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Reduced prevalence of placental malaria in primiparae with blood group O
BACKGROUND: Blood group O protects African children against severe malaria and has reached high prevalence in malarious regions. However, its role in malaria in pregnancy is ambiguous. In 839 delivering Ghanaian women, associations of ABO blood groups with Plasmodium falciparum infection were examin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119177/ https://www.ncbi.nlm.nih.gov/pubmed/25066505 http://dx.doi.org/10.1186/1475-2875-13-289 |
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author | Bedu-Addo, George Gai, Prabhanjan P Meese, Stefanie Eggelte, Teunis A Thangaraj, Kumarasamy Mockenhaupt, Frank P |
author_facet | Bedu-Addo, George Gai, Prabhanjan P Meese, Stefanie Eggelte, Teunis A Thangaraj, Kumarasamy Mockenhaupt, Frank P |
author_sort | Bedu-Addo, George |
collection | PubMed |
description | BACKGROUND: Blood group O protects African children against severe malaria and has reached high prevalence in malarious regions. However, its role in malaria in pregnancy is ambiguous. In 839 delivering Ghanaian women, associations of ABO blood groups with Plasmodium falciparum infection were examined. METHODS: Plasmodium falciparum infection was diagnosed in placental blood samples by microscopy and PCR assays. Present or past infection was defined as the detection of parasitaemia or haemozoin by microscopy, or a positive PCR result. Blood groups were inferred from genotyping rs8176719 (indicating the O allele) and rs8176746/rs8176747 (distinguishing the B allele from the A allele). RESULTS: The majority of women had blood group O (55.4%); present or past P. falciparum infection was seen in 62.3% of all women. Among multiparae, the blood groups had no influence on P. falciparum infection. In contrast, primiparae with blood group O had significantly less present or past infection than women with non-O blood groups (61.5 vs 76.2%, P = 0.007). In multivariate analysis, the odds of present or past placental P. falciparum infection were reduced by 45% in blood group O primiparae (aOR, 0.55 [95% CI, 0.33–0.94]). CONCLUSIONS: The present study shows a clear protective effect of blood group O against malaria in primiparae. This accords with findings in severe malaria and in vitro results. The data underline the relevance of host genetic protection among primiparae, i.e. the high-risk group for malaria in pregnancy, and contribute to the understanding of high O allele frequencies in Africa. |
format | Online Article Text |
id | pubmed-4119177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41191772014-08-03 Reduced prevalence of placental malaria in primiparae with blood group O Bedu-Addo, George Gai, Prabhanjan P Meese, Stefanie Eggelte, Teunis A Thangaraj, Kumarasamy Mockenhaupt, Frank P Malar J Research BACKGROUND: Blood group O protects African children against severe malaria and has reached high prevalence in malarious regions. However, its role in malaria in pregnancy is ambiguous. In 839 delivering Ghanaian women, associations of ABO blood groups with Plasmodium falciparum infection were examined. METHODS: Plasmodium falciparum infection was diagnosed in placental blood samples by microscopy and PCR assays. Present or past infection was defined as the detection of parasitaemia or haemozoin by microscopy, or a positive PCR result. Blood groups were inferred from genotyping rs8176719 (indicating the O allele) and rs8176746/rs8176747 (distinguishing the B allele from the A allele). RESULTS: The majority of women had blood group O (55.4%); present or past P. falciparum infection was seen in 62.3% of all women. Among multiparae, the blood groups had no influence on P. falciparum infection. In contrast, primiparae with blood group O had significantly less present or past infection than women with non-O blood groups (61.5 vs 76.2%, P = 0.007). In multivariate analysis, the odds of present or past placental P. falciparum infection were reduced by 45% in blood group O primiparae (aOR, 0.55 [95% CI, 0.33–0.94]). CONCLUSIONS: The present study shows a clear protective effect of blood group O against malaria in primiparae. This accords with findings in severe malaria and in vitro results. The data underline the relevance of host genetic protection among primiparae, i.e. the high-risk group for malaria in pregnancy, and contribute to the understanding of high O allele frequencies in Africa. BioMed Central 2014-07-28 /pmc/articles/PMC4119177/ /pubmed/25066505 http://dx.doi.org/10.1186/1475-2875-13-289 Text en Copyright © 2014 Bedu-Addo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Bedu-Addo, George Gai, Prabhanjan P Meese, Stefanie Eggelte, Teunis A Thangaraj, Kumarasamy Mockenhaupt, Frank P Reduced prevalence of placental malaria in primiparae with blood group O |
title | Reduced prevalence of placental malaria in primiparae with blood group O |
title_full | Reduced prevalence of placental malaria in primiparae with blood group O |
title_fullStr | Reduced prevalence of placental malaria in primiparae with blood group O |
title_full_unstemmed | Reduced prevalence of placental malaria in primiparae with blood group O |
title_short | Reduced prevalence of placental malaria in primiparae with blood group O |
title_sort | reduced prevalence of placental malaria in primiparae with blood group o |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119177/ https://www.ncbi.nlm.nih.gov/pubmed/25066505 http://dx.doi.org/10.1186/1475-2875-13-289 |
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