Suppr超能文献

人类白细胞抗原 II 类与原发性胆汁性肝硬化易感性的关联:系统评价和荟萃分析。

Association of human leukocyte antigen class II with susceptibility to primary biliary cirrhosis: a systematic review and meta-analysis.

机构信息

Department of Laboratory Diagnostics, Changzheng Hospital, Second Military Medical University, Shanghai, China.

出版信息

PLoS One. 2013 Nov 12;8(11):e79580. doi: 10.1371/journal.pone.0079580. eCollection 2013.

Abstract

PURPOSE

Several previous studies suggested that HLA-Class II may be associated with susceptibility to primary biliary cirrhosis (PBC), but data from individual studies remain controversial. Therefore, a systematic review and meta-analysis is needed to comprehensively evaluate the association between HLA-Class II and PBC risk.

METHODS

All published reports of an association between HLA class II and PBC risk were searched in PubMed, EMBASE (updated to 22 May 2012). ORs with 95% confidence intervals (CIs) were extracted from each included study and the meta-analysis was performed using the fixed- or random-effects model.

RESULTS

A total of 3,732 PBC patients and 11,031 controls from 34 studies were included in the meta-analysis. An assessment of study quality revealed that the majority of studies included (18 studies) were of high quality. The serological group DR8 was found to be a risk factor for PBC (OR = 2.82, 95%CI: 1.84-4.30). At the allelic level, HLA-DR08 and HLA-DR0801 were identified as risk factors for PBC (OR = 2.30, 95%CI: 1.76-3.00; OR = 3.23, 95%CI: 2.22-4.70, respectively), whereas HLA-DR11 and HLA-DR13 were potent protective factors (OR = 0.31, 95%CI: 0.27-0.38; OR = 0.62, 95%CI: 0.48-0.81, respectively). HLA-DQB1 and HLA-DQB10402 conferred a predisposition to PBC development (OR = 3.47, 95%CI: 2.35-5.13), whereas HLA-DQB10604 was protective against PBC (OR = 0.3, 95%CI: 0.18-0.58). No HLA-DPB1 allele was observed to be associated with PBC susceptibility (P > 0.05).

CONCLUSIONS

The present study revealed that HLA-Class II components are closely associated with the development of PBC.

摘要

目的

先前的几项研究表明,HLA-II 类可能与原发性胆汁性肝硬化(PBC)的易感性有关,但来自单个研究的数据仍存在争议。因此,需要进行系统的综述和荟萃分析,以全面评估 HLA-II 类与 PBC 风险之间的关联。

方法

在 PubMed 和 EMBASE(更新至 2012 年 5 月 22 日)中搜索了所有关于 HLA Ⅱ类与 PBC 风险之间关联的已发表报告。从每个纳入的研究中提取 OR 值和 95%置信区间(CI),并使用固定或随机效应模型进行荟萃分析。

结果

共有来自 34 项研究的 3732 名 PBC 患者和 11031 名对照纳入荟萃分析。研究质量评估显示,大多数纳入的研究(18 项研究)质量较高。血清学组 DR8 被认为是 PBC 的危险因素(OR=2.82,95%CI:1.84-4.30)。在等位基因水平上,HLA-DR08 和 HLA-DR0801 被确定为 PBC 的危险因素(OR=2.30,95%CI:1.76-3.00;OR=3.23,95%CI:2.22-4.70),而 HLA-DR11 和 HLA-DR13 是有效的保护因素(OR=0.31,95%CI:0.27-0.38;OR=0.62,95%CI:0.48-0.81)。HLA-DQB1 和 HLA-DQB10402 导致 PBC 发展的易感性增加(OR=3.47,95%CI:2.35-5.13),而 HLA-DQB10604 对 PBC 有保护作用(OR=0.3,95%CI:0.18-0.58)。未观察到 HLA-DPB1 等位基因与 PBC 易感性相关(P>0.05)。

结论

本研究表明,HLA-II 类成分与 PBC 的发生密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee5d/3827176/d16f2847fc0a/pone.0079580.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验