α-Globin mutations and Genetic Variants in γ-globin Promoters are Associated with Unelevated Hemoglobin F Expression of Atypical β 0 -thalassemia/HbE.

Autor: Satthakarn S; Faculty of Allied Health Sciences, Burapha University, Chonburi, Thailand., Panyasai S; Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Thailand. Electronic address: sitthichai.pa@up.ac.th.
Jazyk: angličtina
Zdroj: Archives of medical research [Arch Med Res] 2024 Sep; Vol. 55 (6), pp. 103055. Date of Electronic Publication: 2024 Jul 18.
DOI: 10.1016/j.arcmed.2024.103055
Abstrakt: Background: Excessive expression of hemoglobin F (HbF) is a characteristic feature and important diagnostic marker of β 0 -thalassemia/HbE disease. However, some patients may exhibit low-HbF levels, leading to misdiagnosis and precluding genetic counseling. The genetic factors influencing these differences in HbF expression in this atypical disease are not completely understood.
Aims: To investigate determinants contributing to the non-elevation of HbF expression in β 0 -thalassemia/HbE disease.
Methods: We studied 231 patients with β 0 -thalassemia/HbE confirmed by DNA analysis; classified them into the low-HbF (n = 62) and high-HbF (n = 169) groups; analyzed hematological parameters and hemoglobin levels in both groups; and characterized mutations in β- and α-globin genes and genetic variants in γ-globin promoters.
Results: Both groups showed similar rates of type β 0 -thalassemia mutations but significantly different proportions of α-globin mutations: approximately 88.7% (95% confidence interval [CI] = 66.8-115.5) and 39.1% (95% CI = 30.2-49.7) in the low- and high-HbF groups, respectively. The results revealed single-nucleotide polymorphisms (SNPs) at -158 (C>T) in the G γ-globin promoters and novel SNPs at the 5' untranslated region position 25 (G>A) in A γ-globin promoters. The distribution of CC genotypes of the G γ-globin promoter in the low-HbF group was significantly higher than that in the high-HbF group.
Conclusions: Cases with HbE predominance with low-HbF levels and undetectable HbA may not be as conclusive as those with homozygous HbE until DNA analysis is performed. Concomitant inheritance of α-thalassemia is an important inherent factor modifying HbF expression in a typical β 0 -thalassemia/HbE, and SNPs with the CC genotype in the G γ-globin promoter may indicate unelevated HbF expression in patients with this disease.
(Copyright © 2024 Instituto Mexicano del Seguro Social (IMSS). Published by Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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