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Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19
Polymorphism in human platelet antigen (HPA)-1 and HPA-3 (GPIIb/IIIa), HPA-2 (GPIb/IX), HPA-4 (GPIIIa), HPA-5 (GPIa/IIa), & HPA-15 (CD109) was investigated in 86 COVID-19-infected patients with thrombocytopenia (Group A) and 136 COVID-19-infected patients without thrombocytopenia (Group B). HPA...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658732/ https://www.ncbi.nlm.nih.gov/pubmed/38020117 http://dx.doi.org/10.3389/fmed.2023.1265568 |
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author | Ghaffari, Kazem Rad, Mahsa Ashrafi Moradi Hasan-Abad, Amin Khosravi, Mersedeh Benvidi, Arefeh Iraji, Mahsa Khargh, Heidar Ali Heidari Ghasemi, Ali |
author_facet | Ghaffari, Kazem Rad, Mahsa Ashrafi Moradi Hasan-Abad, Amin Khosravi, Mersedeh Benvidi, Arefeh Iraji, Mahsa Khargh, Heidar Ali Heidari Ghasemi, Ali |
author_sort | Ghaffari, Kazem |
collection | PubMed |
description | Polymorphism in human platelet antigen (HPA)-1 and HPA-3 (GPIIb/IIIa), HPA-2 (GPIb/IX), HPA-4 (GPIIIa), HPA-5 (GPIa/IIa), & HPA-15 (CD109) was investigated in 86 COVID-19-infected patients with thrombocytopenia (Group A) and 136 COVID-19-infected patients without thrombocytopenia (Group B). HPA genotyping was done by the sequence-specific primers PCR method. Lower HPA-3a and higher HPA-3b (P = 0.028) allele frequencies were seen in Group A than in Group B, and homozygosity for HPA 3b (P = 0.038) alleles was more prevalent in Group A than in Group B. The allele and genotype distributions of the other HPA polymorphic variants were similar between the two groups. Univariate analysis identified the CCGGGC (P = 0.016) combined genotype to be negatively associated & the TCGGGC (P = 0.003) and CCGGGC (P = 0.003) to be positively associated with thrombocytopenia. The frequency of anti-HPA-1a and anti-HPA-3a antibodies was significantly higher in all patients compared to other anti-HPAs antibodies (P < 0.05). These results highlight the role of HPAs in the thrombocytopenia of COVID-19 infected patients. This is the first evidence demonstrating the differential association of the six common HPA gene variants and specific HPA genotype combinations with thrombocytopenia in COVID-19-infected patients. |
format | Online Article Text |
id | pubmed-10658732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106587322023-11-06 Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 Ghaffari, Kazem Rad, Mahsa Ashrafi Moradi Hasan-Abad, Amin Khosravi, Mersedeh Benvidi, Arefeh Iraji, Mahsa Khargh, Heidar Ali Heidari Ghasemi, Ali Front Med (Lausanne) Medicine Polymorphism in human platelet antigen (HPA)-1 and HPA-3 (GPIIb/IIIa), HPA-2 (GPIb/IX), HPA-4 (GPIIIa), HPA-5 (GPIa/IIa), & HPA-15 (CD109) was investigated in 86 COVID-19-infected patients with thrombocytopenia (Group A) and 136 COVID-19-infected patients without thrombocytopenia (Group B). HPA genotyping was done by the sequence-specific primers PCR method. Lower HPA-3a and higher HPA-3b (P = 0.028) allele frequencies were seen in Group A than in Group B, and homozygosity for HPA 3b (P = 0.038) alleles was more prevalent in Group A than in Group B. The allele and genotype distributions of the other HPA polymorphic variants were similar between the two groups. Univariate analysis identified the CCGGGC (P = 0.016) combined genotype to be negatively associated & the TCGGGC (P = 0.003) and CCGGGC (P = 0.003) to be positively associated with thrombocytopenia. The frequency of anti-HPA-1a and anti-HPA-3a antibodies was significantly higher in all patients compared to other anti-HPAs antibodies (P < 0.05). These results highlight the role of HPAs in the thrombocytopenia of COVID-19 infected patients. This is the first evidence demonstrating the differential association of the six common HPA gene variants and specific HPA genotype combinations with thrombocytopenia in COVID-19-infected patients. Frontiers Media S.A. 2023-11-06 /pmc/articles/PMC10658732/ /pubmed/38020117 http://dx.doi.org/10.3389/fmed.2023.1265568 Text en Copyright © 2023 Ghaffari, Rad, Moradi Hasan-Abad, Khosravi, Benvidi, Iraji, Khargh and Ghasemi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Ghaffari, Kazem Rad, Mahsa Ashrafi Moradi Hasan-Abad, Amin Khosravi, Mersedeh Benvidi, Arefeh Iraji, Mahsa Khargh, Heidar Ali Heidari Ghasemi, Ali Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title | Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title_full | Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title_fullStr | Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title_full_unstemmed | Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title_short | Association of the human platelet antigens polymorphisms with platelet count in patients with COVID-19 |
title_sort | association of the human platelet antigens polymorphisms with platelet count in patients with covid-19 |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658732/ https://www.ncbi.nlm.nih.gov/pubmed/38020117 http://dx.doi.org/10.3389/fmed.2023.1265568 |
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