Insulin resistance in obesity can be reliably identified from fasting plasma insulin

Background/Objectives: Insulin resistance is the major contributor to cardiometabolic complications of obesity. We aimed to (1) establish cutoff points for insulin resistance from euglycemic hyperinsulinemic clamps (EHCs), (2) identify insulin-resistant obese subjects and (3) predict insulin resista...

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Veröffentlicht in:International Journal of Obesity 2015-12, Vol.39 (12), p.1703-1709
Hauptverfasser: ter Horst, K W, Gilijamse, P W, Koopman, K E, de Weijer, B A, Brands, M, Kootte, R S, Romijn, J A, Ackermans, M T, Nieuwdorp, M, Soeters, M R, Serlie, M J
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Sprache:eng
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Zusammenfassung:Background/Objectives: Insulin resistance is the major contributor to cardiometabolic complications of obesity. We aimed to (1) establish cutoff points for insulin resistance from euglycemic hyperinsulinemic clamps (EHCs), (2) identify insulin-resistant obese subjects and (3) predict insulin resistance from routinely measured variables. Subjects/Methods: We assembled data from non-obese ( n =112) and obese ( n =100) men who underwent two-step EHCs using [6,6- 2 H 2 ]glucose as tracer (insulin infusion dose 20 and 60 mU m −2  min −1 , respectively). Reference ranges for hepatic and peripheral insulin sensitivity were calculated from healthy non-obese men. Based on these reference values, obese men with preserved insulin sensitivity or insulin resistance were identified. Results: Cutoff points for insulin-mediated suppression of endogenous glucose production (EGP) and insulin-stimulated glucose disappearance rate ( R d ) were 46.5% and 37.3 μmol kg − 1  min − 1 , respectively. Most obese men (78%) had EGP suppression within the reference range, whereas only 12% of obese men had R d within the reference range. Obese men with R d 74 pmol l −1 with current insulin immunoassay) may be used for identification of insulin-resistant (or metabolically unhealthy) obese men in research and clinical settings.
ISSN:0307-0565
1476-5497
DOI:10.1038/ijo.2015.125