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Treatment Heterogeneity of Water, Sanitation, Hygiene, and Nutrition Interventions on Child Growth by Environmental Enteric Dysfunction and Pathogen Status for Young Children in Bangladesh.
Butzin-Dozier, Zachary; Ji, Yunwen; Coyle, Jeremy; Malenica, Ivana; McQuade, Elizabeth T Rogawski; Grembi, Jessica Anne; Platts-Mills, James A; Houpt, Eric R; Graham, Jay P; Ali, Shahjahan; Rahman, Md Ziaur; Alauddin, Mohammad; Famida, Syeda L; Akther, Salma; Hossen, Md Saheen; Mutsuddi, Palash; Shoab, Abul K; Rahman, Mahbubur; Islam, Md Ohedul; Miah, Rana; Taniuchi, Mami; Liu, Jie; Alauddin, Sarah; Stewart, Christine P; Luby, Stephen P; Colford, John M; Hubbard, Alan E; Mertens, Andrew N; Lin, Audrie.
Afiliação
  • Butzin-Dozier Z; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Ji Y; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Coyle J; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Malenica I; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • McQuade ETR; Rollins School of Public Health, Emory University, Atlanta, GA USA.
  • Grembi JA; Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA USA.
  • Platts-Mills JA; School of Medicine, University of Virginia, Charlottesville, VA, USA.
  • Houpt ER; School of Medicine, University of Virginia, Charlottesville, VA, USA.
  • Graham JP; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Ali S; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Rahman MZ; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Alauddin M; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Famida SL; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Akther S; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Hossen MS; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Mutsuddi P; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Shoab AK; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Rahman M; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Islam MO; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Miah R; International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
  • Taniuchi M; School of Medicine, University of Virginia, Charlottesville, VA, USA.
  • Liu J; School of Public Health, Qingdao University, Qingdao, China.
  • Alauddin S; Wagner College, Staten Island, NY USA.
  • Stewart CP; Department of Nutrition, University of California Davis, Davis, CA USA.
  • Luby SP; Division of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA USA.
  • Colford JM; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Hubbard AE; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Mertens AN; School of Public Health, University of California, Berkeley, Berkeley, CA USA.
  • Lin A; Department of Microbiology and Environmental Toxicology, University of California, Santa Cruz, Santa Cruz, CA USA.
medRxiv ; 2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38585931
ABSTRACT

Background:

Water, sanitation, hygiene (WSH), nutrition (N), and combined (N+WSH) interventions are often implemented by global health organizations, but WSH interventions may insufficiently reduce pathogen exposure, and nutrition interventions may be modified by environmental enteric dysfunction (EED), a condition of increased intestinal permeability and inflammation. This study investigated the heterogeneity of these treatments' effects based on individual pathogen and EED biomarker status with respect to child linear growth.

Methods:

We applied cross-validated targeted maximum likelihood estimation and super learner ensemble machine learning to assess the conditional treatment effects in subgroups defined by biomarker and pathogen status. We analyzed treatment (N+WSH, WSH, N, or control) randomly assigned in-utero, child pathogen and EED data at 14 months of age, and child LAZ at 28 months of age. We estimated the difference in mean child length for age Z-score (LAZ) under the treatment rule and the difference in stratified treatment effect (treatment effect difference) comparing children with high versus low pathogen/biomarker status while controlling for baseline covariates.

Results:

We analyzed data from 1,522 children, who had median LAZ of -1.56. We found that myeloperoxidase (N+WSH treatment effect difference 0.0007 LAZ, WSH treatment effect difference 0.1032 LAZ, N treatment effect difference 0.0037 LAZ) and Campylobacter infection (N+WSH treatment effect difference 0.0011 LAZ, WSH difference 0.0119 LAZ, N difference 0.0255 LAZ) were associated with greater effect of all interventions on growth. In other words, children with high myeloperoxidase or Campylobacter infection experienced a greater impact of the interventions on growth. We found that a treatment rule that assigned the N+WSH (LAZ difference 0.23, 95% CI (0.05, 0.41)) and WSH (LAZ difference 0.17, 95% CI (0.04, 0.30)) interventions based on EED biomarkers and pathogens increased predicted child growth compared to the randomly allocated intervention.

Conclusions:

These findings indicate that EED biomarker and pathogen status, particularly Campylobacter and myeloperoxidase (a measure of gut inflammation), may be related to impact of N+WSH, WSH, and N interventions on child linear growth.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article