Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/28751
Title: Genetic modifiers of Hb E/β<sup>0 </sup>thalassemia identified by a two-stage genome-wide association study
Authors: Richard Sherva
Orapan Sripichai
Kenneth Abel
Qianli Ma
Johanna Whitacre
Vach Angkachatchai
Wattanan Makarasara
Pranee Winichagoon
Saovaros Svasti
Suthat Fucharoen
Andreas Braun
Lindsay A. Farrer
Boston University School of Medicine
Boston University
Mahidol University
Sequenom Inc.
Human BioMolecular Research Institute
Illumina, Inc.
Innovive, Inc
Keywords: Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 30-Mar-2010
Citation: BMC Medical Genetics. Vol.11, No.1 (2010)
Abstract: Background: Patients with Hb E/β0 thalassemia display remarkable variability in disease severity. To identify genetic modifiers influencing disease severity, we conducted a two-stage genome scan in groups of 207 mild and 305 severe unrelated patients from Thailand with Hb E/β0 thalassemia and normal α-globin genes.Methods: First, we estimated and compared the allele frequencies of approximately 110,000 gene-based single nucleotide polymorphisms (SNPs) in pooled DNAs from different severity groups. The 756 SNPs that showed reproducible allelic differences at P < 0.02 by pooling were selected for individual genotyping.Results: After adjustment for age, gender and geographic region, logistic regression models showed 50 SNPs significantly associated with disease severity (P < 0.05) after Bonferroni adjustment for multiple testing. Forty-one SNPs in a large LD block within the β-globin gene cluster had major alleles associated with severe disease. The most significant was bthal_bg200 (odds ratio (OR) = 5.56, P = 2.6 × 10-13). Seven SNPs in two distinct LD blocks within a region centromeric to the β-globin gene cluster that contains many olfactory receptor genes were also associated with disease severity; rs3886223 had the strongest association (OR = 3.03, P = 3.7 × 10-11). Several previously unreported SNPs were also significantly associated with disease severity.Conclusions: These results suggest that there may be an additional regulatory region centromeric to the β-globin gene cluster that affects disease severity by modulating fetal hemoglobin expression. © 2010 Sherva et al; licensee BioMed Central Ltd.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77950445745&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/28751
ISSN: 14712350
Appears in Collections:Scopus 2006-2010

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.