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Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan
OBJECTIVES: Many researchers have expected pioglitazone to serve as an effective neuroprotective agent against Parkinson’s disease (PD). Therefore, we conducted this cohort study to investigate the association between pioglitazone use and PD by using a large Asian population-based dataset in Taiwan....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119417/ https://www.ncbi.nlm.nih.gov/pubmed/30158237 http://dx.doi.org/10.1136/bmjopen-2018-023302 |
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author | Wu, Hsiu-Feng Kao, Li-Ting Shih, Jui-Hu Kao, Hui-Han Chou, Yu-Ching Li, I-Hsun Kao, Senyeong |
author_facet | Wu, Hsiu-Feng Kao, Li-Ting Shih, Jui-Hu Kao, Hui-Han Chou, Yu-Ching Li, I-Hsun Kao, Senyeong |
author_sort | Wu, Hsiu-Feng |
collection | PubMed |
description | OBJECTIVES: Many researchers have expected pioglitazone to serve as an effective neuroprotective agent against Parkinson’s disease (PD). Therefore, we conducted this cohort study to investigate the association between pioglitazone use and PD by using a large Asian population-based dataset in Taiwan. DESIGN: Retrospective cohort study. SETTING: Taiwan. PARTICIPANTS: 7906 patients with diabetes who had received pioglitazone were defined as the study cohort, and 7906 matched patients with diabetes who had not received pioglitazone were defined as the comparison cohort. PRIMARY AND SECONDARY OUTCOME MEASURES: We tracked each patient individually over a 5-year follow-up period to identify those diagnosed as having PD during this period. We performed Cox proportional hazard regression analyses to evaluate the HRs for PD between the study and comparison cohorts. RESULTS: The findings indicated that among the sampled patients, PD occurred in 257 (1.63%): 119 (1.51%) pioglitazone users and 138 (1.75%) non-users. The adjusted HR for PD within the follow-up period was 0.90 (95% CI: 0.68 to 1.18) in the patients who had received pioglitazone compared with the matched patients who had not received pioglitazone. Moreover, this study revealed that pioglitazone use was not associated with PD incidence in men (HR: 1.06, 95% CI: 0.71 to 1.59) or women (HR: 0.84, 95% CI: 0.61 to 1.15). CONCLUSIONS: This study did not find the relationship between pioglitazone use and PD incidence, regardless of sex, among an Asian population of patients with diabetes. |
format | Online Article Text |
id | pubmed-6119417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-61194172018-09-04 Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan Wu, Hsiu-Feng Kao, Li-Ting Shih, Jui-Hu Kao, Hui-Han Chou, Yu-Ching Li, I-Hsun Kao, Senyeong BMJ Open Urology OBJECTIVES: Many researchers have expected pioglitazone to serve as an effective neuroprotective agent against Parkinson’s disease (PD). Therefore, we conducted this cohort study to investigate the association between pioglitazone use and PD by using a large Asian population-based dataset in Taiwan. DESIGN: Retrospective cohort study. SETTING: Taiwan. PARTICIPANTS: 7906 patients with diabetes who had received pioglitazone were defined as the study cohort, and 7906 matched patients with diabetes who had not received pioglitazone were defined as the comparison cohort. PRIMARY AND SECONDARY OUTCOME MEASURES: We tracked each patient individually over a 5-year follow-up period to identify those diagnosed as having PD during this period. We performed Cox proportional hazard regression analyses to evaluate the HRs for PD between the study and comparison cohorts. RESULTS: The findings indicated that among the sampled patients, PD occurred in 257 (1.63%): 119 (1.51%) pioglitazone users and 138 (1.75%) non-users. The adjusted HR for PD within the follow-up period was 0.90 (95% CI: 0.68 to 1.18) in the patients who had received pioglitazone compared with the matched patients who had not received pioglitazone. Moreover, this study revealed that pioglitazone use was not associated with PD incidence in men (HR: 1.06, 95% CI: 0.71 to 1.59) or women (HR: 0.84, 95% CI: 0.61 to 1.15). CONCLUSIONS: This study did not find the relationship between pioglitazone use and PD incidence, regardless of sex, among an Asian population of patients with diabetes. BMJ Publishing Group 2018-08-29 /pmc/articles/PMC6119417/ /pubmed/30158237 http://dx.doi.org/10.1136/bmjopen-2018-023302 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Urology Wu, Hsiu-Feng Kao, Li-Ting Shih, Jui-Hu Kao, Hui-Han Chou, Yu-Ching Li, I-Hsun Kao, Senyeong Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title | Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title_full | Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title_fullStr | Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title_full_unstemmed | Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title_short | Pioglitazone use and Parkinson’s disease: a retrospective cohort study in Taiwan |
title_sort | pioglitazone use and parkinson’s disease: a retrospective cohort study in taiwan |
topic | Urology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119417/ https://www.ncbi.nlm.nih.gov/pubmed/30158237 http://dx.doi.org/10.1136/bmjopen-2018-023302 |
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