Evidence map›Paper›PMID 23685945›Full record

ArticleJournal of endocrinological investigation2013

Angiotensin-converting enzyme gene insertion/deletion polymorphism with metabolic syndrome in Turkish patients.

S Simsek, S Tekes, A Turkyilmaz, A K Tuzcu, F Kılıc, N N Culcu, B Isık, H Akbas

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Article in Journal of endocrinological investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing 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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

S SimsekDepartment of Medical Biology and Genetics, University of Dicle, Medical School, Diyarbakir, Turkey. seldatsimsek@gmail.com.
S Tekes
A Turkyilmaz
A K Tuzcu
F Kılıc
N N Culcu
B Isık
H Akbas

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe ACE gene has received substantial attention in recent years as candidate for a variety of diseases. The most common polymorphism in ACE gene is the Insertion/Deletion (I/D, rs4646994) polymorphism located on intron 16.

aimWe investigated the association between metabolic syndrome (MS) and the insertion (I) - deletion (D) polymorphisms in the angiotensin converting enzyme (ACE) gene in south-east of Turkey. SUBJECTS AND

methodsOne hundred and sixty subjects, with 101 cases of MS and 59 age- and gender-matched healthy controls were included in the study.

resultsThe frequency of ACE I/D polymorphism was found to be 49.5% for DD, 36.6% for ID, and 13.9% for II in the MSstudy group and 44.1% for DD, 42.4% for ID and 13.5% for II in the control group. Allele frequencies were found to be 0.68% for D and 0.32% for I allele in the study group with MS and 0.65% for D, 0.35% for I allele in the control group. The I/D polymorphism of the ACE gene, DD, ID, and II genotypes occurred with similar frequencies in the study group with MS and the control group with no significant differences (p<0.05). On applying one-way analysis of variance to different ACE gene polymorphic groups in patients with MS were not significantly associated to ACE gene polymorphism and waist circumference, systolic blood pressure, diastolic blood pressure, fasting blood glucose, HDL, and LDL (p<0.05).

conclusionsFurther studies of patients in larger numbers and of different ethnic backgrounds may be necessary to elucidate the association between the ACE I/D gene polymorphism and MS.

Indexed as

Gene DeletionMutagenesis, InsertionalAdultCase-Control StudiesDNAFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansMaleMetabolic SyndromeMiddle AgedPeptidyl-Dipeptidase APolymerase Chain ReactionPolymorphism, GeneticACE protein, humanDNAPeptidyl-Dipeptidase A

Identifiers

PMID23685945

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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.