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Journal article

Association between pharmacological tenofovir adherence measures and subsequent 24-week viral load outcomes for people with HIV in South Africa

Abstract:
Background

Objective measures of antiretroviral therapy (ART) adherence, such as tenofovir (TFV) concentrations, may allow for targeted interventions to prevent future HIV viraemia. We evaluated three TFV adherence measures and their association with current and 24-week viral load (VL) outcomes.

Methods

In a South Africa-based trial, we measured urine TFV using a point-of-care (POC) antibody-based assay and two metrics assessed via liquid-chromatography-mass-spectrometry: quantitative urine TFV and TFV-diphosphate (TFV-DP) concentrations in dried blood spots (DBS). Logistic regression assessed the association between current and subsequent 24-week VL outcomes and these three measures. We also compared the baseline characteristics of individuals with detectable vs. undetectable POC urine TFV results at enrolment.

Results

Of 124 participants, 54.8% female, median age 39 years, 100 (81.5%) had detectable POC urine TFV and 23 (18.5%) did not. Higher TFV-DP concentrations in DBS were negatively associated with viraemia at 24-weeks (OR 0.83, 95% CI 0.725-0.928, p=0.003), whilst a detectable POC urine TFV (OR 0.62, 95% CI 0.22-1.82, p=0.380) and quantitative urine TFV (OR 0.98, 95% CI 0.95-1.00, p=0.153) showed no significant association. Compared to those with detectable POC urine TFV, those with undetectable POC urine TFV were more likely to be viraemic at enrolment (78.3% vs 25.7%, p<0.001) and have a CD4 count <200 cells/uL (34.8% vs 12.9%, p=0.001).

Conclusion

DBS TFV-DP was associated with viraemia at 24-weeks and could help predict future viraemia. Undetectable POC urine TFV was associated with recent ART initiation, current viraemia, and lower CD4 count.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1097/qai.0000000000003866

Authors


Publisher:
Lippincott, Williams & Wilkins
Journal:
Journal of Acquired Immune Deficiency Syndrome More from this journal
Place of publication:
United States
Publication date:
2026-03-26
DOI:
EISSN:
1077-9450
ISSN:
1525-4135
Pmid:
41885097


Language:
English
Pubs id:
2395874
Local pid:
pubs:2395874
Source identifiers:
W7140458433
Deposit date:
2026-05-29
ARK identifier:

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