A comparison of the glycosylation gap and hemoglobin glycation index in patients with diabetes

被引:39
作者
Chalew, SA
McCarter, RJ
Thomas, J
Thomson, JL
Hempe, JM
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Div Pediat Endocrinol, Childrens Hosp New Orleans,Res Inst Children, New Orleans, LA 70118 USA
[2] Childrens Natl Med Ctr, Dept Bioinformat & Stat, Washington, DC 20010 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Dept Publ Hlth & Prevent Med, New Orleans, LA USA
关键词
glucose; hemoglobin A1c; glycated plasma proteins; complications; hemoglobin glycation index; fructosamine; glycosylation gap; diabetes;
D O I
10.1016/j.jdiacomp.2005.01.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Problem: The Glycosylation Gap (GGAP) based on fructosamine (F) measurement and the Hemoglobin Glycation Index (HGI) based on mean blood glucose (MBG) are two indices of between-individual differences in glycated hemoglobin (HbA1c) adjusted for glycemia. We sought to simultaneously compare GGAP with HGI and other estimates of glycemia. Methods: HbA1c, F, and MBG level were obtained at a clinic visit from 62 patients with Type I diabetes. GGAP and HGI were calculated from the data as previously described. The variables were compared by correlation analysis. The concordance of patient classification by GGAP and HGI was compared by weighted kappa test. Results: The mean HbA1c= 11.1 +/- 2.7%, F = 372.0 +/- 136.6 mol/l, MBG = 186.5 +/- 58.4 mg/dl, HGI = 0.0 +/- 2.0, and GGAP = 0.0 +/- 1.9. MBG, HbA1c, and F were all highly correlated with each other. The HGI and GGAP were highly correlated (r = .73, P < .0001) and similar in both magnitude and direction. There was good agreement between HGI and GGAP classifications of patients into high, moderate, and low glycation groups (P < .0075). Conclusions: GGAP and MBG give similar information regarding between-patient differences in HbA1c among patients with diabetes. Thus, biological variation in HbA1c is not an artifact of variability in glucose measurements comprising the MBG. Individual patient factors influence the intracellular glycation of HbA1c in addition to the effect of extracellular glycemia, which is manifested as a between-individual biological variation in HbA1c. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:218 / 222
页数:5
相关论文
共 22 条
[1]  
[Anonymous], BIOL VARIATION PRINC
[2]   Discordance between HbA1c and fructosamine -: Evidence for a glycosylation gap and its relation to diabetic nephropathy [J].
Cohen, RM ;
Holmes, YR ;
Chenier, TC ;
Joiner, CH .
DIABETES CARE, 2003, 26 (01) :163-167
[3]  
Couturier M, 1997, CLIN INVEST MED, V20, P103
[4]  
DCCT Res Grp, 1987, DIABETES CARE, V10, P1
[5]   Investigation of the mechanism underlying the variability of glycated haemoglobin in non-diabetic subjects not related to glycaemia [J].
Gould, BJ ;
Davie, SJ ;
Yudkin, JS .
CLINICA CHIMICA ACTA, 1997, 260 (01) :49-64
[6]  
Hempe JM, 2001, PATHOL LAB MED, P145
[7]  
Hempe JM, 1997, J CAPILLARY ELECTROP, V4, P131
[8]   High and low hemoglobin glycation phenotypes in type 1 diabetes - A challenge for interpretation of glycemic control [J].
Hempe, JM ;
Gomez, R ;
McCarter, RJ ;
Chalew, SA .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2002, 16 (05) :313-320
[9]   GLYCOSYLATED HEMOGLOBIN IN HUMAN AND ANIMAL RED-CELLS - ROLE OF GLUCOSE PERMEABILITY [J].
HIGGINS, PJ ;
GARLICK, RL ;
BUNN, HF .
DIABETES, 1982, 31 (09) :743-748
[10]   SERUM FRUCTOSAMINE AND GLYCATED HEMOGLOBIN MEASUREMENTS IN DIABETIC CONTROL [J].
HINDLE, EJ ;
ROSTRON, GM ;
CLARK, SA ;
GATT, JA .
ARCHIVES OF DISEASE IN CHILDHOOD, 1986, 61 (02) :113-117