A Comparison of Plasma Efavirenz and Tenofovir, Dried Blood Spot Tenofovir-Diphosphate, and Self-Reported Adherence to Predict Virologic Suppression Among South African Women.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 07 2019
Historique:
pubmed: 21 3 2019
medline: 25 2 2020
entrez: 21 3 2019
Statut: ppublish

Résumé

Tenofovir-diphosphate (TFV-DP) in dried blood spots (DBS) is an objective long-term adherence measure, but data are limited on its ability to predict virologic suppression (VS) in people on antiretroviral (ARV) treatment. There are also no data comparing DBS TFV-DP with plasma ARV concentrations as predictors of VS. Women who were on a first-line regimen of tenofovir, emtricitabine, and efavirenz (EFV) were enrolled in a cross-sectional study. Plasma EFV and tenofovir (TFV), DBS TFV-DP assays, and 30-day self-reported adherence were evaluated as predictors of VS (<50 copies/mL) with the area under the curve of receiver operating characteristics and logistic regression. We enrolled 137 women; mean age of 33 years; median 4 years on antiretroviral therapy; 88 (64%) had VS. In receiver operating characteristics analyses: DBS TFV-DP [0.926 (95% CI: 0.876 to 0.976)] had a higher area under the curve than plasma TFV [0.864 (0.797 to 0.932); P = 0.006], whereas plasma EFV [0.903 (0.839-0.967)] was not significantly different from DBS TFV-DP (P = 0.138) or plasma TFV (P = 0.140); all ARV assays performed better than self-report. The association of TFV-DP in DBS with VS strengthened with increasing concentrations [reference <350 fmol/punch: 350-699 fmol/punch aOR 37 (8-178); 700-1249 fmol/punch aOR 47 (13-175); ≥1250 fmol/punch aOR 175 (20-1539)]. "White coat adherence" (defined as DBS TFV-DP <350 fmol/punch with detectable plasma TFV) was only detected in 4 women. Plasma EFV, TFV, and DBS TFV-DP were all strong predictors of VS. EFV or TFV assays have potential for development as point-of-care assays for use as objective adherence measures in resource-limited settings.

Sections du résumé

BACKGROUND
Tenofovir-diphosphate (TFV-DP) in dried blood spots (DBS) is an objective long-term adherence measure, but data are limited on its ability to predict virologic suppression (VS) in people on antiretroviral (ARV) treatment. There are also no data comparing DBS TFV-DP with plasma ARV concentrations as predictors of VS.
METHODS
Women who were on a first-line regimen of tenofovir, emtricitabine, and efavirenz (EFV) were enrolled in a cross-sectional study. Plasma EFV and tenofovir (TFV), DBS TFV-DP assays, and 30-day self-reported adherence were evaluated as predictors of VS (<50 copies/mL) with the area under the curve of receiver operating characteristics and logistic regression.
RESULTS
We enrolled 137 women; mean age of 33 years; median 4 years on antiretroviral therapy; 88 (64%) had VS. In receiver operating characteristics analyses: DBS TFV-DP [0.926 (95% CI: 0.876 to 0.976)] had a higher area under the curve than plasma TFV [0.864 (0.797 to 0.932); P = 0.006], whereas plasma EFV [0.903 (0.839-0.967)] was not significantly different from DBS TFV-DP (P = 0.138) or plasma TFV (P = 0.140); all ARV assays performed better than self-report. The association of TFV-DP in DBS with VS strengthened with increasing concentrations [reference <350 fmol/punch: 350-699 fmol/punch aOR 37 (8-178); 700-1249 fmol/punch aOR 47 (13-175); ≥1250 fmol/punch aOR 175 (20-1539)]. "White coat adherence" (defined as DBS TFV-DP <350 fmol/punch with detectable plasma TFV) was only detected in 4 women.
CONCLUSIONS
Plasma EFV, TFV, and DBS TFV-DP were all strong predictors of VS. EFV or TFV assays have potential for development as point-of-care assays for use as objective adherence measures in resource-limited settings.

Identifiants

pubmed: 30893125
doi: 10.1097/QAI.0000000000002032
pmc: PMC6565450
mid: NIHMS1523043
doi:

Substances chimiques

Alkynes 0
Anti-HIV Agents 0
Anti-Retroviral Agents 0
Benzoxazines 0
Cyclopropanes 0
Organophosphates 0
tenofovir diphosphate 0
Tenofovir 99YXE507IL
Emtricitabine G70B4ETF4S
Adenine JAC85A2161
efavirenz JE6H2O27P8

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

311-318

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI122300
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI068632
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068632
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD074558
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States
Organisme : PEPFAR
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD080465
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106701
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 AI000695
Pays : United States
Organisme : NIMH NIH HHS
ID : R34 MH108393
Pays : United States

Références

J Acquir Immune Defic Syndr. 2013 Mar 1;62(3):275-81
pubmed: 23274933
Br J Clin Pharmacol. 2015 Jul;80(1):146-56
pubmed: 25611810
AIDS. 2018 Aug 24;32(13):1891-1898
pubmed: 29894385
Int J Antimicrob Agents. 2016 Jun;47(6):466-72
pubmed: 27211824
AIDS Res Ther. 2017 Apr 4;14(1):20
pubmed: 28376815
AIDS Behav. 2016 Nov;20(11):2700-2708
pubmed: 27098408
Br J Clin Pharmacol. 2016 Jul;82(1):185-98
pubmed: 26991336
HIV Med. 2017 Jul;18(6):412-418
pubmed: 28444867
J Acquir Immune Defic Syndr. 2016 Aug 1;72 Suppl 2:S189-96
pubmed: 27355508
J Acquir Immune Defic Syndr. 2018 Jan 1;77(1):86-92
pubmed: 28961682
HIV Clin Trials. 2008 Jul-Aug;9(4):238-46
pubmed: 18753118
J Acquir Immune Defic Syndr. 2013 Dec 15;64(5):448-54
pubmed: 24225904
AIDS. 2014 Jan 2;28(1):59-66
pubmed: 24275255
Curr HIV/AIDS Rep. 2018 Feb;15(1):49-59
pubmed: 29380227
AIDS Behav. 2017 Feb;21(2):450-461
pubmed: 27278548
Clin Pharmacokinet. 2014 Nov;53(11):961-73
pubmed: 25204403
AIDS Res Hum Retroviruses. 2015 Apr;31(4):428-32
pubmed: 25328112
AIDS Res Hum Retroviruses. 2013 Feb;29(2):384-90
pubmed: 22935078
AIDS Res Hum Retroviruses. 2016 Jan;32(1):32-43
pubmed: 26414912
Antimicrob Agents Chemother. 2017 Dec 21;62(1):
pubmed: 29038282
PLoS Med. 2018 Mar 30;15(3):e1002547
pubmed: 29601570
Clin Pharmacokinet. 2016 Jul;55(7):861-873
pubmed: 26715213
Clin Infect Dis. 2019 Apr 8;68(8):1335-1342
pubmed: 30137238
Clin Pharmacol Ther. 2015 Oct;98(4):406-16
pubmed: 26044067
Clin J Am Soc Nephrol. 2010 Jun;5(6):1003-9
pubmed: 20299365
J Antimicrob Chemother. 2011 Feb;66(2):240-50
pubmed: 21118913
Transl Behav Med. 2015 Dec;5(4):470-82
pubmed: 26622919
AIDS. 2017 Jul 17;31(11):1647-1650
pubmed: 28657968
Biometrics. 1988 Sep;44(3):837-45
pubmed: 3203132
Antimicrob Agents Chemother. 2016 Aug 22;60(9):5379-86
pubmed: 27353269

Auteurs

Tamsin K Phillips (TK)

Division of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
Centre for Infectious Diseases Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Phumla Sinxadi (P)

Division of Clinical of Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Elaine J Abrams (EJ)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY.
Vagelos College of Physicians and Surgeons, Columbia University, New York, NY.

Allison Zerbe (A)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, NY.

Catherine Orrell (C)

Department of Medicine, Institute of Infectious Disease and Molecular Medicine, Desmond Tutu HIV Centre, University of Cape Town, Cape Town, South Africa.

Nai-Chung Hu (NC)

Centre for Infectious Diseases Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Kirsty Brittain (K)

Division of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
Centre for Infectious Diseases Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Yolanda Gomba (Y)

Centre for Infectious Diseases Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Jennifer Norman (J)

Division of Clinical of Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Lubbe Wiesner (L)

Division of Clinical of Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Landon Myer (L)

Division of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
Centre for Infectious Diseases Epidemiology and Research, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Gary Maartens (G)

Division of Clinical of Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH