Evidence map›Paper›PMID 30743154›Full record

ArticleJournal of the neurological sciences2019

Neural correlates of distinct cognitive phenotypes in early Parkinson's disease.

Ece Bayram, Brent Bluett, Xiaowei Zhuang, Dietmar Cordes, Denise R LaBelle, Sarah J Banks

Abstract read
In one paragraph

Article in Journal of the neurological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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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

6 authors at 3 institutions in 1 country.

Ece BayramCleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA. Electronic address: ebayram@ucsd.edu.
Brent BluettStanford University, Department of Neurology and Neurological Sciences, Palo Alto, CA, USA.
Xiaowei ZhuangCleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
Dietmar CordesCleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
Denise R LaBelleCleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
Sarah J BanksUniversity of California San Diego, Department of Neurosciences, La Jolla, CA, USA.
Cleveland Clinic · USStanford University · USUniversity of California San Diego · US

Funding

Renewal of Centers of Biomedical Research Excellence (COBRE) (Phase 2) CNTN - ResubmissionP20GM109025 · NIGMS · CLEVELAND CLINIC FOUNDATION · PI JESSICA KIRKLAND CALDWELL · 2015 to 2026
$22.8M
NIGMS NIH HHS P20 GM109025
6 · The paper itself

Abstract

objectiveCognitive decline is common in Parkinson's disease (PD), but changes can occur in a variety of cognitive domains. The lack of a single cognitive phenotype complicates diagnosis and tracking. In an earlier study we used a data-driven approach to identify distinct cognitive phenotypes of early PD. Here we identify the morphometric brain differences between those different phenotypes compared with cognitively normal PD participants.

methodsSix different cognitive classes were included (Weak, Typical, Weak-Visuospatial/Strong-Memory, Weak-Visuospatial, Amnestic, Strong). Structural differences between each class and the Typical class were assessed by deformation-based morphometry.

resultsThe different groups evidenced different patterns of atrophy. Weak class had frontotemporal and insular atrophy; Weak-Visuospatial/Strong-Memory class had frontotemporal, insular, parietal, and putamen atrophy; Weak-Visuospatial class had Rolandic operculum; Amnestic class had left frontotemporal, occipital, parietal and insular atrophy when compared to the Typical class. The Strong class did not have any atrophy but had significant differences in left temporal cortex in comparison to the Typical class.

conclusionsStructural neuroimaging differences are evident in PD patients with distinct cognitive phenotypes even very early in the disease process prior to the emergence of frank cognitive impairment. Future studies will elucidate whether these have prognostic value in identifying trajectories toward dementia, or if they represent groups sensitive to different treatments.

Indexed as

AgedAtrophyBrainCognitionCognitive DysfunctionFemaleHumansMagnetic Resonance ImagingMaleMemoryMiddle AgedNeuroimagingNeuropsychological TestsParkinson DiseaseAtrophyCluster analysisCognitive dysfunctionMagnetic resonance imagingNeuroimagingParkinson's disease

Identifiers

PMID30743154
PMCPMC6436969
OpenAlexW2913156557

What OpenQuestion holds

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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.