Comparison of type 1, type 2, and atypical ketosis-prone diabetes at 4 years of diabetes duration☆
Abstract
Context
Atypical ketosis-prone diabetes (KPD) is frequently detected in obese individuals at diagnosis of diabetes, yet its precise pathophysiology is not understood.
Aim
The hypothesis tested in this study states that while individuals with atypical KPD are phenotypically similar to those with type 2 diabetes, metabolically, they behave more like individuals with autoimmune type 1 diabetes.
Methods
Thirty-seven individuals of Black, Hispanic, or White background and a diagnosis of diabetes mellitus for an average duration of 4 years participated in this cross-sectional study. Ten, 12, and 15 subjects had type 1, atypical, and type 2 diabetes, respectively. Insulin secretion was evaluated by a mixed-meal test. Insulin sensitivity and fuel oxidation were assessed by simultaneous euglycemic hyperinsulinemic clamp and indirect calorimetry. Lastly, a 12-h insulin withdrawal test was performed.
Results
Insulin secretion, insulin sensitivity, and the insulin withdrawal tests yielded significant differences for type 1 vs. atypical diabetes and type 1 vs. type 2 diabetes, while there were no significant differences between atypical vs. type 2 diabetes. The indirect calorimetry showed higher-than-normal basal nonprotein respiratory quotients (RQs) and lower-than-normal insulin-stimulated nonprotein RQs across the three study groups.
Conclusions
After 4 years from diabetes diagnosis and while far from optimal glycemic control, atypical KPD resembles type 2 diabetes phenotypically and metabolically as well. Therefore, this study supports the classification of atypical KPD as ketosis-prone type 2 diabetes, and the concept that metabolic inflexibility occurs in the presence of insulin resistance in type 1 and type 2 diabetes.
Keywords: Diabetic ketoacidosis, Glucotoxicity, Hyperglycemic crisis, Insulin resistance, Insulin secretion, Ketosis
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☆ This study was supported by USPHS grant M01-RR000633 from NIH-NCRR-CR to the General Clinical Research Center at UT Southwestern Medical Center at Dallas, TX, USA, and training grant 5 T32 DK07307.
PII: S1056-8727(06)00009-2
doi:10.1016/j.jdiacomp.2006.01.005
© 2006 Elsevier Inc. All rights reserved.
