Evidence map›Paper›PMID 36035955›Full record

ArticleFrontiers in cardiovascular medicine2022

HADH may be the target molecule of early vascular endothelial impairment in T2DM.

Haowen Ye, Ruxin Wang, Jinjing Wei, Ying Wang, Lihong Wang, Xiaofang Zhang

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2022. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. MODY Only Monogenic? A Narrative Review of theInternational journal of molecular sciences · 2024
    Review
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.

Haowen YeDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Jinan University, Guangzhou, China.
Ruxin WangDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Jinan University, Guangzhou, China.
Jinjing WeiDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Jinan University, Guangzhou, China.
Ying WangDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Jinan University, Guangzhou, China.
Lihong WangDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Jinan University, Guangzhou, China.
Xiaofang ZhangDepartment Clinical Experimental Center, First Affiliated Hospital of Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Type 2 diabetes mellitus (T2DM) will significantly increase the risk of atherosclerosis (AS). Vascular endothelial cell dysfunction (VECD) is the foundation of AS. Early identification and intervention of VECD caused by T2DM can help us effectively delay or even suppress the occurrence of AS. Methods: We downloaded the gene expression profiles from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) were identified in R software and weighted gene co-expression network analysis (WGCNA) was performed to further screen the target genes. In addition, we used the receiver operating characteristic curve (ROC curve) to verify the diagnostic efficiency of target genes. Finally, target genes were validated by quantitative polymerase chain reaction (qPCR). Results: Four target genes ( Conclusion:

Indexed as

ASendothelial cell dysfunctionGEOT2DMWGCNA

Identifiers

PMID36035955
PMCPMC9399638

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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.