Cargando…

Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review

Sickle cell disease (SCD) is a genetic disease influenced by ethnicity and regional differences in its clinical course. Recent advances in the management of SCD with newer therapies are being introduced to the Western population. However, many of these treatments are yet to be used in the Arabic SCD...

Descripción completa

Detalles Bibliográficos
Autores principales: Ata, Fateen, Rahhal, Alaa, Malkawi, Lujain, Iqbal, Phool, Khamees, Ibrahim, Alhiyari, Mousa, Yousaf, Zohaib, Qasim, Hana, Alshurafa, Awni, Sardar, Sundus, Javed, Saad, Fernyhough, Liam, Yassin, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9961577/
https://www.ncbi.nlm.nih.gov/pubmed/36851992
http://dx.doi.org/10.2147/PGPM.S391394
_version_ 1784895789154172928
author Ata, Fateen
Rahhal, Alaa
Malkawi, Lujain
Iqbal, Phool
Khamees, Ibrahim
Alhiyari, Mousa
Yousaf, Zohaib
Qasim, Hana
Alshurafa, Awni
Sardar, Sundus
Javed, Saad
Fernyhough, Liam
Yassin, Mohamed
author_facet Ata, Fateen
Rahhal, Alaa
Malkawi, Lujain
Iqbal, Phool
Khamees, Ibrahim
Alhiyari, Mousa
Yousaf, Zohaib
Qasim, Hana
Alshurafa, Awni
Sardar, Sundus
Javed, Saad
Fernyhough, Liam
Yassin, Mohamed
author_sort Ata, Fateen
collection PubMed
description Sickle cell disease (SCD) is a genetic disease influenced by ethnicity and regional differences in its clinical course. Recent advances in the management of SCD with newer therapies are being introduced to the Western population. However, many of these treatments are yet to be used in the Arabic SCD population. Understanding the genetic variations of SCD regionally is essential to anticipate the utilization of new treatments. This systematic review’s main objective is to pool the available data on the genetic composition of SCD in the Arabic population. Data for 44,034 patients was extracted from 184 studies (11 case reports, 8 case series, 56 retrospectives, 107 prospective observational studies, and 2 clinical trials) using PubMed, Scopus, and Google Scholar. Male (49%) and female (51%) patients were equally reported wherever gender was available (N=13105). Various SCD genotypes were reported in a total of 14,257 patients, including Hb SS (77%) Hb Sβ0 (9.9%), and Hb Sβ+ (7.2%), while the rest of the genotypes, including HbSC, HbSD, HbSE, HbSO Arab, Hb S/α-Thal, Hb Sβ0 + α-Thal, and HBS Oman were individually reported in <4% of the cases. Major SCD complications in the Arab population included pain crises (48.25%) followed by neurological complications (33.46%), hepatobiliary complications (25.53%), musculoskeletal complications (24.73%), and hemolytic anemia (23.57%). The treatments reported for SCD included hydroxyurea (20%), blood transfusion (14.32%), and Deferasirox (3.03%). We did not find the use of stem cell transplantation or newer treatments such as L-Glutamine, Voxelotor, Crizanlizumab, or gene therapy reported in any of the studies included in our review. This review highlights the genetic makeup of SCD in Arab countries and its common phenotypic manifestations and will help direct further research on SCD in this region, especially concerning genetic therapy. SYSTEMATIC REVIEW REGISTRATION: The protocol has been registered in the International Prospective Register of Systematic Reviews(PROSPERO):CRD42020218,666. https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=218666.
format Online
Article
Text
id pubmed-9961577
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-99615772023-02-26 Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review Ata, Fateen Rahhal, Alaa Malkawi, Lujain Iqbal, Phool Khamees, Ibrahim Alhiyari, Mousa Yousaf, Zohaib Qasim, Hana Alshurafa, Awni Sardar, Sundus Javed, Saad Fernyhough, Liam Yassin, Mohamed Pharmgenomics Pers Med Review Sickle cell disease (SCD) is a genetic disease influenced by ethnicity and regional differences in its clinical course. Recent advances in the management of SCD with newer therapies are being introduced to the Western population. However, many of these treatments are yet to be used in the Arabic SCD population. Understanding the genetic variations of SCD regionally is essential to anticipate the utilization of new treatments. This systematic review’s main objective is to pool the available data on the genetic composition of SCD in the Arabic population. Data for 44,034 patients was extracted from 184 studies (11 case reports, 8 case series, 56 retrospectives, 107 prospective observational studies, and 2 clinical trials) using PubMed, Scopus, and Google Scholar. Male (49%) and female (51%) patients were equally reported wherever gender was available (N=13105). Various SCD genotypes were reported in a total of 14,257 patients, including Hb SS (77%) Hb Sβ0 (9.9%), and Hb Sβ+ (7.2%), while the rest of the genotypes, including HbSC, HbSD, HbSE, HbSO Arab, Hb S/α-Thal, Hb Sβ0 + α-Thal, and HBS Oman were individually reported in <4% of the cases. Major SCD complications in the Arab population included pain crises (48.25%) followed by neurological complications (33.46%), hepatobiliary complications (25.53%), musculoskeletal complications (24.73%), and hemolytic anemia (23.57%). The treatments reported for SCD included hydroxyurea (20%), blood transfusion (14.32%), and Deferasirox (3.03%). We did not find the use of stem cell transplantation or newer treatments such as L-Glutamine, Voxelotor, Crizanlizumab, or gene therapy reported in any of the studies included in our review. This review highlights the genetic makeup of SCD in Arab countries and its common phenotypic manifestations and will help direct further research on SCD in this region, especially concerning genetic therapy. SYSTEMATIC REVIEW REGISTRATION: The protocol has been registered in the International Prospective Register of Systematic Reviews(PROSPERO):CRD42020218,666. https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=218666. Dove 2023-02-21 /pmc/articles/PMC9961577/ /pubmed/36851992 http://dx.doi.org/10.2147/PGPM.S391394 Text en © 2023 Ata et al. https://creativecommons.org/licenses/by/4.0/This work is published by Dove Medical Press Limited, and licensed under a Creative Commons Attribution License. The full terms of the License are available at http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Ata, Fateen
Rahhal, Alaa
Malkawi, Lujain
Iqbal, Phool
Khamees, Ibrahim
Alhiyari, Mousa
Yousaf, Zohaib
Qasim, Hana
Alshurafa, Awni
Sardar, Sundus
Javed, Saad
Fernyhough, Liam
Yassin, Mohamed
Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title_full Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title_fullStr Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title_full_unstemmed Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title_short Genotypic and Phenotypic Composition of Sickle Cell Disease in the Arab Population - A Systematic Review
title_sort genotypic and phenotypic composition of sickle cell disease in the arab population - a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9961577/
https://www.ncbi.nlm.nih.gov/pubmed/36851992
http://dx.doi.org/10.2147/PGPM.S391394
work_keys_str_mv AT atafateen genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT rahhalalaa genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT malkawilujain genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT iqbalphool genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT khameesibrahim genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT alhiyarimousa genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT yousafzohaib genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT qasimhana genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT alshurafaawni genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT sardarsundus genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT javedsaad genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT fernyhoughliam genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview
AT yassinmohamed genotypicandphenotypiccompositionofsicklecelldiseaseinthearabpopulationasystematicreview