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Vascular dysfunction and body mass index in African adults with HIV

BACKGROUND: Impaired vascular compliance is common among persons with HIV (PWH) and a risk factor for cardiovascular disease (CVD), though many studies documenting this are from regions with a high prevalence of overweight and obesity. The prevalence and characteristics of impaired vascular complian...

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Autores principales: Kaluba, Longa, Chikopela, Theresa, Goma, Fastone, Malambo, Mordecai, Mutale, Wilbroad, Heimburger, Douglas C., Koethe, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896806/
https://www.ncbi.nlm.nih.gov/pubmed/36737679
http://dx.doi.org/10.1186/s12872-023-03093-2
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author Kaluba, Longa
Chikopela, Theresa
Goma, Fastone
Malambo, Mordecai
Mutale, Wilbroad
Heimburger, Douglas C.
Koethe, John R.
author_facet Kaluba, Longa
Chikopela, Theresa
Goma, Fastone
Malambo, Mordecai
Mutale, Wilbroad
Heimburger, Douglas C.
Koethe, John R.
author_sort Kaluba, Longa
collection PubMed
description BACKGROUND: Impaired vascular compliance is common among persons with HIV (PWH) and a risk factor for cardiovascular disease (CVD), though many studies documenting this are from regions with a high prevalence of overweight and obesity. The prevalence and characteristics of impaired vascular compliance among PWH with low body mass index (BMI) is not well described, particularly in sub-Saharan Africa (SSA) where the majority of PWH live, a low BMI is more common, and the burden of CVD is rising. AIM: To assess non-invasive vascular compliance measurements, including augmentation index (AIX), pulse wave velocity (PWV) and pulse waveforms, in underweight, normal weight, and overweight PWH on long-term antiretroviral therapy (ART) in SSA. METHODS: A cross-sectional study among PWH on ART at the University Teaching Hospital in Lusaka, Zambia. All participants had been on a regimen of efavirenz, emtricitabine, and tenofovir disoproxil fumarate for five or more years. Carotid-femoral PWV (cfPWV), carotid-radial PWV (crPWV), and the corresponding augmentation indexes (cfAIX and crAIX), were measured in all participants, in addition to aortic pressure waveforms, classified as type A, B, C and D according to reflected wave timings and amplitude. Multiple linear regression assessed relationships between demographic and clinical factors with vascular measurement endpoints. RESULTS: Ninety one PWH on long-term ART were enrolled; 38 (42%) were underweight (BMI < 18.5 kg/m(2)), 43 (47%) were normal weight (18.5–24.9 kg/m(2)) and 10 (11%) were overweight (> 25 kg/m(2)). Median age was 41, 40 and 40 years, among the three groups, respectively, and the proportion of women increased with BMI level. Overweight participants had a 39% higher cfAIX compared to normal-weight participants, while being underweight was associated with 27% lower cfAIX, after adjusting for age, sex and blood pressure (P = 0.02 and P = 0.01, respectively), but measurements of cfPWV, crPWV and crAIX did not differ. CONCLUSION: Underweight PWH in SSA had lower cfAIX measurements compared to normal weight individuals, indicating less arterial stiffness. However, similar cfPWV, crPWV and crAIX values among the underweight and overweight PWH suggest a low BMI may not confer substantial protection against impaired vascular compliance as a contributor to CVD risk among individuals on ART.
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spelling pubmed-98968062023-02-04 Vascular dysfunction and body mass index in African adults with HIV Kaluba, Longa Chikopela, Theresa Goma, Fastone Malambo, Mordecai Mutale, Wilbroad Heimburger, Douglas C. Koethe, John R. BMC Cardiovasc Disord Research BACKGROUND: Impaired vascular compliance is common among persons with HIV (PWH) and a risk factor for cardiovascular disease (CVD), though many studies documenting this are from regions with a high prevalence of overweight and obesity. The prevalence and characteristics of impaired vascular compliance among PWH with low body mass index (BMI) is not well described, particularly in sub-Saharan Africa (SSA) where the majority of PWH live, a low BMI is more common, and the burden of CVD is rising. AIM: To assess non-invasive vascular compliance measurements, including augmentation index (AIX), pulse wave velocity (PWV) and pulse waveforms, in underweight, normal weight, and overweight PWH on long-term antiretroviral therapy (ART) in SSA. METHODS: A cross-sectional study among PWH on ART at the University Teaching Hospital in Lusaka, Zambia. All participants had been on a regimen of efavirenz, emtricitabine, and tenofovir disoproxil fumarate for five or more years. Carotid-femoral PWV (cfPWV), carotid-radial PWV (crPWV), and the corresponding augmentation indexes (cfAIX and crAIX), were measured in all participants, in addition to aortic pressure waveforms, classified as type A, B, C and D according to reflected wave timings and amplitude. Multiple linear regression assessed relationships between demographic and clinical factors with vascular measurement endpoints. RESULTS: Ninety one PWH on long-term ART were enrolled; 38 (42%) were underweight (BMI < 18.5 kg/m(2)), 43 (47%) were normal weight (18.5–24.9 kg/m(2)) and 10 (11%) were overweight (> 25 kg/m(2)). Median age was 41, 40 and 40 years, among the three groups, respectively, and the proportion of women increased with BMI level. Overweight participants had a 39% higher cfAIX compared to normal-weight participants, while being underweight was associated with 27% lower cfAIX, after adjusting for age, sex and blood pressure (P = 0.02 and P = 0.01, respectively), but measurements of cfPWV, crPWV and crAIX did not differ. CONCLUSION: Underweight PWH in SSA had lower cfAIX measurements compared to normal weight individuals, indicating less arterial stiffness. However, similar cfPWV, crPWV and crAIX values among the underweight and overweight PWH suggest a low BMI may not confer substantial protection against impaired vascular compliance as a contributor to CVD risk among individuals on ART. BioMed Central 2023-02-03 /pmc/articles/PMC9896806/ /pubmed/36737679 http://dx.doi.org/10.1186/s12872-023-03093-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kaluba, Longa
Chikopela, Theresa
Goma, Fastone
Malambo, Mordecai
Mutale, Wilbroad
Heimburger, Douglas C.
Koethe, John R.
Vascular dysfunction and body mass index in African adults with HIV
title Vascular dysfunction and body mass index in African adults with HIV
title_full Vascular dysfunction and body mass index in African adults with HIV
title_fullStr Vascular dysfunction and body mass index in African adults with HIV
title_full_unstemmed Vascular dysfunction and body mass index in African adults with HIV
title_short Vascular dysfunction and body mass index in African adults with HIV
title_sort vascular dysfunction and body mass index in african adults with hiv
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896806/
https://www.ncbi.nlm.nih.gov/pubmed/36737679
http://dx.doi.org/10.1186/s12872-023-03093-2
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