Evidence map›Paper›PMID 35794640›Full record

ArticleJournal of ovarian research2022

Identification of novel candidate biomarkers and immune infiltration in polycystic ovary syndrome.

Zhijing Na, Wen Guo, Jiahui Song, Di Feng, Yuanyuan Fang, Da Li

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 7% of its field
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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  12. Biomarkers in Polycystic Ovary Syndrome.Current opinion in physiology · 2023
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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

6 authors at 1 institution in 1 country.

Zhijing Na *Center of Reproductive Medicine, Shengjing Hospital of China Medical University, No.36, SanHao Street, Shenyang, 110004, China.
Wen Guo *Department of Neurology, The First Hospital of China Medical University, Shenyang, 110002, China.
Jiahui SongCenter of Reproductive Medicine, Shengjing Hospital of China Medical University, No.36, SanHao Street, Shenyang, 110004, China.
Di FengEducation Center for Clinical Skills Practice of China Medical University, Shenyang, 110122, China.
Yuanyuan FangCenter of Reproductive Medicine, Shengjing Hospital of China Medical University, No.36, SanHao Street, Shenyang, 110004, China. fangyy_sj@sina.com.
Da LiCenter of Reproductive Medicine, Shengjing Hospital of China Medical University, No.36, SanHao Street, Shenyang, 110004, China. leeda@ymail.com.
China Medical University · CN

Funding

Fok Ying Tung Education Foundation No. 151039Key Research and Development Program of Liaoning Province NO. 2018225062LiaoNing Revitalization Talents Program No. XLYC1907071National Natural Science Foundation of China No. 82071607Outstanding Scientific Fund of Shengjing Hospital No.202003
6 · The paper itself

Abstract

backgroundIn this study, we aimed to identify novel biomarkers for polycystic ovary syndrome (PCOS) and analyze their potential roles in immune infiltration during PCOS pathogenesis.

methodsFive datasets, namely GSE137684, GSE80432, GSE114419, GSE138518, and GSE155489, were obtained from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were selected from the train datasets. The least absolute shrinkage and selection operator logistic regression model and support vector machine-recursive feature elimination algorithm were combined to screen potential biomarkers. The test datasets validated the expression levels of these biomarkers, and the area under the curve (AUC) was calculated to analyze their diagnostic value. Quantitative real-time PCR was conducted to verify biomarkers' expression in clinical samples. CIBERSORT was used to assess differential immune infiltration, and the correlations of biomarkers with infiltrating immune cells were evaluated.

resultsHerein, 1265 DEGs were identified between PCOS and control groups. The gene sets related to immune response and adaptive immune response were differentially activated in PCOS. The two diagnostic biomarkers of PCOS identified by us were HD domain containing 3 (HDDC3) and syndecan 2 (SDC2; AUC, 0.918 and 0.816, respectively). The validation of hub biomarkers in clinical samples using RT-qPCR was consistent with bioinformatics results. Immune infiltration analysis indicated that decreased activated mast cells (P = 0.033) and increased eosinophils (P = 0.040) may be a part of the pathogenesis of PCOS. HDDC3 was positively correlated with T regulatory cells (P = 0.0064), activated mast cells (P = 0.014), and monocytes (P = 0.024) but negatively correlated with activated memory CD4 T cells (P = 0.016) in PCOS. In addition, SDC2 was positively correlated with activated mast cells (P = 0.0021), plasma cells (P = 0.0051), and M2 macrophages (P = 0.038) but negatively correlated with eosinophils (P = 0.01) and neutrophils (P = 0.031) in PCOS.

conclusionHDDC3 and SDC2 can serve as candidate biomarkers of PCOS and provide new insights into the molecular mechanisms of immune regulation in PCOS.

Indexed as

Polycystic Ovary SyndromeArea Under CurveBiomarkersComputational BiologyFemaleHumansReal-Time Polymerase Chain ReactionBiomarkersBiomarkersCIBERSORTImmune infiltrationMachine learning algorithmPolycystic ovary syndrome

Identifiers

PMID35794640
PMCPMC9258136
OpenAlexW4283829937

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.