Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran

Background: α-thalassemia is one of the common prevente hematological disorders in the Iranian population; knowing its most common mutations can improve the prenatal diagnosis of the disease. To date of this study, no comprehensive data were available on the prevalence of the disease in Chahar Mahal...

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Main Authors: Reihaneh Vallian, Alireza Moafi, Sadeq Vallian, Foroogh Abbasian
Format: Article
Language:fas
Published: Vesnu Publications 2015-08-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/5271
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spelling doaj-93c62836b2744e74a25974fd12ea42e12020-11-25T00:28:49ZfasVesnu Publications مجله دانشکده پزشکی اصفهان1027-75951735-854X2015-08-01333378478551891Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, IranReihaneh Vallian0Alireza Moafi1Sadeq Vallian2Foroogh Abbasian3Student of Medicine, School of Medicine AND Student Research Committee, Isfahan University of Medical Sciences, Isfahan, IranAssociate Professor, Department of Pediatrics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranProfessor, Department of Biology, School of Science, University of Isfahan, Isfahan, IranMolecular Section, Isfahan Genetics Center, Isfahan, IranBackground: α-thalassemia is one of the common prevente hematological disorders in the Iranian population; knowing its most common mutations can improve the prenatal diagnosis of the disease. To date of this study, no comprehensive data were available on the prevalence of the disease in Chahar Mahal va Bakhtiari Province, Iran. For the first time, this study investigated the spectrum of α-thalassemia mutations and their correlation with red blood cell (RBC) indices in this region. Methods: 128 carriers who resided in the Chahar Mahal va Bakhtiari Province were evaluated for α-thalassemia mutations using gap polymerase chain reaction (GAP-PCR), amplification refractory mutation system-polymerase chain reaction (ARMS-PCR), multiplex-ligation-probe-dependent polymerase assay (MLPA) and sequencing methods. The RBC indices were measured. The data were analyzed using chi-square and t tests. Findings: The presence of 6 deletions including α3.7 (83.2%), α20.5 (5.9%), αMED (5%), α4.2 (2.5%), del Hbz-Hba1 (0.8%) and HS-40 (0.8%) as well as the point mutation of Hb-CS (1.7%) on the α-globin gene were approved. Analysis of correlation between different mean corpuscular volume (MCV) measures and α-thalassemia indicated that 78>MCV>75 was correlated with α3.7, α4.2 and Hb-CS mutation and MCV of less than 75 was correlated with α3.7, α20.5, αMED, and del Hbz-Hba1. Among the analyzed mutations, the only mutation with 78 < MCV < 80 or low MCV (< 80) and normal (> 27) mean corpuscular hemoglobin (MCH) was α3.7. Interestingly, mutations with low (< 27) and normal (> 80) MCV were α3.7 and Hb-CS, respectively. Conclusion: Together, the data suggested the presence of a positive relationship between α-thalassemia mutations and RBC indices, which could facilitate rapid and efficient screening for these common mutations in the population of Chahar Mahal va Bakhtiari Province.http://jims.mui.ac.ir/index.php/jims/article/view/5271α-thalassemiaRed blood cell indicesMutationScreening program
collection DOAJ
language fas
format Article
sources DOAJ
author Reihaneh Vallian
Alireza Moafi
Sadeq Vallian
Foroogh Abbasian
spellingShingle Reihaneh Vallian
Alireza Moafi
Sadeq Vallian
Foroogh Abbasian
Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
مجله دانشکده پزشکی اصفهان
α-thalassemia
Red blood cell indices
Mutation
Screening program
author_facet Reihaneh Vallian
Alireza Moafi
Sadeq Vallian
Foroogh Abbasian
author_sort Reihaneh Vallian
title Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
title_short Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
title_full Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
title_fullStr Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
title_full_unstemmed Analysis of Alpha Thalassemia Mutations and its Correlation with Red Blood Cell Indices in Chahar Mahal va Bakhtiari Province, Iran
title_sort analysis of alpha thalassemia mutations and its correlation with red blood cell indices in chahar mahal va bakhtiari province, iran
publisher Vesnu Publications
series مجله دانشکده پزشکی اصفهان
issn 1027-7595
1735-854X
publishDate 2015-08-01
description Background: α-thalassemia is one of the common prevente hematological disorders in the Iranian population; knowing its most common mutations can improve the prenatal diagnosis of the disease. To date of this study, no comprehensive data were available on the prevalence of the disease in Chahar Mahal va Bakhtiari Province, Iran. For the first time, this study investigated the spectrum of α-thalassemia mutations and their correlation with red blood cell (RBC) indices in this region. Methods: 128 carriers who resided in the Chahar Mahal va Bakhtiari Province were evaluated for α-thalassemia mutations using gap polymerase chain reaction (GAP-PCR), amplification refractory mutation system-polymerase chain reaction (ARMS-PCR), multiplex-ligation-probe-dependent polymerase assay (MLPA) and sequencing methods. The RBC indices were measured. The data were analyzed using chi-square and t tests. Findings: The presence of 6 deletions including α3.7 (83.2%), α20.5 (5.9%), αMED (5%), α4.2 (2.5%), del Hbz-Hba1 (0.8%) and HS-40 (0.8%) as well as the point mutation of Hb-CS (1.7%) on the α-globin gene were approved. Analysis of correlation between different mean corpuscular volume (MCV) measures and α-thalassemia indicated that 78>MCV>75 was correlated with α3.7, α4.2 and Hb-CS mutation and MCV of less than 75 was correlated with α3.7, α20.5, αMED, and del Hbz-Hba1. Among the analyzed mutations, the only mutation with 78 < MCV < 80 or low MCV (< 80) and normal (> 27) mean corpuscular hemoglobin (MCH) was α3.7. Interestingly, mutations with low (< 27) and normal (> 80) MCV were α3.7 and Hb-CS, respectively. Conclusion: Together, the data suggested the presence of a positive relationship between α-thalassemia mutations and RBC indices, which could facilitate rapid and efficient screening for these common mutations in the population of Chahar Mahal va Bakhtiari Province.
topic α-thalassemia
Red blood cell indices
Mutation
Screening program
url http://jims.mui.ac.ir/index.php/jims/article/view/5271
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