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Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study

BACKGROUND AND PURPOSE: Hypertension has been associated with Parkinson's disease (PD), but data on antihypertensive drugs and PD are inconclusive. We aim to evaluate antihypertensive drugs for an association with PD in hypertensive patients. METHODS: Hypertensive patients who were free of PD,...

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Autores principales: Lee, Yen-Chieh, Lin, Chin-Hsien, Wu, Ruey-Meei, Lin, Jou-Wei, Chang, Chia-Hsuin, Lai, Mei-Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049613/
https://www.ncbi.nlm.nih.gov/pubmed/24910980
http://dx.doi.org/10.1371/journal.pone.0098961
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author Lee, Yen-Chieh
Lin, Chin-Hsien
Wu, Ruey-Meei
Lin, Jou-Wei
Chang, Chia-Hsuin
Lai, Mei-Shu
author_facet Lee, Yen-Chieh
Lin, Chin-Hsien
Wu, Ruey-Meei
Lin, Jou-Wei
Chang, Chia-Hsuin
Lai, Mei-Shu
author_sort Lee, Yen-Chieh
collection PubMed
description BACKGROUND AND PURPOSE: Hypertension has been associated with Parkinson's disease (PD), but data on antihypertensive drugs and PD are inconclusive. We aim to evaluate antihypertensive drugs for an association with PD in hypertensive patients. METHODS: Hypertensive patients who were free of PD, dementia and stroke were recruited from 2005–2006 using Taiwan National Health Insurance Database. We examined the association between the use of calcium channel blockers (CCBs), angiotensin converting enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs) and the incidence of PD using beta-blockers as the reference. Cox regression model with time-varying medication use was applied. RESULTS: Among 65,001 hypertensive patients with a mean follow-up period of 4.6 years, use of dihydropyridine CCBs, but not non-dihydropyridine CCBs, was associated with a reduced risk of PD (adjusted hazard ratio [aHR] = 0.71; 95% CI, 0.57–0.90). Additionally, use of central-acting CCBs, rather than peripheral-acting ones, was associated with a decreased risk of PD (aHR = .69 [55–0.87]. Further decreased association was observed for higher cumulative doses of felodipine (aHR = 0.54 [0.36–0.80]) and amlodipine (aHR = 0.60 [0.45–0.79]). There was no association between the use of ACEIs (aHR = 0.80 [0.64–1.00]) or ARBs (aHR = 0.86 [0.69–1.08]) with PD. A potentially decreased association was only found for higher cumulative use of ACEIs (HR = 0.52 [0.34–0.80]) and ARBs (HR = 0.52 [0.33–0.80]). CONCLUSIONS: Our study suggests centrally-acting dihydropyridine CCB use and high cumulative doses of ACEIs and ARBs may associate with a decreased incidence of PD in hypertensive patients. Further long-term follow-up studies are needed to confirm the potential beneficial effects of antihypertensive agents in PD.
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spelling pubmed-40496132014-06-18 Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study Lee, Yen-Chieh Lin, Chin-Hsien Wu, Ruey-Meei Lin, Jou-Wei Chang, Chia-Hsuin Lai, Mei-Shu PLoS One Research Article BACKGROUND AND PURPOSE: Hypertension has been associated with Parkinson's disease (PD), but data on antihypertensive drugs and PD are inconclusive. We aim to evaluate antihypertensive drugs for an association with PD in hypertensive patients. METHODS: Hypertensive patients who were free of PD, dementia and stroke were recruited from 2005–2006 using Taiwan National Health Insurance Database. We examined the association between the use of calcium channel blockers (CCBs), angiotensin converting enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs) and the incidence of PD using beta-blockers as the reference. Cox regression model with time-varying medication use was applied. RESULTS: Among 65,001 hypertensive patients with a mean follow-up period of 4.6 years, use of dihydropyridine CCBs, but not non-dihydropyridine CCBs, was associated with a reduced risk of PD (adjusted hazard ratio [aHR] = 0.71; 95% CI, 0.57–0.90). Additionally, use of central-acting CCBs, rather than peripheral-acting ones, was associated with a decreased risk of PD (aHR = .69 [55–0.87]. Further decreased association was observed for higher cumulative doses of felodipine (aHR = 0.54 [0.36–0.80]) and amlodipine (aHR = 0.60 [0.45–0.79]). There was no association between the use of ACEIs (aHR = 0.80 [0.64–1.00]) or ARBs (aHR = 0.86 [0.69–1.08]) with PD. A potentially decreased association was only found for higher cumulative use of ACEIs (HR = 0.52 [0.34–0.80]) and ARBs (HR = 0.52 [0.33–0.80]). CONCLUSIONS: Our study suggests centrally-acting dihydropyridine CCB use and high cumulative doses of ACEIs and ARBs may associate with a decreased incidence of PD in hypertensive patients. Further long-term follow-up studies are needed to confirm the potential beneficial effects of antihypertensive agents in PD. Public Library of Science 2014-06-09 /pmc/articles/PMC4049613/ /pubmed/24910980 http://dx.doi.org/10.1371/journal.pone.0098961 Text en © 2014 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Yen-Chieh
Lin, Chin-Hsien
Wu, Ruey-Meei
Lin, Jou-Wei
Chang, Chia-Hsuin
Lai, Mei-Shu
Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title_full Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title_fullStr Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title_full_unstemmed Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title_short Antihypertensive Agents and Risk of Parkinson's Disease: A Nationwide Cohort Study
title_sort antihypertensive agents and risk of parkinson's disease: a nationwide cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049613/
https://www.ncbi.nlm.nih.gov/pubmed/24910980
http://dx.doi.org/10.1371/journal.pone.0098961
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