Weight gain during pregnancy among women initiating dolutegravir in Botswana.

Botswana Dolutegravir Efavirenz Pregnancy Weight gain

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 28 01 2020
revised: 02 10 2020
accepted: 13 10 2020
entrez: 13 1 2021
pubmed: 14 1 2021
medline: 14 1 2021
Statut: epublish

Résumé

Recent data suggests clinically significant weight gain among non-pregnant HIV-positive adults after starting dolutegravir-based ART (DTG). Excess or insufficient weight gain in pregnancy could adversely impact pregnancy outcomes, but data for pregnant women receiving DTG are limited. The Tsepamo Study captured data at delivery sites in Botswana from 2014 to 2019. HIV testing, HIV treatment information, and weight measurements during antenatal care were abstracted from the maternity obstetric record at delivery. HIV-positive women initiating DTG or efavirenz-based ART (EFV) between conception and 17 weeks gestation and HIV-uninfected women first presenting for antenatal care before 17 weeks gestation were included. We evaluated weekly weight gain, total 18-week weight gain, excess weight gain (>0.59 kg/week), insufficient weight gain (<0.18 kg/week), and weight loss between 18±2 and 36±2 weeks gestation, adjusting for demographic and clinical variables. Baseline characteristics were similar by exposure group, including pre-pregnancy and early pregnancy weight. Compared with EFV, mean weekly weight gain between 18 and 36 weeks gestation was 0.05 (95% CI 0.03, 0.07) kg/week higher for women initiating DTG and 0.12 (0.10, 0.14) kg/week higher for HIV-uninfected women. Mean 18-week weight gain was 1.05 (95% CI 0.61, 1.49) kg higher for women initiating DTG and 2.31 (1.85, 2.77) kg higher for HIV-uninfected women, compared with EFV. Women initiating DTG were more likely to gain excess weight but less likely to gain insufficient weight or lose weight than women initiating EFV. Women initiating DTG compared with EFV during pregnancy gained more weight between 18 and 36 weeks gestation. Neither group gained as much weight as HIV-uninfected women. Initiating DTG compared with EFV during pregnancy could increase the risk of excess weight gain but decrease the risk of insufficient weight gain and weight loss, which could have positive and negative consequences in pregnancy. Our findings are consistent with prior studies in non-pregnant adults.

Sections du résumé

BACKGROUND BACKGROUND
Recent data suggests clinically significant weight gain among non-pregnant HIV-positive adults after starting dolutegravir-based ART (DTG). Excess or insufficient weight gain in pregnancy could adversely impact pregnancy outcomes, but data for pregnant women receiving DTG are limited.
METHODS METHODS
The Tsepamo Study captured data at delivery sites in Botswana from 2014 to 2019. HIV testing, HIV treatment information, and weight measurements during antenatal care were abstracted from the maternity obstetric record at delivery. HIV-positive women initiating DTG or efavirenz-based ART (EFV) between conception and 17 weeks gestation and HIV-uninfected women first presenting for antenatal care before 17 weeks gestation were included. We evaluated weekly weight gain, total 18-week weight gain, excess weight gain (>0.59 kg/week), insufficient weight gain (<0.18 kg/week), and weight loss between 18±2 and 36±2 weeks gestation, adjusting for demographic and clinical variables.
FINDINGS RESULTS
Baseline characteristics were similar by exposure group, including pre-pregnancy and early pregnancy weight. Compared with EFV, mean weekly weight gain between 18 and 36 weeks gestation was 0.05 (95% CI 0.03, 0.07) kg/week higher for women initiating DTG and 0.12 (0.10, 0.14) kg/week higher for HIV-uninfected women. Mean 18-week weight gain was 1.05 (95% CI 0.61, 1.49) kg higher for women initiating DTG and 2.31 (1.85, 2.77) kg higher for HIV-uninfected women, compared with EFV. Women initiating DTG were more likely to gain excess weight but less likely to gain insufficient weight or lose weight than women initiating EFV.
INTERPRETATION CONCLUSIONS
Women initiating DTG compared with EFV during pregnancy gained more weight between 18 and 36 weeks gestation. Neither group gained as much weight as HIV-uninfected women. Initiating DTG compared with EFV during pregnancy could increase the risk of excess weight gain but decrease the risk of insufficient weight gain and weight loss, which could have positive and negative consequences in pregnancy. Our findings are consistent with prior studies in non-pregnant adults.

Identifiants

pubmed: 33437946
doi: 10.1016/j.eclinm.2020.100615
pii: S2589-5370(20)30359-X
pmc: PMC7788432
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100615

Subventions

Organisme : NIAID NIH HHS
ID : K24 AI131928
Pays : United States
Organisme : NICHD NIH HHS
ID : K01 HD100222
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD080471
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW009610
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI131924
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD095766
Pays : United States
Organisme : NICHD NIH HHS
ID : K23 HD088230
Pays : United States

Informations de copyright

© 2020 The Authors.

Déclaration de conflit d'intérêts

No conflicts of interest exist.

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Auteurs

Ellen C Caniglia (EC)

Department of Population Health, New York University School of Medicine, New York, United States.
Harvard T.H. Chan School of Public Health, Boston, United States.

Roger Shapiro (R)

Harvard T.H. Chan School of Public Health, Boston, United States.
Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Modiegi Diseko (M)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Blair J Wylie (BJ)

Beth Israel Deaconess Medical Center, Boston, United States.

Chloe Zera (C)

Beth Israel Deaconess Medical Center, Boston, United States.

Sonya Davey (S)

University of Pennsylvania Perelman School of Medicine, Philadelphia, United States.

Arielle Isaacson (A)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Gloria Mayondi (G)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Judith Mabuta (J)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Rebecca Luckett (R)

Beth Israel Deaconess Medical Center, Boston, United States.

Joseph Makhema (J)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Mompati Mmalane (M)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.

Shahin Lockman (S)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.
Brigham and Women's Hospital, Boston, United States.

Rebecca Zash (R)

Botswana-Harvard AIDS Institute Partnership, Gaborone, Botswana.
Beth Israel Deaconess Medical Center, Boston, United States.

Classifications MeSH