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ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence

Besides their fundamental role in transfusion medicine, ABO and other histo-blood group antigens are associated with the pathogenesis of some human diseases such as malignancy and thrombosis. Reports also show a possible relationship with the risk of asthma and other forms of respiratory atopy. This...

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Autores principales: Uwaezuoke, Samuel N, Eze, Joy N, Ayuk, Adaeze C, Ndu, Ikenna K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067593/
https://www.ncbi.nlm.nih.gov/pubmed/30102298
http://dx.doi.org/10.2147/PHMT.S162570
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author Uwaezuoke, Samuel N
Eze, Joy N
Ayuk, Adaeze C
Ndu, Ikenna K
author_facet Uwaezuoke, Samuel N
Eze, Joy N
Ayuk, Adaeze C
Ndu, Ikenna K
author_sort Uwaezuoke, Samuel N
collection PubMed
description Besides their fundamental role in transfusion medicine, ABO and other histo-blood group antigens are associated with the pathogenesis of some human diseases such as malignancy and thrombosis. Reports also show a possible relationship with the risk of asthma and other forms of respiratory atopy. This paper aims to critically review the current evidence linking ABO histo-blood group with the risk of respiratory atopy in children and adults. A literature search was conducted with PubMed to gather baseline data about this relationship. The search extended to studies published within the past 45 years. First, the molecular mechanism underpinning the role of ABO antigenic system in human diseases comprises a fascinating relationship with von Willebrand factor and several pro-inflammatory and adhesion molecules. Second, specific blood group types vary with asthma phenotypes; severe asthma is associated with B phenotype, while mild and moderate asthma is associated with O and A phenotypes. Third, O phenotype has been linked to allergic rhinitis but only in males. Furthermore, asthma risk is related to O/Lewis negative/secretor phenotypes, while a significant relationship has also been established with B phenotype but not with A and O phenotypes. However, one study failed to establish a significant relationship with any of the ABO blood group antigens. In conclusion, there is no unanimity on the specific histo-blood groups linked to respiratory atopy risk, although asthma phenotypes are associated with specific blood groups. Despite the prospect that this relationship holds for the use of blood-group typing in evaluating respiratory atopy risk in children, more evidence-based studies are still required for its validation.
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spelling pubmed-60675932018-08-10 ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence Uwaezuoke, Samuel N Eze, Joy N Ayuk, Adaeze C Ndu, Ikenna K Pediatric Health Med Ther Review Besides their fundamental role in transfusion medicine, ABO and other histo-blood group antigens are associated with the pathogenesis of some human diseases such as malignancy and thrombosis. Reports also show a possible relationship with the risk of asthma and other forms of respiratory atopy. This paper aims to critically review the current evidence linking ABO histo-blood group with the risk of respiratory atopy in children and adults. A literature search was conducted with PubMed to gather baseline data about this relationship. The search extended to studies published within the past 45 years. First, the molecular mechanism underpinning the role of ABO antigenic system in human diseases comprises a fascinating relationship with von Willebrand factor and several pro-inflammatory and adhesion molecules. Second, specific blood group types vary with asthma phenotypes; severe asthma is associated with B phenotype, while mild and moderate asthma is associated with O and A phenotypes. Third, O phenotype has been linked to allergic rhinitis but only in males. Furthermore, asthma risk is related to O/Lewis negative/secretor phenotypes, while a significant relationship has also been established with B phenotype but not with A and O phenotypes. However, one study failed to establish a significant relationship with any of the ABO blood group antigens. In conclusion, there is no unanimity on the specific histo-blood groups linked to respiratory atopy risk, although asthma phenotypes are associated with specific blood groups. Despite the prospect that this relationship holds for the use of blood-group typing in evaluating respiratory atopy risk in children, more evidence-based studies are still required for its validation. Dove Medical Press 2018-07-27 /pmc/articles/PMC6067593/ /pubmed/30102298 http://dx.doi.org/10.2147/PHMT.S162570 Text en © 2018 Uwaezuoke et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Uwaezuoke, Samuel N
Eze, Joy N
Ayuk, Adaeze C
Ndu, Ikenna K
ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title_full ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title_fullStr ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title_full_unstemmed ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title_short ABO histo-blood group and risk of respiratory atopy in children: a review of published evidence
title_sort abo histo-blood group and risk of respiratory atopy in children: a review of published evidence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067593/
https://www.ncbi.nlm.nih.gov/pubmed/30102298
http://dx.doi.org/10.2147/PHMT.S162570
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