Sickle cell trait and the risk of venous thromboembolism among blacks

Author:

Austin Harland1,Key Nigel S.2,Benson Jane M.3,Lally Cathy1,Dowling Nicole F.3,Whitsett Carolyn4,Hooper W. Craig3

Affiliation:

1. Emory University, Rollins School of Public Health, Atlanta, GA;

2. University of North Carolina, Chapel Hill;

3. Division of Hereditary Blood Disorders, Centers for Disease Control and Prevention, Atlanta, GA;

4. Emory University, School of Medicine, Atlanta, GA

Abstract

AbstractPeople with sickle cell disease have a chronically activated coagulation system and display hemostatic perturbations, but it is unknown whether they experience an increased risk of venous thromboembolism. We conducted a case–control study of venous thromboembolism that included 515 hospitalized black patients and 555 black controls obtained from medical clinics. All subjects were assayed for hemoglobin S and hemoglobin C genotypes. The prevalence of the S allele was 0.070 and 0.032 for case patients and controls, respectively (P < .001). The odds that a patient had sickle cell trait were approximately twice that of a control, indicating that the risk of venous thromboembolism is increased approximately 2-fold among blacks with sickle cell trait compared with those with the wild-type genotype (odds ratio = 1.8 with 95% confidence interval, 1.2-2.9). The odds ratio for pulmonary embolism and sickle cell trait was higher, 3.9 (2.2-6.9). The prevalence of sickle cell disease was also increased among case patients compared with controls. We conclude that sickle cell trait is a risk factor for venous thromboembolism and that the proportion of venous thromboembolism among blacks attributable to the mutation is approximately 7%.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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