Evidence map›Paper›PMID 40842897›Full record

ArticleReports of biochemistry & molecular biology2025

Investigation of Genetic Variations in APLN and APLNR Genes and Their Potential Role in Cardiovascular Diseases.

Nabaa Azhar Abdulmuttaleb, Abdelhameed Abdelkhaliq Oliwi Nasir, Sami Awad Alkubaisy, Osama Akram Mohsein

Abstract read
In one paragraph

Article in Reports of biochemistry & molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nabaa Azhar AbdulmuttalebDepartment of Clinical Laboratories, College of Applied Medical Sciences, University of Kerbala, Iraq.
Abdelhameed Abdelkhaliq Oliwi NasirAl Iraqia University, College of Dentistry, Iraq.
Sami Awad AlkubaisyCenter of Desert Studies, University of Anbar, Iraq.
Osama Akram MohseinDepartment of Medical Laboratory Techniques, Mazaya University College, Thi-Qar, Iraq.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Apelin is a naturally produced ligand for G protein-linked receptors derived from a 77-amino acid pre-propeptide. The effect of apelin on the development of cardiovascular diseases and the relationship between the apelin gene and the apelin receptor. Methods: The case-control study included 100 participants of people suffering from cardiovascular diseases. Samples were collected from patients hospitalized at the Nasiriyah Heart Center between November 10, 2023, and February 15, 2024. The study also included 50 healthy people who did not suffer from cardiovascular disease. The lipid profile was measured by spectrophotometer, and the Apelin level was measured by enzyme-linked immunosorbent assay. Four single nucleotide polymorphisms for Apelin (APLN) and Apelin receptor (APLNR) were chosen, and Sanger sequencing was used to genotype them accurately. Results: The findings indicated that there was no statistically significant difference in age between the two groups. Upon comparing the age demographics of the two groups in the study, the results indicated a lack of statistical significance in the levels of APLN or the lipid profile, despite the case group exhibiting markedly elevated Apelin and lipid levels compared to the control group. After multiple test adjustments (P < 0.05), neither the APLN rs2235310T allele nor the APLNR rs9943582 allele demonstrated an association with an elevated risk of coronary heart disease. Conclusions: The investigation revealed no significant age variations or genetic correlations associated with CHD risk. However, rather than age or genetic differences, elevated apelin and cholesterol levels in the case group indicate these factors as primary contributors to cardiovascular risk.

Indexed as

Apelin ReceptorsCardiacLipid MetabolismPolymorphismRisk factors

Identifiers

PMID40842897
PMCPMC12367213

What Socratic holds

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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 Socratic graph.