Determining the association between systematic lupus erythematosus and the occurrence of primary biliary cirrhosis: a systematic review and meta-analysis.

IF 2.3 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Natchaya Polpichai, Sakditad Saowapa, Shu-Yen Chan, Phuuwadith Wattanachayakul, Pojsakorn Danpanichkul, Panisara Fangsaard, Angkawipa Trongtorsak
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引用次数: 0

Abstract

Background: Autoimmune diseases often coexist; however, the concomitant occurrence of systemic lupus erythematosus (SLE) and primary biliary cirrhosis (PBC) is rare. Therefore, this study aims to provide a comprehensive summary of evidence regarding the co-occurrence of SLE and PBC.

Methods: PubMed, Web of Science, ScienceDirect , and Google Scholar databases were systematically and comprehensively searched for records published up to February 2024. Full-text articles that aligned with the study's aim were included, while those published in languages other than English and those designed as case reports, reviews, conference abstracts, or editorials were excluded. Statistical analyses were performed using Comprehensive Meta-Analysis software, and methodological quality was assessed using the Newcastle-Ottawa Scale.

Results: Only 14 studies that met the inclusion criteria with 3944 PBC and 9414 SLE patients were included for review and analysis. Pooled data analysis revealed that approximately 1.1% of SLE patients have concomitant PBC (range: 0.02-7.5%), while around 2.7% of PBC patients concurrently have SLE (range: 1.3-7.5%). Furthermore, qualitative data analysis indicated that the prevalence of PBC in SLE patients presenting with hepatic dysfunction or abnormal liver enzymes ranges from 2 to 7.5%.

Conclusion: Although the concomitant occurrence of SLE and PBC is rare, the small proportion of patients where these diseases coexist warrants close monitoring by clinicians. This underscores the importance of surveillance to prevent their co-occurrence.

确定系统性红斑狼疮与原发性胆汁性肝硬化发生之间的关联:系统回顾和荟萃分析。
背景:自身免疫性疾病经常同时存在;然而,系统性红斑狼疮(SLE)和原发性胆汁性肝硬化(PBC)同时发生的情况却很少见。因此,本研究旨在全面总结有关系统性红斑狼疮和原发性胆汁性肝硬化并存的证据:方法:系统、全面地检索了 PubMed、Web of Science、ScienceDirect 和 Google Scholar 数据库中截至 2024 年 2 月发表的记录。纳入了符合研究目的的全文文章,但排除了以英语以外的语言发表的文章,以及以病例报告、综述、会议摘要或社论形式发表的文章。统计分析采用 Comprehensive Meta-Analysis 软件进行,方法学质量采用纽卡斯尔-渥太华量表进行评估:只有 14 项研究符合纳入标准,其中包括 3944 名 PBC 患者和 9414 名系统性红斑狼疮患者。汇总数据分析显示,约 1.1% 的系统性红斑狼疮患者同时患有 PBC(范围:0.02%-7.5%),而约 2.7% 的 PBC 患者同时患有系统性红斑狼疮(范围:1.3%-7.5%)。此外,定性数据分析显示,在出现肝功能异常或肝酶异常的系统性红斑狼疮患者中,PBC的发病率为2%至7.5%:结论:虽然系统性红斑狼疮和 PBC 并发的情况很少见,但这两种疾病同时存在的一小部分患者值得临床医生密切监测。结论:尽管系统性红斑狼疮和重型乳腺炎并发的患者很少见,但临床医生仍应密切监测这两种疾病,这也强调了监测以预防并发症的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
4.80%
发文量
269
审稿时长
1 months
期刊介绍: European Journal of Gastroenterology & Hepatology publishes papers reporting original clinical and scientific research which are of a high standard and which contribute to the advancement of knowledge in the field of gastroenterology and hepatology. The journal publishes three types of manuscript: in-depth reviews (by invitation only), full papers and case reports. Manuscripts submitted to the journal will be accepted on the understanding that the author has not previously submitted the paper to another journal or had the material published elsewhere. Authors are asked to disclose any affiliations, including financial, consultant, or institutional associations, that might lead to bias or a conflict of interest.
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