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Effects of Pro12Ala polymorphism of peroxisome proliferator-activated receptor γ2 gene on rosiglitazone response in type 2 diabetes

DC Field Value Language
dc.contributor.author강은석-
dc.contributor.author김철식-
dc.contributor.author김형진-
dc.contributor.author남정모-
dc.contributor.author박소영-
dc.contributor.author안철우-
dc.contributor.author이현철-
dc.contributor.author임승길-
dc.contributor.author차봉수-
dc.date.accessioned2017-05-04T07:39:02Z-
dc.date.available2017-05-04T07:39:02Z-
dc.date.issued2005-
dc.identifier.issn0009-9236-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/147591-
dc.description.abstractOBJECTIVE: The aim of this study was to examine the effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor (PPAR) gamma2 gene on the response to rosiglitazone in patients with type 2 diabetes mellitus. METHODS: A total of 198 patients with type 2 diabetes mellitus were treated with rosiglitazone (4 mg/d) for 12 weeks without a change in previous medications. All patients were genotyped for the PPARgamma2 Pro12Ala polymorphism. RESULTS: The Ala12 allele frequency was 0.04. Of the 198 patients, 183 had the Pro12Pro genotype and 15 had the Pro12Ala genotype. The Ala12Ala genotype was not observed. The decrease in fasting plasma glucose level was significantly greater in subjects with the Ala12 allele than in those without the allele (50.6 +/- 27.8 mg/dL versus 24.3 +/- 41.9 mg/dL, P = .026). In addition, the decrease in hemoglobin A(1c) level was significantly greater in subjects with the Ala12 allele than in those without the allele (1.41% +/- 1.47% versus 0.57% +/- 1.16%, P = .015). There was a significant difference in the response rate to rosiglitazone treatment between the Pro12Pro group and the Pro12Ala variant group (43.72% versus 86.67%, P = .002). CONCLUSION: Patients with the Pro12Ala genotype in the PPARgamma2 gene had a better therapeutic response to rosiglitazone than did patients with the Pro12Pro genotype. The genetic variations in the PPARgamma2 gene can affect the response to rosiglitazone treatment in patients with type 2 diabetes mellitus.-
dc.description.statementOfResponsibilityrestriction-
dc.format.extent202~208-
dc.languageEnglish-
dc.publisherWiley-
dc.relation.isPartOfCLINICAL PHARMACOLOGY & THERAPEUTICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHDiabetes Mellitus, Type 2/genetics*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHHypoglycemic Agents/pharmacology*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPPAR gamma/drug effects*-
dc.subject.MESHPolymorphism, Genetic-
dc.subject.MESHRosiglitazone-
dc.subject.MESHThiazolidinediones/pharmacology*-
dc.titleEffects of Pro12Ala polymorphism of peroxisome proliferator-activated receptor γ2 gene on rosiglitazone response in type 2 diabetes-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Preventive Medicine and Public Health (예방의학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorEun Seok Kang-
dc.contributor.googleauthorSo Young Park-
dc.contributor.googleauthorHyeong Jin Kim-
dc.contributor.googleauthorChul Sik Kim-
dc.contributor.googleauthorChul Woo Ahn-
dc.contributor.googleauthorBong Soo Cha-
dc.contributor.googleauthorSung Kil Lim-
dc.contributor.googleauthorChung Mo Nam-
dc.contributor.googleauthorHyun Chul Lee-
dc.identifier.doi10.1016/j.clpt.2005.04.013-
dc.contributor.localIdA00068-
dc.contributor.localIdA01054-
dc.contributor.localIdA01159-
dc.contributor.localIdA01264-
dc.contributor.localIdA01527-
dc.contributor.localIdA02270-
dc.contributor.localIdA03301-
dc.contributor.localIdA03375-
dc.contributor.localIdA03996-
dc.relation.journalcodeJ00608-
dc.identifier.eissn1532-6535-
dc.identifier.pmid16084854-
dc.identifier.urlhttp://www.nature.com/clpt/journal/v78/n2/full/clpt2005484a.html-
dc.subject.keyword16084854-
dc.contributor.alternativeNameKang, Eun Seok-
dc.contributor.alternativeNameKim, Chul Sik-
dc.contributor.alternativeNameKim, Hyeong Jin-
dc.contributor.alternativeNameNam, Jung Mo-
dc.contributor.alternativeNamePark, So Young-
dc.contributor.alternativeNameAhn, Chul Woo-
dc.contributor.alternativeNameLee, Hyun Chul-
dc.contributor.alternativeNameLim, Sung Kil-
dc.contributor.alternativeNameCha, Bong Soo-
dc.citation.volume78-
dc.citation.number2-
dc.citation.startPage202-
dc.citation.endPage208-
dc.identifier.bibliographicCitationCLINICAL PHARMACOLOGY & THERAPEUTICS, Vol.78(2) : 202-208, 2005-
dc.date.modified2017-05-04-
dc.identifier.rimsid40363-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers

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