Literature DB >> 29431172

Progression and effect of cognitive-behavioral changes in patients with amyotrophic lateral sclerosis.

Meredith Bock1, Y-Nhy Duong1, Anthony Kim1, Isabel Allen1, Jennifer Murphy1, Catherine Lomen-Hoerth1.   

Abstract

BACKGROUND: To prospectively evaluate the progression of cognitive-behavioral function in amyotrophic lateral sclerosis (ALS) and examine the association of cognitive-behavioral deficits with disease progression, patient quality of life (QOL), and caregiver burden.
METHODS: We evaluated cognitive-behavioral function using the Amyotrophic Lateral Sclerosis Cognitive Behavioral Screen at enrollment and after 7 months in a cohort of patients with ALS. Paired t tests were used to evaluate the change in the 2 assessments. Linear regression and Kruskal-Wallis tests were applied to investigate how initial cognitive or behavioral status related to outcomes.
RESULTS: The mean test-retest interval was 6.8 months (SD 1.6). Cognitive status of the study population (n = 49) overall did not change over the study period (p = 0.06) despite progression of motor weakness (p < 0.001), though small subsets of the sample demonstrate cognitive change. Patients initially classified as behaviorally normal showed increased behavioral problems over time (t = -2.8, p = 0.009). Decline in cognitive (β = -1.3, p = 0.03) and behavioral (β = -0.76, p = 0.002) status predicted increasing caregiver burden. Behavioral abnormalities predicted decline in forced vital capacity and ALS Functional Rating Scale-Revised score (p = 0.008, 0.012) in the study population and patient QOL in the most severely affected group (t = 4.3, p = 0.003).
CONCLUSIONS: Cognitive-behavioral change is a key aspect of disease heterogeneity in ALS. Executive function in ALS overall remains stable over 7 months as detected by an administered screening tool. However, patients may develop caregiver-reported behavioral symptoms in that time period. Screening for caregiver-reported symptoms has a particular utility in predicting future clinical decline, increased caregiver burden, and worsening patient QOL.

Entities:  

Year:  2017        PMID: 29431172      PMCID: PMC5800712          DOI: 10.1212/CPJ.0000000000000397

Source DB:  PubMed          Journal:  Neurol Clin Pract        ISSN: 2163-0402


  40 in total

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2.  A cross sectional study on determinants of quality of life in ALS.

Authors:  A Chiò; A Gauthier; A Montuschi; A Calvo; N Di Vito; P Ghiglione; R Mutani
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3.  Verbal fluency and executive dysfunction in amyotrophic lateral sclerosis (ALS).

Authors:  S Abrahams; P N Leigh; A Harvey; G N Vythelingum; D Grisé; L H Goldstein
Journal:  Neuropsychologia       Date:  2000       Impact factor: 3.139

4.  Cognitive change in ALS: a prospective study.

Authors:  S Abrahams; P N Leigh; L H Goldstein
Journal:  Neurology       Date:  2005-04-12       Impact factor: 9.910

Review 5.  Establishing subtypes of the continuum of frontal lobe impairment in amyotrophic lateral sclerosis.

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6.  Cognitive changes predict functional decline in ALS: a population-based longitudinal study.

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7.  Frontotemporal dementia: behavioral symptoms and caregiver distress.

Authors:  J C Mourik; S M Rosso; M F Niermeijer; H J Duivenvoorden; J C Van Swieten; A Tibben
Journal:  Dement Geriatr Cogn Disord       Date:  2004-08-06       Impact factor: 2.959

8.  Caregiver's burden of patients 3 years after stroke assessed by a novel caregiver burden scale.

Authors:  S Elmståhl; B Malmberg; L Annerstedt
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Review 9.  The syndromes of frontotemporal dysfunction in amyotrophic lateral sclerosis.

Authors:  Michael J Strong
Journal:  Amyotroph Lateral Scler       Date:  2008-12

10.  Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.

Authors:  Patricia Lillo; Eneida Mioshi; John R Hodges
Journal:  BMC Neurol       Date:  2012-12-07       Impact factor: 2.474

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1.  Prognostic models for amyotrophic lateral sclerosis: a systematic review.

Authors:  Lu Xu; Bingjie He; Yunjing Zhang; Lu Chen; Dongsheng Fan; Siyan Zhan; Shengfeng Wang
Journal:  J Neurol       Date:  2021-03-10       Impact factor: 4.849

2.  Cognitive impairment across ALS clinical stages in a population-based cohort.

Authors:  Adriano Chiò; Cristina Moglia; Antonio Canosa; Umberto Manera; Rosario Vasta; Maura Brunetti; Marco Barberis; Lucia Corrado; Sandra D'Alfonso; Enrica Bersano; Maria Francesca Sarnelli; Valentina Solara; Jean Pierre Zucchetti; Laura Peotta; Barbara Iazzolino; Letizia Mazzini; Gabriele Mora; Andrea Calvo
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Review 3.  Clinical and Radiological Markers of Extra-Motor Deficits in Amyotrophic Lateral Sclerosis.

Authors:  Foteini Christidi; Efstratios Karavasilis; Michail Rentzos; Nikolaos Kelekis; Ioannis Evdokimidis; Peter Bede
Journal:  Front Neurol       Date:  2018-11-22       Impact factor: 4.003

4.  Modelling disease course in amyotrophic lateral Sclerosis: pseudo-longitudinal insights from cross-sectional health-related quality of life data.

Authors:  Tino Prell; Nayana Gaur; Robert Steinbach; Otto W Witte; Julian Grosskreutz
Journal:  Health Qual Life Outcomes       Date:  2020-05-01       Impact factor: 3.186

5.  Disease aggressiveness signatures of amyotrophic lateral sclerosis in white matter tracts revealed by the D50 disease progression model.

Authors:  Robert Steinbach; Nayana Gaur; Annekathrin Roediger; Thomas E Mayer; Otto W Witte; Tino Prell; Julian Grosskreutz
Journal:  Hum Brain Mapp       Date:  2020-10-26       Impact factor: 5.038

  5 in total

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