Evidence map›Paper›PMID 41978723›Full record

ArticleInternational journal of women's health2026

Integrated Genomic Analysis Reveals New Diagnostic Biomarkers and Immune Mechanisms for Polycystic Ovary Syndrome.

Ning Huang, LuYun Lou

Abstract read
In one paragraph

Article in International journal of women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Ning HuangCixi Integrated Traditional Chinese and Western Medicine Healthcare Group, Ningbo, Zhejiang, 315300, People's Republic of China.
LuYun LouHenghe Central Health Center of Cixi City, Ningbo, Zhejiang, 315300, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Polycystic ovary syndrome (PCOS) is a prevalent endocrine disorder associated with metabolic dysregulation and chronic inflammation. This study employed bioinformatics approaches to analyze the roles of neutrophil extracellular traps (NETs)-related genes (NETRGs) and mitochondria-related genes (MRGs) in PCOS pathogenesis. Methods: Through differential expression analysis, enrichment studies, and machine learning models, we identified 18 differentially expressed neutrophil extracellular trap- and mitophagy-related genes (NETMRDEGs), such as Results: The study identified distinct molecular clusters in PCOS patients based on the expression of NETMRDEGs. Cluster 2 exhibited higher immune infiltration (eg, gamma delta T cells and eosinophils) and severe metabolic dysfunction. The LASSO model achieved superior diagnostic performance (AUC: 0.93) compared to traditional biomarkers such as testosterone (AUC: 0.68). Experimental validation in a PCOS mouse model confirmed elevated expression of hub genes ( Conclusion: The interaction between NETRGs and MRGs forms a "dual-engine" mechanism driving PCOS pathogenesis. This study proposed a novel diagnostic model and therapeutic targets (eg, DNase I and urolithin A), advancing precision medicine for PCOS.

Indexed as

diagnostic modelimmune infiltrationmitochondria-related genesneutrophil extracellular trapspolycystic ovary syndrome

Identifiers

PMID41978723
PMCPMC13070342

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.