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Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information

OBJECTIVE: To estimate the incidence of muscle toxicity in patients receiving statin therapy by examining study populations, drug exposure status and outcome definitions. DESIGN: A retrospective cohort study. SETTING: 16 medical facilities in Japan providing information on laboratory tests performed...

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Autores principales: Chang, Chia-Hsien, Kusama, Makiko, Ono, Shunsuke, Sugiyama, Yuichi, Orii, Takao, Akazawa, Manabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641424/
https://www.ncbi.nlm.nih.gov/pubmed/23585384
http://dx.doi.org/10.1136/bmjopen-2012-002040
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author Chang, Chia-Hsien
Kusama, Makiko
Ono, Shunsuke
Sugiyama, Yuichi
Orii, Takao
Akazawa, Manabu
author_facet Chang, Chia-Hsien
Kusama, Makiko
Ono, Shunsuke
Sugiyama, Yuichi
Orii, Takao
Akazawa, Manabu
author_sort Chang, Chia-Hsien
collection PubMed
description OBJECTIVE: To estimate the incidence of muscle toxicity in patients receiving statin therapy by examining study populations, drug exposure status and outcome definitions. DESIGN: A retrospective cohort study. SETTING: 16 medical facilities in Japan providing information on laboratory tests performed in and claims received by their facilities between 1 April 2004 and 31 December 2010. PARTICIPANTS: A database representing a cohort of 35 903 adult statin (atorvastatin, fluvastatin, pitavastatin, pravastatin, rosuvastatin and simvastatin) users was studied. Use of interacting drugs (fibrates, triazoles, macrolides, amiodarone and ciclosporin) by these patients was determined. MAIN OUTCOME MEASURE: Statin-associated muscle toxicity (the ‘event’) was identified based on a diagnosis of muscle-related disorders (myopathy or rhabdomyolysis) and/or abnormal elevation of creatine kinase (CK) concentrations. Events were excluded if the patients had CK elevation-related conditions other than muscle toxicity. Incidence rates for muscle toxicity were determined per 1000 person-years, with 95% CI determined by Poisson regression. RESULTS: A total of 18 036 patients accounted for 42 193 person-years of statin therapy, and 43 events were identified. The incidence of muscle toxicity in the patients treated with statins was 1.02 (95% CI 0.76 to 1.37)/1000 person-years. The estimates varied when outcome definitions were modified from 0.09/1000 person-years, which met both diagnosis and CK 10× greater than the upper limit of normal range (ULN) criteria, to 2.06/1000 person-years, which met diagnosis or CK 5× ULN criterion. The incidence of muscle toxicity was also influenced by the statin therapies selected, but no significant differences were observed. Among 2430 patients (13.5%) received interacting drugs with statins, only three muscle toxicity cases were observed (incidence: 1.69/1000 person-years). CONCLUSIONS: This database study suggested that statin use is generally well tolerated and safe; however, the risk of muscle toxicity related to the use of interacting drugs requires further exploration.
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spelling pubmed-36414242013-05-06 Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information Chang, Chia-Hsien Kusama, Makiko Ono, Shunsuke Sugiyama, Yuichi Orii, Takao Akazawa, Manabu BMJ Open Epidemiology OBJECTIVE: To estimate the incidence of muscle toxicity in patients receiving statin therapy by examining study populations, drug exposure status and outcome definitions. DESIGN: A retrospective cohort study. SETTING: 16 medical facilities in Japan providing information on laboratory tests performed in and claims received by their facilities between 1 April 2004 and 31 December 2010. PARTICIPANTS: A database representing a cohort of 35 903 adult statin (atorvastatin, fluvastatin, pitavastatin, pravastatin, rosuvastatin and simvastatin) users was studied. Use of interacting drugs (fibrates, triazoles, macrolides, amiodarone and ciclosporin) by these patients was determined. MAIN OUTCOME MEASURE: Statin-associated muscle toxicity (the ‘event’) was identified based on a diagnosis of muscle-related disorders (myopathy or rhabdomyolysis) and/or abnormal elevation of creatine kinase (CK) concentrations. Events were excluded if the patients had CK elevation-related conditions other than muscle toxicity. Incidence rates for muscle toxicity were determined per 1000 person-years, with 95% CI determined by Poisson regression. RESULTS: A total of 18 036 patients accounted for 42 193 person-years of statin therapy, and 43 events were identified. The incidence of muscle toxicity in the patients treated with statins was 1.02 (95% CI 0.76 to 1.37)/1000 person-years. The estimates varied when outcome definitions were modified from 0.09/1000 person-years, which met both diagnosis and CK 10× greater than the upper limit of normal range (ULN) criteria, to 2.06/1000 person-years, which met diagnosis or CK 5× ULN criterion. The incidence of muscle toxicity was also influenced by the statin therapies selected, but no significant differences were observed. Among 2430 patients (13.5%) received interacting drugs with statins, only three muscle toxicity cases were observed (incidence: 1.69/1000 person-years). CONCLUSIONS: This database study suggested that statin use is generally well tolerated and safe; however, the risk of muscle toxicity related to the use of interacting drugs requires further exploration. BMJ Publishing Group 2013-04-11 /pmc/articles/PMC3641424/ /pubmed/23585384 http://dx.doi.org/10.1136/bmjopen-2012-002040 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode
spellingShingle Epidemiology
Chang, Chia-Hsien
Kusama, Makiko
Ono, Shunsuke
Sugiyama, Yuichi
Orii, Takao
Akazawa, Manabu
Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title_full Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title_fullStr Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title_full_unstemmed Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title_short Assessment of statin-associated muscle toxicity in Japan: a cohort study conducted using claims database and laboratory information
title_sort assessment of statin-associated muscle toxicity in japan: a cohort study conducted using claims database and laboratory information
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641424/
https://www.ncbi.nlm.nih.gov/pubmed/23585384
http://dx.doi.org/10.1136/bmjopen-2012-002040
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