Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/23557
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dc.contributor.authorDuran, Cevdet-
dc.date.accessioned2021-12-24T09:10:01Z-
dc.date.available2021-12-24T09:10:01Z-
dc.date.issued2009-01-
dc.identifier.citationDuran, C. vd. (2009). "The investigation of the efficacy of insulin glargine on glycemic control when combined with either repaglinide or acarbose in obese type 2 diabetic patients". Journal of Endocrinological Investigation, 32(1), 69-73.en_US
dc.identifier.issn0391-4097-
dc.identifier.urihttps://doi.org/10.1007/BF03345682-
dc.identifier.urihttps://link.springer.com/article/10.1007%2FBF03345682-
dc.identifier.urihttp://hdl.handle.net/11452/23557-
dc.description.abstractCombinations of insulin and oral antidiabetic drugs (OAD) are often prescribed instead of insulin alone. In this study, the effects of insulin glargine (IG) in combination with repaglinide or acarbose on glycemic parameters were investigated. Obese Type 2 diabetic patients with fasting blood glucose (FBG) levels >= mmol/l and hemoglobin glycated (A1C) >= 9% under maximal CAD combination therapy were enrolled. Previous therapies were discontinued, and patients were randomized into 2 groups. The combinations of IG and repaglinide were administered to group 1, and of IG and acarbose to group 2 for 13 weeks. Twenty Patients in group 1 and 18 patients in group 2 completed the study. A1C levels were significantly decreased from 10.9 +/- 1.4% to 7.7 +/- 1.1% in group 1 and 11.0 +/- 1.4% to 8.1 +/- 1.4% in group 2. FBG levels were significantly decreased from 11.9 +/- 2.7 to 7.1 +/- 2.3 mmol/l in group 1 and 11.1 +/- 2.5 to 6.8 +/- 1.4 mmol/l in group 2. Post-prandial glucose levels were significantly decreased from 15.3 +/- 3.8 to 10.3 +/- 3.0 mmol/l in group 1 and 14.0 +/- 3.1 to 8.9 +/- 2.2 mmol/l in group 2. Intergroup comparisons indicated no significant differences. More weight gain was detected in group 1, compared to the baseline. Syptomatic hypoglycemia incidence was similar in both groups. Severe hypoglycemic attacks were seen in two patients in group 1. Flatulance incidence was higher in acarbose group. Conclusively, repaglinide and acarbose were equally effective when combined with IG for obese Type 2 diabetic patients controlled inadequately with OAD alone. Furthermore, acarbose seems to have advantages over repaglinide concerning weight gain and severe hypoglycemic attacks.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcarboseen_US
dc.subjectInsulin glargineen_US
dc.subjectRepaglinideen_US
dc.subjectSecondary failureen_US
dc.subjectType 2 diabetesen_US
dc.subjectBedtime nph insulinen_US
dc.subjectCombination therapyen_US
dc.subjectPlaceboen_US
dc.subjectHypoglycemiaen_US
dc.subjectMulticenteren_US
dc.subjectMonotherapyen_US
dc.subjectSafetyen_US
dc.subjectTrialen_US
dc.subjectEndocrinology & metabolismen_US
dc.titleThe investigation of the efficacy of insulin glargine on glycemic control when combined with either repaglinide or acarbose in obese type 2 diabetic patientsen_US
dc.typeArticleen_US
dc.identifier.wos000264938300014tr_TR
dc.identifier.scopus2-s2.0-64549112201tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Endokrinoloji ve Metabolizma Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyostatik Anabilim Dalı.tr_TR
dc.identifier.startpage69tr_TR
dc.identifier.endpage73tr_TR
dc.identifier.volume32tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalJournal of Endocrinological Investigationen_US
dc.contributor.buuauthorTuncel, Ercan-
dc.contributor.buuauthorErsoy, Canan-
dc.contributor.buuauthorErcan, İlker-
dc.contributor.buuauthorSelimoğlu, Hadi-
dc.contributor.buuauthorKıyıcı, Sinem-
dc.contributor.buuauthorGüçlü, Metin-
dc.contributor.buuauthorErtürk, Erdinç-
dc.contributor.buuauthorİmamoğlu, Şazi-
dc.contributor.researcheridABF-2367-2020tr_TR
dc.contributor.researcheridABI-4847-2020tr_TR
dc.contributor.researcheridAAJ-6536-2021tr_TR
dc.contributor.researcheridAAH-8861-2021tr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed19337019tr_TR
dc.subject.wosEndocrinology & metabolismen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid7006929833tr_TR
dc.contributor.scopusid6701485882tr_TR
dc.contributor.scopusid6603789069tr_TR
dc.contributor.scopusid15074185600tr_TR
dc.contributor.scopusid12753880400tr_TR
dc.contributor.scopusid15073842600tr_TR
dc.contributor.scopusid7005488796tr_TR
dc.contributor.scopusid6602297533tr_TR
dc.subject.scopusMitiglinide; Sitagliptin; Vogliboseen_US
dc.subject.emtreeAcarboseen_US
dc.subject.emtreeGlucoseen_US
dc.subject.emtreeGlycosylated hemoglobinen_US
dc.subject.emtreeInsulin glargineen_US
dc.subject.emtreeRepaglinideen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBedtime dosageen_US
dc.subject.emtreeBody massen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeControlled clinical trialen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDiastolic blood pressureen_US
dc.subject.emtreeDrug dose increaseen_US
dc.subject.emtreeDrug dose reductionen_US
dc.subject.emtreeDrug dose titrationen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFlatulenceen_US
dc.subject.emtreeGlucose blood levelen_US
dc.subject.emtreeGlycemic controlen_US
dc.subject.emtreeHemoglobin blood levelen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHypoglycemiaen_US
dc.subject.emtreeIncidenceen_US
dc.subject.emtreeInjection site painen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNon insulin dependent diabetes mellitusen_US
dc.subject.emtreeObesityen_US
dc.subject.emtreeRandomized controlled trialen_US
dc.subject.emtreeSide effecten_US
dc.subject.emtreeSystolic blood pressureen_US
dc.subject.emtreeWeight gainen_US
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