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Relationship between assays of glycemia in diabetic subjects with advanced chronic kidney disease
Barry I Freedman1, Zak K Shihabi, Lilian Andries
1Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1053, USA. bfreedma @ wfubmc.edu
Insights
Glycated albumin (GA) and hemoglobin A1c (HbA1c) reflect glycemic control differently in advanced chronic kidney disease (CKD). Reduced glomerular filtration rate (GFR) impacts HbA1c accuracy more than GA in diabetic CKD patients.
Area of Science:
- Nephrology
- Diabetology
- Clinical Chemistry
Background:
- Hemoglobin A1c (HbA1c) is a standard measure of long-term glycemic control.
- Glycated albumin (GA) offers a shorter-term glycemic control assessment, potentially more accurate in dialysis patients.
- Limited comparative data exists for GA and HbA1c in advanced chronic kidney disease (CKD).
Purpose of the Study:
- To compare the accuracy of glycated albumin (GA) and hemoglobin A1c (HbA1c) in assessing glycemic control in diabetic patients with varying stages of chronic kidney disease (CKD).
Main Methods:
- Simultaneous measurement of HbA1c and GA in 303 diabetic subjects.
- Study groups included pre-dialysis CKD stage 4, post-transplant CKD stage 3, and non-nephropathy controls.
- Glomerular filtration rate (GFR) was estimated for all participants.
Main Results:
- The GA:HbA1c ratio significantly differed between non-nephropathy controls and CKD patients (p < 0.001).
- The glucose:HbA1c ratio showed an inverse association with GFR in nephropathy cases (r = -0.13; p = 0.04).
- Glucose:GA ratio did not significantly vary with GFR (r = -0.08; p = 0.24).
Conclusions:
- Reduced GFR in diabetic CKD patients influences the relationship between GA and HbA1c.
- The accuracy of HbA1c in severe nephropathy warrants further investigation.
- HbA1c demonstrates relatively good performance in milder stages of CKD.
Background:
Relative to hemoglobin A(1c) (HbA(1c)), glycated albumin (GA) more accurately reflects recent glycemic control in diabetic patients on hemodialysis and peritoneal dialysis. These assays have yet to be compared in patients with advanced chronic kidney disease (CKD).
Methods:
HbA(1c) and GA were simultaneously measured in 303 diabetic subjects: 70 with CKD prior to dialysis (CKD-stage 4), 184 with CKD after transplantation (TXP-stage 3) and 49 non-nephropathy controls.
Results:
Mean estimated GFR was 76, 46 and 26 ml/min in controls, TXP-3 and CKD-4 cases, respectively. Mean (SD) HbA(1c) (%) and GA (%) concentrations were 7.30 (1.40) and 16.8 (4.9) in controls, 7.28 (1.66) and 21.5 (6.4) in CKD-4 cases, and 7.21 (1.62) and 21.2 (5.5) in TXP-3 cases, respectively. The GA:HbA(1c) ratio differed significantly between non-nephropathy controls and both groups of CKD patients (both p < 0.001), but not between CKD-4 and TXP-3 cases (p = 0.92). The glucose:HbA(1c) ratio was inversely associated with GFR in all 254 nephropathy cases (r = -0.13; p = 0.04), while glucose:GA did not vary significantly based upon GFR (r = -0.08; p = 0.24).
Conclusions:
The relationship between glycated albumin and HbA(1c) is influenced by the presence of reduced GFR in diabetic patients with CKD. The accuracy of the HbA(1c) assay in diabetic subjects with severe nephropathy requires further investigation, although HbA(1c) performs relatively well with milder CKD.
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