Dissociation between insulin resistance and abnormalities in lipoprotein particle concentrations and sizes in normal-weight Chinese adults
Research output: Contribution to journal › Journal article › Research › peer-review
- Tranaes et al_Frontiers in Nutrition_2021_Vol 8_e651199
Final published version, 196 KB, PDF document
Insulin resistance in obesity coincides with abnormalities in lipid profile and lipoprotein subclass distribution and size even before abnormalities in glucose homeostasis manifest. We aimed to assess this relationship in the absence of obesity. Insulin sensitivity (3-h intravenous glucose tolerance test and minimal modeling) and lipoprotein particle concentrations and sizes (proton nuclear magnetic resonance spectroscopy) were evaluated in 15 insulin-resistant and 15 insulin-sensitive lean Asians of Chinese descent with normal glucose tolerance, matched on age, sex, and body mass index. Despite a ~50% lower insulin sensitivity index (Si) in insulin-resistant than in insulin-sensitive subjects, which was accompanied by significantly greater acute insulin response to glucose (AIRg) and fasting insulin concentration but not different fasting glucose concentration, there were no significant differences between groups in the blood lipid profile (p ≥ 0.44) or the lipoprotein subclass concentrations (p ≥ 0.30) and particle sizes (p ≥ 0.43). We conclude that, contrary to observations in subjects with obesity, insulin resistance is not accompanied by unfavorable changes in the plasma lipid profile and lipoprotein particle concentrations and sizes in lean Asians with normal glucose tolerance. Therefore, insulin resistance at the level of glucose metabolism is mechanistically or temporally dissociated from lipid and lipoprotein metabolism.
Trial Registration: clinicaltrials.gov, NCT03264001.
|Journal||Frontiers in Nutrition|
|Number of pages||7|
|Publication status||Published - 2021|
Copyright © 2021 Tranæs, Ding, Chooi, Chan, Choo, Leow and Magkos.
- Faculty of Science - Insulin resistance, Lipoprotein particle size, Obesity phenotypes, Metabolically-unhealthy lean, Nuclear magnetic resonance