Tenofovir concentrations in hair strongly predict virologic suppression in breastfeeding women.


Journal

AIDS (London, England)
ISSN: 1473-5571
Titre abrégé: AIDS
Pays: England
ID NLM: 8710219

Informations de publication

Date de publication:
01 08 2019
Historique:
pubmed: 26 4 2019
medline: 29 7 2020
entrez: 26 4 2019
Statut: ppublish

Résumé

Antiretroviral treatment (ART) adherence is often suboptimal in the perinatal period. We measured hair tenofovir (TFV) concentrations as a metric of adherence in postpartum women to understand patterns and predictors of adherence throughout this critical period. In addition, we examined the association between hair TFV concentrations and virologic outcomes. Between 12/2012 and 09/2016, hair samples were collected longitudinally from delivery through breastfeeding from women on ART in the Promoting Maternal and Infant Survival Everywhere study (NCT01061151) in sub-Saharan Africa. Hair TFV levels were measured using validated methods. Using generalized estimating equations, we estimated the association between hair TFV levels and virologic suppression (<400 copies/ml) over time and assessed predictors of hair TFV levels. Hair TFV levels were measured at 370 visits in 71 women from delivery through a median of 14 months (interquartile range 12-15) of breastfeeding. Levels ranged from below detection (0.002) to 1.067 ng/mg (geometric mean: 0.047). After at least 90 days on ART, 69 women had at least one viral load measured (median 5 measures, range 1-9); 18 (26%) experienced viremia at least once. Each doubling of TFV level more than doubled odds of concurrent virologic suppression [odds ratio 2.35, 95% confidence interval (CI): 1.44-3.84, P = 0.0006] and was associated with 1.43 times the odds of future suppression (95% CI: 0.75-2.73, P = 0.28). Relative to the first 3 months after delivery, hair levels were highest in months 6-12 (1.42-fold higher, 95% CI: 1.09-1.85, P = 0.01). Hair TFV levels strongly predicted concurrent virologic suppression among breastfeeding women. Objective adherence metrics can supplement virologic monitoring to optimize treatment outcomes in this important transition period.

Sections du résumé

BACKGROUND
Antiretroviral treatment (ART) adherence is often suboptimal in the perinatal period. We measured hair tenofovir (TFV) concentrations as a metric of adherence in postpartum women to understand patterns and predictors of adherence throughout this critical period. In addition, we examined the association between hair TFV concentrations and virologic outcomes.
METHODS
Between 12/2012 and 09/2016, hair samples were collected longitudinally from delivery through breastfeeding from women on ART in the Promoting Maternal and Infant Survival Everywhere study (NCT01061151) in sub-Saharan Africa. Hair TFV levels were measured using validated methods. Using generalized estimating equations, we estimated the association between hair TFV levels and virologic suppression (<400 copies/ml) over time and assessed predictors of hair TFV levels.
RESULTS
Hair TFV levels were measured at 370 visits in 71 women from delivery through a median of 14 months (interquartile range 12-15) of breastfeeding. Levels ranged from below detection (0.002) to 1.067 ng/mg (geometric mean: 0.047). After at least 90 days on ART, 69 women had at least one viral load measured (median 5 measures, range 1-9); 18 (26%) experienced viremia at least once. Each doubling of TFV level more than doubled odds of concurrent virologic suppression [odds ratio 2.35, 95% confidence interval (CI): 1.44-3.84, P = 0.0006] and was associated with 1.43 times the odds of future suppression (95% CI: 0.75-2.73, P = 0.28). Relative to the first 3 months after delivery, hair levels were highest in months 6-12 (1.42-fold higher, 95% CI: 1.09-1.85, P = 0.01).
CONCLUSION
Hair TFV levels strongly predicted concurrent virologic suppression among breastfeeding women. Objective adherence metrics can supplement virologic monitoring to optimize treatment outcomes in this important transition period.

Identifiants

pubmed: 31021852
doi: 10.1097/QAD.0000000000002237
pmc: PMC6629471
mid: NIHMS1529025
doi:

Substances chimiques

Anti-HIV Agents 0
Tenofovir 99YXE507IL

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1657-1662

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI069423
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH062246
Pays : United States
Organisme : NIMH NIH HHS
ID : T32 MH019105
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001C
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068632
Pays : United States
Organisme : NIMH NIH HHS
ID : K01 MH119910
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069530
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069518
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027763
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW001081
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069424
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI098472
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106716
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI098472
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068616
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069536
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001I
Pays : United States

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Auteurs

Pamela M Murnane (PM)

Department of Medicine, Center for AIDS Prevention Studies.

Peter Bacchetti (P)

Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco.

Judith S Currier (JS)

Division of Infectious Diseases, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California.

Sean Brummel (S)

Center for Biostatistics in AIDS Research, T.H. Chan School of Public Health, Harvard University, Cambridge, Massachusetts.

Hideaki Okochi (H)

Department of Bioengineering and Therapeutic Sciences, Schools of Pharmacy and Medicine.

Nhi Phung (N)

Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Alexander Louie (A)

Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Karen Kuncze (K)

Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Risa M Hoffman (RM)

Division of Infectious Diseases, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California.

Teacler Nematadzira (T)

Clinical Trials Research Centre, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.

Dean K Soko (DK)

College of Medicine-Johns Hopkins Research Project, Blantyre, Malawi.

Maxensia Owor (M)

Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.

Friday Saidi (F)

University of North Carolina-Lilongwe, Lilongwe, Malawi.

Patricia M Flynn (PM)

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee.

Mary G Fowler (MG)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Monica Gandhi (M)

Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

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