Cargando…

Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine

BACKGROUND: Hemophilia A is an X-linked recessive bleeding disorder caused by mutations in FVIII gene with an incidence of 1 in 5,000 to 10,000 live born males. The Inv22 mutation is a major cause of the disease worldwide, accounting for up to 40%–50% of severe FVIII mutations. The aim of the presen...

Descripción completa

Detalles Bibliográficos
Autores principales: Mahmoud Abu Arra, Caesar, Samarah, Fekri, Sudqi Abu Hasan, Nael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533029/
https://www.ncbi.nlm.nih.gov/pubmed/33062376
http://dx.doi.org/10.1155/2020/3428648
_version_ 1783590049509539840
author Mahmoud Abu Arra, Caesar
Samarah, Fekri
Sudqi Abu Hasan, Nael
author_facet Mahmoud Abu Arra, Caesar
Samarah, Fekri
Sudqi Abu Hasan, Nael
author_sort Mahmoud Abu Arra, Caesar
collection PubMed
description BACKGROUND: Hemophilia A is an X-linked recessive bleeding disorder caused by mutations in FVIII gene with an incidence of 1 in 5,000 to 10,000 live born males. The Inv22 mutation is a major cause of the disease worldwide, accounting for up to 40%–50% of severe FVIII mutations. The aim of the present study was to screen Inv22 of the FVIII gene in Palestinian patients with severe HA and reveal its role as a predisposing factor for the development of inhibitors. MATERIALS AND METHODS: A cohort of 77 HA individuals including 5 carrier females from 52 unrelated families registered at governmental hemophilia centers in the West Bank area of Palestine was investigated. The demographic data and the clinical history were retrieved from medical files. Molecular analysis of Inv22 mutation in severe HA (30 cases) from Palestine was performed using the subcycling polymerase reaction (S-PCR). FVIII coagulant activities were carried out on an aPTT-based 1-stage clotting assay. FVIII inhibitors were quantified using the Nijmegen modification of the Bethesda assay. RESULT: Overall, 41.7% (30/72) of the studied cases were classified as having severe HA, 22.2% (16/72) had moderate HA, and 36.1% (26/72) had mild HA. Five randomly selected carrier mothers were screened for the Inv22 mutation to confirm its transmission to their sons. The Inv22 mutation was detected in 11 severe HA patients (36.6%). Among the severe HA patients with positive Inv22, 45.5% (5/11) had developed inhibitors. The current study showed that there was no association (p=0.53) between inhibitor development and the Inv22 mutation. CONCLUSION: Findings on Inv22 are in agreement with worldwide reports, being a major genetic mutation in severe HA. The S-PCR is a simple, rapid, and cost-effective method for the diagnosis of Inv22 in severe HA patients. Although the Inv22 mutation was associated with 36.6% of severe HA phenotype cases, it was not a major predisposing factor for inhibitor formation.
format Online
Article
Text
id pubmed-7533029
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-75330292020-10-13 Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine Mahmoud Abu Arra, Caesar Samarah, Fekri Sudqi Abu Hasan, Nael Scientifica (Cairo) Research Article BACKGROUND: Hemophilia A is an X-linked recessive bleeding disorder caused by mutations in FVIII gene with an incidence of 1 in 5,000 to 10,000 live born males. The Inv22 mutation is a major cause of the disease worldwide, accounting for up to 40%–50% of severe FVIII mutations. The aim of the present study was to screen Inv22 of the FVIII gene in Palestinian patients with severe HA and reveal its role as a predisposing factor for the development of inhibitors. MATERIALS AND METHODS: A cohort of 77 HA individuals including 5 carrier females from 52 unrelated families registered at governmental hemophilia centers in the West Bank area of Palestine was investigated. The demographic data and the clinical history were retrieved from medical files. Molecular analysis of Inv22 mutation in severe HA (30 cases) from Palestine was performed using the subcycling polymerase reaction (S-PCR). FVIII coagulant activities were carried out on an aPTT-based 1-stage clotting assay. FVIII inhibitors were quantified using the Nijmegen modification of the Bethesda assay. RESULT: Overall, 41.7% (30/72) of the studied cases were classified as having severe HA, 22.2% (16/72) had moderate HA, and 36.1% (26/72) had mild HA. Five randomly selected carrier mothers were screened for the Inv22 mutation to confirm its transmission to their sons. The Inv22 mutation was detected in 11 severe HA patients (36.6%). Among the severe HA patients with positive Inv22, 45.5% (5/11) had developed inhibitors. The current study showed that there was no association (p=0.53) between inhibitor development and the Inv22 mutation. CONCLUSION: Findings on Inv22 are in agreement with worldwide reports, being a major genetic mutation in severe HA. The S-PCR is a simple, rapid, and cost-effective method for the diagnosis of Inv22 in severe HA patients. Although the Inv22 mutation was associated with 36.6% of severe HA phenotype cases, it was not a major predisposing factor for inhibitor formation. Hindawi 2020-09-25 /pmc/articles/PMC7533029/ /pubmed/33062376 http://dx.doi.org/10.1155/2020/3428648 Text en Copyright © 2020 Caesar Mahmoud Abu Arra et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mahmoud Abu Arra, Caesar
Samarah, Fekri
Sudqi Abu Hasan, Nael
Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title_full Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title_fullStr Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title_full_unstemmed Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title_short Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
title_sort factor viii intron 22 inversion in severe hemophilia a patients in palestine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533029/
https://www.ncbi.nlm.nih.gov/pubmed/33062376
http://dx.doi.org/10.1155/2020/3428648
work_keys_str_mv AT mahmoudabuarracaesar factorviiiintron22inversioninseverehemophiliaapatientsinpalestine
AT samarahfekri factorviiiintron22inversioninseverehemophiliaapatientsinpalestine
AT sudqiabuhasannael factorviiiintron22inversioninseverehemophiliaapatientsinpalestine