Alterations of the microbiome across body sites in systemic lupus erythematosus: A systematic review and meta-analysis

Author:

Wang Yiyu12,Wu Hong12,Yan Chengrui3,Huang Ronggui12,Li Kaidi12,Du Yujie12,Jin Xue12,Zhu Gaoqi3,Zeng Hanjun3,Li Baozhu124ORCID

Affiliation:

1. Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, China

2. Anhui Provincial Laboratory of Inflammatory and Immune Diseases, Hefei, China

3. Haiheng Community Health Service Center HETDA, Hefei, China

4. The Second Hospital of Anhui Medical University, Hefei, China

Abstract

Background Systemic lupus erythematosus (SLE) is a complex autoimmune disease with unclear etiology. Growing evidence suggests the microbiome plays a role in SLE pathogenesis. However, findings are inconsistent across studies due to factors like small sample sizes and geographical variations. A comprehensive meta-analysis is needed to elucidate microbiome alterations in SLE. Objective This study aimed to provide a systematic overview of microbiota dysbiosis across body sites in SLE through a meta-analysis of alpha diversity indices, beta diversity indices, and abundance taxa of microbiome. Methods A literature search was conducted across four databases to identify relevant studies comparing SLE patients and healthy controls. Extracted data encompassed alpha and beta diversity metrics, as well as bacterial, fungal, and viral abundance across gut, oral, skin, and other microbiota. Study quality was assessed using the Newcastle-Ottawa Scale. Standardized mean differences and pooled effect sizes were calculated through meta-analytical methods. Results The analysis showed reduced alpha diversity and distinct beta diversity in SLE, particularly in the gut microbiota. Taxonomic analysis revealed compositional variations in bacteria from the gut and oral cavity. However, results for fungi, viruses, and bacteria from other sites were inconsistent due to limited studies. Conclusions This meta-analysis offers a comprehensive perspective on microbiome dysbiosis in SLE patients across diverse body sites and taxa. The observed variations underscore the microbiome’s potential role in SLE pathogenesis. Future research should address geographical variations, employ longitudinal designs, and integrate multi-omics approaches.

Funder

National Natural Science Foundation of China

Research Fund of Anhui Institute of translational medicine

Science Research Project of Anhui Educational Committee

Center for Big Data and Population Health of IHM

Clinical medical research transformation project in Anhui Province

Publisher

SAGE Publications

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