{"title":"Dysbiosis in PCOS: A Systematic Review of Microbiome Alterations Across Body Sites with GRADE Assessment of Evidence Quality.","authors":"Navjot Kaur, Nisha Yadav, Sarika Sachan, Priya Sharma, Preeti Khetarpal","doi":"10.1152/physiolgenomics.00072.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Polycystic Ovary Syndrome (PCOS) is a prevalent endocrine-metabolic disorder that adversely affects reproductive, metabolic, and cardiovascular health in females, leading to menstrual irregularities and an increased risk of endometrial malignancies. Emerging research evidence suggests that the gut and extra gastrointestinal microbiome dysbiosis may play a significant role in the pathophysiology of PCOS. This systematic review aims to elucidate the microbiome dysbiosis patterns in PCOS patients compared to healthy controls. A systematic search was conducted across PubMed, Scopus, and Web of Science from inception until February 28<sup>th</sup>, 2025, encompassing all original cross-sectional, cohort, or case-control studies that examined the gut, oral, blood, and lower genital tract (LGT) microbiomes of PCOS patients (cases) against healthy females (controls). Of the 4,377 studies identified, 64 were assessed for eligibility through full-text screening, and ultimately, 29 studies met inclusion criteria and were included into the systematic review. The results revealed inconsistent patterns in alpha and beta diversity, with reports of increased, decreased, or unchanged microbial diversity across studies. Key alterations were observed at different taxonomic levels, such as phylum, family, genus, and species. The most significant bacterial alterations include changes in the relative abundance of various bacterial taxa such as <i>Bacteroidetes</i>, <i>Firmicutes</i>, <i>Actinobacteria</i>, <i>Proteobacteria</i>, <i>Verrucomicrobia</i>, <i>Gammaproteobacteria</i>, <i>Fusobacteria</i>, <i>Eubacterium</i>, <i>Streptococcus</i>, <i>Paraprevotella</i>, <i>Tucibacter</i>, and <i>Tenericutes</i>. These findings indicate that complex dysbiotic microbial shifts may be involved in the pathogenesis of PCOS. As per the GRADE assessment, the quality of evidence is low for most of the studies. This systematic review supports the role of microbial dysbiosis in PCOS pathogenesis, however, additional research is required to elucidate these interactions to guide the development of therapeutic strategies in the future.</p>","PeriodicalId":20129,"journal":{"name":"Physiological genomics","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1152/physiolgenomics.00072.2025","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Polycystic Ovary Syndrome (PCOS) is a prevalent endocrine-metabolic disorder that adversely affects reproductive, metabolic, and cardiovascular health in females, leading to menstrual irregularities and an increased risk of endometrial malignancies. Emerging research evidence suggests that the gut and extra gastrointestinal microbiome dysbiosis may play a significant role in the pathophysiology of PCOS. This systematic review aims to elucidate the microbiome dysbiosis patterns in PCOS patients compared to healthy controls. A systematic search was conducted across PubMed, Scopus, and Web of Science from inception until February 28th, 2025, encompassing all original cross-sectional, cohort, or case-control studies that examined the gut, oral, blood, and lower genital tract (LGT) microbiomes of PCOS patients (cases) against healthy females (controls). Of the 4,377 studies identified, 64 were assessed for eligibility through full-text screening, and ultimately, 29 studies met inclusion criteria and were included into the systematic review. The results revealed inconsistent patterns in alpha and beta diversity, with reports of increased, decreased, or unchanged microbial diversity across studies. Key alterations were observed at different taxonomic levels, such as phylum, family, genus, and species. The most significant bacterial alterations include changes in the relative abundance of various bacterial taxa such as Bacteroidetes, Firmicutes, Actinobacteria, Proteobacteria, Verrucomicrobia, Gammaproteobacteria, Fusobacteria, Eubacterium, Streptococcus, Paraprevotella, Tucibacter, and Tenericutes. These findings indicate that complex dysbiotic microbial shifts may be involved in the pathogenesis of PCOS. As per the GRADE assessment, the quality of evidence is low for most of the studies. This systematic review supports the role of microbial dysbiosis in PCOS pathogenesis, however, additional research is required to elucidate these interactions to guide the development of therapeutic strategies in the future.
多囊卵巢综合征(PCOS)是一种常见的内分泌代谢紊乱,对女性的生殖、代谢和心血管健康产生不利影响,导致月经不规则和子宫内膜恶性肿瘤的风险增加。新的研究证据表明,肠道和胃肠道外微生物群失调可能在多囊卵巢综合征的病理生理中发挥重要作用。本系统综述旨在阐明PCOS患者与健康对照者的微生物群落失调模式。系统检索PubMed、Scopus和Web of Science从成立到2025年2月28日,包括所有原始的横断面、队列或病例对照研究,这些研究检查了PCOS患者(病例)与健康女性(对照组)的肠道、口腔、血液和下生殖道(LGT)微生物组。在确定的4377项研究中,64项研究通过全文筛选进行了资格评估,最终,29项研究符合纳入标准并被纳入系统评价。结果显示α和β多样性的模式不一致,在研究中有增加、减少或不变的微生物多样性报告。在门、科、属和种等不同的分类水平上观察到关键的变化。最显著的细菌变化包括各种细菌分类群的相对丰度的变化,如拟杆菌门、厚壁菌门、放线菌门、变形菌门、Verrucomicrobia、γ变形菌门、梭菌门、真细菌、链球菌、拟杆菌门、Tucibacter和Tenericutes。这些发现表明,复杂的益生菌转移可能参与多囊卵巢综合征的发病机制。根据GRADE评估,大多数研究的证据质量很低。本系统综述支持微生物生态失调在多囊卵巢综合征发病机制中的作用,然而,需要进一步的研究来阐明这些相互作用,以指导未来治疗策略的发展。
期刊介绍:
The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.