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Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study

A link between infection, inflammation, neurodevelopment and adult illnesses has been proposed. The objective of this study was to examine the association between infection burden during childhood – a critical period of development for the immune and nervous systems – and subsequent systemic inflamm...

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Autores principales: MACKINNON, N., ZAMMIT, S., LEWIS, G., JONES, P. B., KHANDAKER, G. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851035/
https://www.ncbi.nlm.nih.gov/pubmed/29198208
http://dx.doi.org/10.1017/S0950268817002710
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author MACKINNON, N.
ZAMMIT, S.
LEWIS, G.
JONES, P. B.
KHANDAKER, G. M.
author_facet MACKINNON, N.
ZAMMIT, S.
LEWIS, G.
JONES, P. B.
KHANDAKER, G. M.
author_sort MACKINNON, N.
collection PubMed
description A link between infection, inflammation, neurodevelopment and adult illnesses has been proposed. The objective of this study was to examine the association between infection burden during childhood – a critical period of development for the immune and nervous systems – and subsequent systemic inflammatory markers and general intelligence. In the Avon Longitudinal Study of Parents and Children, a prospective birth cohort in England, we examined the association of exposure to infections during childhood, assessed at seven follow-ups between age 1·5 and 7·5 years, with subsequent: (1) serum interleukin 6 and C-reactive protein (CRP) levels at age 9; (2) intelligence quotient (IQ) at age 8. We also examined the relationship between inflammatory markers and IQ. Very high infection burden (90+ percentile) was associated with higher CRP levels, but this relationship was explained by body mass index (adjusted odds ratio (OR) 1·19; 95% confidence interval (CI) 0·95–1·50), maternal occupation (adjusted OR 1·23; 95% CI 0·98–1·55) and atopic disorders (adjusted OR 1·24; 95% CI 0·98–1·55). Higher CRP levels were associated with lower IQ; adjusted β = −0·79 (95% CI −1·31 to −0·27); P = 0·003. There was no strong evidence for an association between infection and IQ. The findings indicate that childhood infections do not have an independent, lasting effect on circulating inflammatory marker levels subsequently in childhood; however, elevated inflammatory markers may be harmful for intellectual development/function.
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spelling pubmed-58510352018-03-16 Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study MACKINNON, N. ZAMMIT, S. LEWIS, G. JONES, P. B. KHANDAKER, G. M. Epidemiol Infect Original Papers A link between infection, inflammation, neurodevelopment and adult illnesses has been proposed. The objective of this study was to examine the association between infection burden during childhood – a critical period of development for the immune and nervous systems – and subsequent systemic inflammatory markers and general intelligence. In the Avon Longitudinal Study of Parents and Children, a prospective birth cohort in England, we examined the association of exposure to infections during childhood, assessed at seven follow-ups between age 1·5 and 7·5 years, with subsequent: (1) serum interleukin 6 and C-reactive protein (CRP) levels at age 9; (2) intelligence quotient (IQ) at age 8. We also examined the relationship between inflammatory markers and IQ. Very high infection burden (90+ percentile) was associated with higher CRP levels, but this relationship was explained by body mass index (adjusted odds ratio (OR) 1·19; 95% confidence interval (CI) 0·95–1·50), maternal occupation (adjusted OR 1·23; 95% CI 0·98–1·55) and atopic disorders (adjusted OR 1·24; 95% CI 0·98–1·55). Higher CRP levels were associated with lower IQ; adjusted β = −0·79 (95% CI −1·31 to −0·27); P = 0·003. There was no strong evidence for an association between infection and IQ. The findings indicate that childhood infections do not have an independent, lasting effect on circulating inflammatory marker levels subsequently in childhood; however, elevated inflammatory markers may be harmful for intellectual development/function. Cambridge University Press 2017-12-04 /pmc/articles/PMC5851035/ /pubmed/29198208 http://dx.doi.org/10.1017/S0950268817002710 Text en © Cambridge University Press 2017 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
MACKINNON, N.
ZAMMIT, S.
LEWIS, G.
JONES, P. B.
KHANDAKER, G. M.
Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title_full Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title_fullStr Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title_full_unstemmed Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title_short Association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
title_sort association between childhood infection, serum inflammatory markers and intelligence: findings from a population-based prospective birth cohort study
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851035/
https://www.ncbi.nlm.nih.gov/pubmed/29198208
http://dx.doi.org/10.1017/S0950268817002710
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