Weight Changes and Adverse Pregnancy Outcomes With Dolutegravir- and Tenofovir Alafenamide Fumarate-Containing Antiretroviral Treatment Regimens During Pregnancy and Postpartum

dc.contributor.authorHoffman R.M.
dc.contributor.authorBrummel S.
dc.contributor.authorZiemba L.
dc.contributor.authorChinula L.
dc.contributor.authorMcCarthy K.
dc.contributor.authorFairlie L.
dc.contributor.authorJean-Philippe P.
dc.contributor.authorChakhtoura N.
dc.contributor.authorJohnston B.
dc.contributor.authorKrotje C.
dc.contributor.authorNematadzira T.G.
dc.contributor.authorNakayiwa F.
dc.contributor.authorNdyanabangi V.
dc.contributor.authorHanley S.
dc.contributor.authorTheron G.
dc.contributor.authorViolari A.
dc.contributor.authorJoão E.
dc.contributor.authorCorrea M.D.
dc.contributor.authorHofer C.B.
dc.contributor.authorNavanukroh O.
dc.contributor.authorAurpibul L.
dc.contributor.authorNevrekar N.
dc.contributor.authorZash R.
dc.contributor.authorShapiro R.
dc.contributor.authorStringer J.S.A.
dc.contributor.authorCurrier J.S.
dc.contributor.authorSax P.
dc.contributor.authorLockman S.
dc.contributor.correspondenceHoffman R.M.
dc.contributor.otherMahidol University
dc.date.accessioned2024-06-25T18:14:38Z
dc.date.available2024-06-25T18:14:38Z
dc.date.issued2024-06-14
dc.description.abstractBACKGROUND: We evaluated associations between antepartum weight change and adverse pregnancy outcomes and between antiretroviral therapy (ART) regimens and week 50 postpartum body mass index in IMPAACT 2010. METHODS: Women with human immunodeficiency virus (HIV)-1 in 9 countries were randomized 1:1:1 at 14-28 weeks' gestational age (GA) to start dolutegravir (DTG) + emtricitabine (FTC)/tenofovir alafenamide fumarate (TAF) versus DTG + FTC/tenofovir disoproxil fumarate (TDF) versus efavirenz (EFV)/FTC/TDF. Insufficient antepartum weight gain was defined using Institute of Medicine guidelines. Cox-proportional hazards regression models were used to evaluate the association between antepartum weight change and adverse pregnancy outcomes: stillbirth (≥20 weeks' GA), preterm delivery (<37 weeks' GA), small size for GA (<10th percentile), and a composite of these endpoints. RESULTS: A total of 643 participants were randomized: 217 to the DTG + FTC/TAF, 215 to the DTG + FTC/TDF, and 211 to the EFV/FTC/TDF arm. Baseline medians were as follows: GA, 21.9 weeks; HIV RNA, 903 copies/mL; and CD4 cell count, 466/μL. Insufficient weight gain was least frequent with DTG + FTC/TAF (15.0%) versus DTG + FTC/TDF (23.6%) and EFV/FTC/TDF (30.4%). Women in the DTG + FTC/TAF arm had the lowest rate of composite adverse pregnancy outcome. Low antepartum weight gain was associated with higher hazard of composite adverse pregnancy outcome (hazard ratio, 1.44 [95% confidence interval, 1.04-2.00]) and small size for GA (1.48 [.99-2.22]). More women in the DTG + FTC/TAF arm had a body mass index ≥25 (calculated as weight in kilograms divided by height in meters squared) at 50 weeks postpartum (54.7%) versus the DTG + FTC/TDF (45.2%) and EFV/FTC/TDF (34.2%) arms. CONCLUSIONS: Antepartum weight gain on DTG regimens was protective against adverse pregnancy outcomes typically associated with insufficient weight gain, supportive of guidelines recommending DTG-based ART for women starting ART during pregnancy. Interventions to mitigate postpartum weight gain are needed.
dc.identifier.citationClinical infectious diseases : an official publication of the Infectious Diseases Society of America Vol.78 No.6 (2024) , 1617-1628
dc.identifier.doi10.1093/cid/ciae001
dc.identifier.eissn15376591
dc.identifier.pmid38180851
dc.identifier.scopus2-s2.0-85196228429
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/98987
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleWeight Changes and Adverse Pregnancy Outcomes With Dolutegravir- and Tenofovir Alafenamide Fumarate-Containing Antiretroviral Treatment Regimens During Pregnancy and Postpartum
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85196228429&origin=inward
oaire.citation.endPage1628
oaire.citation.issue6
oaire.citation.startPage1617
oaire.citation.titleClinical infectious diseases : an official publication of the Infectious Diseases Society of America
oaire.citation.volume78
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationFHI 360
oairecerif.author.affiliationFrontier Science &amp; Technology Research Foundation, Inc.
oairecerif.author.affiliationUniversity of the Witwatersrand Faculty of Health Sciences
oairecerif.author.affiliationUNC Project-Malawi
oairecerif.author.affiliationUniversity of Zimbabwe
oairecerif.author.affiliationHarvard T.H. Chan School of Public Health
oairecerif.author.affiliationUniversidade Federal de Minas Gerais
oairecerif.author.affiliationBeth Israel Deaconess Medical Center
oairecerif.author.affiliationUNC School of Medicine
oairecerif.author.affiliationNational Institute of Child Health and Human Development (NICHD)
oairecerif.author.affiliationBrigham and Women's Hospital
oairecerif.author.affiliationUniversity of the Witwatersrand, Johannesburg
oairecerif.author.affiliationUniversity of KwaZulu-Natal
oairecerif.author.affiliationNational Institutes of Health (NIH)
oairecerif.author.affiliationJohns Hopkins University
oairecerif.author.affiliationDavid Geffen School of Medicine at UCLA
oairecerif.author.affiliationStellenbosch University
oairecerif.author.affiliationChiang Mai University
oairecerif.author.affiliationUniversidade Federal do Rio de Janeiro
oairecerif.author.affiliationHospital Federal dos Servidores do Estado
oairecerif.author.affiliationBaylor College of Medicine Children's Foundation
oairecerif.author.affiliationMU-JHU Care Limited

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