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Risk of insulin resistance with statin therapy in individuals without dyslipidemia: A propensity-matched analysis in a registry population

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dc.contributor.authorHyun, Myung Han-
dc.contributor.authorJang, Jae Won-
dc.contributor.authorChoi, Byoung Geol-
dc.contributor.authorNa, Jin Oh-
dc.contributor.authorChoi, Cheol Ung-
dc.contributor.authorKim, Jin Won-
dc.contributor.authorKim, Eung Ju-
dc.contributor.authorRha, Seung-Woon-
dc.contributor.authorPark, Chang Gyu-
dc.contributor.authorLee, Eunmi-
dc.contributor.authorSeo, Hong Seog-
dc.date.accessioned2021-08-30T22:24:40Z-
dc.date.available2021-08-30T22:24:40Z-
dc.date.created2021-06-18-
dc.date.issued2020-06-
dc.identifier.issn0305-1870-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/55537-
dc.description.abstractSeveral studies suggest the higher vulnerability of individuals with lower low-density lipoprotein cholesterol (LDL-C) levels to diabetes mellitus. However, the discordance between high and low baseline LDL-C levels shown by statin-induced insulin resistance is not fully understood. This study aimed to explore the relationship between baseline LDL-C levels and the risk of statin-induced insulin resistance during statin therapy. In total, 2660 (451 with dyslipidemia and 2209 without dyslipidemia) consecutive patients were enrolled. Their baseline clinical data were adjusted using a propensity score matching analysis, using the logistic regression model. Insulin resistance index was based on the homeostatic model assessment-insulin resistance (HOMA-IR) and was monitored for a median of 2 years. Among the individuals who received statin therapy, those with and without dyslipidemia showed significantly decreased LDL-C levels (all P < .0001) and significantly increased fasting plasma insulin levels (Delta = +24.1%, P = .0230; Delta = +30.1%, P < .0001); however, their glycated haemoglobin A1c and fasting blood glucose levels did not change (all P > .05). Although HOMA-IR was positively associated with statin therapy in individuals with and without dyslipidemia, statistically significant difference during follow-ups was observed only in individuals without dyslipidemia (Delta = +15.6%, P = .1609; Delta = 24.0%; P = .0001). Insulin resistance was higher in statin users without baseline dyslipidemia than in those with dyslipidemia. Thus, statin therapy could increase the risk of statin-induced insulin resistance in individuals with normal baseline cholesterol levels.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectMETABOLIC SYNDROME-
dc.subjectPLASMA-GLUCOSE-
dc.subjectCHOLESTEROL-
dc.subjectEZETIMIBE-
dc.subjectSIMVASTATIN-
dc.subjectATORVASTATIN-
dc.subjectPRAVASTATIN-
dc.subjectABSORPTION-
dc.subjectFAT-
dc.subjectINHIBITION-
dc.titleRisk of insulin resistance with statin therapy in individuals without dyslipidemia: A propensity-matched analysis in a registry population-
dc.typeArticle-
dc.contributor.affiliatedAuthorNa, Jin Oh-
dc.contributor.affiliatedAuthorChoi, Cheol Ung-
dc.contributor.affiliatedAuthorKim, Jin Won-
dc.contributor.affiliatedAuthorKim, Eung Ju-
dc.contributor.affiliatedAuthorRha, Seung-Woon-
dc.contributor.affiliatedAuthorSeo, Hong Seog-
dc.identifier.doi10.1111/1440-1681.13272-
dc.identifier.scopusid2-s2.0-85080096315-
dc.identifier.wosid000530851800004-
dc.identifier.bibliographicCitationCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, v.47, no.6, pp.947 - 954-
dc.relation.isPartOfCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY-
dc.citation.titleCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY-
dc.citation.volume47-
dc.citation.number6-
dc.citation.startPage947-
dc.citation.endPage954-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusMETABOLIC SYNDROME-
dc.subject.keywordPlusPLASMA-GLUCOSE-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordPlusEZETIMIBE-
dc.subject.keywordPlusSIMVASTATIN-
dc.subject.keywordPlusATORVASTATIN-
dc.subject.keywordPlusPRAVASTATIN-
dc.subject.keywordPlusABSORPTION-
dc.subject.keywordPlusFAT-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordAuthordyslipidemia-
dc.subject.keywordAuthorinsulin resistance-
dc.subject.keywordAuthorstatin-
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