# BMI-stratified phenotypes of polycystic ovary syndrome: advances in gut microbiota research and personalized management strategies

**Authors:** Bisha Su, Yining Cao, Lin Ma, Jian Huang

PMC · DOI: 10.3389/fendo.2026.1734041 · Frontiers in Endocrinology · 2026-02-06

## TL;DR

This review explores how PCOS differs in obese and non-obese women, focusing on gut microbiota and personalized treatment strategies.

## Contribution

The paper highlights mechanistic differences in gut microbiota between BMI-stratified PCOS subgroups and proposes tailored interventions.

## Key findings

- Obese PCOS is linked to more severe gut microbiota dysbiosis and metabolic abnormalities.
- Non-obese PCOS primarily shows reproductive endocrine dysfunction with less pronounced metabolic issues.
- Personalized strategies like probiotics and fecal microbiota transplantation show promise for PCOS management.

## Abstract

Polycystic ovary syndrome (PCOS) is a heterogeneous endocrine-metabolic disorder affecting 11%-13% of women of reproductive age. Based on body mass index (BMI), patients can be phenotypically classified into obese and non-obese subgroups: the obese PCOS is characterized by insulin resistance, hyperandrogenemia, and metabolic syndrome, with more pronounced metabolic risks; non-obese PCOS primarily manifests as reproductive endocrine dysfunction. In recent years, studies have shown that the Gut microbiota plays a key role in the pathogenesis of PCOS, and dysbiosis in the obese subgroup is generally more pronounced, potentially amplifying metabolic abnormalities through pathways such as short-chain fatty acids, bile acid disturbances, and endotoxin-related low-grade inflammation. This review systematically summarizes the clinically heterogeneous features of BMI-stratified PCOS and its gut microbiota characteristics, with a focus on elucidating the mechanistic differences between obese and non-obese individuals in terms of inflammation, metabolites, and endocrine regulatory pathways. Based on current evidence, individualized intervention strategies targeting different BMI subtypes are proposed, including dietary and lifestyle modifications, interventions with probiotics/prebiotics/synbiotics, and exploration of emerging precision microbiome therapies such as fecal microbiota transplantation. The interaction between BMI and gut microbiota provides new directions for stratified management and personalized treatment of PCOS; however, high-quality longitudinal and interventional studies are still needed to clarify causal relationships and optimize microbiota-targeted strategies.

## Linked entities

- **Diseases:** Polycystic ovary syndrome (MONDO:0008487), metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** ERBB4 (erb-b2 receptor tyrosine kinase 4) [NCBI Gene 2066] {aka ALS19, HER4, p180erbB4}, HSD3B2 (hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2) [NCBI Gene 3284] {aka HSD3B, HSDB, SDR11E2}, DENND1A (DENN domain containing 1A) [NCBI Gene 57706] {aka FAM31A, KIAA1608}, PYY (peptide YY) [NCBI Gene 5697] {aka PYY-I, PYY1}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, GPBAR1 (G protein-coupled bile acid receptor 1) [NCBI Gene 151306] {aka BG37, GPCR19, GPR131, M-BAR, TGR5}, GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, XBP1 (X-box binding protein 1) [NCBI Gene 7494] {aka TREB-5, TREB5, XBP-1, XBP2}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** type 2 diabetes (MESH:D003924), metabolic and hormonal abnormalities (MESH:C566454), miscarriage (MESH:D000022), inflammatory bowel disease (MESH:D015212), GM (MESH:C562602), systemic (MESH:D015619), ovulatory dysfunction (MESH:D006331), visceral obesity (MESH:D056128), impaired glucose tolerance (MESH:D018149), acne (MESH:D000152), chronic (MESH:D002908), reproductive axis dysfunction (MESH:C566610), HA (MESH:D017588), endotoxemia (MESH:D019446), PCOS (MESH:D011085), hypertension (MESH:D006973), lipid metabolism disorders (MESH:D052439), sex hormone abnormalities (MESH:D012729), cardiovascular diseases (MESH:D002318), gestational hypertension (MESH:D046110), T (MESH:D001260), infertility (MESH:D007246), endocrine and metabolic disorder (MESH:D004700), weight loss (MESH:D015431), IR (MESH:D007333), Non-obese (MESH:D009765), overweight (MESH:D050177), metabolic and reproductive abnormalities (MESH:D060737), metabolic abnormalities (MESH:D008659), hirsutism (MESH:D006628), chronic inflammation (MESH:D007249), metabolic disturbances (MESH:D024821), dyslipidemia (MESH:D050171), GM dysbiosis (MESH:D064806), preeclampsia (MESH:D011225)
- **Chemicals:** tauroursodeoxycholic acid (MESH:C031655), Prebiotics (MESH:D056692), LPS (MESH:D008070), DHEA (MESH:D003687), lipid (MESH:D008055), acetate (MESH:D000085), tryptophan (MESH:D014364), SCFA (MESH:D005232), dextrin (-), Bile acid (MESH:D001647), oligosaccharides (MESH:D009844), butyrate (MESH:D002087), propionate (MESH:D011422), carbohydrate (MESH:D002241), fatty acid (MESH:D005227), Metformin (MESH:D008687), free fatty acids (MESH:D005230), testosterone (MESH:D013739), glycocholic acid (MESH:D006000), taurocholic acid (MESH:D013656), GABA (MESH:D005680), glycochenodeoxycholic acid (MESH:D005999), fat (MESH:D005223), T (MESH:D014316), triglycerides (MESH:D014280), clomiphene (MESH:D002996), fructooligosaccharides (MESH:C116580)
- **Species:** Shigella (genus) [taxon 620], gut metagenome (species) [taxon 749906], Akkermansia muciniphila (species) [taxon 239935], Bacteroides fragilis (species) [taxon 817], Lactococcus (lactic streptococci, genus) [taxon 1357], Homo sapiens (human, species) [taxon 9606], Faecalibacterium prausnitzii (species) [taxon 853], Parabacteroides distasonis (species) [taxon 823], Escherichia coli (E. coli, species) [taxon 562], Anaerobutyricum hallii (species) [taxon 39488], Prevotella (genus) [taxon 838], Mus musculus (house mouse, species) [taxon 10090], Coprococcus (genus) [taxon 33042]
- **Mutations:** rs569675099, rs12000707

## Full text

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## Figures

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## References

99 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920190/full.md

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Source: https://tomesphere.com/paper/PMC12920190