Abstract
Background: High-intensity statin therapy is typically used in patients with acute myocardial infarction (AMI) for secondary prevention. However, there have been consistent concerns regarding its association with diabetes mellitus. We investigated the effect of high-intensity atorvastatin and rosuvastatin on new-onset diabetes mellitus (NODM) and cardiovascular outcomes over a 3-year follow-up period. Methods: Data from the Korea Acute Myocardial Infarction Registry were collected from November 2011 to October 2015, and 13,104 patients with AMI were enrolled from major cardiovascular centers. Among them, 2221 patients without diabetes who had been administered with high-intensity atorvastatin (40–80 mg) and rosuvastatin (20 mg) were investigated. The atorvastatin and rosuvastatin groups were evaluated for the incidence of NODM and major adverse cardiac events (MACE) including death, myocardial infarction, and revascularization cases in the following 3 years. Results: Baseline characteristics were comparable between the two groups. Event-free survival rate of NODM was not significantly different between the atorvastatin and rosuvastatin groups (92.5% vs. 90.8%, respectively; Log-rank P-value = 0.550). The event-free survival rate of MACE was also not significantly different between atorvastatin and rosuvastatin groups (89.0% vs. 89.6%, respectively; Log rank P-value = 0.662). Multivariate Cox analysis revealed that statin type was not a prognostic factor in the development of NODM and MACE. Conclusions: Administering high-intensity atorvastatin and rosuvastatin in patients with AMI produced comparable effects on NODM and clinical outcomes, suggesting their clinical equivalence in secondary prevention.
Original language | English |
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Article number | 11 |
Journal | BMC Pharmacology and Toxicology |
Volume | 22 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2021 Dec |
Bibliographical note
Funding Information:This research was supported by a fund (2016-ER6304–02) by Research of Korea Centers for Disease Control and Prevention.
Funding Information:
This study was done with the support of Korean Circulation Society (KCS). The KAMIR study group of the KSC was as follows: Woong Chol Kang, Gachon University Gil Medical Center, Incheon; Kiyuk Chang, Catholic University Hospital, Seoul; Seung Ho Hur, Keimyung University Dongsan Medical Center, Daegu; Seung Woon Rha, Korea University Guro Hospital, Seoul; Kwang-Soo Cha, Pusan National University Hospital, Busan; Hyeon Cheol Gwon, Samsung Medical Center, Seoul; Seok Kyu Oh, Wonkwang University Hospital, Iksan; Jei Keon Chae, Chonbuk National University Hospital, Jeonju; Kyung-Kook Hwang, Chungbuk National University Hospital, Chungju; Chong Jin Kim, East West Neo Medical Center, Seoul; Jung Han Yoon, Wonju Severance Christian Hospital, Wonju; Jin Yong Hwang, Gyeongsang National University Hospital, Jinju; Doo Il Kim, Inje University Busan Paik Hospital, Busan; Seung Jae Joo, Jeju National University Hospital, Jeju. We would like to thank Editage (www.editage.co.kr) for English language editing.
Funding Information:
This study was done with the support of Korean Circulation Society (KCS). The KAMIR study group of the KSC was as follows: Woong Chol Kang, Gachon University Gil Medical Center, Incheon; Kiyuk Chang, Catholic University Hospital, Seoul; Seung Ho Hur, Keimyung University Dongsan Medical Center, Daegu; Seung Woon Rha, Korea University Guro Hospital, Seoul; Kwang-Soo Cha, Pusan National University Hospital, Busan; Hyeon Cheol Gwon, Samsung Medical Center, Seoul; Seok Kyu Oh, Wonkwang University Hospital, Iksan; Jei Keon Chae, Chonbuk National University Hospital, Jeonju; Kyung-Kook Hwang, Chungbuk National University Hospital, Chungju; Chong Jin Kim, East West Neo Medical Center, Seoul; Jung Han Yoon, Wonju Severance Christian Hospital, Wonju; Jin Yong Hwang, Gyeongsang National University Hospital, Jinju; Doo Il Kim, Inje University Busan Paik Hospital, Busan; Seung Jae Joo, Jeju National University Hospital, Jeju.
Publisher Copyright:
© 2021, The Author(s).
All Science Journal Classification (ASJC) codes
- Pharmacology
- Pharmacology (medical)