Evidence map›Paper›PMID 39841754›Full record

ArticleArquivos brasileiros de cardiologia2025

Influence of Insertion/Deletion Polymorphism of the Angiotensin Converting Enzyme Gene on Adiposity and Cardiac Function in Patients with Heart Failure.

Marla Darlene Machado Vale, Édina Caroline Ternus Ribeiro, Ingrid da Silveira Knobloch, Ida Vanessa Doederlein Schwartz, Fernanda Sperb-Ludwig, Gabriela Corrêa Souza

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Article in Arquivos brasileiros de cardiologia, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Marla Darlene Machado ValePrograma de Pós-Graduação em Alimentação, Nutrição e Saúde - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil.ORCID 0009-0004-7024-0701
Édina Caroline Ternus RibeiroHospital de Clínicas de Porto Alegre, Porto Alegre, RS - Brasil.ORCID 0000-0001-7017-0599
Ingrid da Silveira KnoblochPrograma de Pós-Graduação em Ciências da Saúde - Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS - Brasil.
Ida Vanessa Doederlein SchwartzHospital de Clínicas de Porto Alegre, Porto Alegre, RS - Brasil.
Fernanda Sperb-LudwigPrograma de Pós-Graduação em Genética e Biologia Molecular - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil.
Gabriela Corrêa SouzaPrograma de Pós-Graduação em Alimentação, Nutrição e Saúde - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil.ORCID 0000-0002-3620-4334

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism (rs4340) is associated with the pathogenesis of heart failure (HF). This polymorphism may contribute to a greater propensity for severe HF and excess weight.

objectiveTo evaluate adiposity, cardiac function, and their association with ACE I/D polymorphism in HF patients.

methodsCross-sectional study with ambulatory individuals ≥18 years diagnosed with HF. Genetic analysis was performed using polymerase chain reaction followed by agarose gel electrophoresis. Left ventricular ejection fraction (LVEF) was determined by echocardiography. Nutritional status was assessed using body mass index, while adiposity was analyzed using bioelectrical impedance analysis (BIA), waist circumference, waist-to-hip ratio, and waist-to-height ratio. The adopted significance level was 5% (p < 0.05).

resultsSeventy-one individuals were included, with a mean age of 55.8 ± 13.0 years, predominantly male (66.2%), with functional class I and II (90.9%), and a median LVEF of 30% (24-40). The prevalence of overweight was 38%, class I obesity was 23.9%, and class II and III obesity was 12.7%, with 50.7% exhibiting excess adiposity as assessed by BIA. A total of 88 D alleles and 54 I alleles of the ACE gene were identified. Regarding ACE genotypes, 38.1% were DD, 47.8% were ID, and 14.1% were II. In the multivariate analysis, the D allele (DD + ID genotypes versus II) was associated with LVEF (PR 0.995; 95% CI 0.991-1.000; p = 0.048) and with the etiology of HF (dilated cardiomyopathy: PR 1.283; 95% CI 1.039-1.583; p = 0.021). No independent association was found with adiposity.

conclusionThe presence of the D allele of the ACE polymorphism is associated with LVEF and HF etiology. Despite overweight being prevalent in the sample, no independent associations were found.

Indexed as

AdiposityHeart FailureINDEL MutationPeptidyl-Dipeptidase APolymorphism, GeneticAdultAgedBody Mass IndexCross-Sectional StudiesFemaleGenotypeHumansMaleMiddle AgedPolymerase Chain ReactionStroke VolumePeptidyl-Dipeptidase A

Identifiers

PMID39841754
PMCPMC11841369

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