Evidence map›Paper›PMID 40289511›Full record

ArticleScience progress

Association of angiotensin I converting enzyme gene I/D polymorphism and coronary artery disease in the Pakistani population.

Nusrat Saba, Sadia Rehman, Saeeda Munir, Amna Noor

Abstract read
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Article in Science progress. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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

4 authors.

Nusrat SabaInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.ORCID 0000-0002-1577-9972
Sadia RehmanInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Saeeda MunirInstitute of Biomedical and Genetic Engineering, Islamabad, Pakistan.
Amna NoorRawalpindi Medical University Rawalpindi, Rawalpindi, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveThe aim of this study was to investigate the association between angiotensin I converting enzyme gene polymorphism and coronary artery disease in the Pakistani population, given the early onset and aggressive nature of coronary artery disease in this region.MethodsA case-control study was conducted involving 540 Pakistani patients with established coronary artery disease and 224 healthy controls. DNA samples were amplified using polymerase chain reaction with primers targeting the insertion (I)/deletion (D) sites of intron 16 of the angiotensin I converting enzyme gene. The polymerase chain reaction products were analyzed for the presence of 490-bp (II), 190-bp (DD), or both (ID) fragments.ResultsThe frequency of the homozygous insertion (II) genotype was 9% in the control group and 25% in coronary artery disease patients, while the homozygous deletion (DD) genotype was 26% in controls and 24% in patients. A significant association was found between the angiotensin I converting enzyme II genotype and coronary artery disease (odds ratio = 7.963,

Indexed as

Coronary Artery DiseaseINDEL MutationPeptidyl-Dipeptidase APolymorphism, GeneticAdultAgedCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPakistanACE protein, humanPeptidyl-Dipeptidase AAngiotensin I converting enzymeangiotensin I converting enzyme I/D polymorphismcoronary artery diseasegenetic predispositionPakistani population

Identifiers

PMID40289511
PMCPMC12035323

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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.