Evidence map›Paper›PMID 40159225›Full record

ArticleJournal of atherosclerosis and thrombosis2025

Sex-Specific Association between HO-1 (GT)n Promoter Polymorphism and Large-Artery Atherosclerosis Stroke.

Jintao Li, Junting Chen, Jia Wen, Kailin Cheng, Xiaoli Fu, Shuen Li, Zhu Shi

Abstract read
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2025. 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

7 authors.

Jintao LiDepartment of Neurology and Stroke Center, The 10th Affiliate Hospital, Southern Medical University.
Junting ChenDepartment of Neurology, Houjie Hospital of Dongguan.
Jia WenThe 1st Clinical Medical School, Southern Medical University.
Kailin ChengDepartment of Neurology and Stroke Center, The 10th Affiliate Hospital, Southern Medical University.
Xiaoli FuDepartment of Neurology and Stroke Center, The 10th Affiliate Hospital, Southern Medical University.
Shuen LiDepartment of Neurology and Stroke Center, The 10th Affiliate Hospital, Southern Medical University.
Zhu ShiDepartment of Neurology and Stroke Center, The 10th Affiliate Hospital, Southern Medical University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsOxidative stress is a central factor in the pathogenesis of atherosclerosis and potentially exhibits sexual dimorphism. The induction of heme oxygenase-1 (HO-1) serves as a crucial mechanism against reactive oxygen species toxicity in the vascular wall, and this induction is regulated by the promoter (GT)n repeat length. We aim to investigate whether or not HO-1 gene (GT)n polymorphism is associated with the occurrence of large-artery atherosclerotic (LAA) stroke.

methodsWe consecutively recruited stroke patients, with a control group comprising age- and sex-matched non-stroke individuals. HO-1 (GT)n genotypes were determined using DNA extracted from the peripheral leukocytes. HO-1 (GT)n polymorphism was classified as short [S, ≤ 24 (GT)n], medium [M, 25 ≤ (GT)n <31], or long [L, 31 ≤ (GT)n]. Clinical data were collected, and stroke patients were categorized into LAA and non-LAA groups according to the TOAST classification. A multivariable logistic regression analysis was conducted to evaluate the association between HO-1 (GT)n variants and LAA occurrence stratified by sex.

resultsThere was no significant difference in the distribution of HO-1 (GT)n genotypes between the stroke and non-stroke populations. However, the proportion of S/S genotype was significantly lower in the LAA stroke patients than in the non-LAA stroke patients (7.08% vs. 21.78%, p<0.001). A multivariable logistic regression analysis indicated that non-SS genotypes were associated with a significantly increased risk of LAA compared to the S/S genotype patients (odds ratio [OR] 3.35, 95% confidence interval [CI] 1.98-5.67, p<0.001). After stratification by sex, the protective effect of the HO-1 (GT)n S/S genotype was highly significant in men (OR 5.50, 95% CI 2.67-11.34, p<0.001), whereas the association was not significant in women (OR 1.60, 95% CI 0.75-3.34, p = 0.228).

conclusionShort (GT)n variants in HO-1 may confer significant protection against LAA stroke in men but not in women.

Indexed as

AtherosclerosisGenetic Predisposition to DiseaseHeme Oxygenase-1Polymorphism, GeneticPolymorphism, Single NucleotidePromoter Regions, GeneticStrokeAgedCase-Control StudiesFemaleGenotypeHumansMaleMiddle AgedPrognosisRisk FactorsHeme Oxygenase-1HMOX1 protein, humanHO-1 geneLarger-artery atherosclerosisOxidative stressPolymorphismSexual dimorphismStroke

Identifiers

PMID40159225
PMCPMC12416964

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.