Evidence map›Paper›PMID 39484734›Full record

ArticlePsychiatry and clinical neurosciences2025

Risk of subsequent Parkinson's disease among patients with bipolar disorder or major depression: A nationwide longitudinal study in Taiwan.

Mao-Hsuan Huang, Chih-Ming Cheng, Ju-Wei Hsu, Ya-Mei Bai, Tung-Ping Su, Cheng-Ta Li, Shih-Jen Tsai, Yee-Lam E Chan, Mu-Hong Chen

Abstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Bipolar Disorder as a Long-Term Risk Factor for Parkinson's Disease: A Nationwide Case-Control Study.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mao-Hsuan HuangDepartment of Psychiatry, Taipei Veterans General Hospital, Yuanshan and Suao Branch, Ilan, Taiwan.ORCID https://orcid.org/0000-0002-7970-3758
Chih-Ming ChengDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-8334-0438
Ju-Wei HsuDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Ya-Mei BaiDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Tung-Ping SuDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Cheng-Ta LiDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-0670-1153
Shih-Jen TsaiDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Yee-Lam E ChanDepartment of Psychiatry, General Cheng Hsin Hospital, Taipei, Taiwan.
Mu-Hong ChenDivision of Psychiatry, Faculty of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-6516-1073

Funding

Hsinchu Science Park Bureau, Ministry of Science and Technology, Taiwan 107-2314-B-075-063-MY3Hsinchu Science Park Bureau, Ministry of Science and Technology, Taiwan 112-2314-B-A19-001 -Hsinchu Science Park Bureau, Ministry of Science and Technology, Taiwan 113-2314-B-A19-001 -Kaohsiung Veterans General Hospital, Tri-Service General Hospital, Academia Sinica Joint Research Program VTA112-V1-6-1Kaohsiung Veterans General Hospital, Tri-Service General Hospital, Academia Sinica Joint Research Program VTA113-V1-5-1Ministry of Science and Technology, Taiwan MOST 109-2314-B-010-050-MY3Ministry of Science and Technology, Taiwan MOST110-2314-B-075-024-MY3Ministry of Science and Technology, Taiwan MOST110-2314-B-075-026Ministry of Science and Technology, Taiwan MOST 111-2314-B-075-013Ministry of Science and Technology, Taiwan MOST111-2314-B-075-014-MY2Ministry of Science and Technology, Taiwan NSTC111-2314-B-A49-089-MY2Ministry of Science and Technology, Taiwan NSTC 113-2314-B-075-042Taipei Veterans General Hospital V103E10-001Taipei Veterans General Hospital V104E10-002Taipei Veterans General Hospital V105A-049Taipei Veterans General Hospital V105E10-001-MY2-1Taipei Veterans General Hospital V106B020Taipei Veterans General Hospital V107C-181Taipei Veterans General Hospital V113C-010Taipei Veterans General Hospital V113C-011Taipei Veterans General Hospital V113C-039Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST112-G1-8-1Veterans General Hospitals and University System of Taiwan Joint Research Program VGHUST113-G1-8-1Yen Tjing Ling Medical Foundation CI-113-32, CI-113-30
6 · The paper itself

Abstract

aimBipolar disorder (BD) and major depression have been associated with an increased risk of developing Parkinson's disease (PD); however, few studies have directly compared the risk of PD development between patients with BD and major depression while considering relevant risk factors and psychotropic medications.

methodsUsing the Taiwan National Health Insurance Research Database, 21,186 patients with BD, 21,188 patients with major depression, and 42,374 controls were enrolled between 2001 and 2009, and followed until the end of 2011. Individuals who developed PD during the follow-up period were identified. Cox regression models were used to analyze the hazard ratio (HR) of developing PD, adjusting for demographic factors, comorbidities, and psychotropic medication usage.

resultsBoth patients with BD [HR 8.63, 95% confidence interval (CI) 6.35-11.72] and those with major depression (HR 5.68, 95% CI 4.15-7.78) had an elevated risk of subsequent PD compared to the controls. Patients with BD were associated with a 51% increased risk of subsequent PD compared with patients with major depression. Long-term treatment with antiepileptic mood stabilizers was associated with increased PD risk among patients with late-onset BD and high Charlson comorbidity index scores. Lithium was not associated with an increased PD risk.

conclusionsThe study highlights an elevated PD risk in patients with BD and major depression compared to the controls, with BD patients at highest risk. Further research is needed to elucidate the complex interplay between psychotropic medications and neurodegenerative processes in BD, aiming to optimize therapeutic strategies and improve patient outcomes.

Indexed as

Bipolar DisorderMajor Depressive DisorderParkinson DiseaseAgedAnticonvulsantsFemaleHumansLongitudinal StudiesMaleMiddle AgedRisk FactorsTaiwanAnticonvulsantsbipolar disorderlithiummood stabilizersparkinsonism

Identifiers

PMID39484734
PMCPMC11693976

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.