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Identification of Individuals With Insulin Resistance Using Routine Clinical Measurements

Stern, Steven; Williams, Ken; Ferrannini, Eleuterio; DeFronzo, Ralph; Bogardus, Clifton; Stern, Michael

Description

Insulin resistance is a treatable precursor of diabetes and potentially of cardiovascular disease as well. To identify insulin-resistant patients, we developed decision rules from measurements of obesity, fasting glucose, insulin, lipids, and blood pressure and family history in 2,321 (2,138 nondiabetic) individuals studied with the euglycemic insulin clamp technique at 17 European sites; San Antonio, Texas; and the Pima Indian reservation. The distribution of whole-body glucose disposal...[Show more]

dc.contributor.authorStern, Steven
dc.contributor.authorWilliams, Ken
dc.contributor.authorFerrannini, Eleuterio
dc.contributor.authorDeFronzo, Ralph
dc.contributor.authorBogardus, Clifton
dc.contributor.authorStern, Michael
dc.date.accessioned2015-12-13T23:04:16Z
dc.identifier.issn0012-1797
dc.identifier.urihttp://hdl.handle.net/1885/85297
dc.description.abstractInsulin resistance is a treatable precursor of diabetes and potentially of cardiovascular disease as well. To identify insulin-resistant patients, we developed decision rules from measurements of obesity, fasting glucose, insulin, lipids, and blood pressure and family history in 2,321 (2,138 nondiabetic) individuals studied with the euglycemic insulin clamp technique at 17 European sites; San Antonio, Texas; and the Pima Indian reservation. The distribution of whole-body glucose disposal appeared to be bimodal, with an optimal insulin resistance cutoff of <28 μmol/min·kg lean body mass. Using recursive partitioning, we developed three types of classification tree models: the first, based on clinical measurements and all available laboratory determinations, had an area under the receiver operator characteristic curve (aROC) of 90.0% and generated a simple decision rule: diagnose insulin resistance if any of the following conditions are met: BMI >28.9 kg/m2, homeostasis model assessment of insulin resistance (HOMA-IR) >4.65, or BMI >27.5 kg/m2 and HOMA-IR >3.60. The fasting serum insulin concentrations corresponding to these HOMA-IR cut points were 20.7 and 16.3 μU/ml, respectively. This rule had a sensitivity and specificity of 84.9 and 78.7%, respectively. The second model, which included clinical measurements but no laboratory determinations, had an aROC of 85.0% and generated a decision rule that had a sensitivity and specificity of 78.7 and 79.6%, respectively. The third model, which included clinical measurements and lipid measurements but not insulin (and thus excluded HOMA-IR as well), had a similar aROC (85.1%), sensitivity (81.3%), and specificity (76.3%). Thus, insulin-resistant individuals can be identified using simple decision rules that can be tailored to specific needs.
dc.publisherAmerican Diabetes Association
dc.sourceDiabetes
dc.subjectKeywords: glucose; insulin; lipid; blood pressure; cardiovascular disease; clinical trial; comparative study; controlled clinical trial; controlled study; diabetes mellitus; diagnostic accuracy; diagnostic approach route; disease classification; family history; glu
dc.titleIdentification of Individuals With Insulin Resistance Using Routine Clinical Measurements
dc.typeJournal article
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.citationvolume54
dc.date.issued2005
local.identifier.absfor030499 - Medicinal and Biomolecular Chemistry not elsewhere classified
local.identifier.ariespublicationMigratedxPub13632
local.type.statusPublished Version
local.contributor.affiliationStern, Steven, College of Business and Economics, ANU
local.contributor.affiliationWilliams, Ken, University of Texas
local.contributor.affiliationFerrannini, Eleuterio, National Research Council (CNR) Institute of Clinical Physiology
local.contributor.affiliationDeFronzo, Ralph, University of Texas
local.contributor.affiliationBogardus, Clifton, National Institutes of Health
local.contributor.affiliationStern, Michael, University of Texas
local.description.embargo2037-12-31
local.bibliographicCitation.issue2
local.bibliographicCitation.startpage333
local.bibliographicCitation.lastpage339
local.identifier.doi10.2337/diabetes.54.2.333
dc.date.updated2015-12-12T07:54:59Z
local.identifier.scopusID2-s2.0-12744262843
CollectionsANU Research Publications

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