Cargando…

Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant

INTRODUCTION: Sub-dermal hormone implants, such as levonorgestrel (LNG), are a safe and desirable form of long-acting contraception, but their use among HIV-positive women on antiretroviral therapy (ART) may be compromised given the potential for a cytochrome P450 3A-mediated drug–drug interaction....

Descripción completa

Detalles Bibliográficos
Autores principales: Scarsi, Kimberly, Lamorde, Mohammed, Darin, Kristin, Dilly Penchala, Sujan, Else, Laura, Nakalema, Shadia, Byakika-Kibwika, Pauline, Khoo, Saye, Cohn, Susan, Merry, Concepta, Back, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International AIDS Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224805/
https://www.ncbi.nlm.nih.gov/pubmed/25393993
http://dx.doi.org/10.7448/IAS.17.4.19484
_version_ 1782343408580296704
author Scarsi, Kimberly
Lamorde, Mohammed
Darin, Kristin
Dilly Penchala, Sujan
Else, Laura
Nakalema, Shadia
Byakika-Kibwika, Pauline
Khoo, Saye
Cohn, Susan
Merry, Concepta
Back, David
author_facet Scarsi, Kimberly
Lamorde, Mohammed
Darin, Kristin
Dilly Penchala, Sujan
Else, Laura
Nakalema, Shadia
Byakika-Kibwika, Pauline
Khoo, Saye
Cohn, Susan
Merry, Concepta
Back, David
author_sort Scarsi, Kimberly
collection PubMed
description INTRODUCTION: Sub-dermal hormone implants, such as levonorgestrel (LNG), are a safe and desirable form of long-acting contraception, but their use among HIV-positive women on antiretroviral therapy (ART) may be compromised given the potential for a cytochrome P450 3A-mediated drug–drug interaction. Our study aimed to characterize the pharmacokinetics of LNG released from a sub-dermal implant over six months in HIV-positive Ugandan women on nevirapine (NVP)- or efavirenz (EFV)-based ART. MATERIAL AND METHODS: This non-randomized, parallel group study compared LNG pharmacokinetics between HIV-positive Ugandan women not yet eligible for ART (control group, n=18) and those on stable NVP- (n=20) or EFV- (n=20) based ART. The two-rod (75 mg/rod) LNG sub-dermal implant was inserted at study enrolment. LNG sampling was obtained pre-implant and at weeks 1, 4, 12 and 24 post-insertion. LNG concentrations were analyzed using a validated LC-MS/MS method, with an assay calibration range of 50–1500 pg/mL. Safety monitoring, including a pregnancy test, was conducted at each study visit. RESULTS: At enrolment, participants had a mean age of 31 years; CD4+ cell counts were similar between the control, NVP and EFV groups (758, 645 and 568 cells/mm(3), respectively; p=0.09); all women in the NVP and EFV groups had an undetectable HIV-RNA. Women in the control group had a higher baseline body weight (73 kg) compared to those in the NVP (63 kg; p=0.03) or EFV groups (60 kg; p<0.01). By linear regression, weight was a significant predictor of LNG concentrations (1 kg increase in weight=5 pg/mL decrease in LNG, p=0.03). LNG concentrations are reported in the table. CONCLUSIONS: Over a 24-week period, LNG concentrations were 40–54% lower in women on EFV-based ART, despite their having a significantly lower body weight, compared to those not on ART. In women on NVP-based ART, LNG concentrations were 32–39% higher than those observed in the control group, a difference partially explained by body weight. These data confirm a significant drug interaction occurs between the LNG implant and EFV, adding to growing concern for reduced contraceptive efficacy with their combined use. In contrast, these data support use of the LNG implant with NVP-based ART.
format Online
Article
Text
id pubmed-4224805
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher International AIDS Society
record_format MEDLINE/PubMed
spelling pubmed-42248052014-11-13 Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant Scarsi, Kimberly Lamorde, Mohammed Darin, Kristin Dilly Penchala, Sujan Else, Laura Nakalema, Shadia Byakika-Kibwika, Pauline Khoo, Saye Cohn, Susan Merry, Concepta Back, David J Int AIDS Soc Oral Presentation – Abstract O131 INTRODUCTION: Sub-dermal hormone implants, such as levonorgestrel (LNG), are a safe and desirable form of long-acting contraception, but their use among HIV-positive women on antiretroviral therapy (ART) may be compromised given the potential for a cytochrome P450 3A-mediated drug–drug interaction. Our study aimed to characterize the pharmacokinetics of LNG released from a sub-dermal implant over six months in HIV-positive Ugandan women on nevirapine (NVP)- or efavirenz (EFV)-based ART. MATERIAL AND METHODS: This non-randomized, parallel group study compared LNG pharmacokinetics between HIV-positive Ugandan women not yet eligible for ART (control group, n=18) and those on stable NVP- (n=20) or EFV- (n=20) based ART. The two-rod (75 mg/rod) LNG sub-dermal implant was inserted at study enrolment. LNG sampling was obtained pre-implant and at weeks 1, 4, 12 and 24 post-insertion. LNG concentrations were analyzed using a validated LC-MS/MS method, with an assay calibration range of 50–1500 pg/mL. Safety monitoring, including a pregnancy test, was conducted at each study visit. RESULTS: At enrolment, participants had a mean age of 31 years; CD4+ cell counts were similar between the control, NVP and EFV groups (758, 645 and 568 cells/mm(3), respectively; p=0.09); all women in the NVP and EFV groups had an undetectable HIV-RNA. Women in the control group had a higher baseline body weight (73 kg) compared to those in the NVP (63 kg; p=0.03) or EFV groups (60 kg; p<0.01). By linear regression, weight was a significant predictor of LNG concentrations (1 kg increase in weight=5 pg/mL decrease in LNG, p=0.03). LNG concentrations are reported in the table. CONCLUSIONS: Over a 24-week period, LNG concentrations were 40–54% lower in women on EFV-based ART, despite their having a significantly lower body weight, compared to those not on ART. In women on NVP-based ART, LNG concentrations were 32–39% higher than those observed in the control group, a difference partially explained by body weight. These data confirm a significant drug interaction occurs between the LNG implant and EFV, adding to growing concern for reduced contraceptive efficacy with their combined use. In contrast, these data support use of the LNG implant with NVP-based ART. International AIDS Society 2014-11-02 /pmc/articles/PMC4224805/ /pubmed/25393993 http://dx.doi.org/10.7448/IAS.17.4.19484 Text en © 2014 Scarsi K et al; licensee International AIDS Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oral Presentation – Abstract O131
Scarsi, Kimberly
Lamorde, Mohammed
Darin, Kristin
Dilly Penchala, Sujan
Else, Laura
Nakalema, Shadia
Byakika-Kibwika, Pauline
Khoo, Saye
Cohn, Susan
Merry, Concepta
Back, David
Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title_full Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title_fullStr Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title_full_unstemmed Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title_short Efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
title_sort efavirenz- but not nevirapine-based antiretroviral therapy decreases exposure to the levonorgestrel released from a sub-dermal contraceptive implant
topic Oral Presentation – Abstract O131
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224805/
https://www.ncbi.nlm.nih.gov/pubmed/25393993
http://dx.doi.org/10.7448/IAS.17.4.19484
work_keys_str_mv AT scarsikimberly efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT lamordemohammed efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT darinkristin efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT dillypenchalasujan efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT elselaura efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT nakalemashadia efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT byakikakibwikapauline efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT khoosaye efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT cohnsusan efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT merryconcepta efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant
AT backdavid efavirenzbutnotnevirapinebasedantiretroviraltherapydecreasesexposuretothelevonorgestrelreleasedfromasubdermalcontraceptiveimplant