Evidence map›Paper›PMID 34479502›Full record

ArticleBMC neurology2021

Impairment of the visuospatial working memory in the patients with Parkinson's Disease: an fMRI study.

Shoji Kawashima, Yoko Shimizu, Yoshino Ueki, Noriyuki Matsukawa

Open access · goldAbstract read
In one paragraph

Article in BMC neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Visual memory in Parkinson's Disease: a non-graphomotor approach to assessment.Journal of neural transmission (Vienna, Austria : 1996) · 2026
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  4. Review
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  10. Combined brain topological metrics with machine learning to distinguish essential tremor and tremor-dominant Parkinson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  11. Review
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  14. Endogenous PTEN-Induced Kinase 1 Regulates Dendritic Architecture and Spinogenesis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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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

4 authors at 1 institution in 1 country.

Shoji KawashimaDepartment of Neurology and Neuroscience, Graduate School of Medical Science, Nagoya City University, 1 Kawasumi, Mizuho-ku, 467-8601, Nagoya, Japan. shojiyuto@wf6.so-net.ne.jp.
Yoko ShimizuDepartment of Rehabilitation Medicine, Graduate School of Medical Science, Nagoya City University, 1 Kawasumi, Mizuho-ku, 467-8601, Nagoya, Japan.
Yoshino UekiDepartment of Rehabilitation Medicine, Graduate School of Medical Science, Nagoya City University, 1 Kawasumi, Mizuho-ku, 467-8601, Nagoya, Japan.
Noriyuki MatsukawaDepartment of Neurology and Neuroscience, Graduate School of Medical Science, Nagoya City University, 1 Kawasumi, Mizuho-ku, 467-8601, Nagoya, Japan.
Nagoya City University · JP

Funding

This study was supported in part by Grants-in-Aid for Scientific Research on Priority Areas 15K16362
6 · The paper itself

Abstract

backgroundMild cognitive impairment (MCI) is a common symptom in the patients with Parkinson's disease (PD). The characteristics of cognitive impairment in PD are executive function (including working memory) and visuo-perceptual processing. The visuospatial n-back test has the merit of minimizing the influence of educational biases involved in the verbal n-back test. Furthermore, it can assess both visuospatial recognition and working memory in a single test.

methodsWe aimed to clarify the advantage of the visuospatial n-back test as a tool for detecting impairments of working memory in PD. We enrolled 28 right-handed patients with PD (18 males, 10 females) and 12 age-matched healthy controls (HC; 7 males, 5 females). Thirteen patients were classified as MCI (PD-MCI), and 15 as cognitively normal PD (PD-CN). Using functional MRI (fMRI), we explored the specific brain regions associated with the performance of the n-back test in the PD-MCI, PD-CN, and HC groups. The 0-back test assesses visuospatial recognition, while the 1-back and 2-back tests assess visuospatial working memory. Group comparisons were performed for three loads of this test.

resultsPatients with PD performed significantly worse in terms of the correct answer rates of all n-back tests compared with HC. fMRI analyses performed during the 2-back test revealed reduced activation in the bilateral dorsolateral prefrontal cortex, middle frontal gyrus (MFG), and parietal lobule in the PD group compared with the HC group. In contrast, the fMRI result during the 0-back test showed only a marginal difference in the frontal lobe. On comparisons of task performance between the PD-MCI and PD-CN groups, we found that the correct answer rate in the 2-back test was lower in the PD-MCI group than in the PD-CN group. However, scores of the 0-back and 1-back tests were not significantly different between the two groups. The fMRI findings revealed that activations within the middle frontal gyrus (MFG) and inferior parietal lobule (IPL) during the 2-back test were reduced in the patients with PD-MCI when compared to those with PD-CN.

conclusionsThis study reports reduced activation of the MFG and IPL in patients with PD-MCI. These regions may be associated with the pathophysiology of working memory impairment in patients with PD, which involves fronto-striatal network dysfunction.

Indexed as

Cognitive DysfunctionParkinson DiseaseBrainFemaleHumansMagnetic Resonance ImagingMaleMemory, Short-TermNeuropsychological Testsfunctional MRIMild cognitive impairmentn-back testParkinson’s diseaseworking memory

Identifiers

PMID34479502
PMCPMC8414685
OpenAlexW3113125494

What OpenQuestion holds

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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.