{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,10]],"date-time":"2026-03-10T23:11:53Z","timestamp":1773184313038,"version":"3.50.1"},"reference-count":41,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,1]]},"abstract":"<jats:sec>\n            <jats:title>Objective<\/jats:title>\n            <jats:p>In AIDS Clinical Trials Group study A5338, concomitant rifampicin, isoniazid, and efavirenz was associated with more rapid plasma medroxyprogesterone acetate (MPA) clearance compared to historical controls without tuberculosis or HIV therapy. We characterized the pharmacogenetics of this interaction.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Methods<\/jats:title>\n            <jats:p>In A5338, women receiving efavirenz-based HIV therapy and rifampicin plus isoniazid for tuberculosis underwent pharmacokinetic evaluations over 12\u2009weeks following a 150-mg intramuscular injection of depot MPA. Data were interpreted with nonlinear mixed-effects modelling. Associations between individual pharmacokinetic parameters and polymorphisms relevant to rifampicin, isoniazid, efavirenz, and MPA were assessed.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Results<\/jats:title>\n            <jats:p>Of 62 A5338 participants in four African countries, 44 were evaluable for pharmacokinetic associations, with 17 <jats:italic toggle=\"yes\">CYP2B6<\/jats:italic> normal, 21 intermediate, and 6 poor metabolizers, and 5 <jats:italic toggle=\"yes\">NAT2<\/jats:italic> rapid, 20 intermediate, and 19 slow acetylators. There were no associations between either <jats:italic toggle=\"yes\">CYP2B6<\/jats:italic> or <jats:italic toggle=\"yes\">NAT2<\/jats:italic> genotype and MPA <jats:italic toggle=\"yes\">C<\/jats:italic>\n                                 <jats:sub>min<\/jats:sub> at week 12, apparent clearance, <jats:italic toggle=\"yes\">C<\/jats:italic>\n                                 <jats:sub>max<\/jats:sub>, area under the concentration-time curve (AUC) or half-life, or unexplained interindividual variability in clearance, and uptake rate constant or mean transit time of the slow-release fraction (<jats:italic toggle=\"yes\">P<\/jats:italic>\u2009&gt;\u20090.05 for each). In exploratory analyses, none of 28 polymorphisms in 14 genes were consistently associated with MPA pharmacokinetic parameters, and none withstood correction for multiple testing.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p>Study A5338 suggested that more frequent depot MPA dosing may be appropriate for women receiving rifampicin, isoniazid, and efavirenz. The present results suggest that knowledge of <jats:italic toggle=\"yes\">CYP2B6<\/jats:italic> metabolizer or <jats:italic toggle=\"yes\">NAT2<\/jats:italic> acetylator status does not inform individualized DMPA dosing in this setting.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1097\/fpc.0000000000000448","type":"journal-article","created":{"date-parts":[[2021,8,9]],"date-time":"2021-08-09T18:38:01Z","timestamp":1628534281000},"page":"24-30","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":6,"title":["Pharmacogenetics of interaction between depot medroxyprogesterone acetate and efavirenz, rifampicin, and isoniazid during treatment of HIV and tuberculosis"],"prefix":"10.1097","volume":"32","author":[{"given":"David W.","family":"Haas","sequence":"first","affiliation":[{"name":"Department of Medicine, Vanderbilt University School of Medicine"},{"name":"Department of Internal Medicine, Meharry Medical College, Nashville, Tennessee, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rosie","family":"Mngqibisa","sequence":"additional","affiliation":[{"name":"Enhancing Care Foundation, Durban International CRS, Wentworth Hospital, Durban"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jose","family":"Francis","sequence":"additional","affiliation":[{"name":"Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Helen","family":"McIlleron","sequence":"additional","affiliation":[{"name":"Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jennifer A.","family":"Robinson","sequence":"additional","affiliation":[{"name":"Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michelle A.","family":"Kendall","sequence":"additional","affiliation":[{"name":"Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, Massachusetts"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paxton","family":"Baker","sequence":"additional","affiliation":[{"name":"Vanderbilt Technologies for Advanced Genomics, Vanderbilt University Medical Center, Nashville, TN, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sajeeda","family":"Mawlana","sequence":"additional","affiliation":[{"name":"Enhancing Care Foundation, Durban International CRS, Wentworth Hospital, Durban"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sharlaa","family":"Badal-Faesen","sequence":"additional","affiliation":[{"name":"Clinical HIV Research Unit, Department of Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francis","family":"Angira","sequence":"additional","affiliation":[{"name":"Kenya Medical Research Institute, Center for Global Health Research (KEMRI\/CGHR)\/Emory-CDC CTU, Kisumu, Kenya"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ayotunde","family":"Omoz-Oarhe","sequence":"additional","affiliation":[{"name":"Botswana Clinical Trials Unit, Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wadzanai P.","family":"Samaneka","sequence":"additional","affiliation":[{"name":"Parirenyatwa CRS, University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Paolo","family":"Denti","sequence":"additional","affiliation":[{"name":"Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Susan E.","family":"Cohn","sequence":"additional","affiliation":[{"name":"Northwestern University Feinberg School of Medicine, Infectious Diseases Division, Chicago, Illinois, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"name":"for the AIDS Clinical Trials Group A5338 Study Team","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","published-online":{"date-parts":[[2021,8,6]]},"reference":[{"key":"R3-20250808","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1111\/1471-0528.14408","article-title":"Maternal and perinatal mortality and morbidity associated with tuberculosis during pregnancy and the postpartum period: a systematic review and meta-analysis.","volume":"124","author":"Sobhy","year":"2017","journal-title":"BJOG"},{"issue":"Suppl 2","key":"R5-20250808","doi-asserted-by":"crossref","first-page":"S216","DOI":"10.1093\/infdis\/jis009","article-title":"Prevention, diagnosis, and treatment of tuberculosis in children and mothers: evidence for action for maternal, neonatal, and child health 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