Evidence map›Paper›PMID 30125297›Full record

ArticlePloS one2018

Cognition among individuals along a spectrum of increased risk for Parkinson's disease.

Lana M Chahine, Liz Urbe, Chelsea Caspell-Garcia, Dag Aarsland, Roy Alcalay, Paolo Barone, David Burn, Alberto J Espay, Jamie L Hamilton, Keith A Hawkins and 9 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Neuroimaging in Glucocerebrosidase-Associated Parkinsonism: A Systematic Review.Movement disorders : official journal of the Movement Disorder Society · 2022
    Pooled it
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  13. Parkinson disease-associated cognitive impairment.Nature reviews. Disease primers · 2021
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  14. Observational
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  19. The Neuropsychiatry of Parkinson Disease: A Perfect Storm.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry · 2019
    Review
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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

19 authors at 16 institutions in 3 countries.

Lana M ChahineUniversity of Pittsburgh, Pittsburgh, PA, United States of America.ORCID 0000-0003-2521-7196
Liz UrbeThe University of Iowa, Iowa City, Iowa, United States of America.
Chelsea Caspell-GarciaThe University of Iowa, Iowa City, Iowa, United States of America.
Dag AarslandDepartment of Old Age Psychiatry, Institute of Psychiatry, Psychology & Neuroscience, King's College London, England.
Roy AlcalayColumbia University Medical Center, Department of Neurology, New York, NY, United States of America.
Paolo BaroneDepartment of Medicine and Surgery, Center for Neurodegenerative Diseases, University of Salerno, Fisciano, Italy.
David BurnInstitute for Ageing and Health, Newcastle University, Newcastle, United Kingdom.
Alberto J EspayDepartment of Neurology, University of Cincinnati Academic Health Center, Cincinnati, OH, United States of America.
Jamie L HamiltonThe Michael J. Fox Foundation for Parkinson's Research, New York, NY, United States of America.
Keith A HawkinsDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, United States of America.
Shirley LaschInstitute for Neurodegenerative Disorders, New Haven, CT, United States of America.
James B LeverenzCleveland Clinic, Cleveland, OH, United States of America.
Irene LitvanUCSD Movement Disorder Center, Department of Neurosciences, University of California San Diego, San Diego, CA, United States of America.
Irene RichardDepartments of Neurology and Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, NY, United States of America.
Andrew SiderowfDepartment of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States of America.
Christopher S CoffeyThe University of Iowa, Iowa City, Iowa, United States of America.
Tanya SimuniNorthwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Daniel WeintraubDepartment of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA, United States of America.
Parkinson’s Progression Markers Initiative
University of Iowa · USCleveland Clinic · USColumbia University Irving Medical Center · USInstitute for Neurodegenerative Disorders · USKing's College London · GBMental Illness Research, Education and Clinical Centers · USMichael J. Fox Foundation · USNewcastle Hospitals - Campus for Ageing and Vitality · GBNorthwestern University · USUniversity of California San Diego · USUniversity of Cincinnati Medical Center · USUniversity of Pennsylvania · USUniversity of Pittsburgh · USUniversity of Rochester · USUniversity of Salerno · ITYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSeveral characteristics associated with increased risk for Parkinson's disease (PD) have been identified, including specific genotypes and various non-motor symptoms. Characterizing non-motor features, such as cognitive abilities, among individuals considered at-risk for PD is essential to improving prediction of future neurodegeneration.

methodsParticipants belonging to the following cohorts of the Parkinson Progression Markers Initiative (PPMI) study were included: de novo PD with dopamine transporter binding deficit (n = 423), idiopathic REM sleep behavior disorder (RBD, n = 39), hyposmia (n = 26) and non-PD mutation carrier (NMC; Leucine-rich repeat kinase 2 (LRRK2) G2019S (n = 88) and glucocerebrosidase (GBA) gene (n = 38) mutations)). Inclusion criteria enriched the RBD and hyposmia cohorts, but not the NMC cohort, with individuals with dopamine transporter binding deficit. Baseline neuropsychological performance was compared, and analyses were adjusted for age, sex, education, and depression.

resultsThe RBD cohort performed significantly worse than the hyposmia and NMC cohorts on Symbol Digit Modality Test (mean (SD) 32.4 (9.16) vs. 41.8 (9.98), p = 0.002 and vs. 45.2 (10.9), p<0.001) and Judgment of Line Orientation (11.3 (2.36) vs.12.9 (1.87), p = 0.004 and vs. 12.9 (1.87), p<0.001). The RBD cohort also performed worse than the hyposmia cohort on the Montreal Cognitive Assessment (25.5 (4.13) vs. 27.3 (1.71), p = 0.02). Hyposmics did not differ from PD or NMC cohorts on any cognitive test score.

conclusionAmong individuals across a spectrum of risk for PD, cognitive function is worse among those with the characteristic most strongly associated with future risk of PD or dementia with Lewy bodies, namely RBD.

Indexed as

CognitionDisease SusceptibilityAdultAgedAged, 80 and overBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedMutationNeuropsychological TestsParkinson DiseaseRisk AssessmentRisk FactorsBiomarkers

Identifiers

PMID30125297
PMCPMC6101368
OpenAlexW2888291381

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.