Improved Detection of Abnormal Glucose Tolerance in Africans: The Value of Combining Hemoglobin A1c With Glycated Albumin

In African-born Blacks living in America, we determined by BMI category 1) prevalence of abnormal glucose tolerance (Abnl-GT) and 2) diagnostic value and reproducibility of hemoglobin A_1c (HbA_1c), fructosamine, and glycated albumin (GA).

Participants (n = 416; male, 66%; BMI 27.7 ± 4.5 kg/m² [mean ± SD]) had an oral glucose tolerance test with HbA_1c, GA, and fructosamine assayed. These glycemic markers were repeated 11 ± 7 days later. Abnl-GT diagnosis required 0 h ≥5.6 mmol/L (≥100 mg/dL) and/or 2 h ≥7.8 mmol/L (≥140 mg/dL). Thresholds for HbA_1c, GA, and fructosamine were the values at the 75th percentile for the population (39 mmol/mol [5.7%], 14.2%, and 234 μmol/L, respectively).

Abnl-GT prevalence in the nonobese was 34% versus 42% in the obese (P = 0.124). Reproducibility was excellent for HbA_1c and GA (both ≥ 0.8), but moderate for fructosamine ( = 0.6). Focusing on HbA_1c and GA in the nonobese, we found as single tests the sensitivities of HbA_1c and GA were 36% versus 37% (P = 0.529). Combining HbA_1c and GA, sensitivity increased to 58% because GA identified 37% of Africans with Abnl-GT not detected by HbA_1c (P value for both tests vs. HbA_1c alone was <0.001). For the obese, sensitivities for HbA_1c, GA, and the combined tests were 60%, 27%, and 67%, respectively. Combined test sensitivity did not differ from HbA_1c alone (P = 0.25) because GA detected only 10% of obese Africans with Abnl-GT not detected by HbA_1c.

Adding GA to HbA_1c improves detection of Abnl-GT in nonobese Africans.