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In people with sickle cell trait (SCT; found in ≈10% of blacks), hemoglobin A (HbA) accounts for 60% to 70% of hemoglobin in erythrocytes and hemoglobin S (HbS) accounts for the remainder. Some research suggests that erythrocytes with HbS have shortened life spans, which could lead to lower glycosylated hemoglobin (HbA1c) levels. In this retrospective cohort study, researchers identified 367 people with SCT and 4253 self-identified African-Americans without SCT in two community-based populations; concurrent measures of HbA1c, fasting blood glucose, and 2-hour postprandial glucose levels were available from 10 to 25 years of follow-up.
For all fasting glucose level categories (in 10-mg/dL groups, from <80 mg/dL to ≥150 mg/dL), mean HbA1c leve…