Effect on growth of exposure to maternal antiretroviral therapy in breastmilk versus extended infant nevirapine prophylaxis among HIV-exposed perinatally uninfected infants in the PROMISE randomized trial.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 03 03 2021
accepted: 04 07 2021
entrez: 20 8 2021
pubmed: 21 8 2021
medline: 24 11 2021
Statut: epublish

Résumé

Malnutrition is highly prevalent in HIV-exposed perinatally uninfected infants (HEUs) increasing the risk of morbidity and mortality throughout the life course. We set out to compare the effect of postnatal exposure to maternal antiretroviral therapy (mART) in breastmilk versus infant Nevirapine prophylaxis (iNVP) on somatic growth of HEUs in the randomized PROMISE trial. We randomized 2431 mothers with HIV and their 2444 HEUs from six African countries and India 6-14 days after delivery to mART or iNVP for prevention of breastmilk HIV transmission. The mART regimen contained tenofovir/emtricitabine (99%) plus lopinavir/ritonavir. Infant growth parameters were compared at postnatal week 10, 26, 74 and 104 using World Health Organization (WHO) z-scores for length-for-age (LAZ), weight-for-age (WAZ), and head circumference-for-age (HCAZ). Week 26 LAZ was the primary endpoint measure. Student T-tests compared mean LAZ, WAZ, and HCAZ; estimated mean and 95% confidence interval (CI) are presented. Maternal and infant baseline characteristics were comparable between study arms. The estimated median breastfeeding duration was 70 weeks. After a mean follow-up of 88 weeks, mean LAZ and WAZ were below the WHO reference population mean at all timepoints, whereas mean HCAZ was not. The mART and iNVP arms did not differ for the primary outcome measure of LAZ at week 26 (p-value = 0.39; estimated mean difference (95%CI) of -0.05 (-0.18, 0.07)) or any of the other secondary growth outcome measures or timepoints (all p-values≥0.16). Secondary analyses of the primary outcome measure adjusting for week 0 LAZ and other covariates did not change these results (all p-values≥0.09). However, infants assigned to mART were more likely to have stunting compared to iNVP infants at week 26 (odds ratio (95% CI): 1.28 (1.05, 1.57)). In HEUs, growth effects from postnatal exposure to mART compared to iNVP were comparable for measures on length, weight and head circumference with no clinically relevant differences between the groups. Despite breastfeeding into the second year of life, length and weight were below reference population means at all ages in both arms. Further investment is needed to optimize postnatal growth of infants born to women with HIV. ClinicalTrials.gov number NCT01061151.

Sections du résumé

BACKGROUND
Malnutrition is highly prevalent in HIV-exposed perinatally uninfected infants (HEUs) increasing the risk of morbidity and mortality throughout the life course. We set out to compare the effect of postnatal exposure to maternal antiretroviral therapy (mART) in breastmilk versus infant Nevirapine prophylaxis (iNVP) on somatic growth of HEUs in the randomized PROMISE trial.
METHODS AND FINDINGS
We randomized 2431 mothers with HIV and their 2444 HEUs from six African countries and India 6-14 days after delivery to mART or iNVP for prevention of breastmilk HIV transmission. The mART regimen contained tenofovir/emtricitabine (99%) plus lopinavir/ritonavir. Infant growth parameters were compared at postnatal week 10, 26, 74 and 104 using World Health Organization (WHO) z-scores for length-for-age (LAZ), weight-for-age (WAZ), and head circumference-for-age (HCAZ). Week 26 LAZ was the primary endpoint measure. Student T-tests compared mean LAZ, WAZ, and HCAZ; estimated mean and 95% confidence interval (CI) are presented. Maternal and infant baseline characteristics were comparable between study arms. The estimated median breastfeeding duration was 70 weeks. After a mean follow-up of 88 weeks, mean LAZ and WAZ were below the WHO reference population mean at all timepoints, whereas mean HCAZ was not. The mART and iNVP arms did not differ for the primary outcome measure of LAZ at week 26 (p-value = 0.39; estimated mean difference (95%CI) of -0.05 (-0.18, 0.07)) or any of the other secondary growth outcome measures or timepoints (all p-values≥0.16). Secondary analyses of the primary outcome measure adjusting for week 0 LAZ and other covariates did not change these results (all p-values≥0.09). However, infants assigned to mART were more likely to have stunting compared to iNVP infants at week 26 (odds ratio (95% CI): 1.28 (1.05, 1.57)).
CONCLUSIONS
In HEUs, growth effects from postnatal exposure to mART compared to iNVP were comparable for measures on length, weight and head circumference with no clinically relevant differences between the groups. Despite breastfeeding into the second year of life, length and weight were below reference population means at all ages in both arms. Further investment is needed to optimize postnatal growth of infants born to women with HIV.
CLINICAL TRIAL REGISTRATION
ClinicalTrials.gov number NCT01061151.

Identifiants

pubmed: 34415933
doi: 10.1371/journal.pone.0255250
pii: PONE-D-21-06961
pmc: PMC8378741
doi:

Substances chimiques

Anti-Retroviral Agents 0
Nevirapine 99DK7FVK1H

Banques de données

ClinicalTrials.gov
['NCT01061151']

Types de publication

Comparative Study Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0255250

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI068632
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069530
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069518
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069436
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001I
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI068632
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001C
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069463
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068616
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106716
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069436
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Lynda Stranix-Chibanda (L)

University of Zimbabwe Faculty of Medicine and Health Sciences, Child and Adolescent Health Unit, Harare, Zimbabwe.
University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.

Camlin Tierney (C)

Harvard T.H. Chan School of Public Health, Center for Biostatistics in AIDS Research in the Department of Biostatistics, Boston, MA, United States of America.

Mauricio Pinilla (M)

Harvard T.H. Chan School of Public Health, Center for Biostatistics in AIDS Research in the Department of Biostatistics, Boston, MA, United States of America.

Kathleen George (K)

FHI 360, Durham, NC, United States of America.

Jim Aizire (J)

Makerere University-Johns Hopkins University Research Programme, Kampala, Uganda.
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States of America.

Godwin Chipoka (G)

University of North Carolina Project, Lilongwe, Malawi.

Macpherson Mallewa (M)

College of Medicine-Johns Hopkins University Project, Blantyre, Malawi.

Megeshinee Naidoo (M)

University of KwaZulu-Natal, Centre Aids Prevention Research South Africa (CAPRISA), Durban, South Africa.

Teacler Nematadzira (T)

University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.

Bangani Kusakara (B)

University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.

Avy Violari (A)

Perinatal HIV Research Unit, Johannesburg, South Africa.

Tapiwa Mbengeranwa (T)

University of Zimbabwe Clinical Trials Research Centre, Harare, Zimbabwe.

Boniface Njau (B)

Kilimanjaro Christian Medical Center, Moshi, United Republic of Tanzania.

Lee Fairlie (L)

Wits Reproductive Health and HIV Institute, University of the Witwatersrand, Johannesburg, South Africa.

Gerard Theron (G)

Department of Obstetrics and Gynaecology, Stellenbosch University, Cape Town, South Africa.

Mwangelwa Mubiana-Mbewe (M)

Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.

Sandhya Khadse (S)

Department of Obstetrics and Gynaecology, BJ Government Medical College, Pune, India.

Renee Browning (R)

Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States of America.

Mary Glenn Fowler (MG)

Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.

George K Siberry (GK)

Office of HIV/AIDS, United States Agency for International Development, Washington, DC, United States of America.

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