Evidence map›Paper›PMID 40391054›Full record

ArticleTexas Heart Institute journal

A Proposed Genetic Risk Score for Dilated Cardiomyopathy Susceptibility in the Chinese Han Population.

Jianjun Lan, Lin Wang, Guoyuan Qiu, Shihai Wang, Chao Yang, Mengnian Ran, Hongyu Li, Shiyang Li

Abstract read
In one paragraph

Article in Texas Heart Institute journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Jianjun LanDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.
Lin WangDepartment of Psychiatry, the Third People's Hospital of Panzhihua, Panzhihua, China.
Guoyuan QiuClinical Laboratory Center, Panzhihua Central Hospital, Panzhihua, China.
Shihai WangDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.
Chao YangDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.
Mengnian RanDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.
Hongyu LiDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.
Shiyang LiDivision of Cardiology, Panzhihua Central Hospital, Panzhihua, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dilated cardiomyopathy (DCM) is one of the most common types of cardiomyopathies. The current study constructs a proposed genetic risk score and assesses its potential as a predictive tool for individual DCM susceptibility. Methods: A total of 1,000 patients with idiopathic DCM and 828 control participants from the study institution were enrolled. The top 25 up-regulated and down-regulated genes from tandem mass spectrometry analysis of 6 hearts with DCM and 7 control hearts (from a study by Chen et al) were selected for logistic analysis using whole-exome sequencing data. Statistically significant variants were prepared for genetic risk score construction. The predictive power of the genetic risk score and a composite variable for DCM risk were evaluated using receiver operating characteristic curve analysis. Results: A total of 5 variants associated with DCM susceptibility were identified to develop the genetic risk score. A score of at least 6.4 was more strongly associated with increased risk of DCM (odds ratio, 2.4; Conclusion: The genetic risk score, which consists of 5 variants, could effectively identify individuals at high risk of DCM in the study population and aid in the implementation of early prevention strategies in clinical practice.

Indexed as

Cardiomyopathy, DilatedEast Asian PeopleGenetic Predisposition to DiseaseAdultCase-Control StudiesChinaFemaleGenetic Risk ScoreHumansMaleMiddle AgedPhenotypeRisk AssessmentRisk FactorsROC CurveCardiomyopathy, dilatedgenetic risk scoreprediction algorithmsrisk

Identifiers

PMID40391054
PMCPMC12086268

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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.