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Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya

BACKGROUND: Milk lactoferrin is a multi‐functional, iron‐binding glycoprotein with immunomodulatory effects, protecting infants against infectious diseases. AIMS: This study explored how maternal inflammation/infection and iron‐deficiency anemia (IDA) might influence human milk lactoferrin. Lactofer...

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Autores principales: Fujita, Masako, Wander, Katherine, Paredes Ruvalcaba, Nerli, Odo, Amelia Ngozi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078565/
https://www.ncbi.nlm.nih.gov/pubmed/36181360
http://dx.doi.org/10.1002/ajhb.23812
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author Fujita, Masako
Wander, Katherine
Paredes Ruvalcaba, Nerli
Odo, Amelia Ngozi
author_facet Fujita, Masako
Wander, Katherine
Paredes Ruvalcaba, Nerli
Odo, Amelia Ngozi
author_sort Fujita, Masako
collection PubMed
description BACKGROUND: Milk lactoferrin is a multi‐functional, iron‐binding glycoprotein with immunomodulatory effects, protecting infants against infectious diseases. AIMS: This study explored how maternal inflammation/infection and iron‐deficiency anemia (IDA) might influence human milk lactoferrin. Lactoferrin might be elevated with maternal inflammation resulting from infectious disease processes. Conversely, lactoferrin might decrease with IDA, corresponding to scarce maternal iron for transfer in milk. In these two hypothesized scenarios, the degree of lactoferrin elevation or decrease might vary with infant vulnerability to infectious diseases or malnutrition. Alternatively, lactoferrin might be unassociated with inflammation/infection or IDA if mothers could buffer it against these conditions. MATERIALS & METHODS: We used cross‐sectional data from Ariaal mothers of northern Kenya (n = 200) to evaluate associations between milk lactoferrin and maternal inflammation/infection, IDA, infant age/sex, and the mother‐infant variable interactions in multivariate regression models. RESULTS: Maternal inflammation was associated with higher lactoferrin for younger infants (<~5 months of age) but with lower lactoferrin for older infants. Maternal IDA was unassociated with lactoferrin alone or in interaction with infant variables. DISCUSSION & CONCLUSION: Results suggest that mothers of vulnerable young infants deliver more lactoferrin when they have inflammation/infection but mothers with older infants do not, and that maternal delivery of lactoferrin is unaffected by their IDA. Longitudinal research should verify these findings.
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spelling pubmed-100785652023-04-07 Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya Fujita, Masako Wander, Katherine Paredes Ruvalcaba, Nerli Odo, Amelia Ngozi Am J Hum Biol Short Reports BACKGROUND: Milk lactoferrin is a multi‐functional, iron‐binding glycoprotein with immunomodulatory effects, protecting infants against infectious diseases. AIMS: This study explored how maternal inflammation/infection and iron‐deficiency anemia (IDA) might influence human milk lactoferrin. Lactoferrin might be elevated with maternal inflammation resulting from infectious disease processes. Conversely, lactoferrin might decrease with IDA, corresponding to scarce maternal iron for transfer in milk. In these two hypothesized scenarios, the degree of lactoferrin elevation or decrease might vary with infant vulnerability to infectious diseases or malnutrition. Alternatively, lactoferrin might be unassociated with inflammation/infection or IDA if mothers could buffer it against these conditions. MATERIALS & METHODS: We used cross‐sectional data from Ariaal mothers of northern Kenya (n = 200) to evaluate associations between milk lactoferrin and maternal inflammation/infection, IDA, infant age/sex, and the mother‐infant variable interactions in multivariate regression models. RESULTS: Maternal inflammation was associated with higher lactoferrin for younger infants (<~5 months of age) but with lower lactoferrin for older infants. Maternal IDA was unassociated with lactoferrin alone or in interaction with infant variables. DISCUSSION & CONCLUSION: Results suggest that mothers of vulnerable young infants deliver more lactoferrin when they have inflammation/infection but mothers with older infants do not, and that maternal delivery of lactoferrin is unaffected by their IDA. Longitudinal research should verify these findings. John Wiley & Sons, Inc. 2022-10-01 2022-12 /pmc/articles/PMC10078565/ /pubmed/36181360 http://dx.doi.org/10.1002/ajhb.23812 Text en © 2022 The Authors. American Journal of Human Biology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Reports
Fujita, Masako
Wander, Katherine
Paredes Ruvalcaba, Nerli
Odo, Amelia Ngozi
Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title_full Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title_fullStr Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title_full_unstemmed Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title_short Human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern Kenya
title_sort human milk lactoferrin variation in relation to maternal inflammation and iron deficiency in northern kenya
topic Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078565/
https://www.ncbi.nlm.nih.gov/pubmed/36181360
http://dx.doi.org/10.1002/ajhb.23812
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