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A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients
BACKGROUND: Parvovirus B19 is the causative agent for erythema infectiosum, and also as a potentially life-threatening infectious agent, it is mainly presented in high erythrocyte turnover patients. Sickle cell disease (SCD) is an inherited monogenic hematological disorder resulting from the mutatio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709306/ https://www.ncbi.nlm.nih.gov/pubmed/33292852 http://dx.doi.org/10.1186/s41182-020-00284-x |
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author | Soltani, Saber Zakeri, Armin Tabibzadeh, Alireza Zandi, Milad Ershadi, Elham Akhavan Rezayat, Sara Khaseb, Sanaz Zakeri, Amir mohammad Ashtar Nakhaei, Mohammadvala Afzali, Shervin Farahani, Abbas |
author_facet | Soltani, Saber Zakeri, Armin Tabibzadeh, Alireza Zandi, Milad Ershadi, Elham Akhavan Rezayat, Sara Khaseb, Sanaz Zakeri, Amir mohammad Ashtar Nakhaei, Mohammadvala Afzali, Shervin Farahani, Abbas |
author_sort | Soltani, Saber |
collection | PubMed |
description | BACKGROUND: Parvovirus B19 is the causative agent for erythema infectiosum, and also as a potentially life-threatening infectious agent, it is mainly presented in high erythrocyte turnover patients. Sickle cell disease (SCD) is an inherited monogenic hematological disorder resulting from the mutations in the hemoglobin β-chain gene. Thalassemia is a hereditary hematological syndrome that happens in consequence of deficiencies in the production of one or more globin chains. We summarize current knowledge about the prevalence rates of the parvovirus B19 infection in sickle cell anemia and thalassemia patients. METHODS: Several online databases were searched including, Scopus, EMBASE, Web of Science, Google Scholar, and PubMed, which were performed amidst 2009–2019 by using distinct keywords: “Thalassemia,” “Parvovirus,” “Anemia,” “Sickle cell anemia,” “parvoviridae,” “parvoviridae infection,” and “parvovirus B19.” RESULTS: Search results indicated 4 and 7 studies for the prevalence of the parvovirus B19 in β-thalassemia and SCD, respectively. Among the β-thalassemia patients, the B19V seroprevalence for IgG and IgM were ranged from 18.2–81% and 14.5–41.1%, respectively; meanwhile, B19V DNA positively results was 4–15.3%. Moreover, in the SCD group, the extent of B19V IgG was varied from 37.6 to 65.9% and that of IgM was in a range of 2.9–30%, and the DNA detection rate was 4–54%. CONCLUSION: B19V seroprevalence changes in several conditions including, different epidemiological features, socio-economic status, and overpopulation. Age can expand the incidence of anti-B19V IgG/IgM in SCD and beta-thalassemia patients. Reinfection and diverse genotypes are relevant factors in the seroprevalence of B19v. The patients’ immunological-hematological station and higher abundance of transfusions can affect the B19V seroprevalence in SCD and beta-thalassemia group. Further investigations in this field could be suggested to better understand the virus distribution in this susceptible population of patients. |
format | Online Article Text |
id | pubmed-7709306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77093062020-12-02 A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients Soltani, Saber Zakeri, Armin Tabibzadeh, Alireza Zandi, Milad Ershadi, Elham Akhavan Rezayat, Sara Khaseb, Sanaz Zakeri, Amir mohammad Ashtar Nakhaei, Mohammadvala Afzali, Shervin Farahani, Abbas Trop Med Health Review BACKGROUND: Parvovirus B19 is the causative agent for erythema infectiosum, and also as a potentially life-threatening infectious agent, it is mainly presented in high erythrocyte turnover patients. Sickle cell disease (SCD) is an inherited monogenic hematological disorder resulting from the mutations in the hemoglobin β-chain gene. Thalassemia is a hereditary hematological syndrome that happens in consequence of deficiencies in the production of one or more globin chains. We summarize current knowledge about the prevalence rates of the parvovirus B19 infection in sickle cell anemia and thalassemia patients. METHODS: Several online databases were searched including, Scopus, EMBASE, Web of Science, Google Scholar, and PubMed, which were performed amidst 2009–2019 by using distinct keywords: “Thalassemia,” “Parvovirus,” “Anemia,” “Sickle cell anemia,” “parvoviridae,” “parvoviridae infection,” and “parvovirus B19.” RESULTS: Search results indicated 4 and 7 studies for the prevalence of the parvovirus B19 in β-thalassemia and SCD, respectively. Among the β-thalassemia patients, the B19V seroprevalence for IgG and IgM were ranged from 18.2–81% and 14.5–41.1%, respectively; meanwhile, B19V DNA positively results was 4–15.3%. Moreover, in the SCD group, the extent of B19V IgG was varied from 37.6 to 65.9% and that of IgM was in a range of 2.9–30%, and the DNA detection rate was 4–54%. CONCLUSION: B19V seroprevalence changes in several conditions including, different epidemiological features, socio-economic status, and overpopulation. Age can expand the incidence of anti-B19V IgG/IgM in SCD and beta-thalassemia patients. Reinfection and diverse genotypes are relevant factors in the seroprevalence of B19v. The patients’ immunological-hematological station and higher abundance of transfusions can affect the B19V seroprevalence in SCD and beta-thalassemia group. Further investigations in this field could be suggested to better understand the virus distribution in this susceptible population of patients. BioMed Central 2020-12-02 /pmc/articles/PMC7709306/ /pubmed/33292852 http://dx.doi.org/10.1186/s41182-020-00284-x Text en © The Author(s) 2020 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/. |
spellingShingle | Review Soltani, Saber Zakeri, Armin Tabibzadeh, Alireza Zandi, Milad Ershadi, Elham Akhavan Rezayat, Sara Khaseb, Sanaz Zakeri, Amir mohammad Ashtar Nakhaei, Mohammadvala Afzali, Shervin Farahani, Abbas A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title | A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title_full | A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title_fullStr | A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title_full_unstemmed | A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title_short | A literature review on the parvovirus B19 infection in sickle cell anemia and β-thalassemia patients |
title_sort | literature review on the parvovirus b19 infection in sickle cell anemia and β-thalassemia patients |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709306/ https://www.ncbi.nlm.nih.gov/pubmed/33292852 http://dx.doi.org/10.1186/s41182-020-00284-x |
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