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Cardiovascular Outcomes in African Americans with Sickle Cell Trait and Chronic Kidney Disease
Kabir O Olaniran1, Nwamaka D Eneanya2, Andrew S Allegretti3
1Division of Nephrology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA, kolaniran@mgh.harvard.edu.
Insights
Sickle cell trait (SCT) increases coronary artery disease (CAD) risk in African American men with chronic kidney disease (CKD). This risk mirrors that seen in sickle cell disease (SCD) patients, highlighting a sex-specific cardiovascular impact.
Area of Science:
- Nephrology
- Cardiology
- Genetics
Background:
- Sickle cell trait (SCT) is prevalent in African Americans and often considered benign.
- Recent studies link SCT to increased risks of chronic kidney disease (CKD) and cardiovascular disease (CVD).
- Existing knowledge on SCT is largely derived from sickle cell disease (SCD) data, where sex influences outcomes.
Purpose of the Study:
- To investigate the effect of SCT on cardiovascular risk in African American patients with CKD.
- To examine the interaction between SCT and sex regarding cardiovascular risk in this population.
Main Methods:
- A retrospective cohort study involving 217 African American CKD patients with SCT and 404 matched controls without SCT.
- Data collected from January 2005 to December 2017 across two centers.
- Primary outcomes included incident coronary artery disease (CAD), incident stroke, and all-cause mortality, with analysis of sex-SCT interaction.
Main Results:
- No significant differences in primary outcomes were observed between SCT patients and controls overall.
- A significant interaction between SCT and sex was found for CAD risk (p < 0.01).
- Stratified analysis revealed no increased CAD risk in females, but a significantly elevated risk in males with SCT (HR 2.13; 95% CI 1.17-3.86).
Conclusions:
- Sickle cell trait is associated with increased coronary artery disease risk specifically in African American males with CKD.
- This observed risk pattern in males with SCT parallels findings in males with sickle cell disease.
- Further research is warranted to validate these sex-specific cardiovascular findings in SCT.
Background:
Sickle cell trait (SCT) is common among African Americans and has been historically considered to be benign. Recently, SCT has been associated with an increased risk for chronic kidney disease (CKD) and cardiovascular disease in the general population. Our understanding of SCT has been extrapolated largely from data of patients with sickle cell disease (SCD). Notably, in SCD, the outcomes differ by sex. The effect of SCT on cardiovascular risk in the African American CKD population is unknown, and the interaction between SCT and sex on cardiovascular risk has not been investigated.
Methods:
We performed a 2-center retrospective cohort study of all African American patients with SCT using international classification of disease diagnosis codes and CKD (using the 2012 Kidney Disease Improving Global Outcomes criteria) with at least 1 year of follow-up between January 2005 and December 2017. A reference group of -African American CKD patients without SCT was used as a comparator during the same period. SCT patients and the reference patients were matched at baseline for age, sex, comorbidities, and proteinuria. Primary outcomes were incident coronary artery disease (CAD), incident stroke, and all-cause mortality. Analysis of effect modification between sex and SCT on primary outcomes was performed.
Results:
We identified 621 African American CKD patients, 217 SCT patients, and 404 reference patients. The mean age was 56 ± 13 years and 66% were female. The mean estimated glomerular filtration rate was 69 ± 30 mL/min. The mean follow-up time was 8 ± 4 years. There were no significant differences in the primary outcomes comparing SCT patients to matched controls. The interaction term between SCT and sex, however, was significant in the CAD model (p < 0.01). Stratification by sex showed no increased risk in females but a significantly increased risk for CAD in male SCT patients (hazard ratio [HR] 2.14; 95% CI 1.18-3.86), which persisted after multivariable analysis (HR 2.13; 95% CI 1.17-3.86).
Conclusion:
SCT is associated with an increased risk for CAD in African American males with CKD. The excess risk in males with SCT appears to follow the same pattern as risk in males with SCD. Larger studies are needed to confirm these findings.
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