Literature DB >> 35585776

Utility of the ALSFRS-R for predicting ALS and comorbid disease neuropathology: The Veterans Affairs Biorepository Brain Bank.

Leigh E Colvin1, Zachariah W Foster1, Thor D Stein1,2,3,4,5, Manisha Thakore-James1,6, Mohammad Kian Salajegheh1,7, Kendall Carr1, Keith R Spencer1, Nazifa Abdul Rauf1, Latease Adams1, James G Averill8, Sean E Walker8, Ian Robey8, Victor E Alvarez1,2,3,4,6, Bertrand R Huber1,2,3,4,6, Ann C McKee1,2,3,4,5,6, Neil W Kowall1,2,3,6, Christopher B Brady1,2,6,7.   

Abstract

INTRODUCTION/AIMS: The amyotrophic lateral sclerosis (ALS) functional rating scale-revised (ALSFRS-R) is commonly used to track ALS disease progression; however, there are gaps in the literature regarding the extent to which the ALSFRS-R relates to underlying central nervous system (CNS) pathology. The current study explored the association between ALSFRS-R (total and subdomain) scores and postmortem neuropathology (both ALS-specific and comorbid disease).
METHODS: Within our sample of 93 military veterans with autopsy-confirmed ALS, we utilized hierarchical cluster analysis (HCA) to identify discrete profiles of motor dysfunction based on ALSFRS-R subdomain scores. We examined whether emergent clusters were associated with neuropathology. Separate analyses of variance and covariance with post-hoc comparisons were performed to examine relevant cluster differences.
RESULTS: Analyses revealed significant correlations between ALSFRS-R total and subdomain scores with some, but not all, neuropathological variables. The HCA illustrated three groups: Cluster 1-predominantly diffuse functional impairment; Cluster 2-spared respiratory/bulbar and impaired motor function; and Cluster 3-spared bulbar and impaired respiratory, and fine and gross motor function. Individuals in Cluster 1 (and to a lesser degree, Cluster 3) exhibited greater accumulation of ALS-specific neuropathology and less comorbid neuropathology than those in Cluster 2. DISCUSSION: These results suggest that discrete patterns of motor dysfunction based on ALSFRS-R subdomain scores are related to postmortem neuropathology. Findings support use of ALSFRS-R subdomain scores to capture the heterogeneity of clinical presentation and disease progression in ALS, and may assist researchers in identifying endophenotypes for separate assessment in clinical trials. Published 2022. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  amyotrophic lateral sclerosis; cluster analysis; functional rating scale; neuropathology

Mesh:

Year:  2022        PMID: 35585776      PMCID: PMC9308705          DOI: 10.1002/mus.27635

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.852


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Authors:  Julian Grosskreutz; Jörn Kaufmann; Julia Frädrich; Reinhard Dengler; Hans-Jochen Heinze; Thomas Peschel
Journal:  BMC Neurol       Date:  2006-04-25       Impact factor: 2.474

6.  Assessment of the factorial validity and reliability of the ALSFRS-R: a revision of its measurement model.

Authors:  Leonhard A Bakker; Carin D Schröder; Michael A van Es; Paul Westers; Johanna M A Visser-Meily; Leonard H van den Berg
Journal:  J Neurol       Date:  2017-06-12       Impact factor: 4.849

7.  Longitudinal evaluation of cerebral and spinal cord damage in Amyotrophic Lateral Sclerosis.

Authors:  Milena de Albuquerque; Lucas Melo T Branco; Thiago Junqueira R Rezende; Helen Maia Tavares de Andrade; Anamarli Nucci; Marcondes Cavalcante França
Journal:  Neuroimage Clin       Date:  2017-01-24       Impact factor: 4.881

8.  Clinical Significance of TDP-43 Neuropathology in Amyotrophic Lateral Sclerosis.

Authors:  Matthew D Cykowski; Suzanne Z Powell; Leif E Peterson; Joan W Appel; Andreana L Rivera; Hidehiro Takei; Ellen Chang; Stanley H Appel
Journal:  J Neuropathol Exp Neurol       Date:  2017-05-01       Impact factor: 3.685

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Journal:  Orphanet J Rare Dis       Date:  2009-02-03       Impact factor: 4.123

10.  Combinatory Biomarker Use of Cortical Thickness, MUNIX, and ALSFRS-R at Baseline and in Longitudinal Courses of Individual Patients With Amyotrophic Lateral Sclerosis.

Authors:  Anna M Wirth; Andrei Khomenko; Dobri Baldaranov; Ines Kobor; Ohnmar Hsam; Thomas Grimm; Siw Johannesen; Tim-Henrik Bruun; Wilhelm Schulte-Mattler; Mark W Greenlee; Ulrich Bogdahn
Journal:  Front Neurol       Date:  2018-07-30       Impact factor: 4.003

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