Evidence map›Paper›PMID 29756003›Full record

ArticleMovement disorders clinical practice

Onset and Remission of Psychosis in Parkinson's Disease: Pharmacologic and Motoric Markers.

Jared Thomas Hinkle, Kate Perepezko, Catherine C Bakker, Martinus P G Broen, Kathleen Chin, Ted M Dawson, Vanessa Johnson, Zoltan Mari, Cherie L Marvel, Kelly A Mills and 8 more

Open access · greenAbstract read
In one paragraph

Article in Movement disorders clinical practice. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Lewy Body Degenerations as Neuropsychiatric Disorders.The Psychiatric clinics of North America · 2020
    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

18 authors at 3 institutions in 2 countries.

Jared Thomas HinkleMedical Scientist Training Program, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Kate PerepezkoDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Catherine C BakkerMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Martinus P G BroenDepartment of Neurology, Maastricht University Medical Centre, Maastricht, the Netherlands.
Kathleen ChinDepartment of Neurology, Johns Hopkins School of Medicine, Baltimore MD, United States.
Ted M DawsonMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Vanessa JohnsonDepartment of Neurology, Johns Hopkins School of Medicine, Baltimore MD, United States.
Zoltan MariMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Cherie L MarvelDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Kelly A MillsMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Alexander PantelyatMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Olga PletnikovaMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Liana S RosenthalMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Melissa D ShepardDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Daniel A StevensMedical Scientist Training Program, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Juan C TroncosoMorris K. Udall Parkinson's Disease Research Center, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Jiangxia WangDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Gregory M PontoneDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Johns Hopkins University · USJohns Hopkins Medicine · USMaastricht University Medical Centre · NL

Funding

Project 2 MeasurementU19AG033655 · NIA · JOHNS HOPKINS UNIVERSITY · PI Abhay Moghekar · 2014 to 2026
$51.5M
UNDERSTANDING NO SIGNALING RESULTING IN NEUROPROTECTION.P50DA000266 · NIDA · JOHNS HOPKINS UNIVERSITY · PI BARABAN, JAY M · 1985 to 2017
$45.2M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
Understanding Mechanisms of a-synuclein pathologyP50NS038377 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DAWSON, TED M. · 1998 to 2019
$38.8M
'T V ASSESSMENT - MEMORY DISORDERED PATIENTS'P50AG005146 · NIA · JOHNS HOPKINS UNIVERSITY · PI ALBERT, MARILYN S. · 1985 to 2019
$37.6M
Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Ji Yi · 1985 to 2026
$22.1M
Parthanatos, AIF and PAAN-1 in Neuronal InjuryR37NS067525 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DAWSON, TED M., DAWSON, VALINA L. · 2015 to 2021
$5.3M
Johns Hopkins Medicine Biomarker Discovery in Parkinson's DiseaseU01NS082133 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DAWSON, TED M. · 2012 to 2016
$4.1M
HIV-Related Neuroplasticity and Attention-to-Reward as Predictors of Real World FunctionR01DA041264 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MARVEL, CHERIE L · 2016 to 2020
$2.1M
Altered Amyloid Processing HIVR01MH096636 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HAUGHEY, NORMAN J · 2013 to 2017
$2.0M
Unfolded Protein Response in Alpha-synucleinopathiesR01NS086074 · NINDS · UNIVERSITY OF MINNESOTA · PI LEE, MICHAEL K · 2014 to 2018
$1.7M
Anxiety in Parkinson's: Use of quantitative methods to guide rational treatmentK23AG044441 · NIA · JOHNS HOPKINS UNIVERSITY · PI PONTONE, GREGORY MICHAEL · 2014 to 2018
$1.0M
NEI NIH HHS P30 EY001765NIA NIH HHS K23 AG044441NIA NIH HHS P50 AG005146NIA NIH HHS U19 AG033655NIDA NIH HHS P50 DA000266NIDA NIH HHS R01 DA041264NIGMS NIH HHS T32 GM007309NIMH NIH HHS R01 MH096636NINDS NIH HHS P50 NS038377NINDS NIH HHS R01 NS086074NINDS NIH HHS R25 NS079185NINDS NIH HHS R37 NS067525NINDS NIH HHS U01 NS082133
6 · The paper itself

Abstract

backgroundPsychosis is among the most disabling complications of Parkinson's disease (PD). The chronicity of PD psychosis remains understudied and the relative importance of dopaminergic therapy versus the disease process itself in engendering psychosis remains unclear.

objectivesTo examine pharmacologic and motoric correlates of PD psychosis onset and remission in a longitudinally monitored PD cohort.

methodsWe analyzed data from 165 participants enrolled in a longitudinal PD study through the Morris K. Udall Parkinson's Disease Research Center of Excellence at Johns Hopkins University. Evaluations included formal psychiatric assessment and were conducted at two-year intervals. Regression with generalized estimated equations (GEE) was used to produce unadjusted and adjusted estimates for time-varying longitudinal associations between psychosis and putative risk factors.

resultsSixty-two participants (37.6%) were diagnosed with psychosis during at least one evaluation. Of forty-nine participants with psychosis followed over multiple evaluations, 13 (26.5%) demonstrated remission despite significant Hoehn & Yahr stage increase (p=0.009); two of these cases later relapsed. Multivariable regression with GEE identified dementia diagnosis, akinesia-rigidity, anticholinergic usage, and levodopa-carbidopa dose to be significantly associated with psychosis, while disease duration was not. A sub-analysis of 30 incident psychosis cases suggested that dopamine agonist dose was lowered after psychosis onset with a compensatory increase in levodopa-carbidopa dosage.

conclusionsOur findings suggest that in the context of standard therapy, PD-related psychotic disorder can remit at a frequency of approximately 27%. Additionally, akinetic-rigid motor impairment was more strongly associated with psychosis than disease duration, independent of cognitive impairment and medications.

Indexed as

HallucinationsMotor subtypesParkinson’s diseasePsychosisRemission

Identifiers

PMID29756003
PMCPMC5945218
OpenAlexW2755129626

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.