without AD or cataract. Through analysis of the exomic sequence of the 3 individuals from the same family, we identified that with respect to AD, there were 162 genes mutated in both this patient and his father but not in his mother. In addition, we found 10 genes mutated in this patient only without in his parents according to cataract.

Conclusion: This research suggests that coinheritance of mutations in these genes may correlate with AD, and the pathogenesis of AD complicated with cataracts was related to genetic factors.


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