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 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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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. |
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ISSN: | 0307-0565 1476-5497 |
DOI: | 10.1038/ijo.2015.125 |