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Dysfunctional pancreatic beta-cells of critical stress play a more prominent role in the development of stress diabetes in critically burned Korean subjects

DC Field Value Language
dc.contributor.author이병완-
dc.date.accessioned2015-04-23T17:02:31Z-
dc.date.available2015-04-23T17:02:31Z-
dc.date.issued2010-
dc.identifier.issn0026-0495-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/101712-
dc.description.abstractThe purposes of this study are to identify the predictive parameters for the development of stress-induced hyperglycemia and to investigate the glucose metabolic homeostasis in critically burned Korean subjects. We conducted a prospective cross-sectional study of adult patients with glucose management targeting fasting and postprandial blood glucose levels less than 140 and 200 mg/dL, respectively, in patients with unrecognized diabetes. Clinical and laboratory stress parameters and insulin secretory and sensitivity parameters were assessed. Stimulated C-peptide and 24-hour urinary free cortisol predicted new-onset stress diabetes requiring insulin therapy. The subjects requiring insulin therapy were leaner and more insulin sensitive than insulin-free subjects, without significance. Glycated hemoglobin, stimulated C-peptide, homeostasis model assessment of insulin resistance, and age had a significant influence on the mean daily dose of insulin. Our present data showed that Korean subjects with dysfunctional pancreatic beta-cells of critical stress are prone to become stress diabetic and require more insulin to control the hyperglycemia-
dc.description.statementOfResponsibilityopen-
dc.format.extent1307~1315-
dc.relation.isPartOfMETABOLISM-CLINICAL AND EXPERIMENTAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAnalysis of Variance-
dc.subject.MESHAsian Continental Ancestry Group-
dc.subject.MESHBurns/complications*-
dc.subject.MESHBurns/metabolism-
dc.subject.MESHBurns/physiopathology-
dc.subject.MESHCross-Sectional Studies-
dc.subject.MESHDiabetes Mellitus, Type 2/etiology*-
dc.subject.MESHDiabetes Mellitus, Type 2/metabolism-
dc.subject.MESHDiabetes Mellitus, Type 2/physiopathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHHyperglycemia/etiology*-
dc.subject.MESHHyperglycemia/metabolism-
dc.subject.MESHHyperglycemia/physiopathology-
dc.subject.MESHInsulin/blood-
dc.subject.MESHInsulin Resistance-
dc.subject.MESHInsulin-Secreting Cells/metabolism*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPancreas/metabolism-
dc.subject.MESHPancreas/physiopathology*-
dc.subject.MESHPostprandial Period-
dc.subject.MESHProspective Studies-
dc.subject.MESHStress, Physiological*-
dc.titleDysfunctional pancreatic beta-cells of critical stress play a more prominent role in the development of stress diabetes in critically burned Korean subjects-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorLee Byung-Wan-
dc.contributor.googleauthorHur Jun-
dc.contributor.googleauthorHae-Jun Yim-
dc.contributor.googleauthorJae-Bong Park-
dc.contributor.googleauthorHeungjeong Woo-
dc.contributor.googleauthorHyung-Joon Yoo-
dc.identifier.doi10.1016/j.metabol.2009.11.022-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02796-
dc.relation.journalcodeJ02223-
dc.identifier.eissn1532-8600-
dc.identifier.pmid20045532-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0026049509005101-
dc.contributor.alternativeNameLee, Byung Wan-
dc.contributor.affiliatedAuthorLee, Byung Wan-
dc.citation.volume59-
dc.citation.number9-
dc.citation.startPage1307-
dc.citation.endPage1315-
dc.identifier.bibliographicCitationMETABOLISM-CLINICAL AND EXPERIMENTAL, Vol.59(9) : 1307-1315, 2010-
dc.identifier.rimsid46682-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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