Present and Future: Crosstalks Between Polycystic Ovary Syndrome and Gut Metabolites Relating to Gut Microbiota
Overview
Authors
Affiliations
Polycystic ovary syndrome (PCOS) is a common disease, affecting 8%-13% of the females of reproductive age, thereby compromising their fertility and long-term health. However, the pathogenesis of PCOS is still unclear. It is not only a reproductive endocrine disease, dominated by hyperandrogenemia, but also is accompanied by different degrees of metabolic abnormalities and insulin resistance. With a deeper understanding of its pathogenesis, more small metabolic molecules, such as bile acids, amino acids, and short-chain fatty acids, have been reported to be involved in the pathological process of PCOS. Recently, the critical role of gut microbiota in metabolism has been focused on. The gut microbiota-related metabolic pathways can significantly affect inflammation levels, insulin signaling, glucose metabolism, lipid metabolism, and hormonal secretions. Although the abnormalities in gut microbiota and metabolites might not be the initial factors of PCOS, they may have a significant role in the pathological process of PCOS. The dysbiosis of gut microbiota and disturbance of gut metabolites can affect the progression of PCOS. Meanwhile, PCOS itself can adversely affect the function of gut, thereby contributing to the aggravation of the disease. Inhibiting this vicious cycle might alleviate the symptoms of PCOS. However, the role of gut microbiota in PCOS has not been fully explored yet. This review aims to summarize the potential effects and modulative mechanisms of the gut metabolites on PCOS and suggests its potential intervention targets, thus providing more possible treatment options for PCOS in the future.
Polycystic Ovarian Syndrome: A Review of Multi-omics Analyses.
Naqvi I, Bandyopadhyay A, Panda A, Hareramadas B Reprod Sci. 2025; 32(3):618-646.
PMID: 39875694 DOI: 10.1007/s43032-025-01789-8.
The gut microbiota: emerging biomarkers and potential treatments for infertility-related diseases.
Wang M, Zheng L, Ma S, Zhao D, Xu Y Front Cell Infect Microbiol. 2024; 14:1450310.
PMID: 39391885 PMC: 11464459. DOI: 10.3389/fcimb.2024.1450310.
Arvanitakis K, Chatzikalil E, Kalopitas G, Patoulias D, Popovic D, Metallidis S J Clin Med. 2024; 13(14).
PMID: 39064282 PMC: 11278502. DOI: 10.3390/jcm13144243.
Li M, Chang Q, Luo Y, Pan J, Hu Y, Liu B Front Cell Dev Biol. 2024; 12:1384233.
PMID: 38872933 PMC: 11169812. DOI: 10.3389/fcell.2024.1384233.
Zhou M, Yu J, Li X, Ruan Z, Yu S J Cell Mol Med. 2024; 28(8):e18258.
PMID: 38546608 PMC: 10977384. DOI: 10.1111/jcmm.18258.