Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.

<h4>Background</h4>Although Idiopathic Parkinson's disease (IPD) develops in considerable patients with drug-induced Parkinsonism (DIP), the association hasn't been well defined. We aimed to evaluate the underlying association and risk factors of DIP and IPD.<h4>Methods&l...

Full description

Bibliographic Details
Main Authors: Sohyun Jeong, Hyemin Cho, Yun Joong Kim, Hyeo-Il Ma, Sunmee Jang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0247354
id doaj-7fb505ebbf3f4b92a9cc8fefa074cbd7
record_format Article
spelling doaj-7fb505ebbf3f4b92a9cc8fefa074cbd72021-03-12T05:31:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01163e024735410.1371/journal.pone.0247354Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.Sohyun JeongHyemin ChoYun Joong KimHyeo-Il MaSunmee Jang<h4>Background</h4>Although Idiopathic Parkinson's disease (IPD) develops in considerable patients with drug-induced Parkinsonism (DIP), the association hasn't been well defined. We aimed to evaluate the underlying association and risk factors of DIP and IPD.<h4>Methods</h4>A retrospective cohort study using National Health Insurance Claims data in 2011-2016 was conducted. New-onset DIP patients in 2012 were selected and matched with active controls having diabetes mellitus at a 1:4 ratio by age, sex, and Charlson's Comorbidity Index score. Comorbidity, causative drugs, and prescription days were evaluated as covariates.<h4>Results</h4>A total of 441 DIP were selected. During the 4-year follow up, 14 IPD events in the DM group but 62 events in the DIP group were observed (adjusted hazard ratio, HR: 18.88, 95% CI, 9.09-39.22, adjusting for comorbidities and causative drugs). IPD diagnosis in DIP was observed high in males compared to females (15.58/13.24%). The event was the most within the 1st year follow-up, mean days 453 (SD 413.36). Subgroup analysis in DIP showed calcium channel blocker (verapamil, diltiazem, and flunarizine) was significantly associated with increased IPD risk (HR: 2.24, 95% CI, 1.27-3.93).<h4>Conclusion</h4>Increased IPD in DIP patients might not be from the causal toxicity of antidopaminergic effects but from a trigger by the causative drugs on the DIP patients who already had subclinical IPD pathology. DIP can serve as a strong proxy for IPD incidence. Subjects who develop DIP should be monitored carefully for potential IPD incidence.https://doi.org/10.1371/journal.pone.0247354
collection DOAJ
language English
format Article
sources DOAJ
author Sohyun Jeong
Hyemin Cho
Yun Joong Kim
Hyeo-Il Ma
Sunmee Jang
spellingShingle Sohyun Jeong
Hyemin Cho
Yun Joong Kim
Hyeo-Il Ma
Sunmee Jang
Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
PLoS ONE
author_facet Sohyun Jeong
Hyemin Cho
Yun Joong Kim
Hyeo-Il Ma
Sunmee Jang
author_sort Sohyun Jeong
title Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
title_short Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
title_full Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
title_fullStr Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
title_full_unstemmed Drug-induced Parkinsonism: A strong predictor of idiopathic Parkinson's disease.
title_sort drug-induced parkinsonism: a strong predictor of idiopathic parkinson's disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description <h4>Background</h4>Although Idiopathic Parkinson's disease (IPD) develops in considerable patients with drug-induced Parkinsonism (DIP), the association hasn't been well defined. We aimed to evaluate the underlying association and risk factors of DIP and IPD.<h4>Methods</h4>A retrospective cohort study using National Health Insurance Claims data in 2011-2016 was conducted. New-onset DIP patients in 2012 were selected and matched with active controls having diabetes mellitus at a 1:4 ratio by age, sex, and Charlson's Comorbidity Index score. Comorbidity, causative drugs, and prescription days were evaluated as covariates.<h4>Results</h4>A total of 441 DIP were selected. During the 4-year follow up, 14 IPD events in the DM group but 62 events in the DIP group were observed (adjusted hazard ratio, HR: 18.88, 95% CI, 9.09-39.22, adjusting for comorbidities and causative drugs). IPD diagnosis in DIP was observed high in males compared to females (15.58/13.24%). The event was the most within the 1st year follow-up, mean days 453 (SD 413.36). Subgroup analysis in DIP showed calcium channel blocker (verapamil, diltiazem, and flunarizine) was significantly associated with increased IPD risk (HR: 2.24, 95% CI, 1.27-3.93).<h4>Conclusion</h4>Increased IPD in DIP patients might not be from the causal toxicity of antidopaminergic effects but from a trigger by the causative drugs on the DIP patients who already had subclinical IPD pathology. DIP can serve as a strong proxy for IPD incidence. Subjects who develop DIP should be monitored carefully for potential IPD incidence.
url https://doi.org/10.1371/journal.pone.0247354
work_keys_str_mv AT sohyunjeong druginducedparkinsonismastrongpredictorofidiopathicparkinsonsdisease
AT hyemincho druginducedparkinsonismastrongpredictorofidiopathicparkinsonsdisease
AT yunjoongkim druginducedparkinsonismastrongpredictorofidiopathicparkinsonsdisease
AT hyeoilma druginducedparkinsonismastrongpredictorofidiopathicparkinsonsdisease
AT sunmeejang druginducedparkinsonismastrongpredictorofidiopathicparkinsonsdisease
_version_ 1714787531753521152