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Effects of rosiglitazone and metformin on inflammatory markers and adipokines: decrease in interleukin-18 is an independent factor for the improvement of homeostasis model assessment-beta in type 2 diabetes mellitus.

DC Field Value Language
dc.contributor.authorKim, HJ-
dc.contributor.authorKang, ES-
dc.contributor.authorKim, DJ-
dc.contributor.authorKim, SH-
dc.contributor.authorAhn, CW-
dc.contributor.authorCha, BS-
dc.contributor.authorNam, M-
dc.contributor.authorChung, CH-
dc.contributor.authorLee, KW-
dc.contributor.authorNam, CM-
dc.contributor.authorLee, HC-
dc.date.accessioned2011-01-21T04:40:15Z-
dc.date.available2011-01-21T04:40:15Z-
dc.date.issued2007-
dc.identifier.issn0300-0664-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/1241-
dc.description.abstractOBJECTIVE: We examined the individual pharmacological effects of the addition of rosiglitazone and metformin to glimepiride on inflammatory markers and adipokines in patients with type 2 diabetes mellitus. We analysed the relationships between these variables, the measurements of insulin sensitivity and beta-cell function in patients treated with rosiglitazone plus glimepiride.



DESIGN AND PATIENTS: One hundred twenty (120) patients with type 2 diabetes mellitus were randomized and treated with glimepiride plus rosiglitazone or glimepiride plus metformin for 12 weeks. The plasma concentrations of the inflammatory markers and adipokines were measured at baseline and after 12 weeks.



MEASUREMENTS: Markers of insulin sensitivity and beta-cell function were determined by the quantitative insulin sensitivity check index (QUICKI) and the homeostasis model assessment of beta-cell function (HOMA-beta), respectively. Plasma concentrations of adiponectin were measured by radioimmunoassay. Plasma concentrations of resistin, tumour necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-18 (IL-18) were measured using ELISA.



RESULTS: Improvements in fasting insulin level, QUICKI and HOMA-beta were noted in the rosiglitazone-treated group. Only the QUICKI value improved in the metformin-treated group. Adiponectin concentrations significantly increased in the rosiglitazone-treated group after 12 weeks. Significant decreases in resistin, C-reactive protein, TNF-alpha, IL-6 and IL-18 were seen in the rosiglitazone-treated patients but not in the metformin-treated patients. The independent risk factor for the HOMA-beta change according to stepwise multivariate regression analysis was a change in IL-18.



CONCLUSIONS: Rosiglitazone, but not metformin, improved the plasma concentrations of inflammatory markers and adipokines in patients with type 2 diabetes mellitus. A decrease in IL-18 is an independent factor for the improvement of HOMA-beta in type 2 diabetes mellitus.
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dc.language.isoen-
dc.subject.MESHAdiponectin/blood-
dc.subject.MESHAnalysis of Variance-
dc.subject.MESHBiological Markers/blood-
dc.subject.MESHBlood Glucose/analysis-
dc.subject.MESHC-Reactive Protein/analysis-
dc.subject.MESHDiabetes Mellitus, Type 2/blood-
dc.subject.MESHDiabetes Mellitus, Type 2/drug therapy*-
dc.subject.MESHDiabetes Mellitus, Type 2/immunology-
dc.subject.MESHDrug Administration Schedule-
dc.subject.MESHHomeostasis-
dc.subject.MESHHumans-
dc.subject.MESHHypoglycemic Agents/therapeutic use*-
dc.subject.MESHInsulin/blood-
dc.subject.MESHInsulin Resistance-
dc.subject.MESHInterleukin-18/blood*-
dc.subject.MESHInterleukin-6/blood-
dc.subject.MESHMetformin/therapeutic use*-
dc.subject.MESHMultivariate Analysis-
dc.subject.MESHResistin/blood-
dc.subject.MESHSulfonylurea Compounds/therapeutic use*-
dc.subject.MESHThiazolidinediones/therapeutic use*-
dc.subject.MESHTime Factors-
dc.subject.MESHTumor Necrosis Factor-alpha/blood-
dc.titleEffects of rosiglitazone and metformin on inflammatory markers and adipokines: decrease in interleukin-18 is an independent factor for the improvement of homeostasis model assessment-beta in type 2 diabetes mellitus.-
dc.typeArticle-
dc.identifier.pmid17224000-
dc.identifier.urlhttp://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0300-0664&date=2007&volume=66&issue=2&spage=282-
dc.contributor.affiliatedAuthor김, 대중-
dc.contributor.affiliatedAuthor이, 관우-
dc.type.localJournal Papers-
dc.identifier.doi10.1111/j.1365-2265.2006.02723.x-
dc.citation.titleClinical endocrinology-
dc.citation.volume66-
dc.citation.number2-
dc.citation.date2007-
dc.citation.startPage282-
dc.citation.endPage289-
dc.identifier.bibliographicCitationClinical endocrinology, 66(2):282-289, 2007-
dc.identifier.eissn1365-2265-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
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