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Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh

CONTEXT: β-thalassemia is one of the most common heterogeneous inherited single gene disorders. The disease results from one or more of 380 different mutations in the β-globin gene. Uttar Pradesh (U.P.) is the most populous state of India, comprising various ethnic groups and Bareilly is one of the...

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Autores principales: Christopher, Ajay F., Kumari, Anita, Chaudhary, Sunali, Hora, Sandhya, Ali, Ziledar, Agrawal, Satish C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758729/
https://www.ncbi.nlm.nih.gov/pubmed/24019624
http://dx.doi.org/10.4103/0971-6866.116119
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author Christopher, Ajay F.
Kumari, Anita
Chaudhary, Sunali
Hora, Sandhya
Ali, Ziledar
Agrawal, Satish C.
author_facet Christopher, Ajay F.
Kumari, Anita
Chaudhary, Sunali
Hora, Sandhya
Ali, Ziledar
Agrawal, Satish C.
author_sort Christopher, Ajay F.
collection PubMed
description CONTEXT: β-thalassemia is one of the most common heterogeneous inherited single gene disorders. The disease results from one or more of 380 different mutations in the β-globin gene. Uttar Pradesh (U.P.) is the most populous state of India, comprising various ethnic groups and Bareilly is one of the largest cities situated in Western U.P. AIMS: To examine the prevalence of five common β-thalassemian mutations: Intervening Sequence IVS 1-5 (c. 92 + 5 G > C), codon 8/9 (c. 27_28insG), codon 41/42 (c. 124_127delTTCT), IVS 1-1 (c. 92 + 1 G > T) and codon 26 G-A (c. 79G > A) in Western U.P. SETTINGS AND DESIGN: Patients attending camps organized by the Thalassemia Society, Bareilly were selected for the study. MATERIALS AND METHODS: A total of 48 blood samples were collected from the patients of transfusion dependent β-thalassemia from July 2011 to May 2012. All the samples were analyzed for five common mutations by using the Amplification Refractory Mutation System (ARMS)-hot start-polymerase chain reaction (PCR) technique. RESULTS: Among the five common mutations prevalent in India, we were able to detect all except codon 26 G-A (c. 79G > A), which is prevalent in northeast India. These four mutations accounted for 58% of the total number of our patients. The IVS 1-5 (G-C) was found to be the most common mutation with a frequency of 46% and the 2 (nd)most common mutation was Fr8/9 (+G) with a frequency of 21%. The frequency of other mutations was IVS1-1 (12%) and Cd 41/42 (4%). CONCLUSION: This study provides evidence that the pattern of mutations in Western U.P. is different from the rest of India and even from the neighboring states (Delhi and Punjab). To the best of our knowledge, mutation Fr8/9, the 2(nd)most common mutation in our study has never been reported to be so common from anywhere in India. Some mutations, which are prevalent in other regions are absent in our region (mutation for ε-globin). Hence, these findings can be called unique to Western U.P.
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spelling pubmed-37587292013-09-09 Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh Christopher, Ajay F. Kumari, Anita Chaudhary, Sunali Hora, Sandhya Ali, Ziledar Agrawal, Satish C. Indian J Hum Genet Original Article CONTEXT: β-thalassemia is one of the most common heterogeneous inherited single gene disorders. The disease results from one or more of 380 different mutations in the β-globin gene. Uttar Pradesh (U.P.) is the most populous state of India, comprising various ethnic groups and Bareilly is one of the largest cities situated in Western U.P. AIMS: To examine the prevalence of five common β-thalassemian mutations: Intervening Sequence IVS 1-5 (c. 92 + 5 G > C), codon 8/9 (c. 27_28insG), codon 41/42 (c. 124_127delTTCT), IVS 1-1 (c. 92 + 1 G > T) and codon 26 G-A (c. 79G > A) in Western U.P. SETTINGS AND DESIGN: Patients attending camps organized by the Thalassemia Society, Bareilly were selected for the study. MATERIALS AND METHODS: A total of 48 blood samples were collected from the patients of transfusion dependent β-thalassemia from July 2011 to May 2012. All the samples were analyzed for five common mutations by using the Amplification Refractory Mutation System (ARMS)-hot start-polymerase chain reaction (PCR) technique. RESULTS: Among the five common mutations prevalent in India, we were able to detect all except codon 26 G-A (c. 79G > A), which is prevalent in northeast India. These four mutations accounted for 58% of the total number of our patients. The IVS 1-5 (G-C) was found to be the most common mutation with a frequency of 46% and the 2 (nd)most common mutation was Fr8/9 (+G) with a frequency of 21%. The frequency of other mutations was IVS1-1 (12%) and Cd 41/42 (4%). CONCLUSION: This study provides evidence that the pattern of mutations in Western U.P. is different from the rest of India and even from the neighboring states (Delhi and Punjab). To the best of our knowledge, mutation Fr8/9, the 2(nd)most common mutation in our study has never been reported to be so common from anywhere in India. Some mutations, which are prevalent in other regions are absent in our region (mutation for ε-globin). Hence, these findings can be called unique to Western U.P. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3758729/ /pubmed/24019624 http://dx.doi.org/10.4103/0971-6866.116119 Text en Copyright: © Indian Journal of Human Genetics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Christopher, Ajay F.
Kumari, Anita
Chaudhary, Sunali
Hora, Sandhya
Ali, Ziledar
Agrawal, Satish C.
Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title_full Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title_fullStr Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title_full_unstemmed Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title_short Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh
title_sort unique pattern of mutations in β-thalassemia patients in western uttar pradesh
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758729/
https://www.ncbi.nlm.nih.gov/pubmed/24019624
http://dx.doi.org/10.4103/0971-6866.116119
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