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A comparison of osteoprotegerin with adiponectin and high-sensitivity C-reactive protein (hsCRP) as a marker for insulin resistance

Authors :
Niamh Devlin
Eoin P. O'Sullivan
Colin Davenport
Paula M O'Shea
Grainne Kelleher
Christopher J. Thompson
Lakshmi Penugonda
Amar Agha
Rachel K Crowley
David T. Ashley
Diarmuid Smith
Donal J. O’Gorman
Source :
Metabolism: clinical and experimental. 62(1)
Publication Year :
2011

Abstract

Insulin resistance (IR) is associated with low adiponectin and elevated high sensitivity C-reactive protein (hsCRP). Osteoprotegerin (OPG) has been shown to be elevated in type 2 diabetes, but whether it reflects underlying IR is unclear. We aimed to compare the ability of serum OPG with adiponectin and hsCRP to act as a marker for IR in individuals with normal and abnormal glucose tolerance.115 men underwent a 75 g oral glucose tolerance test. OPG, hsCRP and adiponectin were measured using ELISA. IR was assessed using the homeostasis model assessment of insulin resistance (HOMA-IR).Men with abnormal glucose tolerance (n=38) were older (58.3±11.2 vs 47.3±11.4 years, P.001), had higher body mass index (BMI) (31.1±2.9 vs 27.9±3.2 kg/m(2), P.001) and were more insulin resistant (median (I.Q.) HOMA-IR 5.88 (3.38) vs 1.13 (1.14), P.001) than those with normal glucose tolerance (n=77). After adjustment for age and BMI, OPG (6.28 (2.32) vs 5.16 (1.86) pmol/L, P.001) and hsCRP (2.07 (5.47) vs 0.78 (1.05) mg/L, P.001) were higher and adiponectin (3.02±1.17 vs 4.78±2.38 μg/mL, P.001) was lower in those with AGT. After adjustment for age and BMI, adiponectin (r=-0.317, P.001) and hsCRP (r=0.318, P.001), but not OPG (r=0.126, P=.196) correlated with HOMA-IR. On multiple linear regression analysis, adiponectin and hsCRP but not OPG were independent predictors of HOMA-IR.OPG is higher in individuals with abnormal glucose tolerance, but unlike adiponectin and hsCRP, does not correlate with HOMA-IR, suggesting its elevation within this cohort of individuals is due to factors other than insulin resistance.

Details

ISSN :
15328600
Volume :
62
Issue :
1
Database :
OpenAIRE
Journal :
Metabolism: clinical and experimental
Accession number :
edsair.doi.dedup.....efc1ee5c0a1d4b1c4140a8bfc116da8e