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dc.contributor.authorProtopsaltis, I. D.en
dc.contributor.authorNikolopoulos, Georgios K.en
dc.contributor.authorDimou, Eftihiaen
dc.contributor.authorBrestas, Parisen
dc.contributor.authorKokkoris, Steliosen
dc.contributor.authorKorantzopoulos, Panagiotisen
dc.contributor.authorMelidonis, Andreasen
dc.creatorProtopsaltis, I. D.en
dc.creatorNikolopoulos, Georgios K.en
dc.creatorDimou, Eftihiaen
dc.creatorBrestas, Parisen
dc.creatorKokkoris, Steliosen
dc.creatorKorantzopoulos, Panagiotisen
dc.creatorMelidonis, Andreasen
dc.date.accessioned2018-06-22T09:53:00Z
dc.date.available2018-06-22T09:53:00Z
dc.date.issued2007
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41612
dc.description.abstractBackground: There is no consistent evidence regarding the prognostic value of metabolic syndrome (MS) in predicting all-cause mortality and coronary heart disease (CHD) risk among type 2 diabetic patients. We sought to investigate whether individual or various combinations of MS components have a different predictive value than the presence of MS in this setting. Methods: Six hundred type 2 diabetic patients (mean age 60.4 ± 9 years, 54% males) without known CHD were prospectively followed-up for a mean period of 10.06 years. The presence of MS was examined using the National Cholesterol Education Program (NCEP) definition. Statistical analyses were performed using Kaplan-Meier estimator and Cox proportional Hazard models. Results: MS was present in 62.4% of the patients while 142 died during follow-up. Significant predictors for all-cause mortality were the presence of MS (HR 1.75), sex (HR 1.69), age (HR 1.09), and diabetes duration (HR 1.02). Regarding CHD incidents, HDL (HR 0.98), systolic blood pressure (HR 1.01), sex (HR 2.05), and total cholesterol (HR 1.005) were significant predictors while the presence of MS was not. Subjects fulfilling the triad consisting of diabetes, hypertension, and low HDL or the combination of diabetes, hypertension, low HDL, and high triglyceride levels had the highest probability for developing CHD events (HR 1.79, 1.73, respectively). Conclusions: The presence of MS in type 2 diabetic patients without known CHD reduces the 10-year survival while specific combinations of its components have different impact on CHD risk. © 2006 Elsevier Ireland Ltd. All rights reserved.en
dc.language.isoengen
dc.sourceAtherosclerosisen
dc.subjectArticleen
dc.subjectHumanen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectAdulten
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectFollow upen
dc.subjectPredictive value of testsen
dc.subjectPriority journalen
dc.subjectTreatment outcomeen
dc.subjectPrognosisen
dc.subjectProspective studyen
dc.subjectSurvivalen
dc.subjectDiabetesen
dc.subjectMortalityen
dc.subjectTime factorsen
dc.subjectMaleen
dc.subjectStatistical analysisen
dc.subjectSystolic blood pressureen
dc.subjectHypertensionen
dc.subjectRisken
dc.subjectDisease durationen
dc.subjectCardiovascular risken
dc.subjectCoronary diseaseen
dc.subjectHigh density lipoproteinen
dc.subjectTriacylglycerolen
dc.subjectKaplan meier methoden
dc.subjectCholesterolen
dc.subjectCholesterol blood levelen
dc.subjectIschemic heart diseaseen
dc.subjectTriacylglycerol blood levelen
dc.subjectCoronary artery diseaseen
dc.subjectProportional hazards modelen
dc.subjectPredictor variableen
dc.subjectProbabilityen
dc.subjectMetabolic syndrome xen
dc.subjectEducation programen
dc.subjectDiabetes mellitusen
dc.subjectDiabetic patienten
dc.subjectMetabolic syndromeen
dc.subjectNon insulin dependent diabetes mellitusen
dc.subjectType 2en
dc.subjectCombination of componentsen
dc.subjectMorbidityen
dc.subjectSexen
dc.titleMetabolic syndrome and its components as predictors of all-cause mortality and coronary heart disease in type 2 diabetic patientsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.atherosclerosis.2006.09.019
dc.description.volume195
dc.description.issue1
dc.description.startingpage189
dc.description.endingpage194
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidNikolopoulos, Georgios K.[0000-0002-3307-0246]
dc.gnosis.orcid0000-0002-3307-0246


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