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银屑病的遗传学:精准医学的基础

Genetics of psoriasis: a basis for precision medicine.

作者信息

Ran Delin, Cai Minglong, Zhang Xuejun

机构信息

Institute of Dermatology and Department of Dermatology of the First Affiliated Hospital, Anhui Medical University, Hefei, China.

Key Laboratory of Dermatology, Anhui Medical University, Ministry of Education, Hefei, China.

出版信息

Precis Clin Med. 2019 Jun 24;2(2):120-130. doi: 10.1093/pcmedi/pbz011. eCollection 2019 Jun.

Abstract

Psoriasis is an inflammatory skin disease with a background of polygenic inheritance. Both environmental and genetic factors are involved in the etiology of the disease. In the last two decades, numerous studies have been conducted through linkage analysis, genome-wide association study (GWAS), and direct sequencing to explore the role of genetic variation in disease pathogenesis and progression. To date, >80 psoriasis susceptibility genes have been identified, including , , , and . Some genetic markers have been applied in disease prediction, clinical diagnosis, treatment, and new drug development, which could further explain the pathogenesis of psoriasis and promote the development of precision medicine. This review summarizes related research on genetic variation in psoriasis and explores implications of the findings in clinical application and the promotion of a personalized medicine project.

摘要

银屑病是一种具有多基因遗传背景的炎症性皮肤病。环境因素和遗传因素均参与该疾病的病因。在过去二十年中,通过连锁分析、全基因组关联研究(GWAS)和直接测序进行了大量研究,以探索遗传变异在疾病发病机制和进展中的作用。迄今为止,已鉴定出80多个银屑病易感基因,包括……。一些遗传标记已应用于疾病预测、临床诊断、治疗和新药开发,这可以进一步解释银屑病的发病机制并促进精准医学的发展。本文综述总结了银屑病遗传变异的相关研究,并探讨了这些研究结果在临床应用中的意义以及对个性化医疗项目的推动作用。

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