Cited 22 times in
LPIN1 genetic variation is associated with rosiglitazone response in type 2 diabetic patients
DC Field | Value | Language |
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dc.contributor.author | 한승진 | - |
dc.contributor.author | 강은석 | - |
dc.contributor.author | 김경섭 | - |
dc.contributor.author | 남정모 | - |
dc.contributor.author | 박세은 | - |
dc.contributor.author | 안철우 | - |
dc.contributor.author | 이현철 | - |
dc.contributor.author | 차봉수 | - |
dc.date.accessioned | 2015-05-19T16:40:37Z | - |
dc.date.available | 2015-05-19T16:40:37Z | - |
dc.date.issued | 2008 | - |
dc.identifier.issn | 1096-7192 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/106738 | - |
dc.description.abstract | Lipin1 protein, a product of the LPIN1 gene, is required for normal adipose tissue development and metabolism. Lipin1 deficiency results in immature adipocyte development in cases of mouse fatty liver dystrophy and human lipodystrophy. Recently, pioglitazone has been reported to increase human adipocyte lipin1 expression. We evaluated the effects of LPIN1 polymorphisms on rosiglitazone response in patients with type 2 diabetes (T2DM). A total of 262 patients were treated with 12 weeks of rosiglitazone (4 mg/day) in addition to their previous drug regimen medications. Six single nucleotide polymorphisms (SNPs) at the LPIN1 locus were genotyped: rs11693809, rs10192566, rs2278513, rs2577262, rs2716610, and rs1050800. Because rs11693809, rs10192566, and rs2278513 are in nearly complete linkage disequilibrium (D'>0.958, r(2) >0.882), we analyzed rs10192566, rs2577262, rs2716610, and rs1050800. Rs10192566 was significantly associated with rosiglitazone treatment response. Patients with the G allele in rs10192566 had a larger decrease in fasting plasma glucose, 2-h postprandial glucose, and HbA1c than those without. This genetic effect remained significant after adjustment for age, sex, and initial body weight. No other SNPs were associated with response. These data suggest that LPIN1 genetic variations can affect rosiglitazone treatment response in T2DM. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 96~100 | - |
dc.relation.isPartOf | MOLECULAR GENETICS AND METABOLISM | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Blood Glucose/analysis | - |
dc.subject.MESH | Cohort Studies | - |
dc.subject.MESH | Diabetes Mellitus, Type 2/drug therapy* | - |
dc.subject.MESH | Diabetes Mellitus, Type 2/genetics* | - |
dc.subject.MESH | Diabetes Mellitus, Type 2/metabolism | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Genetic Variation* | - |
dc.subject.MESH | Glycated Hemoglobin A/metabolism | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hypoglycemic Agents/administration & dosage* | - |
dc.subject.MESH | Linkage Disequilibrium | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Nuclear Proteins/genetics* | - |
dc.subject.MESH | Nuclear Proteins/metabolism | - |
dc.subject.MESH | Phosphatidate Phosphatase | - |
dc.subject.MESH | Polymorphism, Single Nucleotide | - |
dc.subject.MESH | Thiazolidinediones/administration & dosage* | - |
dc.title | LPIN1 genetic variation is associated with rosiglitazone response in type 2 diabetic patients | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Biochemistry & Molecular Biology (생화학,분자생물학) | - |
dc.contributor.googleauthor | Eun Seok Kang | - |
dc.contributor.googleauthor | Se Eun Park | - |
dc.contributor.googleauthor | Seung Jin Han | - |
dc.contributor.googleauthor | So Hun Kim | - |
dc.contributor.googleauthor | Chung Mo Nam | - |
dc.contributor.googleauthor | Chul Woo Ahn | - |
dc.contributor.googleauthor | Bong Soo Cha | - |
dc.contributor.googleauthor | Kyung Sub Kim | - |
dc.contributor.googleauthor | Hyun Chul Lee | - |
dc.identifier.doi | 10.1016/j.ymgme.2008.06.011 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01264 | - |
dc.contributor.localId | A04302 | - |
dc.contributor.localId | A00068 | - |
dc.contributor.localId | A00297 | - |
dc.contributor.localId | A01521 | - |
dc.contributor.localId | A02270 | - |
dc.contributor.localId | A03301 | - |
dc.contributor.localId | A03996 | - |
dc.relation.journalcode | J02258 | - |
dc.identifier.eissn | 1096-7206 | - |
dc.identifier.pmid | 18693052 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S1096719208001923 | - |
dc.subject.keyword | Genetic association | - |
dc.subject.keyword | Lipin | - |
dc.subject.keyword | SNP | - |
dc.subject.keyword | Rosiglitazone | - |
dc.subject.keyword | Type 2 diabetes | - |
dc.subject.keyword | Pharmacogenetics | - |
dc.contributor.alternativeName | Han, Seung Jin | - |
dc.contributor.alternativeName | Kang, Eun Seok | - |
dc.contributor.alternativeName | Kim, Kyung Sup | - |
dc.contributor.alternativeName | Nam, Jung Mo | - |
dc.contributor.alternativeName | Park, Se Eun | - |
dc.contributor.alternativeName | Ahn, Chul Woo | - |
dc.contributor.alternativeName | Lee, Hyun Chul | - |
dc.contributor.alternativeName | Cha, Bong Soo | - |
dc.contributor.affiliatedAuthor | Nam, Jung Mo | - |
dc.contributor.affiliatedAuthor | Han, Seung Jin | - |
dc.contributor.affiliatedAuthor | Kang, Eun Seok | - |
dc.contributor.affiliatedAuthor | Kim, Kyung Sup | - |
dc.contributor.affiliatedAuthor | Park, Se Eun | - |
dc.contributor.affiliatedAuthor | Ahn, Chul Woo | - |
dc.contributor.affiliatedAuthor | Lee, Hyun Chul | - |
dc.contributor.affiliatedAuthor | Cha, Bong Soo | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 95 | - |
dc.citation.number | 1-2 | - |
dc.citation.startPage | 96 | - |
dc.citation.endPage | 100 | - |
dc.identifier.bibliographicCitation | MOLECULAR GENETICS AND METABOLISM, Vol.95(1-2) : 96-100, 2008 | - |
dc.identifier.rimsid | 49335 | - |
dc.type.rims | ART | - |
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