Sex differences in hypertension among people living with HIV after initiation of antiretroviral therapy.

HIV blood pressure dolutegravir incident hypertension lopinavir protease inhibitors sex differences

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 29 07 2022
accepted: 31 10 2022
entrez: 5 12 2022
pubmed: 6 12 2022
medline: 6 12 2022
Statut: epublish

Résumé

Hypertension is common in people living with HIV (PLWH) on antiretroviral therapy (ART). In the general population and in experimental animal models, the incidence of hypertension is greater in males than in females, especially during the premenopausal period. However, it is not known whether there are sex differences in hypertension associated with HIV and ART, and the factors contributing to incident hypertension among PLWH have not been well characterized. In this study, we aimed to determine the time course, sex differences and factors associated with incident hypertension in PLWH initiating ART. We conducted a retrospective study in which we used programmatic data from the ART registry to identify sex differences in the determinants of incident hypertension among PLWH initiating the ART regimen from Livingstone University Teaching Hospital in Zambia and followed for 8 years. Males developed hypertension earlier, 2 years after initiating ART, compared to 6 years in females. In multivariable analysis, increasing age, baseline systolic blood pressure and baseline mean arterial pressure (MAP) were associated with increased risk for developing incident hypertension. Also, participants who switched to the integrase strand transfer inhibitor, dolutegravir (DTG) or the protease inhibitor, lopinavir boosted with ritonavir were 2 and 3 times more likely to develop hypertension when compared to those on non-nucleoside reverse transcriptase inhibitors (NNRTIs). However, these relationships were abrogated by sex, as self-reported male sex was the major contributor in predicting incident hypertension. While none of the factors remained significantly associated with incident hypertension upon multivariate analysis among females, body mass index (BMI), and use of protease inhibitors remained strongly associated with hypertension among males. Our results indicate that the use of protease inhibitors and BMI are important predictors of incident hypertension among males. Thus, blood pressure and BMI should be closely monitored, particularly in males living with HIV on protease inhibitors. In addition, identifying specific factors that protect females from developing hypertension early is important but remains to be determined.

Sections du résumé

Background UNASSIGNED
Hypertension is common in people living with HIV (PLWH) on antiretroviral therapy (ART). In the general population and in experimental animal models, the incidence of hypertension is greater in males than in females, especially during the premenopausal period. However, it is not known whether there are sex differences in hypertension associated with HIV and ART, and the factors contributing to incident hypertension among PLWH have not been well characterized. In this study, we aimed to determine the time course, sex differences and factors associated with incident hypertension in PLWH initiating ART.
Methods and results UNASSIGNED
We conducted a retrospective study in which we used programmatic data from the ART registry to identify sex differences in the determinants of incident hypertension among PLWH initiating the ART regimen from Livingstone University Teaching Hospital in Zambia and followed for 8 years. Males developed hypertension earlier, 2 years after initiating ART, compared to 6 years in females. In multivariable analysis, increasing age, baseline systolic blood pressure and baseline mean arterial pressure (MAP) were associated with increased risk for developing incident hypertension. Also, participants who switched to the integrase strand transfer inhibitor, dolutegravir (DTG) or the protease inhibitor, lopinavir boosted with ritonavir were 2 and 3 times more likely to develop hypertension when compared to those on non-nucleoside reverse transcriptase inhibitors (NNRTIs). However, these relationships were abrogated by sex, as self-reported male sex was the major contributor in predicting incident hypertension. While none of the factors remained significantly associated with incident hypertension upon multivariate analysis among females, body mass index (BMI), and use of protease inhibitors remained strongly associated with hypertension among males.
Conclusion UNASSIGNED
Our results indicate that the use of protease inhibitors and BMI are important predictors of incident hypertension among males. Thus, blood pressure and BMI should be closely monitored, particularly in males living with HIV on protease inhibitors. In addition, identifying specific factors that protect females from developing hypertension early is important but remains to be determined.

Identifiants

pubmed: 36465432
doi: 10.3389/fcvm.2022.1006789
pmc: PMC9715396
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1006789

Subventions

Organisme : FIC NIH HHS
ID : D43 TW009744
Pays : United States

Informations de copyright

Copyright © 2022 Masenga, Povia, Mutengo, Hamooya, Nzala, Heimburger, Munsaka, Elijovich, Patel and Kirabo.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Sepiso K Masenga (SK)

HAND Research Group, School of Medicine and Health Sciences, Mulungushi University, Livingstone, Zambia.
School of Medicine, University of Zambia, Lusaka, Zambia.

Joreen P Povia (JP)

HAND Research Group, School of Medicine and Health Sciences, Mulungushi University, Livingstone, Zambia.

Katongo H Mutengo (KH)

HAND Research Group, School of Medicine and Health Sciences, Mulungushi University, Livingstone, Zambia.

Benson M Hamooya (BM)

HAND Research Group, School of Medicine and Health Sciences, Mulungushi University, Livingstone, Zambia.

Selestine Nzala (S)

School of Medicine, University of Zambia, Lusaka, Zambia.

Douglas C Heimburger (DC)

School of Medicine, University of Zambia, Lusaka, Zambia.
Department of Medicine, Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States.

Sody M Munsaka (SM)

Department of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.

Fernando Elijovich (F)

Department of Medicine, Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States.

Kaushik P Patel (KP)

Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, NE, United States.

Annet Kirabo (A)

Department of Medicine, Vanderbilt Institute for Global Health, Vanderbilt University Medical Center, Nashville, TN, United States.

Classifications MeSH