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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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 |
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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 |
work_keys_str_mv |
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