Perturbations in gut microbiota composition in patients with polycystic ovary syndrome: a systematic review and meta-analysis

多囊卵巢 医学 荟萃分析 科克伦图书馆 观察研究 内科学 α多样性 肠道菌群 梅德林 系统回顾 检查表 生物 生态学 免疫学 物种多样性 肥胖 胰岛素抵抗 生物化学 古生物学
作者
Pan Li,Ping Shuai,Sj Shen,Huimin Zheng,Ping Sun,Renfang Zhang,Shanwei Lan,Zixin Lan,Thisun Jayawardana,Yumei Yang,Jianhui Zhao,Yuping Liu,Xia Chen,Emad El‐Omar,Zhengwei Wan
出处
期刊:BMC Medicine [BioMed Central]
卷期号:21 (1): 302-302 被引量:78
标识
DOI:10.1186/s12916-023-02975-8
摘要

BACKGROUND: The results of human observational studies on the correlation between gut microbiota perturbations and polycystic ovary syndrome (PCOS) have been contradictory. This study aimed to perform the first systematic review and meta-analysis to evaluate the specificity of the gut microbiota in PCOS patients compared to healthy women. METHODS: ) for alpha diversity were calculated. Qualitative syntheses of beta-diversity and microbe alterations were performed. RESULTS: Twenty-eight studies (n = 1022 patients, n = 928 control) that investigated gut microbiota by collecting stool samples were included, with 26 and 27 studies having provided alpha-diversity and beta-diversity results respectively. A significant decrease in microbial evenness and phylogenetic diversity was observed in PCOS patients when compared with control participants (Shannon index: SMD = - 0.27; 95% CI, - 0.37 to - 0.16; phylogenetic diversity: SMD = - 0.39; 95% CI, -- 0.74 to - 0.03). We also found that reported beta-diversity was inconsistent between studies. Despite heterogeneity in bacterial relative abundance, we observed depletion of Lachnospira and Prevotella and enrichment of Bacteroides, Parabacteroides, Lactobacillus, Fusobacterium, and Escherichia/Shigella in PCOS. Gut dysbiosis in PCOS, which might be characterized by the reduction of short-chain fatty acid (SCFA)-producing and bile-acid-metabolizing bacteria, suggests a shift in balance to favor pro-inflammatory rather than anti-inflammatory bacteria. CONCLUSIONS: Gut dysbiosis in PCOS is associated with decreased diversity and alterations in bacteria involved in microbiota-host crosstalk. TRIAL REGISTRATION: PROSPERO registration: CRD42021285206, May 22, 2023.
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