HETEROGENEITY OF HEMOGLOBIN A(1D) - ASSESSMENT AND PARTIAL CHARACTERIZATION OF 2 NEW MINOR HEMOGLOBINS, A(1D3A) AND A(1D3B), INCREASED IN UREMIC AND DIABETIC-PATIENTS, RESPECTIVELY

Citation
E. Bisse et al., HETEROGENEITY OF HEMOGLOBIN A(1D) - ASSESSMENT AND PARTIAL CHARACTERIZATION OF 2 NEW MINOR HEMOGLOBINS, A(1D3A) AND A(1D3B), INCREASED IN UREMIC AND DIABETIC-PATIENTS, RESPECTIVELY, Journal of chromatography B. Biomedical applications, 687(2), 1996, pp. 349-356
Citations number
17
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Journal of chromatography B. Biomedical applications
ISSN journal
15726495 → ACNP
Volume
687
Issue
2
Year of publication
1996
Pages
349 - 356
Database
ISI
SICI code
Abstract
We have separated and quantified two new minor hemoglobins named HbA(1 d3a) and HbA(1d3b). The level of HbA(1d3a) was significantly higher in uremic than in non-uremic patients (3.00 +/- 0.50% vs. 1.28 +/- 0.26% of total hemoglobin). It correlated well with carbamylated hemoglobin (r = 0.80, n = 81, p < 0.002) and with plasma urea concentration (r = 0.78, n = 81, p < 0.002). These data and the electrospray ionization mass spectrometric analysis provide strong evidence that HbA(1d3a) is an alpha-chain modified by carbamylation. The HbA(1d3a) level in diabe tic patients was found to be 1.6-fold that in non-diabetic subjects (3 .00 +/- 0.49 vs. 1.90 +/- 0.33). This was attributed to HbA(1d3) modif ied by glycation. Indeed HbA(1d3b) correlated significantly with HbA(1 c) (r = 0.71, p < 0.002) and with serum glucose level (r = 0.62, p < 0 .002). These two new minor hemoglobins may serve as complements for th e objective assessment of averaged long-term uremia and glycemia in ur emic and diabetic patients.