Literature DB >> 33314770

Baseline neuropsychological profiles in prion disease predict survival time.

Saranya E Sundaram1,2, Adam M Staffaroni1, Nicole C Walker1,3, Kaitlin B Casaletto1, Megan Casey1, Aili Golubjatnikov1, Stacy Metcalf1, Kelly O'Leary1, Katherine Wong1, Kendra Benisano1, Sven Forner1, Marta Gonzalez Catalan1,2, Isabel E Allen4, Howard J Rosen1, Joel H Kramer1, Michael D Geschwind1.   

Abstract

OBJECTIVE: Few studies have captured the neuropsychological profile of sporadic Creutzfeldt-Jakob disease (sCJD) with neuropsychological testing, and little is known about cognitive predictors of survival. We characterized baseline neuropsychological performance in sCJD and investigated associations with survival.
METHODS: sCJD participants who completed the MMSE (n = 118), 61 sCJD of whom also completed a neuropsychological battery at baseline, and 135 age-matched healthy controls, were included. Composite scores of global cognition, memory, executive functions, visuospatial, and language were derived. Cox proportional hazard models estimated survival time, controlling for age and education. Additional models adjusted for Barthel Index and PRNP codon 129 polymorphism.
RESULTS: sCJD participants performed significantly worse than controls on all cognitive tasks and composites with most showing very large effect sizes. The three tests showing the largest group differences were delayed verbal recall (Hedges'g = 4.08, P < 0.0001), Stroop Inhibition (Hedges'g = 3.14, P < 0.0001), and Modified Trails (Hedges'g = 2.94, P < 0.0001). Memory (95%) and executive functioning (87%) composites were most commonly impaired. Poorer global (HR = 0.65, P < 0.0001), visuospatial (HR = 0.82, P < 0.0001), and memory (HR = 0.82, P = 0.01) composites predicted shorter survival. Visuospatial cognition remained a significant predictor even after adjusting for all other cognitive composites; each standard deviation decrease in visuospatial cognition was associated with an 18% higher chance of death (HR = 0.82, P < 0.003). Global (HR = 0.68, P = 0.03) and visuospatial (HR = 0.82, P = 0.001) composites remained significant predictors after controlling for Barthel Index and codon 129.
INTERPRETATION: sCJD participants exhibit a broad range of cognitive impairments, with memory and executive functioning deficits in the vast majority. Neuropsychological assessment, particularly of visuospatial abilities, informs prognostication in sCJD.
© 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

Entities:  

Year:  2020        PMID: 33314770     DOI: 10.1002/acn3.51115

Source DB:  PubMed          Journal:  Ann Clin Transl Neurol        ISSN: 2328-9503            Impact factor:   4.511


  2 in total

1.  The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy.

Authors:  Anna Rita Giovagnoli; Giuseppe Di Fede; Giacomina Rossi; Fabio Moda; Marina Grisoli; Orso Bugiani
Journal:  Neurol Sci       Date:  2022-01-28       Impact factor: 3.307

2.  Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease.

Authors:  Akın Nihat; Janice M Ranson; Dominique Harris; Kirsty McNiven; TzeHow Mok; Peter Rudge; John Collinge; David J Llewellyn; Simon Mead
Journal:  Brain Commun       Date:  2022-08-02
  2 in total

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