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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.author김병극-
dc.contributor.author김종윤-
dc.contributor.author박성하-
dc.contributor.author이상학-
dc.contributor.author이찬주-
dc.date.accessioned2022-12-22T04:14:41Z-
dc.date.available2022-12-22T04:14:41Z-
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.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAmlodipine / therapeutic use-
dc.subject.MESHAtherosclerosis* / complications-
dc.subject.MESHCardiovascular Diseases* / complications-
dc.subject.MESHFasting-
dc.subject.MESHGlucose-
dc.subject.MESHHeart Diseases* / complications-
dc.subject.MESHHumans-
dc.subject.MESHHydroxymethylglutaryl-CoA Reductase Inhibitors* / adverse effects-
dc.subject.MESHHypertension* / chemically induced-
dc.subject.MESHHypertension* / complications-
dc.subject.MESHHypertension* / drug therapy-
dc.subject.MESHInsulin Resistance*-
dc.subject.MESHPrediabetic State* / complications-
dc.subject.MESHRosuvastatin Calcium-
dc.subject.MESHTelmisartan / therapeutic use-
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.googleauthorChan Joo Lee-
dc.contributor.googleauthorJung-Hoon Sung-
dc.contributor.googleauthorTae-Soo Kang-
dc.contributor.googleauthorSungha Park-
dc.contributor.googleauthorSang-Hak Lee-
dc.contributor.googleauthorJong-Youn Kim-
dc.contributor.googleauthorByeong-Kuek Kim-
dc.identifier.doi10.1097/MD.0000000000030496-
dc.contributor.localIdA00493-
dc.contributor.localIdA00926-
dc.contributor.localIdA01512-
dc.contributor.localIdA02833-
dc.contributor.localIdA03238-
dc.relation.journalcodeJ02214-
dc.identifier.eissn1536-5964-
dc.identifier.pmid36086748-
dc.contributor.alternativeNameKim, Byeong Keuk-
dc.contributor.affiliatedAuthor김병극-
dc.contributor.affiliatedAuthor김종윤-
dc.contributor.affiliatedAuthor박성하-
dc.contributor.affiliatedAuthor이상학-
dc.contributor.affiliatedAuthor이찬주-
dc.citation.volume101-
dc.citation.number36-
dc.citation.startPagee30496-
dc.identifier.bibliographicCitationMEDICINE, Vol.101(36) : e30496, 2022-09-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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