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Measurement of Hba(1C) in patients with chronic renal failure
Randie R Little1, Curt L Rohlfing, Alethea L Tennill
1Department of Pathology and Anatomical Sciences, University of Missouri School of Medicine, One Hospital Dr., Columbia, MO 65212, USA. littler@health.missouri.edu
Insights
Diabetic patients with chronic renal failure (CRF) may have inaccurate HbA1c results. While most methods are accurate, healthcare providers should interpret HbA1c cautiously due to shortened erythrocyte survival in CRF.
Area of Science:
- Clinical Chemistry
- Nephrology
- Endocrinology
Background:
- Carbamylated hemoglobin (carbHb) may interfere with HbA1c measurements.
- Shortened erythrocyte survival in chronic renal failure (CRF) can lead to low HbA1c results.
Purpose of the Study:
- Evaluate carbHb's effect on HbA1c measurements.
- Compare HbA1c with glycated albumin (GA) in patients with and without renal disease.
- Determine if CRF causes clinically significant bias in HbA1c results.
Main Methods:
- Assessed 11 assay methods for HbA1c measurement.
- Included patients with and without renal failure and diabetes.
- Used estimated glomerular filtration rate (eGFR) to assess renal disease severity.
- Employed multiple regression analysis to evaluate eGFR's impact on HbA1c.
- Compared HbA1c and GA in renal failure patients.
Main Results:
- Some methods showed statistically significant eGFR effects, but none were clinically significant.
- HbA1c results were approximately 1.5% lower in renal failure patients compared to GA, assuming GA reflects glycemic control better.
Conclusions:
- Most methods accurately measure HbA1c in renal failure patients.
- Healthcare providers must interpret HbA1c results cautiously in CRF patients.
- Shortened erythrocyte survival is a key factor influencing HbA1c interpretation in renal failure.
Background:
Carbamylated hemoglobin (carbHb) is reported to interfere with measurement and interpretation of HbA(1c) in diabetic patients with chronic renal failure (CRF). There is also concern that HbA1c may give low results in these patients due to shortened erythrocyte survival.
Methods:
We evaluated the effect of carbHb on HbA(1c) measurements and compared HbA(1c) with glycated albumin (GA) in patients with and without renal disease to test if CRF causes clinically significant bias in HbA(1c) results by using 11 assay methods. Subjects included those with and without renal failure and diabetes. Each subject's estimated glomerular filtration rate (eGFR) was used to determine the presence and degree of the renal disease. A multiple regression model was used to determine if the relationship between HbA(1c) results obtained from each test method and the comparative method was significantly (p<0.05) affected by eGFR. These methods were further evaluated for clinical significance by using the difference between the eGRF quartiles of >7% at 6 or 9% HbA(1c). The relationship between HbA(1c) and glycated albumin (GA) in patients with and without renal failure was also compared.
Results:
Some methods showed small but statistically significant effects of eGFR; none of these differences were clinically significant. If GA is assumed to better reflect glycemic control, then HbA(1c) was approximately 1.5% HbA(1c) lower in patients with renal failure.
Conclusions:
Although most methods can measure HbA(1c) accurately in patients with renal failure, healthcare providers must interpret these test results cautiously in these patients due to the propensity for shortened erythrocyte survival in renal failure.
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