Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers. (3rd March 2020)

• Record Type: Journal Article
• Authors: Manco, Licínio; Bento, Celeste; Relvas, Luís; Cunha, Elisabete; Pereira, Janet; Moreira, Valeria; Alvarez, Manuela; Maia, Tabita; Ribeiro, M. Letícia
• Is Part Of: Hemoglobin. Volume 44:Number 2(2020)
• Page Start: 113
• Page End: 117
• Publication Date: 2020-03-03
• Subjects: β-Thalassemia (β-thal) carriers -- genetic risk score (GRS) -- Hb F -- multi-locus -- quantitative trait loci (QTL); Hemoglobinopathy -- Periodicals; Hemoglobin -- Periodicals; Hematology -- Periodicals; Thalassemia -- Periodicals; Blood -- Diseases -- Periodicals; 612.1111
• DOI: 10.1080/03630269.2020.1753766
• Languages: English
• ISSNs: 0363-0269

Abstract

Abstract: Hb F production is under the influence of major quantitative trait loci (QTL). The present study aims: i) to replicate the association with Hb F for representative genetic variants in the three major Hb F QTLs in a Portuguese sample of β-thalassemia (β-thal) carriers; and ii) to test different genetic multi-locus models to account for the genetic component of Hb F variation. A population sample of 79 Portuguese β-thal carriers (39 males, 40 females), aged between 2 to 70 years old, were genotyped for polymorphisms in the locus control region (LCR)-5' hypersensitive site 4 (5'HS4) rs16912979, Xmn I- HBG2 rs7482144, BCL11A rs1427407 and HMIP rs66650371, using standard biomolecular procedures. Univariate linear regression models were used to test for genetic associations with Hb F. The minor alleles of the individual variants BCL11A rs1427407 (T) (0.165), HMIP rs66650371 (3 bp del) (0.247) and Xmn I- HBG2 rs7482144 (T) (0.196), were found to be significantly associated with increased levels of Hb F ( p = 0.029, p = 0.002 and p = 0.0004, respectively), explaining about 6.0, 12.0 and 15.0% of Hb F variation, respectively. In a multiple linear regression approach, the three loci accounted for about 30.0% of Hb F variance. Two genetic risk scores (GRS), rationalizing the number of minor alleles into a single genetic variable, explained about 30.0 and 32.0% of the Hb F variation. In conclusion, we replicated in β-thal carriers previously reported associations with Hb F. Multi-locus models combining three representative variants of Hb F influencing QTLs can explain a larger amount of Hb F variability.