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Burden of malaria infection among individuals of varied blood groups in Kenya
BACKGROUND: The ABO blood groups consist of A, B, and H carbohydrate antigens, which regulate protein activities during malaria infection in humans. Understanding the interplay between the malaria parasite and blood group antigens is essential in understanding new interventions to reduce the global...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438094/ https://www.ncbi.nlm.nih.gov/pubmed/36050680 http://dx.doi.org/10.1186/s12936-022-04251-1 |
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author | Yeda, Redemptah Okudo, Charles Owiti, Eunice Biwot, Gladys Momanyi, Cliff Korir, Winnie Mitsanze, Thoya Tegerei, Caroline Juma, Dennis Opot, Benjamin Mwakio, Edwin Chemwor, Gladys Okoth, Raphael Ochora, Douglas O. Cheruiyot, Agnes C. Roth, Amanda Akala, Hoseah M. Andagalu, Ben |
author_facet | Yeda, Redemptah Okudo, Charles Owiti, Eunice Biwot, Gladys Momanyi, Cliff Korir, Winnie Mitsanze, Thoya Tegerei, Caroline Juma, Dennis Opot, Benjamin Mwakio, Edwin Chemwor, Gladys Okoth, Raphael Ochora, Douglas O. Cheruiyot, Agnes C. Roth, Amanda Akala, Hoseah M. Andagalu, Ben |
author_sort | Yeda, Redemptah |
collection | PubMed |
description | BACKGROUND: The ABO blood groups consist of A, B, and H carbohydrate antigens, which regulate protein activities during malaria infection in humans. Understanding the interplay between the malaria parasite and blood group antigens is essential in understanding new interventions to reduce the global burden of malaria. This study assessed the burden of malaria infection among individuals with varying blood groups seeking treatment at selected hospitals in Kenya. METHODS: A total of 366 samples from an ongoing malaria surveillance study were diagnosed for malaria by microscopy and further typed for blood group using ABO blood grouping. Age and sex were recorded in a data sheet, and analysed using R software version 4. Groups’ proportions (blood group, malaria infection, age and sex) were compared using Pearson’s Chi-square and Fischer exact tests. Wilcoxon and Kruskal-Wallis tests were performed and P-value < 0.05 was considered significant after Bonferroni correction for multiple comparisons. To understand the effect of each blood group on parasitaemia, multivariate logistic regression was used to model ABO blood group in relation to parasitaemia. RESULTS: Of the 366 samples analysed, 312 were malaria positive, mean age was 9.83 years (< 5 years n = 152 (48.41%), 6 to 17 years n = 101 (32.16%) and > 18 years n = 61 (19.43%)). Malaria prevalence was higher among females than males, 54.46% and 45.54%, respectively. Kisumu enrolled the highest number 109 (35%)) of malaria cases, Kombewa 108 (35%), Malindi 32 (10%), Kisii 28 (9%), Marigat 23 (7%), and Kericho 12 (4%). Blood group O(+) was the most prevalent among the enrolled individuals (46.50%), A(+) (27.71%), B(+) (21.02%) and AB(+) (4.78%) respectively. Compared to blood group O+, blood group B(+) individuals were (14%) were more likely to habour Plasmodium falciparum infection as opposed to A(+) and AB(+) individuals, that were 7% and 20%, respectively,. Those living in malaria-endemic zones presented with higher parasite densities compared to those living in malaria-epidemic (p = 0.0061). Individuals bearing B + blood group are more likely to habour high parasitaemia compared to O + blood group bearers (OR = 4.47, CI = 1.53–13.05, p = 0.006). CONCLUSION: Individuals of blood group B harbour high parasitaemia compared with the blood group O, Additionally, blood group A and B present with symptoms at lower parasitaemia than blood group O. Regardles of malaria transmission zones, individuals from endemic zones showed up with high parasitaemia and among them were more individuals of blood groups A and B than individuals of blood group O. Implying that these individuals were more at risk and require additional attention and effective case management. GARPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04251-1. |
format | Online Article Text |
id | pubmed-9438094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94380942022-09-03 Burden of malaria infection among individuals of varied blood groups in Kenya Yeda, Redemptah Okudo, Charles Owiti, Eunice Biwot, Gladys Momanyi, Cliff Korir, Winnie Mitsanze, Thoya Tegerei, Caroline Juma, Dennis Opot, Benjamin Mwakio, Edwin Chemwor, Gladys Okoth, Raphael Ochora, Douglas O. Cheruiyot, Agnes C. Roth, Amanda Akala, Hoseah M. Andagalu, Ben Malar J Research BACKGROUND: The ABO blood groups consist of A, B, and H carbohydrate antigens, which regulate protein activities during malaria infection in humans. Understanding the interplay between the malaria parasite and blood group antigens is essential in understanding new interventions to reduce the global burden of malaria. This study assessed the burden of malaria infection among individuals with varying blood groups seeking treatment at selected hospitals in Kenya. METHODS: A total of 366 samples from an ongoing malaria surveillance study were diagnosed for malaria by microscopy and further typed for blood group using ABO blood grouping. Age and sex were recorded in a data sheet, and analysed using R software version 4. Groups’ proportions (blood group, malaria infection, age and sex) were compared using Pearson’s Chi-square and Fischer exact tests. Wilcoxon and Kruskal-Wallis tests were performed and P-value < 0.05 was considered significant after Bonferroni correction for multiple comparisons. To understand the effect of each blood group on parasitaemia, multivariate logistic regression was used to model ABO blood group in relation to parasitaemia. RESULTS: Of the 366 samples analysed, 312 were malaria positive, mean age was 9.83 years (< 5 years n = 152 (48.41%), 6 to 17 years n = 101 (32.16%) and > 18 years n = 61 (19.43%)). Malaria prevalence was higher among females than males, 54.46% and 45.54%, respectively. Kisumu enrolled the highest number 109 (35%)) of malaria cases, Kombewa 108 (35%), Malindi 32 (10%), Kisii 28 (9%), Marigat 23 (7%), and Kericho 12 (4%). Blood group O(+) was the most prevalent among the enrolled individuals (46.50%), A(+) (27.71%), B(+) (21.02%) and AB(+) (4.78%) respectively. Compared to blood group O+, blood group B(+) individuals were (14%) were more likely to habour Plasmodium falciparum infection as opposed to A(+) and AB(+) individuals, that were 7% and 20%, respectively,. Those living in malaria-endemic zones presented with higher parasite densities compared to those living in malaria-epidemic (p = 0.0061). Individuals bearing B + blood group are more likely to habour high parasitaemia compared to O + blood group bearers (OR = 4.47, CI = 1.53–13.05, p = 0.006). CONCLUSION: Individuals of blood group B harbour high parasitaemia compared with the blood group O, Additionally, blood group A and B present with symptoms at lower parasitaemia than blood group O. Regardles of malaria transmission zones, individuals from endemic zones showed up with high parasitaemia and among them were more individuals of blood groups A and B than individuals of blood group O. Implying that these individuals were more at risk and require additional attention and effective case management. GARPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12936-022-04251-1. BioMed Central 2022-09-01 /pmc/articles/PMC9438094/ /pubmed/36050680 http://dx.doi.org/10.1186/s12936-022-04251-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yeda, Redemptah Okudo, Charles Owiti, Eunice Biwot, Gladys Momanyi, Cliff Korir, Winnie Mitsanze, Thoya Tegerei, Caroline Juma, Dennis Opot, Benjamin Mwakio, Edwin Chemwor, Gladys Okoth, Raphael Ochora, Douglas O. Cheruiyot, Agnes C. Roth, Amanda Akala, Hoseah M. Andagalu, Ben Burden of malaria infection among individuals of varied blood groups in Kenya |
title | Burden of malaria infection among individuals of varied blood groups in Kenya |
title_full | Burden of malaria infection among individuals of varied blood groups in Kenya |
title_fullStr | Burden of malaria infection among individuals of varied blood groups in Kenya |
title_full_unstemmed | Burden of malaria infection among individuals of varied blood groups in Kenya |
title_short | Burden of malaria infection among individuals of varied blood groups in Kenya |
title_sort | burden of malaria infection among individuals of varied blood groups in kenya |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438094/ https://www.ncbi.nlm.nih.gov/pubmed/36050680 http://dx.doi.org/10.1186/s12936-022-04251-1 |
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