Evidence map›Paper›PMID 36118846›Full record

ArticleFrontiers in genetics2022

Molecular subtype identification and predictive power of N6-methyladenosine regulator in unexplained recurrent pregnancy loss.

Jiahui Huo, Qian Chen, Yutong Zhang, Nuo Li, Zhiyu Fu, Ning Ma, Nan Zheng, Nan Cui, Lu Li

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

9 authors.

Jiahui HuoDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Qian ChenDepartment of Reproductive Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yutong ZhangDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Nuo LiDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Zhiyu FuDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Ning MaDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Nan ZhengDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.
Nan CuiDepartment of Reproductive Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Lu LiDepartment of Social Medicine and Health Care Management, School of Public Health, Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The etiology of recurrent pregnancy loss (RPL) is complicated and effective clinical preventive measures are lacking. Identifying biomarkers for RPL has been challenging, and to date, little is known about the role of N6-methyladenosine (m6A) regulators in RPL. Expression data for m6A regulators in 29 patients with RPL and 29 healthy controls were downloaded from the Gene Expression Omnibus (GEO) database. To establish a diagnostic model for unexplained RPL, differential gene expression analysis was conducting for 36 m6A regulators using least absolute shrinkage and selection operator (LASSO) regression. Unsupervised cluster analysis was conducted on hub genes, and probable mechanisms were explored using gene set enrichment analysis (GSEA) and gene ontology (GO) analysis. Correlations between m6A-related differentially expressed genes and immune infiltration were analyzed using single-sample GSEA. A total of 18 m6A regulators showed significant differences in expression in RPL: 10 were upregulated and eight were downregulated. Fifteen m6A regulators were integrated and used to construct a diagnostic model for RPL that had good predictive efficiency and robustness in differentiating RPL from control samples, with an overall area under the curve (AUC) value of 0.994. Crosstalk was identified between 10 hub genes, miRNAs, and transcription factors (TFs). For example,

Indexed as

diagnostic modelimmune cell infiltrationN6-methyladenosinerecurrent pregnancy lossYTHDF2

Identifiers

PMID36118846
PMCPMC9478558

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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.