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Continuous Glucose Monitoring Metrics in the Assessment of Glycemia in Moderate-to-Advanced CKD in Diabetes
James Ling1, Jack K C Chung Ng1, Eric S H Lau1
1Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Sha Tin, New Territories, Hong Kong SAR, China.
Insights
Glycated hemoglobin A1c (HbA1c) reliability decreases in advanced chronic kidney disease (CKD). Continuous glucose monitoring (CGM) metrics offer valuable insights into glycemic control and variability, complementing HbA1c.
Area of Science:
- Nephrology
- Endocrinology
- Metabolic Diseases
Background:
- Glycated hemoglobin A1c (HbA1c) accuracy is compromised in advanced chronic kidney disease (CKD) due to altered red blood cell turnover.
- Continuous glucose monitoring (CGM) is increasingly recommended for assessing glycemic control in CKD patients.
- The relationship between HbA1c and CGM-derived glycemic metrics in moderate-to-advanced CKD requires further investigation.
Purpose of the Study:
- To evaluate the correlation between HbA1c and CGM metrics of average glycemia and glucose variability (GV) in patients with moderate-to-advanced CKD.
- To determine the reliability of HbA1c as a sole indicator of glycemic control in different stages of CKD.
- To explore the potential utility of CGM-derived indices as adjuncts to HbA1c monitoring in CKD management.
Main Methods:
- Ninety patients with diabetes across CKD stages G3b, G4, and G5 (nondialysis) were enrolled.
- Blood samples for HbA1c and blinded CGM data were collected concurrently.
- Correlations between HbA1c, glucose management indicator (GMI), time-in-range (TIR), and glucose variability metrics were analyzed.
Main Results:
- Correlation between HbA1c and GMI significantly attenuated with advancing CKD stages (G3b: r=0.68; G4: r=0.52; G5: r=0.22).
- HbA1c correlated with TIR and % time > 13.9 mmol/l in G3b and G4 CKD, but not in G5.
- Estimated glomerular filtration rate (eGFR) was a significant determinant of the bias between GMI and HbA1c.
Conclusions:
- CGM-derived glycemic indices can supplement HbA1c monitoring for improved glycemic management in CKD, particularly with eGFR < 30 ml/min/1.73 m².
- Time in hypoglycemia and glucose variability are critical targets for glycemic optimization in CKD, which are not adequately reflected by HbA1c.
- HbA1c alone is an unreliable measure of glycemic control in advanced CKD.
Introduction:
Glycated hemoglobin A1c (HbA1c) has reduced reliability in advanced chronic kidney disease (CKD) owing to factors influencing red cell turnover. Recent guidelines support the use of continuous glucose monitoring (CGM) in glycemic assessment in these patients. We evaluated relationships between HbA1c and CGM metrics of average glycemia and glucose variability (GV) in moderate-to-advanced CKD.
Methods:
There were a total of 90 patients with diabetes in CKD stages G3b (n = 33), G4 (n = 43), and G5 (nondialysis) (n = 14) (age [mean ± SD] 65.4 ± 9.0 years, estimated glomerular filtration rate [eGFR] 26.1 ± 9.6 ml/min per 1.73 m2, and HbA1c 7.4 ± 0.8%). CGM metrics were estimated from blinded CGM (Medtronic Ipro2 with Enlite sensor) and compared with HbA1c in the same week.
Results:
Correlations between glucose management indicator (GMI) and HbA1c attenuated with advancing CKD (G3b [r = 0.68, P < 0.0001], G4 [r = 0.52, P < 0.001], G5 [r = 0.22, P = 0.44], P = 0.01 for CKD stage). In G3b and G4, HbA1c correlated significantly with time-in-range (TIR) (3.9-10.0 mmol/l) (r = -0.55 and r = -0.54, respectively) and % time > 13.9 mmol/l (r = 0.53 and r = 0.44, respectively), but not in G5. HbA1c showed no correlation with % time <3.0 mmol/l (r = -0.045, P = 0.67) or % coefficient of variation (CV) (r = -0.05, P = 0.64) in any CKD stage. Only eGFR was a significant determinant of bias for the difference between GMI and HbA1c (difference -0.28%, 95% CI [-0.52 to -0.03] per 15 ml/min per 1.73 m2 decrement, P = 0.03).
Conclusion:
CGM-derived indices might serve as an adjunct to HbA1c monitoring to guide glycemic management, especially in those with eGFR <30 ml/min per 1.73 m2. Time in hypoglycemia and glycemic variability are relevant glycemic targets for optimization not reflected by HbA1c.
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