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Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study

BACKGROUND: Limited epidemiological evidence suggests that low maternal iron status and anaemia in pregnancy may increase the risk of childhood respiratory and allergic outcomes. OBJECTIVES: To investigate the relation between maternal haemoglobin concentrations in pregnancy and childhood respirator...

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Autores principales: Shaheen, S. O., Macdonald‐Wallis, C., Lawlor, D. A., Henderson, A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725736/
https://www.ncbi.nlm.nih.gov/pubmed/28940397
http://dx.doi.org/10.1111/cea.13034
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author Shaheen, S. O.
Macdonald‐Wallis, C.
Lawlor, D. A.
Henderson, A. J.
author_facet Shaheen, S. O.
Macdonald‐Wallis, C.
Lawlor, D. A.
Henderson, A. J.
author_sort Shaheen, S. O.
collection PubMed
description BACKGROUND: Limited epidemiological evidence suggests that low maternal iron status and anaemia in pregnancy may increase the risk of childhood respiratory and allergic outcomes. OBJECTIVES: To investigate the relation between maternal haemoglobin concentrations in pregnancy and childhood respiratory and allergic outcomes. METHODS: In the Avon Longitudinal Study of Parents and Children (ALSPAC), we examined associations of maternal haemoglobin concentrations (g/dL) in pregnancy with hayfever, eczema, wheezing, doctor‐diagnosed asthma, allergic sensitisation and total IgE at 7 years, and with lung function at 8‐9 years in the offspring, after controlling for potential confounders (N = 3234‐5335). RESULTS: Maternal haemoglobin was not associated with offspring hayfever, eczema, wheezing or asthma. However, the first haemoglobin measurement in pregnancy (<18 weeks' gestation) and the last measurement (>28 weeks' gestation) were negatively associated with allergic sensitisation (adjusted odds ratio [95% CI] per g/dL 0.91 [0.83 to 0.99] and 0.90 [0.83 to 0.98], respectively). The last haemoglobin measurement was also negatively associated with total IgE (adjusted geometric mean ratio 0.94 [0.88 to 0.99]). Anaemia (haemoglobin <11 g/dL) in late pregnancy was negatively associated with forced vital capacity (difference in standard deviation score −0.07 [−0.13 to −0.01]). CONCLUSIONS AND CLINICAL RELEVANCE: Lower maternal haemoglobin in pregnancy may be a risk factor for allergic sensitisation, elevated IgE and lower FVC in childhood, which may reflect effects of lower prenatal iron status. However, maternal haemoglobin was not associated with risk of childhood asthma or other allergic disorders.
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spelling pubmed-57257362017-12-18 Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study Shaheen, S. O. Macdonald‐Wallis, C. Lawlor, D. A. Henderson, A. J. Clin Exp Allergy ORIGINAL ARTICLES BACKGROUND: Limited epidemiological evidence suggests that low maternal iron status and anaemia in pregnancy may increase the risk of childhood respiratory and allergic outcomes. OBJECTIVES: To investigate the relation between maternal haemoglobin concentrations in pregnancy and childhood respiratory and allergic outcomes. METHODS: In the Avon Longitudinal Study of Parents and Children (ALSPAC), we examined associations of maternal haemoglobin concentrations (g/dL) in pregnancy with hayfever, eczema, wheezing, doctor‐diagnosed asthma, allergic sensitisation and total IgE at 7 years, and with lung function at 8‐9 years in the offspring, after controlling for potential confounders (N = 3234‐5335). RESULTS: Maternal haemoglobin was not associated with offspring hayfever, eczema, wheezing or asthma. However, the first haemoglobin measurement in pregnancy (<18 weeks' gestation) and the last measurement (>28 weeks' gestation) were negatively associated with allergic sensitisation (adjusted odds ratio [95% CI] per g/dL 0.91 [0.83 to 0.99] and 0.90 [0.83 to 0.98], respectively). The last haemoglobin measurement was also negatively associated with total IgE (adjusted geometric mean ratio 0.94 [0.88 to 0.99]). Anaemia (haemoglobin <11 g/dL) in late pregnancy was negatively associated with forced vital capacity (difference in standard deviation score −0.07 [−0.13 to −0.01]). CONCLUSIONS AND CLINICAL RELEVANCE: Lower maternal haemoglobin in pregnancy may be a risk factor for allergic sensitisation, elevated IgE and lower FVC in childhood, which may reflect effects of lower prenatal iron status. However, maternal haemoglobin was not associated with risk of childhood asthma or other allergic disorders. John Wiley and Sons Inc. 2017-10-16 2017-12 /pmc/articles/PMC5725736/ /pubmed/28940397 http://dx.doi.org/10.1111/cea.13034 Text en © 2017 The Authors. Clinical & Experimental Allergy Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Shaheen, S. O.
Macdonald‐Wallis, C.
Lawlor, D. A.
Henderson, A. J.
Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title_full Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title_fullStr Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title_full_unstemmed Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title_short Haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: Birth cohort study
title_sort haemoglobin concentrations in pregnancy and respiratory and allergic outcomes in childhood: birth cohort study
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725736/
https://www.ncbi.nlm.nih.gov/pubmed/28940397
http://dx.doi.org/10.1111/cea.13034
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