322 226

Cited 17 times in

Impact of pitavastatin on new-onset diabetes mellitus compared to atorvastatin and rosuvastatin: a distributed network analysis of 10 real-world databases

Authors
 Won-Woo Seo  ;  Seung In Seo  ;  Yerim Kim  ;  Jong Jin Yoo  ;  Woon Geon Shin  ;  Jinseob Kim  ;  Seng Chan You  ;  Rae Woong Park  ;  Young Min Park  ;  Kyung-Jin Kim  ;  Sang Youl Rhee  ;  Meeyoung Park  ;  Eun-Sun Jin  ;  Sung Eun Kim 
Citation
 CARDIOVASCULAR DIABETOLOGY, Vol.21(1) : 82, 2022-05 
Journal Title
CARDIOVASCULAR DIABETOLOGY
Issue Date
2022-05
MeSH
Atorvastatin / adverse effects ; Cohort Studies ; Diabetes Mellitus* / diagnosis ; Diabetes Mellitus* / drug therapy ; Diabetes Mellitus* / epidemiology ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors* / adverse effects ; Multicenter Studies as Topic ; Quinolines ; Retrospective Studies ; Rosuvastatin Calcium / adverse effects
Keywords
Common data model ; Diabetes mellitus ; Pitavastatin ; Statin
Abstract
Background: Statin treatment increases the risk of new-onset diabetes mellitus (NODM); however, data directly comparing the risk of NODM among individual statins is limited. We compared the risk of NODM between patients using pitavastatin and atorvastatin or rosuvastatin using reliable, large-scale data.

Methods: Data of electronic health records from ten hospitals converted to the Observational Medical Outcomes Partnership Common Data Model (n = 14,605,368 patients) were used to identify new users of pitavastatin, atorvastatin, or rosuvastatin (atorvastatin + rosuvastatin) for ≥ 180 days without a previous history of diabetes or HbA1c level ≥ 5.7%. We conducted a cohort study using Cox regression analysis to examine the hazard ratio (HR) of NODM after propensity score matching (PSM) and then performed an aggregate meta-analysis of the HR.

Results: After 1:2 PSM, 10,238 new pitavastatin users (15,998 person-years of follow-up) and 18,605 atorvastatin + rosuvastatin users (33,477 person-years of follow-up) were pooled from 10 databases. The meta-analysis of the HRs demonstrated that pitavastatin resulted in a significantly reduced risk of NODM than atorvastatin + rosuvastatin (HR 0.72; 95% CI 0.59-0.87). In sub-analysis, pitavastatin was associated with a lower risk of NODM than atorvastatin or rosuvastatin after 1:1 PSM (HR 0.69; CI 0.54-0.88 and HR 0.74; CI 0.55-0.99, respectively). A consistently low risk of NODM in pitavastatin users was observed when compared with low-to-moderate-intensity atorvastatin + rosuvastatin users (HR 0.78; CI 0.62-0.98).

Conclusions: In this retrospective, multicenter active-comparator, new-user, cohort study, pitavastatin reduced the risk of NODM compared with atorvastatin or rosuvastatin.
Files in This Item:
T202203417.pdf Download
DOI
10.1186/s12933-022-01524-6
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
Yonsei Authors
You, Seng Chan(유승찬) ORCID logo https://orcid.org/0000-0002-5052-6399
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191415
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links