Evidence map›Paper›PMID 40995065›Full record

ArticleHuman mutation2025

Identification of ARHGAP9 as a Key Diagnostic Marker for Abdominal Aortic Aneurysm by Multiomics and Experimental Validation.

Zhe Peng, Kun Li, Shile Wu, Baozhang Chen, Xiaonan Wang, Liang Chen, Xinsheng Wang, Hao Zhang, Biao Wu

Abstract read
In one paragraph

Article in Human mutation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Zhe PengDepartment of General Surgery, Qinghai Province People's Hospital, Xining, Qinghai, China.ORCID https://orcid.org/0000-0002-3431-4409
Kun LiDepartment of Vascular Surgery, Changhai Hospital, Shanghai, China.ORCID https://orcid.org/0009-0006-1648-8508
Shile WuDepartment of General Surgery, Qinghai Province People's Hospital, Xining, Qinghai, China.ORCID https://orcid.org/0009-0008-5798-1133
Baozhang ChenDepartment of General Surgery, Qinghai Province People's Hospital, Xining, Qinghai, China.ORCID https://orcid.org/0009-0007-7372-923X
Xiaonan WangDepartment of Vascular Surgery, Changhai Hospital, Shanghai, China.ORCID https://orcid.org/0009-0001-1315-9534
Liang ChenDepartment of Vascular Surgery, Changhai Hospital, Shanghai, China.ORCID https://orcid.org/0009-0001-7414-3923
Xinsheng WangDepartment of General Surgery, Qinghai Province People's Hospital, Xining, Qinghai, China.ORCID https://orcid.org/0009-0005-4631-3808
Hao ZhangDepartment of Vascular Surgery, 967 Hospital of the Joint Logistics Support Force of PLA, Dalian, Liaoning, China.ORCID https://orcid.org/0009-0000-8387-2477
Biao WuDepartment of Vascular Surgery, Changhai Hospital, Shanghai, China.ORCID https://orcid.org/0009-0008-9870-268X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abdominal aortic aneurysm (AAA) is a serious vascular condition that significantly endangers the lives of patients. Although there have been improvements in early detection and treatment methods, considerable challenges persist regarding the timely identification and evaluation of risk associated with this disease. Therefore, there is an immediate requirement for novel biomarkers that can enhance the early diagnosis and risk evaluation of AAA, thus allowing for more accurate and individualized medical interventions. In this study, we identified key diagnostic markers for AAA using various machine learning algorithms, and we explored the functions of these genes in AAA through gene enrichment analysis. A diagnostic model for AAA was constructed based on multiple machine learning algorithms, with the random forest algorithm highlighting the central role of ARHGAP9. In vitro experiments confirmed the influence of ARHGAP9 on vascular smooth muscle cells (VSMCs). Our findings indicate that the key genes identified are associated with the immune microenvironment and metabolism in AAA samples. The validated diagnostic model exhibited excellent predictive performance. Knockdown of ARHGAP9 significantly inhibited the proliferative capacity of VSMCs. In conclusion, our results suggest that ARHGAP9 may serve as a diagnostic and therapeutic marker for AAA.

Indexed as

Aortic Aneurysm, AbdominalBiomarkersGTPase-Activating ProteinsCell ProliferationHumansMachine LearningMaleMultiomicsMuscle, Smooth, VascularMyocytes, Smooth MuscleBiomarkersGTPase-Activating Proteinsabdominal aortic aneurysmARHGAP9biomarkermachine learning

Identifiers

PMID40995065
PMCPMC12457051

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.