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Effects of high-intensity statin combined with telmisartan versus amlodipine on glucose metabolism in hypertensive atherosclerotic cardiovascular disease patients with impaired fasting glucose: A randomized multicenter trial

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dc.contributor.authorLee, Chan Joo-
dc.contributor.authorSung, Jung-Hoon-
dc.contributor.authorKang, Tae-Soo-
dc.contributor.authorPark, Sungha-
dc.contributor.authorLee, Sang-Hak-
dc.contributor.authorKim, Jong-Youn-
dc.contributor.authorKim, Byeong-Kuek-
dc.date.accessioned2022-12-22T04:14:41Z-
dc.date.available2022-12-22T04:14:41Z-
dc.date.created2023-03-22-
dc.date.issued2022-09-
dc.identifier.issn0025-7974-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/192078-
dc.description.abstractBackground: There is lacking evidence that telmisartan can improve insulin resistance in patients on high-intensity statins. This study compared the effects of telmisartan and amlodipine on glucose metabolism in hypertensive atherosclerotic cardiovascular disease (ASCVD) patients with impaired fasting glucose (IFG) requiring high-intensity rosuvastatin therapy. Methods: Ninety-nine patients were randomly assigned to 2 groups [telmisartan-statin group (n=48) and amlodipine-statin group (n=51)] as add-on therapy to high-intensity rosuvastatin therapy (20 mg). The primary endpoint was to assess insulin resistance using the homeostatic model assessment (HOMA-IR) value at week 24. The secondary endpoint was the change in glucose metabolism indices from baseline to week 24. Results: The HOMA-IR at week 24 (2.4 [interquartile range, 1.8-3.8] versus 2.7 [1.7-3.7]; P = .809) and changes in the HOMA-IR from baseline to week 24 (-7.0 [-29.0 to 21.0] versus -5.5 [-53.3 to 27.3]; P = .539) were not significantly different between 2 groups. However, the fasting glucose level at week 24 was significantly lower in the telmisartan-statin group than in the amlodipine-statin group (107.7 +/- 13.4 mg/dL versus 113.3 +/- 12.4 mg/dL; P = .039) and significantly decreased in the telmisartan-statin group (-3.2 +/- 8.6% versus 3.8 +/- 13.2%; P = .003). The proportion of patients with fasting glucose >= 100 mg/dL (71.1% versus 89.6%; P = .047) or new-onset diabetes mellitus (12.5% versus 31.4%, P = .044) at week 24 was also significantly lower in the telmisartan-statin group than in the amlodipine-statin group. Conclusion: In comparison to amlodipine, telmisartan did not decrease the HOMA-IR. However, telmisartan preserved insulin secretion, led to a regression from IFG to euglycemia and prevented new-onset diabetes mellitus in ASCVD patients with IFG requiring high-intensity statins.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherLippincott Williams & Wilkins-
dc.relation.isPartOfMedicine-
dc.relation.isPartOfMEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleEffects of high-intensity statin combined with telmisartan versus amlodipine on glucose metabolism in hypertensive atherosclerotic cardiovascular disease patients with impaired fasting glucose: A randomized multicenter trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorLee, Chan Joo-
dc.contributor.googleauthorSung, Jung-Hoon-
dc.contributor.googleauthorKang, Tae-Soo-
dc.contributor.googleauthorPark, Sungha-
dc.contributor.googleauthorLee, Sang-Hak-
dc.contributor.googleauthorKim, Jong-Youn-
dc.contributor.googleauthorKim, Byeong-Kuek-
dc.identifier.doi10.1097/MD.0000000000030496-
dc.relation.journalcodeJ02214-
dc.identifier.eissn1536-5964-
dc.identifier.pmid36086748-
dc.subject.keywordangiotensin-II-receptor blockers-
dc.subject.keywordcalcium channel blocker-
dc.subject.keyworddiabetes mellitus-
dc.subject.keywordimpaired fasting glucose-
dc.subject.keywordinsulin resistance-
dc.subject.keywordstatin-
dc.contributor.alternativeNameKim, Byeong Keuk-
dc.contributor.affiliatedAuthorLee, Chan Joo-
dc.contributor.affiliatedAuthorPark, Sungha-
dc.contributor.affiliatedAuthorLee, Sang-Hak-
dc.contributor.affiliatedAuthorKim, Jong-Youn-
dc.contributor.affiliatedAuthorKim, Byeong-Kuek-
dc.identifier.scopusid2-s2.0-85138127206-
dc.identifier.wosid000851993100031-
dc.citation.volume101-
dc.citation.number36-
dc.citation.startPageE30496-
dc.identifier.bibliographicCitationMedicine, Vol.101(36) : E30496, 2022-09-
dc.identifier.rimsid77982-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorangiotensin-II-receptor blockers-
dc.subject.keywordAuthorcalcium channel blocker-
dc.subject.keywordAuthordiabetes mellitus-
dc.subject.keywordAuthorimpaired fasting glucose-
dc.subject.keywordAuthorinsulin resistance-
dc.subject.keywordAuthorstatin-
dc.subject.keywordPlusINSULIN-RESISTANCE-
dc.subject.keywordPlusCLINICAL-TRIALS-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusINDIVIDUALS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusSECRETION-
dc.subject.keywordPlusBLOCKERS-
dc.subject.keywordPlusCOHORT-
dc.subject.keywordPlusADULTS-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.identifier.articlenoe30496-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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