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
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
e0255250Subventions
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.
Références
PLoS One. 2016 Apr 06;11(4):e0151762
pubmed: 27049853
N Engl J Med. 2015 Aug 27;373(9):795-807
pubmed: 26192873
Pediatr Infect Dis J. 2016 Jan;35(1):71-7
pubmed: 26741583
Lancet. 2008 Jan 19;371(9608):243-60
pubmed: 18207566
PLoS One. 2013 May 29;8(5):e64636
pubmed: 23734210
Pediatr Infect Dis J. 2015 Aug;34(8):851-7
pubmed: 25961889
JAMA. 2006 Aug 16;296(7):794-805
pubmed: 16905785
J Acquir Immune Defic Syndr. 2019 Dec 1;82(4):377-385
pubmed: 31567725
ISRN Pediatr. 2012;2012:763591
pubmed: 22701801
AIDS. 2020 Feb 1;34(2):215-225
pubmed: 31634154
Public Health Nutr. 2013 Sep;16(9):1548-57
pubmed: 23507372
HIV Clin Trials. 2018 Dec;19(6):209-224
pubmed: 30890061
J Acquir Immune Defic Syndr. 2021 Jan 1;86(1):81-90
pubmed: 33027153
Curr HIV/AIDS Rep. 2019 Dec;16(6):501-513
pubmed: 31732866
J Acquir Immune Defic Syndr. 2018 Apr 1;77(4):383-392
pubmed: 29239901
J Acquir Immune Defic Syndr. 2011 Feb 1;56(2):131-8
pubmed: 21124227
Lancet. 2013 Aug 3;382(9890):427-451
pubmed: 23746772
Lancet. 2007 Jan 6;369(9555):60-70
pubmed: 17208643
Pediatr Infect Dis J. 2017 Sep;36(9):869-876
pubmed: 28198792
BMC Pediatr. 2015 Jun 06;15:66
pubmed: 26048411
Matern Child Nutr. 2019 Jul;15(3):e12776
pubmed: 30609287
Lancet Child Adolesc Health. 2019 Apr;3(4):234-244
pubmed: 30773459
N Engl J Med. 2016 Nov 3;375(18):1726-1737
pubmed: 27806243