| Literature DB >> 27829299 |
Gift D Pule1, Valentina J Ngo Bitoungui2, Bernard Chetcha Chemegni2, Andre P Kengne3, Ambroise Wonkam1.
Abstract
High level of Hb F has been shown to improve survival in sickle cell disease. Among 453 Cameroonians with sickle cell disease, we have investigated 18 selected single-nucleotide polymorphisms (SNPs) in novel and suggestive loci associated with Hb F level identified through a genomewide association study in sickle cell disease patients in Tanzania, and whole-genome sequencing of a population from Sardinia. Seven of 10 variants reported in Sardinians were either monomorphic or very rare in the Cameroonians. No associations were observed with any SNPs and Hb F levels in Cameroonians affected by sickle cell disease. The present study illustrates the complexity of replicating Hb F-promoting variants association results across populations.Entities:
Keywords: Cameroon; Hb F; Sardinia; Tanzania; sickle cell disease
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Year: 2016 PMID: 27829299 DOI: 10.1080/03630269.2016.1251453
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849