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PTPN22 C1858T 与银屑病风险:荟萃分析。

PTPN22 C1858T and the risk of psoriasis: a meta-analysis.

机构信息

Department of Dermatology, Show-Chwan Memorial Hospital, Changhua, Taiwan.

出版信息

Mol Biol Rep. 2012 Aug;39(8):7861-70. doi: 10.1007/s11033-012-1630-z. Epub 2012 Apr 28.

Abstract

Psoriasis is a chronic autoimmune skin disease with both environmental and genetic risk factors. Previous studies of the association between psoriasis and PTPN22 C1858T (rs2476601), a gain of function variant associated with a stronger inhibitory effect of T-lymphocytes, have produced inconsistent results. The purpose of the current study is to evaluate the association between PTPN22 C1858T and psoriasis using meta-analysis to: (1) have a sufficient sample size for detecting a weak association; and (2) to explore the heterogeneity between studies. A meta-analysis based on random-effects model was performed with ten studies (3,334 psoriasis cases and 5,753 controls) identified from a literature search. A non-significantly positive association between psoriasis and the PTPN22 T1858 was observed [summary allelic odds ratio (OR) = 1.15, 95 % confidence interval (CI): 1.00-1.33] and the association appears stronger among subjects with psoriatic arthritis (summary allelic OR = 1.23, 95 % CI: 1.00-1.52). A null association between PTPN22 T1858 and early-onset psoriasis was observed (summary allelic OR = 1.08, 95 % CI: 0.92-1.28). The current analysis showed a non-significantly positive association between psoriasis and the PTPN22 T1858 allele, and the association appeared stronger among subjects with psoriatic arthritis. Future studies of psoriasis should incorporate gene-environment interaction in the analysis and pay attention to the heterogeneity of psoriasis cases and bias associated with population stratification.

摘要

银屑病是一种慢性自身免疫性皮肤病,具有环境和遗传风险因素。先前关于银屑病与 PTPN22 C1858T(rs2476601)之间关联的研究,该基因的功能变体与 T 淋巴细胞的抑制作用更强有关,结果不一致。本研究的目的是通过荟萃分析评估 PTPN22 C1858T 与银屑病之间的关联,以:(1)有足够的样本量来检测弱关联;(2) 探讨研究之间的异质性。对从文献检索中确定的十项研究(3334 例银屑病病例和 5753 例对照)进行基于随机效应模型的荟萃分析。观察到银屑病与 PTPN22 T1858 之间存在非显著正相关[综合等位基因优势比(OR)=1.15,95%置信区间(CI):1.00-1.33],并且在患有银屑病关节炎的患者中这种关联更强[综合等位基因 OR = 1.23,95%CI:1.00-1.52]。观察到 PTPN22 T1858 与早发性银屑病之间不存在关联[综合等位基因 OR = 1.08,95%CI:0.92-1.28]。本分析显示银屑病与 PTPN22 T1858 等位基因之间存在非显著正相关,并且在患有银屑病关节炎的患者中这种关联更强。未来的银屑病研究应在分析中纳入基因-环境相互作用,并注意银屑病病例的异质性和与人群分层相关的偏倚。

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