Evidence map›Paper›PMID 33910166›Full record

ArticleAging2021

Bioinformatics analysis of the molecular mechanism of obesity in polycystic ovary syndrome.

Jiaojiao Zhou, Xiaolin Huang, Bingshuang Xue, Yuhe Wei, Fei Hua

Open access · greenAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.8field-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

5 citing papers in PubMed, 21 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Jiaojiao ZhouDepartment of Endocrinology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, China.
Xiaolin HuangDepartment of Endocrinology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, China.
Bingshuang XueDepartment of Endocrinology, The Affiliated Wujin Hospital of Jiangsu University, Changzhou, Jiangsu 213017, China.
Yuhe WeiDepartment of Endocrinology, The Affiliated Wujin Hospital of Jiangsu University, Changzhou, Jiangsu 213017, China.
Fei HuaDepartment of Endocrinology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, China.
Jiangsu University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity is an important part of polycystic ovary syndrome (PCOS) pathologies. The present study utilized the bioinformatics method to identify the molecular mechanism of obesity status in PCOS.

methodsSix transcriptome profiles of adipose tissue were obtained from online databases. The background correction and normalization were performed, and the DEGs were detected with the settings

resultsA total of 37 DGEs were found between obesity PCOS and healthy controls, and 8 of them were tested significant in the third database. The expression patterns of the 8 detected DGEs were then measured in another two datasets based on lean/obesity PCOS patients and healthy controls. The gene CHRDL1 was found to be in linear regression with the BMI index in PCOS patients (

conclusionIn summary, the present study identified CHRDL1 as a candidate gene responsible for the obesity of PCOS patients.

Indexed as

Body Mass IndexBone Morphogenetic Protein 4Eye ProteinsFemaleHumansInsulin-Like Growth Factor INerve Tissue ProteinsObesityPolycystic Ovary SyndromeSignal TransductionBMP4 protein, humanBone Morphogenetic Protein 4CHRDL1 protein, humanEye ProteinsIGF1 protein, humanInsulin-Like Growth Factor INerve Tissue ProteinsbioinformaticsCHRDL1obesityPCOS

Identifiers

PMID33910166
PMCPMC8148487
OpenAlexW3157033578

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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.