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Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population
BACKGROUND: The pathophysiology underlying primary adult immune thrombocytopenic purpura (ITP) has not yet been identified. However, many mechanisms affect the immune system, causing defective tolerance to self-platelets and megakaryocytes. Cluster of differentiation 40 (CD40) contributes to both hu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9492531/ https://www.ncbi.nlm.nih.gov/pubmed/35920091 http://dx.doi.org/10.5045/br.2022.2022057 |
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author | Ellithy, Hend Nabil Yousry, Sherif Mohamed Abdel-Aal, Asmaa Tawadros, Lelian Momen, Nouran |
author_facet | Ellithy, Hend Nabil Yousry, Sherif Mohamed Abdel-Aal, Asmaa Tawadros, Lelian Momen, Nouran |
author_sort | Ellithy, Hend Nabil |
collection | PubMed |
description | BACKGROUND: The pathophysiology underlying primary adult immune thrombocytopenic purpura (ITP) has not yet been identified. However, many mechanisms affect the immune system, causing defective tolerance to self-platelets and megakaryocytes. Cluster of differentiation 40 (CD40) contributes to both humoral and cell-mediated immune responses. METHODS: This case‒control study was conducted to detect rs4810485G>T and rs1883832C>T polymorphisms of CD40 in Egyptian patients with persistent/chronic ITP to clarify their possible association with chronic disease evolution. This study included 50 patients with persistent/chronic ITP and 50 healthy controls. Genotyping was performed using the polymerase chain reaction‒restriction fragment length polymorphism technique. RESULTS: Genotyping of rs1883832 and rs4810485 revealed no statistically significant differences between the two groups. However, combined gene polymorphism genotyping showed a statistically significant difference between the two groups (P<0.01). CONCLUSION: Our results indicate a strong association between the combined polymorphism of both genes and susceptibility to developing ITP among adult Egyptian patients. Targeting this pathway using novel therapeutic approaches is promising. |
format | Online Article Text |
id | pubmed-9492531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis |
record_format | MEDLINE/PubMed |
spelling | pubmed-94925312022-09-30 Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population Ellithy, Hend Nabil Yousry, Sherif Mohamed Abdel-Aal, Asmaa Tawadros, Lelian Momen, Nouran Blood Res Original Article BACKGROUND: The pathophysiology underlying primary adult immune thrombocytopenic purpura (ITP) has not yet been identified. However, many mechanisms affect the immune system, causing defective tolerance to self-platelets and megakaryocytes. Cluster of differentiation 40 (CD40) contributes to both humoral and cell-mediated immune responses. METHODS: This case‒control study was conducted to detect rs4810485G>T and rs1883832C>T polymorphisms of CD40 in Egyptian patients with persistent/chronic ITP to clarify their possible association with chronic disease evolution. This study included 50 patients with persistent/chronic ITP and 50 healthy controls. Genotyping was performed using the polymerase chain reaction‒restriction fragment length polymorphism technique. RESULTS: Genotyping of rs1883832 and rs4810485 revealed no statistically significant differences between the two groups. However, combined gene polymorphism genotyping showed a statistically significant difference between the two groups (P<0.01). CONCLUSION: Our results indicate a strong association between the combined polymorphism of both genes and susceptibility to developing ITP among adult Egyptian patients. Targeting this pathway using novel therapeutic approaches is promising. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2022-09-30 2022-09-30 /pmc/articles/PMC9492531/ /pubmed/35920091 http://dx.doi.org/10.5045/br.2022.2022057 Text en © 2022 Korean Society of Hematology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ellithy, Hend Nabil Yousry, Sherif Mohamed Abdel-Aal, Asmaa Tawadros, Lelian Momen, Nouran Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title | Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title_full | Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title_fullStr | Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title_full_unstemmed | Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title_short | Association of CD40 gene polymorphisms and immune thrombocytopenic purpura in the adult Egyptian population |
title_sort | association of cd40 gene polymorphisms and immune thrombocytopenic purpura in the adult egyptian population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9492531/ https://www.ncbi.nlm.nih.gov/pubmed/35920091 http://dx.doi.org/10.5045/br.2022.2022057 |
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