Evidence map›Paper›PMID 42118761›Full record

ArticlePLOS global public health2026

Determinants of left ventricular hypertrophy in a cohort attending a medical clinic: A comparative analysis stratified by sex.

Sydney Mulamfu, David Chisompola, Martin Chakulya, John Nzobokela, Phinnoty Mwansa, Benson M Hamooya, Joreen P Povia, Sepiso K Masenga

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Article in PLOS global public health, 2026. 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

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2 · The registry

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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

8 authors.

Sydney MulamfuDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.
David ChisompolaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.ORCID https://orcid.org/0000-0002-3765-0635
Martin ChakulyaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.
John NzobokelaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.
Phinnoty MwansaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.ORCID https://orcid.org/0009-0004-9244-7287
Benson M HamooyaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.
Joreen P PoviaDepartment of Health Economics, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.
Sepiso K MasengaDepartment of Cardiovascular Science and Metabolic Diseases, Livingstone Center for Prevention and Translational Science, Livingstone, Zambia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Left ventricular hypertrophy (LVH) is a significant cardiovascular complication in sub-Saharan Africa. However, sex-specific determinants of LVH in this population remain poorly understood. This study aimed to identify factors associated with LVH in a cohort attending medical clinic, stratified by sex. We conducted a cross-sectional analysis of 333 adults attending an outpatient clinic at Livingstone Teaching Hospital, Zambia. LVH was diagnosed by echocardiography. Data on demographics, clinical history (HIV, TB, hypertension) and metabolic profiles were collected. Univariable and multivariable logistic regression models were used to identify predictors of LVH in the overall cohort and in sex-stratified subgroups. p < 0.05 was considered statistically significant. Data from 333 participants were analysed. LVH was diagnosed in 75 participants (22.5%). In the overall cohort, independent factors associated with LVH were older age (AOR: 1.06 per year, 95% CI: 1.03-1.09, p < 0.0001), female sex (AOR: 2.31, 95% CI: 1.13-4.68, p = 0.020), hypertension (AOR: 2.52, 95% CI: 1.36-4.66, p = 0.003), and heart failure (AOR: 7.50, 95% CI: 1.85-30.3, p = 0.005). Sex-stratified analysis revealed distinct profiles: in males, LVH was significantly associated with older age (AOR: 1.06, 95% CI: 1.00-1.13, p = 0.030), hypertension (AOR: 3.70, 95% CI: 1.03-13.2, p = 0.044), and heart failure (AOR: 18.3, 95% CI: 1.60-209.0, p = 0.019), whereas in females, factors associated with LVH included older age (AOR: 1.06, 95% CI: 1.03-1.09, p < 0.0001), hypertension (AOR: 2.50, 95% CI: 1.21-5.18, p = 0.013), waist circumference (AOR: 1.05 per cm, 95% CI: 1.00-1.10, p = 0.047), and elevated cholesterol-HDL ratio (AOR: 1.53, 95% CI: 1.02-2.30, p = 0.036). LVH in this cohort was associated with age, female sex, hypertension, and heart failure. Factors associated with LVH differed by sex, with metabolic factors playing a more prominent role in women and hemodynamic factors in men. These findings underscore the importance of sex-specific cardiovascular risk assessment and tailored management strategies.

Identifiers

PMID42118761
PMCPMC13166945

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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.