Evidence map›Paper›PMID 32032471›Full record

ArticleAnnals of clinical and translational neurology2020

White matter hyperintensities and risk of levodopa-induced dyskinesia in Parkinson's disease.

Seok Jong Chung, Han Soo Yoo, Yang Hyun Lee, Jin Ho Jung, KyoungWon Baik, Byoung Seok Ye, Young H Sohn, Phil Hyu Lee

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Dopamine transporter availability based on white matter hyperintensity during early to mid-stage Parkinson's disease and multiple system atrophy: a case control study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  2. Article
  3. The impact of cerebral small vessel disease burden and its imaging markers on gait, postural control, and cognition in Parkinson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
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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

8 authors at 1 institution in 1 country.

Seok Jong ChungDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-6086-3199
Han Soo YooDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-7846-6271
Yang Hyun LeeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Jin Ho JungDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
KyoungWon BaikDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-7215-375X
Byoung Seok YeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Young H SohnDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Phil Hyu LeeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.ORCID 0000-0001-9931-8462
Yonsei University · KR

Funding

Ministry of Education NRF-2018R1D1A1B07048959Ministry of Science, ICT and Future Planning NRF-2019R1A2C2085462National Research Foundation of Korea
6 · The paper itself

Abstract

objectiveTo investigate whether the burden of white matter hyperintensities (WMHs) is associated with the risk of developing levodopa-induced dyskinesia (LID) in Parkinson's disease (PD).

methodsAccording to the Clinical Research Center for Dementia of South Korea WMH visual rating scale, 336 patients with drug-naïve early stage PD (follow-up >3 years) were divided into two groups of PD with minimal WMHs (PD-WMH-; n = 227) and moderate-to-severe WMHs (PD-WMH+; n = 109). The Cox regression model was used to estimate the hazard ratio for the development of LID in the PD-WMH + group compared with the PD-WMH- group, while adjusting for age at PD onset, sex, striatal dopamine depletion, and PD medication dose. Additionally, we assessed the effects of WMH burden rated by the Scheltens scale and regional WMH distribution on the development of LID.

resultsPatients in the PD-WMH + group were older and had more severe parkinsonian motor signs despite comparable striatal dopamine transporter availability than those in the PD-WMH- group. Patients in the PD-WMH + group had a higher risk of developing LID (hazard ratio, 2.66; P < 0.001) than those in the PD-WMH- group after adjustment for other confounding factors. A greater WMH burden was associated with earlier occurrence of LID (hazard ratio, 1.04; P = 0.001), although the effects of WMHs on LID development did not exhibit region-specific patterns.

interpretationThe present study demonstrates that the burden of WMHs is associated with occurrence of LID in patients with PD, suggesting comorbid WMHs as a risk factor for LID.

Indexed as

AgedComorbidityDopamine AgentsDyskinesia, Drug-InducedFemaleHumansLeukoaraiosisLevodopaMagnetic Resonance ImagingMaleMiddle AgedParkinson DiseasePositron-Emission TomographyProportional Hazards ModelsRetrospective StudiesRiskDopamine AgentsLevodopa

Identifiers

PMID32032471
PMCPMC7034502
OpenAlexW3004671348

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.