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Front Med (Lausanne). 2021 Jun 29;8:645550. doi: 10.3389/fmed.2021.645550. eCollection 2021.
2
The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database Analysis.不同主要种族群体高尿酸血症和痛风的流行病学与遗传学:文献综述及人群遗传学二级数据库分析
J Pers Med. 2021 Mar 22;11(3):231. doi: 10.3390/jpm11030231.
3
Combining Understanding of Immunological Mechanisms and Genetic Variants Toward Development of Personalized Medicine for Psoriasis Patients.结合对免疫机制和基因变异的理解以开发针对银屑病患者的个性化药物。
Front Genet. 2019 May 3;10:395. doi: 10.3389/fgene.2019.00395. eCollection 2019.
4
ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study.ABCG2 基因在全基因组关联研究中导致痛风和高尿酸血症的发生。
Sci Rep. 2018 Feb 16;8(1):3137. doi: 10.1038/s41598-018-21425-7.
5
Impact of HOTAIR Gene Polymorphism and Environmental Risk on Oral Cancer.HOTAIR 基因多态性和环境风险对口腔癌的影响。
J Dent Res. 2018 Jun;97(6):717-724. doi: 10.1177/0022034517749451. Epub 2018 Jan 3.
6
The Genetic Basis of Psoriasis.银屑病的遗传学基础。
Int J Mol Sci. 2017 Nov 25;18(12):2526. doi: 10.3390/ijms18122526.
7
A comprehensive analysis of the association of common variants of ABCG2 with gout.对 ABCG2 常见变异与痛风关联性的综合分析。
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8
Autoimmune aspects of psoriasis: Heritability and autoantigens.银屑病的自身免疫方面:遗传性和自身抗原。
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ABCG2 polymorphisms in gout: insights into disease susceptibility and treatment approaches.痛风中的ABCG2基因多态性:对疾病易感性和治疗方法的见解。
Pharmgenomics Pers Med. 2017 Apr 20;10:129-142. doi: 10.2147/PGPM.S105854. eCollection 2017.

基因多态性对银屑病易感性的影响。

Impact of Gene Polymorphism on the Predisposition to Psoriasis.

作者信息

Huang Yu-Huei, See Lai-Chu, Chang Ya-Ching, Chung Wen-Hung, Chang Lun-Ching, Yang Shun-Fa, Su Shih-Chi

机构信息

Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.

Department of Dermatology, Chang Gung Memorial Hospital, Linkou Branch, Taoyuan 333, Taiwan.

出版信息

Genes (Basel). 2021 Oct 12;12(10):1601. doi: 10.3390/genes12101601.

DOI:10.3390/genes12101601
PMID:34680995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8535938/
Abstract

Psoriasis is a chronic inflammatory disease which is caused by the interaction between genetic and environmental factors. Evidence shows an association of psoriasis with co-morbidities including cardiovascular diseases, metabolic syndrome and hyperuricemia. Genome-wide association studies have revealed that the gene encoding ATP-binding cassette G2 protein was associated with inflammation and higher serum urate concentrations. In this study, we aimed to evaluate the role of gene polymorphisms on the susceptibility to psoriasis. The genotype distribution of two single nucleotide polymorphisms (SNPs), rs2231142 and rs2231137, was examined in 410 psoriasis patients and 1,089 gender-matched non-psoriasis controls. We found that heterozygotes (GT) for rs2231142 was associated with a decreased risk of psoriasis ( = 0.001; adjusted OR = 0.532; 95% CI, 0.370-0.765) after adjusting for age, as compared with homozygotes for the major allele (GG). Subjects who carried at least one polymorphic allele (homozygote or heterozygote for the minor allele) were less susceptible to psoriasis ( = 0.002; adjusted OR = 0.594; 95% CI, 0.249-0.823) and bearing higher serum urate levels ( = 0.026) than those homozygous for the major allele. Our results indicated that the gene polymorphism was associated with the risk of psoriasis.

摘要

银屑病是一种由遗传和环境因素相互作用引起的慢性炎症性疾病。有证据表明银屑病与包括心血管疾病、代谢综合征和高尿酸血症在内的合并症有关。全基因组关联研究表明,编码ATP结合盒G2蛋白的基因与炎症和较高的血清尿酸浓度有关。在本研究中,我们旨在评估基因多态性在银屑病易感性中的作用。在410例银屑病患者和1089例性别匹配的非银屑病对照中检测了两个单核苷酸多态性(SNP)rs2231142和rs2231137的基因型分布。我们发现,与主要等位基因纯合子(GG)相比,rs2231142的杂合子(GT)在调整年龄后与银屑病风险降低相关(P = 0.001;调整后的OR = 0.532;95%CI,0.370 - 0.765)。携带至少一个多态性等位基因(次要等位基因的纯合子或杂合子)的受试者比主要等位基因纯合子的受试者对银屑病的易感性更低(P = 0.002;调整后的OR = 0.594;95%CI,0.249 - 0.823),且血清尿酸水平更高(P = 0.026)。我们的结果表明该基因多态性与银屑病风险相关。