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

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dc.contributor.authorWon‑Woo Seo-
dc.contributor.authorSeung In Seo-
dc.contributor.authorYerim Kim-
dc.contributor.authorJong Jin Yoo-
dc.contributor.authorWoon Geon Shin-
dc.contributor.authorJinseob Kim-
dc.contributor.authorSeng Chan You-
dc.contributor.authorRae Woong Park-
dc.contributor.authorYoung Min Park-
dc.contributor.authorKyung‑Jin Kim-
dc.contributor.authorSang Youl Rhee-
dc.contributor.authorMeeyoung Park-
dc.contributor.authorEun‑Sun Jin-
dc.contributor.authorSung Eun Kim-
dc.date.accessioned2022-06-13T04:32:47Z-
dc.date.available2022-06-13T04:32:47Z-
dc.date.issued2022-05-23-
dc.identifier.citationCardiovascular Diabetology. Vol 21(1):82ko_KR
dc.identifier.issn1475-2840-
dc.identifier.urihttps://hdl.handle.net/10371/181271-
dc.description.abstractStatin 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.
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.
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; CI0.62–0.98).
In this retrospective, multicenter active-comparator, new-user, cohort study, pitavastatin reduced the risk of NODM compared with atorvastatin or rosuvastatin.
ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectDiabetes mellitus-
dc.subjectPitavastatin-
dc.subjectStatin-
dc.subjectCommon data model-
dc.titleImpact of pitavastatin on new-onset diabetes mellitus compared to atorvastatin and rosuvastatin: a distributed network analysis of 10 real-world databasesko_KR
dc.typeArticleko_KR
dc.identifier.doihttps://doi.org/10.1186/s12933-022-01524-6ko_KR
dc.citation.journaltitleCardiovascular Diabetologyko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2022-05-29T03:32:56Z-
dc.citation.number1ko_KR
dc.citation.startpage82ko_KR
dc.citation.volume21ko_KR
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