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Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi

Environmental enteric dysfunction (EED) is common and contributes to linear growth faltering (stunting) and mortality among children in low-resource settings. A few studies on the environmental causes of EED have been conducted but the exact exposures that cause or predispose children to EED are con...

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Autores principales: Liu, Zhifei, Fan, Yue-Mei, Ashorn, Per, Chingwanda, Chilungamo, Maleta, Kenneth, Hallamaa, Lotta, Hyöty, Heikki, Chaima, David, Ashorn, Ulla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9517768/
https://www.ncbi.nlm.nih.gov/pubmed/36078607
http://dx.doi.org/10.3390/ijerph191710891
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author Liu, Zhifei
Fan, Yue-Mei
Ashorn, Per
Chingwanda, Chilungamo
Maleta, Kenneth
Hallamaa, Lotta
Hyöty, Heikki
Chaima, David
Ashorn, Ulla
author_facet Liu, Zhifei
Fan, Yue-Mei
Ashorn, Per
Chingwanda, Chilungamo
Maleta, Kenneth
Hallamaa, Lotta
Hyöty, Heikki
Chaima, David
Ashorn, Ulla
author_sort Liu, Zhifei
collection PubMed
description Environmental enteric dysfunction (EED) is common and contributes to linear growth faltering (stunting) and mortality among children in low-resource settings. A few studies on the environmental causes of EED have been conducted but the exact exposures that cause or predispose children to EED are context-specific and not clear. This study aimed to assess associations between selected environmental exposures and EED markers among 620 18-month-old children. This was a secondary analysis of data from Malawian children who participated in a randomized controlled trial (iLiNS-DYAD, registered at clinicaltrials.gov as NCT01239693) from birth to 18 months of age. Data on environmental exposures, including drinking water source, sanitation, exposure to animals, housing materials, season, residential area, and food insecurity were collected at enrolment. Biomarkers of EED included concentrations of calprotectin, regenerating 1B protein (REG1B), and alpha-1-antitrypsin from stool samples to assess intestinal inflammation, repair, and permeability, respectively. We performed bivariate and multivariable analyses to assess associations between environmental exposures and EED biomarkers. Adjusting for possible confounders, we did not find associations between the selected environmental exposures and the three biomarkers. These results do not provide support for our hypothesis that the studied adverse environmental exposures are associated with increased concentrations of children’s EED markers in rural Malawi.
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spelling pubmed-95177682022-09-29 Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi Liu, Zhifei Fan, Yue-Mei Ashorn, Per Chingwanda, Chilungamo Maleta, Kenneth Hallamaa, Lotta Hyöty, Heikki Chaima, David Ashorn, Ulla Int J Environ Res Public Health Article Environmental enteric dysfunction (EED) is common and contributes to linear growth faltering (stunting) and mortality among children in low-resource settings. A few studies on the environmental causes of EED have been conducted but the exact exposures that cause or predispose children to EED are context-specific and not clear. This study aimed to assess associations between selected environmental exposures and EED markers among 620 18-month-old children. This was a secondary analysis of data from Malawian children who participated in a randomized controlled trial (iLiNS-DYAD, registered at clinicaltrials.gov as NCT01239693) from birth to 18 months of age. Data on environmental exposures, including drinking water source, sanitation, exposure to animals, housing materials, season, residential area, and food insecurity were collected at enrolment. Biomarkers of EED included concentrations of calprotectin, regenerating 1B protein (REG1B), and alpha-1-antitrypsin from stool samples to assess intestinal inflammation, repair, and permeability, respectively. We performed bivariate and multivariable analyses to assess associations between environmental exposures and EED biomarkers. Adjusting for possible confounders, we did not find associations between the selected environmental exposures and the three biomarkers. These results do not provide support for our hypothesis that the studied adverse environmental exposures are associated with increased concentrations of children’s EED markers in rural Malawi. MDPI 2022-09-01 /pmc/articles/PMC9517768/ /pubmed/36078607 http://dx.doi.org/10.3390/ijerph191710891 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Zhifei
Fan, Yue-Mei
Ashorn, Per
Chingwanda, Chilungamo
Maleta, Kenneth
Hallamaa, Lotta
Hyöty, Heikki
Chaima, David
Ashorn, Ulla
Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title_full Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title_fullStr Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title_full_unstemmed Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title_short Lack of Associations between Environmental Exposures and Environmental Enteric Dysfunction among 18-Month-Old Children in Rural Malawi
title_sort lack of associations between environmental exposures and environmental enteric dysfunction among 18-month-old children in rural malawi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9517768/
https://www.ncbi.nlm.nih.gov/pubmed/36078607
http://dx.doi.org/10.3390/ijerph191710891
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