Limitation of the validity of the homeostasis model assessment as an index of insulin resistance in Korea
Authors
Eun Seok Kang ; Yong Seok Yun ; Seok Won Park ; Hyeung Jin Kim ; Chul Woo Ahn ; Young Duk Song ; Bong Soo Cha ; Sung Kil Lim ; Kyung Rae Kim ; Hyun Chul Lee
Citation
METABOLISM-CLINICAL AND EXPERIMENTAL, Vol.54(2) : 206-211, 2005
Adult ; Blood Glucose/metabolism ; Body Mass Index ; Diabetes Mellitus, Type 2/blood ; Female ; Glucose Clamp Technique ; Glucose Intolerance/blood ; Homeostasis/physiology* ; Humans ; Insulin/blood ; Insulin Resistance/physiology* ; Islets of Langerhans/physiology ; Kinetics ; Korea ; Male ; Middle Aged ; Models, Biological ; Pancreatic Function Tests ; Reproducibility of Results
Keywords
15690315
Abstract
Homeostasis model assessment of insulin resistance (HOMA-IR) is a less invasive, inexpensive, and less labor-intensive method to measure insulin resistance (IR) as compared with the glucose clamp test. The aim of this study was to evaluate the validity of HOMA-IR by comparing it with the euglycemic clamp test in determining IR. We assessed the validity of HOMA-IR by comparing it with the total glucose disposal rate measured by the 3-hour euglycemic-hyperinsulinemic clamp in subjects with type 2 diabetes (n = 47), impaired glucose tolerance (n = 21), and normal glucose tolerance (n = 22). There was a strong inverse correlation (r = −0.558; P < .001) between the log-transformed HOMA-IR and the total glucose disposal rate. There was moderate agreement between the 2 methods in the categorization according to the IR (weighted κ = 0.294). The magnitude of the correlation coefficients was smaller in the subjects with a lower body mass index (BMI <25.0 kg/m2, r = −0.441 vs BMI ≥25.0 kg/m2, r = −0.615; P = .032), a lower HOMA-beta cell function (HOMA-β <60.0, r = −0.527 vs HOMA-β ≥60.0, r = −0.686; P = .016), and higher fasting glucose levels (fasting glucose ≤5.66 mmol/L, r = −0.556 vs fasting glucose >5.66 mmol/L, r = −0.520; P = .039). The limitation of the validity of the HOMA-IR should be carefully considered in subjects with a lower BMI, a lower beta cell function, and high fasting glucose levels such as lean type 2 diabetes mellitus with insulin secretory defects.