Evidence mapPaperPMID 40134784Full record

ReviewFrontiers in cellular and infection microbiology2025

Gut microbiota: an emerging target connecting polycystic ovarian syndrome and insulin resistance.

Yufeng Mei, Wanzhen Li, Bingqi Wang, Zhenni Chen, Xinyi Wu, Yingrui Lin, Min Wang

Abstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yufeng MeiDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Wanzhen LiDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Bingqi WangDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhenni ChenDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xinyi WuDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yingrui LinDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Min WangDepartment of Laboratory Medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycystic ovary syndrome (PCOS) is a highly heterogeneous metabolic disorder, with oligomenorrhea and hirsutism as patients' primary complaints. Hyperinsulinemia is a crucial pathophysiological mechanism in the development of PCOS, with 50-70% of patients exhibiting insulin resistance (IR). This condition not only exacerbates ovulatory dysfunction but also leads to various adverse metabolic outcomes, such as dyslipidemia and diabetes, and increases the risk of cardiovascular events both before and after menopause. Gut microbiota is a microbial community within the host that possesses significant metabolic potential and is shaped by external environmental factors, the neuro-immune network, and metabolism. Recent studies have shown that gut microbiota dysbiosis is closely related to the development and progression of PCOS. Despite the growing recognition of the potential role of gut microbiota in the pathogenesis and treatment of PCOS, its clinical application remains in its infancy. Currently, most clinical guidelines and expert consensus still emphasize traditional therapeutic approaches, such as hormonal treatments, lifestyle modifications, and insulin sensitizers. However, accumulating evidence suggests that gut microbiota may influence the metabolic and reproductive health of PCOS patients through various mechanisms. Therefore, understanding the role of gut microbiota between PCOS and IR is essential. This review describes the changes in the gut microbiota of IR-PCOS patients, examines the potential mechanisms by which the gut microbiota contributes to IR in PCOS patients, and updates the evidence supporting the gut microbiota as a potential metabolic regulatory target in IR-PCOS. In summary, gut microbiota dysbiosis may be involved in the development and progression of IR in PCOS patients, and improving gut microbiota may offer metabolic stability benefits.

Indexed as

Gastrointestinal MicrobiomeInsulin ResistancePolycystic Ovary SyndromeDysbiosisFemaleHumansgut microbiotainsulin resistancemetabolic disordersPCOSpotential therapy target

Identifiers

PMID40134784
PMCPMC11933006

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.