Rare Diseases Symptoms Automatic Extraction

Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia.

[alpha-thalassemia]

Stroke is a catastrophic complication of sickle cell anaemia (SCA) and is one of the leading causes of death in both adults and children with SCA. Evidence suggests that some genetic polymorphisms could be related to stroke development, but their association remains controversial. Here, we performed genotyping of five published single nucleotide polymorphisms, the α-thalassemia genotype, the G6PD A (-) variant deficiency, and the β(S) haplotype in a large series of SCA patients with well-defined stroke phenotypes. Of 261 unrelated SCA patients included in the study, 67 (9.5 %) presented a documented, primary stroke event. Markers of haemolysis (red blood cell (RBC) counts, p=0.023; reticulocyte counts, p=0.003; haemoglobin (Hb) levels, p<0.001; indirect bilirubin levels, p=0.006; lactate dehydrogenase (LDH) levels, p=0.001) were associated with stroke susceptibility. Genetically, only the β(S) haplotype (odds ratio (OR) 2.9, 95 % confidence interval (CI) 1.56 to 4.31; p=0.003) and the α(3.7kb)-thalassemia genotype (OR 0.31, 95 % CI 0.11 to 0. 83; p=0.02) were associated with increased and decreased stroke risk, respectively. In multivariate analysis, the β(S) haplotype was independently associated with stroke development (OR 2.26, 95 % CI 1.16 to 4.4; p=0.016). Our findings suggest that only the β(S) haplotypes and the α(3.7kb)-thalassemia genotype modulate the prevalence of stroke in our SCA population. Genetic heterogeneity among different populations may account for the irreproducibility amongst different studies.

Diseases presenting "large series" symptom

  • alpha-thalassemia
  • cushing syndrome
  • cutaneous mastocytosis
  • erdheim-chester disease
  • homocystinuria without methylmalonic aciduria
  • kallmann syndrome
  • lymphangioleiomyomatosis
  • sneddon syndrome
  • typhoid

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