Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia

Ann Hematol. 2019 Dec;98(12):2673-2681. doi: 10.1007/s00277-019-03783-y. Epub 2019 Sep 2.

Abstract

Sickle cell anemia (SCA) is an autosomal recessive monogenic disease with significant clinical variability. Cerebrovascular disease, particularly ischemic stroke, is one of the most severe complications of SCA in children. This study aimed to investigate the influence of genetic variants on the levels of fetal hemoglobin (Hb F) and biochemical parameters related with chronic hemolysis, as well as on ischemic stroke risk, in ninety-one unrelated SCA patients, children of sub-Saharan progenitors. Our results show that a higher Hb F level has an inverse relationship with the occurrence of stroke, since the group of patients who suffered stroke presents a significantly lower mean Hb F level (5.34 ± 4.57% versus 9.36 ± 6.48%; p = 0.024). Furthermore, the co-inheritance of alpha-thalassemia improves the chronic hemolytic pattern, evidenced by a decreased reticulocyte count (8.61 ± 3.58% versus 12.85 ± 4.71%; p < 0.001). In addition, our findings have confirmed the importance of HBG2 and BCL11A loci in the regulation of Hb F expression in sub-Saharan African SCA patients, as rs7482144_A, rs11886868_C, and rs4671393_A alleles are significantly associated with a considerable increase in Hb F levels (p = 0.019, p = 0.026, and p = 0.028, respectively). Concerning KLF1, twelve different variants were identified, two of them novel. Seventy-three patients (80.2%) presented at least one variant in this gene. However, no correlation was observed between the presence of these variants and Hb F level, severity of hemolysis, or stroke occurrence, which is consistent with their in silico-predicted minor functional consequences. Thus, we conclude that the prevalence of functional KLF1 variants in a sub-Saharan African background does not seem to be relevant to SCA clinical modulation.

Keywords: Cerebrovascular disease; Fetal hemoglobin; Genetic risk factors; KLF1 gene; Sickle cell anemia.

Publication types

  • Clinical Trial

MeSH terms

  • Adolescent
  • Anemia, Sickle Cell* / complications
  • Anemia, Sickle Cell* / ethnology
  • Anemia, Sickle Cell* / genetics
  • Anemia, Sickle Cell* / metabolism
  • Black People*
  • Brain Ischemia* / ethnology
  • Brain Ischemia* / etiology
  • Brain Ischemia* / genetics
  • Brain Ischemia* / metabolism
  • Child
  • Child, Preschool
  • Female
  • Fetal Hemoglobin* / biosynthesis
  • Fetal Hemoglobin* / genetics
  • Gene Expression Regulation*
  • Genetic Loci
  • Humans
  • Male
  • Stroke* / ethnology
  • Stroke* / etiology
  • Stroke* / genetics
  • Stroke* / metabolism

Substances

  • Fetal Hemoglobin