|
|
||||||||
Clinical |
Departments of Internal Medicine,1 Pathology,2 Pediatrics,3 and Biostatistical Sciences,4 Wake Forest University School of Medicine, Winston–Salem, North Carolina, USA
Correspondence to: B.I. Freedman, Section on Nephrology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston–Salem, North Carolina 27157-1053 USA. bfreedma{at}wfubmc.edu
Background: Relative to hemoglobin A1c
(HbA1c), percentage of glycated albumin (GA%) more accurately
reflects recent glycemic control in diabetic hemodialysis (HD)
patients.
Methods: To determine the accuracy of glycemic assays
in a larger sample including patients on peritoneal dialysis (PD),
HbA1c and GA% were measured in 519 diabetic subjects: 55 on PD, 415
on HD, and 49 non-nephropathy controls.
Results: Mean ± SD serum glucose levels were
higher in HD and PD patients relative to non-nephropathy controls (HD 169.7
± 62 mg/dL, PD 168.6 ± 66 mg/dL, controls 146.1 ± 66
mg/dL; p = 0.03 HD vs controls, p = 0.13 PD vs controls).
GA% was also higher in HD and PD patients (HD 20.6% ± 8.0%, PD 19.0%
± 5.7%, controls 15.7% ± 7.7%; p < 0.02 HD vs
controls and PD vs controls). HbA1c was paradoxically lower in
dialysis patients (HD 6.78% ± 1.6%, PD 6.87% ± 1.4%, controls
7.3% ± 1.4%; p = 0.03 HD vs controls, p = 0.12 PD vs
controls). The serum glucose/HbA1c ratio differed significantly
between dialysis patients and controls (p < 0.0001 HD vs controls,
p = 0.002 PD vs controls), while serum glucose/GA% ratio was similar
across groups (p = 0.96 HD vs controls, p = 0.64 PD vs
controls). In best-fit multivariate models with HbA1c or GA% as
outcome variable, dialysis status was a significant predictor of
HbA1c but not GA%.
Conclusions: The relationship between HbA1c
and GA% differs in diabetic patients with end-stage renal disease who perform
either PD or HD compared to those without nephropathy. HbA1c
significantly underestimates glycemic control in peritoneal and hemodialysis
patients relative to GA%.
KEY WORDS: Diabetes mellitus; end-stage renal disease; glycated albumin; glycemic control; hemoglobin A1c.
Received 21 October 2008; accepted 3 March 2009.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |