dc.contributor.author |
Manne-Goehler, Jennifer
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|
dc.contributor.author |
Fabian, June
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dc.contributor.author |
Sokhela, Simiso
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|
dc.contributor.author |
Akpomiemie, Godspower
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|
dc.contributor.author |
Rahim, Nicholas
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|
dc.contributor.author |
Lalla-Edward, Samanta Tresha
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|
dc.contributor.author |
Brennan, Alana T.
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dc.contributor.author |
Siedner, Mark J.
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dc.contributor.author |
Hill, Andrew
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|
dc.contributor.author |
Venter, Willem Daniel Francois
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|
dc.date.accessioned |
2025-01-21T10:15:21Z |
|
dc.date.available |
2025-01-21T10:15:21Z |
|
dc.date.issued |
2024-07 |
|
dc.description |
DATA AVAILABILITY STATEMENT :
The data that support the findings of this study are available on request from the
corresponding author. The data are not publicly available due to privacy or ethical
restrictions. |
en_US |
dc.description |
SUPPORTING INFORMATION : TABLE S1. Baseline characteristics of primary analytical sample at 48 weeks by treatment group.
TABLE S2. Baseline characteristics of primary analytical sample at 96 weeks by treatment group.
TABLE S3. Baseline characteristics of primary analytical sample at 192 weeks by treatment group.
TABLE S4. Baseline characteristics of primary analytical sample at 48 weeks.
TABLE S5. Baseline characteristics of primary analytical sample at 96 weeks.
TABLE S6. Baseline characteristics of primary analytical sample at 192 weeks.
TABLE S7. Baseline characteristics of secondary analytical sample at 48 weeks by treatment group.
TABLE S8. Baseline characteristics of secondary analytical sample at 96 weeks by treatment group.
TABLE S9. Baseline characteristics of secondary analytical sample at 192 weeks by treatment group.
TABLE S10. Changes in systolic and diastolic blood pressure (mmHg) from baseline to weeks 48 and 96, by ADVANCE treatment groups.
TABLE S11. Changes in systolic and diastolic blood pressure (mmHg) from baseline to week 192, by ADVANCE treatment groups.
TABLE S12. Proportion with treatment emergent hypertension and grade at weeks 48, 96, and 192, by ADVANCE treatment group.
TABLE S13. Linear regression models of the association of individual-level characteristics and change in systolic blood pressure (mmHg) from baseline to week 48, adjusted and unadjusted.
TABLE S14. Linear regression models of the association of individual-level characteristics and change in diastolic blood pressure (mmHg) from baseline, adjusted and unadjusted.
TABLE S15. Linear regression models of the association of individual-level characteristics and change in diastolic blood pressure (mmHg) from baseline to week 48, adjusted and unadjusted.
TABLE S16. Poisson regression models of the association of individual-level characteristics and risk of emergent-hypertension up until week 48, adjusted and unadjusted.
TABLE S17. Sex-stratified linear regression models of the association of individual-level characteristics and change in systolic blood pressure (mmHg) from baseline to week 48, adjusted and unadjusted.
TABLE S18. Sex-stratified Poisson regression models of the association of individual-level characteristics and risk of emergent-hypertension up until week 48, adjusted and unadjusted.
TABLE S19. Poisson regression models of the association of individual-level characteristics and risk of baseline hypertension, adjusted and unadjusted.
TABLE S20. Adjusted Cox-hazard model of time until hypertension diagnosis.
TABLE S21. Urine albumin:creatinine change and SBP change at 48 and 96 weeks by group.
FIGURE S1. Kaplan-Meier curves of time until hypertension incidence, by treatment group. |
en_US |
dc.description.abstract |
INTRODUCTION : Recent evidence has raised questions about whether newer HIV treatment regimens, including dolutegravir
(DTG) and tenofovir alafenamide (TAF), are associated with increases in blood pressure (BP).
METHODS : We assessed changes in BP by treatment regimen and evaluated the relative contribution of kidney function and
weight gain to these changes among participants in the ADVANCE phase-3 trial clinical trial in South Africa (study dates:
January 2017–February 2022). Our primary outcome of interest was a change in systolic BP (SBP) at 96 and 192 weeks,
among those not receiving antihypertensive medication. The secondary outcome was treatment-emergent hypertension at
these same time points, defined as BP ≥140/90 mmHg on two occasions, or initiation of antihypertensive medication after
week 4 among individuals without hypertension at enrolment. We used linear regression to evaluate the relationship between
change in estimated glomerular filtration rate (eGFR) and change in SBP; and Poisson regression to evaluate the relationship
between change in eGFR and treatment-emergent hypertension at each time point. All models were adjusted for age, sex,
treatment group and change in body mass index (BMI).
RESULTS : Over 96 weeks, the average changes in SBP were 1.7 mmHg (95% CI: 0.0−3.4), −0.5 mmHg (95% CI: −2.2 to 1.7)
and −2.1 mmHg (95% CI: −3.8 to 0.4) in the TAF/emtricitabine (FTC)/DTG, tenofovir disoproxil fumarate (TDF)/FTC/DTG
and TDF/FTC/efavirenz (EFV) groups, respectively. This difference was significant for the TAF/FTC/DTG compared to the
TDF/FTC/EFV group (p = 0.002). Over 96 weeks, 18.2% (95% CI: 13.4–22.9), 15.4% (95% CI: 11.0–19.9) and 13.3% (95% CI:
8.9–17.6) of participants developed treatment-emergent hypertension, respectively. In adjusted models, there was no significant
relationship between change in eGFR and either outcome. Change in BMI was significantly associated with an increase in
SBP, while age was associated with an increased risk of treatment-emergent hypertension. Adjustment for BMI also mitigated
the unadjusted relationship between HIV treatment regimen and SBP where present.
CONCLUSIONS : In the ADVANCE cohort, weight gain and age accounted for increases in BP and risk of treatment-emergent
hypertension. HIV treatment programmes may need to integrate the management of obesity and hypertension into routine
care. |
en_US |
dc.description.department |
School of Health Systems and Public Health (SHSPH) |
en_US |
dc.description.librarian |
am2024 |
en_US |
dc.description.sdg |
SDG-03:Good heatlh and well-being |
en_US |
dc.description.sponsorship |
National Institute of Diabetes and Digestive and Kidney Diseases,
SA MRC, UNITAID, USAID, ViiV Healthcare |
en_US |
dc.description.uri |
https://onlinelibrary.wiley.com/journal/17582652 |
en_US |
dc.identifier.citation |
Manne-Goehler, J., Fabian, J., Sokhela, S. et al. 2024, 'Blood pressure increases are associated with weight gain and not antiretroviral regimen or kidney function : a secondary analysis from the ADVANCE trial in South Africa', Journal of the International AIDS Society, vol. 27, art. e26268, pp. 43-49. https://DOI.org/10.1002/jia2.26268. |
en_US |
dc.identifier.issn |
1758-2652 |
|
dc.identifier.other |
10.1002/jia2.26268 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/100214 |
|
dc.language.iso |
en |
en_US |
dc.publisher |
Wiley |
en_US |
dc.rights |
© 2024 The Author(s).
This is an open access article under the terms of the Creative Commons Attribution License. |
en_US |
dc.subject |
Hypertension |
en_US |
dc.subject |
Tenofovir alafenamide |
en_US |
dc.subject |
Obesity |
en_US |
dc.subject |
Kidney function |
en_US |
dc.subject |
Human immunodeficiency virus (HIV) |
en_US |
dc.subject |
SDG-03: Good health and well-being |
en_US |
dc.subject |
Dolutegravir (DTG) |
en_US |
dc.title |
Blood pressure increases are associated with weight gain and not antiretroviral regimen or kidney function : a secondary analysis from the ADVANCE trial in South Africa |
en_US |
dc.type |
Article |
en_US |