Hb E1c as an indicator for the presence of Hb AE phenotype in diabetic patients.

Since the observation of a “fast-moving” hemoglobin (Hb) in diabetic blood specimens by Rahbar in 1968 [1] and the subsequent structural identification of the glucose-“modified” Hb [2], the measurement of erythrocyte glycoHb (Hb A1c) has served as the monitor for long-term glucose control for patients with diabetes mellitus [3]. Column chromatography was one of the first methodologies used for the quantification of Hb A1c [4]. Recent modifications of the methodology, including shorter column size and faster turnaround time, have resulted in the application of automated HPLC for Hb A1c analysis. As column chromatography has always been a major tool for the investigation of human Hb variants, the use of automated HPLC systems for the analysis of Hb A1c in clinical laboratories renders an extra opportunity for detecting abnormal Hbs in clinical blood specimens, e.g., Hb Manitoba, Hb GCoushatta, Hb Turriff, and Hb Sherwood Forest [5–7]. The presence of an abnormal Hb will result in the formation of its own minor glycoHb; the total glycoHb in the red cells of a Hb variant trait carrier is then the sum of the glycoHb A and the glycoHb variant. For example, the total glycoHb in a sickle cell trait carrier (Hb AS) is Hb A1c 1 Hb S1c. We describe in this report the chromatographic property of the minor glycoHb E (a2b2 ) in an automated HPLC system, and the usefulness of the detection of the Hb E1c peak in the HPLC chromatogram as the indicator for the presence of Hb E in the patient. This study involved EDTA whole-blood specimens specifically for Hb A1c analysis. Hospital in-house specimens arrived in the authors’ NUH Referral Laboratories within 2 h, whereas referral samples were delivered overnight by courier. The general protocol was: (a) Hb A1c assay by HPLC, and (b) hemoglobinopathy studies on specimens whose HPLC chromatograms suggested the presence of abnormal Hb peaks. Hb A1c assay of the red cell hemolysates of the specimens was carried out with an automated Diamat HPLC system (BioRad), which involved a spherical cation-exchange gel column and a 5-min step-gradient created by a single-piston pump and three phosphate buffers of increasing ionic concentration. Chromatography was carried out at 10 °C, and the elution of Hb fractions was monitored at 415 nm and 690 nm. A built-in integrator performed the data analysis. Hemoglobinopathy studies were carried out according to established procedures, including: (a) the initial detection and identification of abnormal Hbs by alkaline and acid electrophoreses on Helena’s cellulose acetate and citrate agar plates, and (b) the quantification of Hb fractions (Hb A, F, A2, and E) in red cell hemolysates by a Variant cationexchange HPLC system (BioRad) programmed with a 6.5-min gradient. Both the Diamat and Variant systems had previously been evaluated in the authors’ laboratory; the latter elutes Hb E and Hb A2 as a single major peak [8, 9]. Criteria for designating Hb AE phenotype to a blood specimen were: (a) the presence of a slow-moving Hb variant in the Hb E/Hb A2 position on alkaline cellulose acetate gel, (b) one single Hb A/Hb E band on acid agar plate, (c) a major Hb E/Hb A2 peak at the end portion of the Variant HPLC chromatogram, and (d) positive test for unstable Hb by the isopropanol assay [10]. A total of 3144 Hb A1c blood specimens (48% NUH inpatients, 47% local outpatients, 5% others) was analyzed in the first 6 months of this year. Fig. 1A is a Hb AA Diamat HPLC chromatogram, showing a minor Hb A1c peak eluted at 2.8 min and a major Hb A peak at 4.0 min. Fig. 1B is the Diamat HPLC chromatogram on another specimen, where an asymmetrical Hb A1c peak with a “right shoulder” was observed. Hemoglobinopathy studies on this specimen revealed the presence of a slowmoving Hb variant, most likely Hb E, with the following properties: electrophoretic mobility in the E/A2 position on alkaline cellulose acetate gel, identical electrophoretic mobility as Hb A on acid citrate gel, coelution with Hb A2 on cation-exchange chromatography, and positive isopropanol unstable Hb test. During a 6-month period, nine Hb A1c blood specimens were found to have the asymmetrical Hb A1c peak with a “right shoulder;” all these specimens were confirmed by hemoglobinopathy studies to have the phenotype of Hb AE. The ethnic origins of the nine Hb E trait carriers were: six Malays, two East Indians, and one Indonesian. Their hematological data were: RBC 5 4.4 3 10/L (3.91–5.91); Hb 5 109 g/L (97–138); mean cell volume (MCV) 5 77.7 fL (68.9–86.1); mean cell Hb (MCH) 5 24.6 pg (21.1–27.4); mean cell Hb concentration (MCHC) 5 317 g/L (298– 340). The average percentage of Hb (E1A2) in seven of the nine samples (as quantified by the Variant HPLC) was 28.3% (25.5–31.0%). The “right shoulder” peak had an elution time of 3.0–3.1 min. Its identity was inferred from the analysis of a patient who had been diagnosed to be Hb EE (or Hb E-b°-thalassemia), with only Hb E and no Hb A, MCV 5 65.1 fL, and MCH 5 23.1 pg. Fig. 1C shows the Hb EE chromatogram: 2.8% Hb F (at 2.0 min), 4.2% minor peak (at 3.0 min), and 92.6% Hb E (at 4 min). The 4.2% minor Hb eluted at 3.0 min was Hb E1c, as Hb E was the only major Hb in this sample. Thus, it could be inferred that the Hb E1c in the Hb AE blood specimens was eluted as the “right shoulder” in the chromatogram, since the elution time of Hb E1c (3.0 min) was slightly behind that of Hb A1c (2.8 min). No similar “right shoulder” was observed in the analysis of red cell hemolysates from trait carriers of Hb S (a2b2 ) and Hb D (a2b2 ). The chromatographic properties of the red cell Hbs from diabetic individuals have been well studied [11]; those of Hb E can be found in a review by Huisman [12]. Cation-exchange HPLC with a SynChropak CM300 column and a sodium acetate gradient resolves Hb E1c completely behind the Hb F fractions (F1 and FO) but in front of the other major Hbs (A and E). Hb E is well known to coelute with the normal minor Hb A2 (a2d2) on both anion and cation exchangers (unless a Technical Briefs