Evidence map›Paper›PMID 40783527›Full record

ArticleBiomedical engineering online2025

Cholesterol homeostasis and pathway enrichment in post-revascularization recovery.

Syed Abdullah Basit, Nehad M Alajez, Tanvir Alam

Abstract read
In one paragraph

Article in Biomedical engineering online, 2025. 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

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2 · The registry

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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.

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4 · The record

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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

3 authors.

Syed Abdullah BasitCollege of Science and Engineering, Hamad Bin Khalifa University (HBKU), Qatar Foundation (QF), Doha, Qatar.
Nehad M AlajezTranslational Oncology Research Center (TORC), Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation (QF), Doha, Qatar.
Tanvir AlamCollege of Science and Engineering, Hamad Bin Khalifa University (HBKU), Qatar Foundation (QF), Doha, Qatar. talam@hbku.edu.qa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHeart revascularization is a critical intervention for restoring myocardial perfusion in patients with ischemic cardiovascular disease. While the procedure alleviates ischemia, it also triggers systemic metabolic and transcriptional changes, particularly in lipid metabolism.

methodsIn this pilot study, we utilized RNA-seq data from 4 revascularized patients and 5 control participants from the Qatar Biobank (QBB) to investigate the effects of revascularization on cholesterol biosynthesis and metabolic pathways. Differential gene expression analysis was performed to identify key regulatory genes, followed by pathway enrichment and Gene Ontology analyses.

resultsThirteen differentially expressed genes, including ABCG1, EBP, and LPCAT3, were identified as potentially involved in cholesterol regulation, lipid remodeling, and sterol metabolism. Notably, ABCG1, EBP, and LPCAT3 showed significant downregulation. Correlation analysis revealed strong associations between gene expression and clinical parameters, with ABCG1 expression negatively correlating with triglyceride levels (r = - 0.89, p = 0.001).

conclusionThis exploratory study provides preliminary evidence that heart revascularization may affect cholesterol-related metabolic pathways. While the small sample size (n = 4 revascularized patients) limits generalizability, these findings generate important hypotheses regarding post-revascularization metabolic adaptation and establish a foundation for larger validation studies. Future research with expanded cohorts is essential to confirm these preliminary observations and their therapeutic implications.

Indexed as

CholesterolHomeostasisMyocardial RevascularizationAgedATP Binding Cassette Transporter, Subfamily G, Member 1FemaleGene Expression ProfilingGene Expression RegulationHumansMaleMiddle AgedPilot ProjectsATP Binding Cassette Transporter, Subfamily G, Member 1CholesterolCholesterol biosynthesisCoronary artery diseaseHeart revascularizationQatar BiobankRNA-Seq analysis

Identifiers

PMID40783527
PMCPMC12335785

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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.