Relating CYP2B6 genotype and efavirenz resistance among post-partum women living with HIV with high viremia in Uganda: a nested cross-sectional study.


Journal

AIDS research and therapy
ISSN: 1742-6405
Titre abrégé: AIDS Res Ther
Pays: England
ID NLM: 101237921

Informations de publication

Date de publication:
31 03 2023
Historique:
received: 03 01 2023
accepted: 24 03 2023
medline: 4 4 2023
entrez: 2 4 2023
pubmed: 3 4 2023
Statut: epublish

Résumé

We investigated the association between CYP2B6 polymorphisms and efavirenz drug resistance among women living with HIV who started on antiretroviral therapy during pregnancy and with high viremia during post-partum. This was a cross-sectional study of women with viral loads greater than 1000 copies/ml who were at least 6 weeks postpartum. Sanger sequencing was used to detect resistant mutations, as well as host genotyping, and efavirenz resistance was compared among the metabolizer genotypes. Over the course of one year (July 2017-July 2018), 322 women were screened, with 110 (34.2%) having viral loads of 1000 copies/ml and 62 having whole blood available for genotyping. Fifty-nine of these women had both viral resistance and human host genotypic results. Efavirenz resistance according to metabolizer genotype was; 47% in slow, 34% in extensive and 28% in intermediate metabolizers, but the difference was not statistically significant due to the small sample size. There was no statistically significant difference in EFV resistance between EFV metabolizer genotypes in women who started antiretroviral therapy during pregnancy and had high viremia in the postpartum period. However, a numerical trend was discovered, which calls for confirmation in a large, well-designed, statistically powered study.

Sections du résumé

BACKGROUND
We investigated the association between CYP2B6 polymorphisms and efavirenz drug resistance among women living with HIV who started on antiretroviral therapy during pregnancy and with high viremia during post-partum.
METHODS
This was a cross-sectional study of women with viral loads greater than 1000 copies/ml who were at least 6 weeks postpartum. Sanger sequencing was used to detect resistant mutations, as well as host genotyping, and efavirenz resistance was compared among the metabolizer genotypes.
RESULTS
Over the course of one year (July 2017-July 2018), 322 women were screened, with 110 (34.2%) having viral loads of 1000 copies/ml and 62 having whole blood available for genotyping. Fifty-nine of these women had both viral resistance and human host genotypic results. Efavirenz resistance according to metabolizer genotype was; 47% in slow, 34% in extensive and 28% in intermediate metabolizers, but the difference was not statistically significant due to the small sample size.
CONCLUSIONS
There was no statistically significant difference in EFV resistance between EFV metabolizer genotypes in women who started antiretroviral therapy during pregnancy and had high viremia in the postpartum period. However, a numerical trend was discovered, which calls for confirmation in a large, well-designed, statistically powered study.

Identifiants

pubmed: 37004096
doi: 10.1186/s12981-023-00514-2
pii: 10.1186/s12981-023-00514-2
pmc: PMC10064798
doi:

Substances chimiques

Cytochrome P-450 CYP2B6 EC 1.14.14.1
Anti-HIV Agents 0
efavirenz JE6H2O27P8
Benzoxazines 0
CYP2B6 protein, human EC 1.14.14.1

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

20

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI069911
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Allan Buzibye (A)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda. abuzibye@idi.co.ug.

Kara Wools-Kaloustian (K)

School of Medicine, Infectious Diseases, Indiana University, Indianapolis, IN, USA.

Adeniyi Olagunju (A)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Ellon Twinomuhwezi (E)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

Constantin Yiannoutsos (C)

Fairbanks School of Public Health, Indiana University, Indianapolis, IN, USA.

Andrew Owen (A)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Megan Neary (M)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Joshua Matovu (J)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

Grace Banturaki (G)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

Barbara Castelnuovo (B)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

Mohammed Lamorde (M)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

Saye Khoo (S)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Catriona Waitt (C)

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Agnes Kiragga (A)

Research Department, Infectious Diseases Institute, College of Health Sciences, Makerere University, P. O. Box 22418, Kampala, Uganda.

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Classifications MeSH