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Attention impairment in motor functional neurological disorders: a neuropsychological study

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023752%3A_____%2F22%3A43920906" target="_blank" >RIV/00023752:_____/22:43920906 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00064165:_____/22:10449344 RIV/00216208:11110/22:10449344 RIV/00216208:11210/22:10449344 RIV/00216208:11230/22:10449344

  • Výsledek na webu

    <a href="https://link.springer.com/article/10.1007/s00415-022-11211-x" target="_blank" >https://link.springer.com/article/10.1007/s00415-022-11211-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00415-022-11211-x" target="_blank" >10.1007/s00415-022-11211-x</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Attention impairment in motor functional neurological disorders: a neuropsychological study

  • Popis výsledku v původním jazyce

    Objective Our objective was to assess cognitive functioning across multiple cognitive domains using a standardised neuropsychological battery in patients with motor functional neurological disorders (mFND). Methods Thirty patients with clinically established mFND and 30 age-, sex- and education-matched control subjects underwent a thorough neuropsychological assessment evaluating (1) attention including processing speed, (2) executive functions including working memory, (3) short-term memory, (4) speech and language and (5) visuospatial functions. Performance validity tests (PVT) and self-report measures of depression, anxiety and cognitive complaints were included in the assessment. Only patients with valid test performance were included in the analysis. Results Three patients scored below the cut-off scores in PVT. Patients performed significantly worse than controls in the following areas: (1) the attention domain which included a slow processing speed (p = 0.005, Cohen&apos;s d = 0.89), (2) executive functions (p = 0.01, Cohen&apos;s d = 0.88) and (3) speech and language domains (p = 0.025, Cohen&apos;s d = 0.77). Patients with mFND showed greater intra-individual variability in cognitive performance (p = 0.005, Cohen&apos;s d = 0.94). Cognitive impairments were independent of depressive symptoms, which were higher in mFND patients. Conclusion This study revealed both subjective and objective cognitive impairment in patients with mFND. The neuropsychological profile in mFND was characterised primarily by attentional impairment including a slow processing speed and a high intra-individual variability in cognitive performance. Cognitive impairment was associated with a valid test performance, highlighting that the deficits observed were not likely to be explained by a lack of effort in the patient group. Attention is considered to play a key role in mFND pathophysiology, and the results suggest that such impairments are objectively measurable.

  • Název v anglickém jazyce

    Attention impairment in motor functional neurological disorders: a neuropsychological study

  • Popis výsledku anglicky

    Objective Our objective was to assess cognitive functioning across multiple cognitive domains using a standardised neuropsychological battery in patients with motor functional neurological disorders (mFND). Methods Thirty patients with clinically established mFND and 30 age-, sex- and education-matched control subjects underwent a thorough neuropsychological assessment evaluating (1) attention including processing speed, (2) executive functions including working memory, (3) short-term memory, (4) speech and language and (5) visuospatial functions. Performance validity tests (PVT) and self-report measures of depression, anxiety and cognitive complaints were included in the assessment. Only patients with valid test performance were included in the analysis. Results Three patients scored below the cut-off scores in PVT. Patients performed significantly worse than controls in the following areas: (1) the attention domain which included a slow processing speed (p = 0.005, Cohen&apos;s d = 0.89), (2) executive functions (p = 0.01, Cohen&apos;s d = 0.88) and (3) speech and language domains (p = 0.025, Cohen&apos;s d = 0.77). Patients with mFND showed greater intra-individual variability in cognitive performance (p = 0.005, Cohen&apos;s d = 0.94). Cognitive impairments were independent of depressive symptoms, which were higher in mFND patients. Conclusion This study revealed both subjective and objective cognitive impairment in patients with mFND. The neuropsychological profile in mFND was characterised primarily by attentional impairment including a slow processing speed and a high intra-individual variability in cognitive performance. Cognitive impairment was associated with a valid test performance, highlighting that the deficits observed were not likely to be explained by a lack of effort in the patient group. Attention is considered to play a key role in mFND pathophysiology, and the results suggest that such impairments are objectively measurable.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30210 - Clinical neurology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/NV16-29651A" target="_blank" >NV16-29651A: Diagnostické neurofyziologické a laboratorní markery a patofyziologické mechanismy funkčních poruch hybnosti</a><br>

  • Návaznosti

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Ostatní

  • Rok uplatnění

    2022

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Journal of Neurology

  • ISSN

    0340-5354

  • e-ISSN

    1432-1459

  • Svazek periodika

    269

  • Číslo periodika v rámci svazku

    11

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    10

  • Strana od-do

    5981-5990

  • Kód UT WoS článku

    000826269600001

  • EID výsledku v databázi Scopus

    2-s2.0-85134478587