4.4 Article

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

Journal

MUSCLE & NERVE
Volume 66, Issue 2, Pages 167-174

Publisher

WILEY
DOI: 10.1002/mus.27635

Keywords

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

Funding

  1. Department of Veterans Affairs, Veterans Health Administration - Biomedical Laboratory Research and Development Merit Awards, Veterans Affairs Biorepository Brain Bank and Gulf War Veterans' Illnesses Biorepository - Clinical Sciences Research and Developm [BX002466, BX003063, I01-CX001038]
  2. National Institute on Aging [R56AG057768, RF1AG054156]
  3. National Institute on Aging Boston University AD Center [0572063345-5, P30AG13846]

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This study examined the association between ALSFRS-R scores and postmortem neuropathology in military veterans with autopsy-confirmed ALS. The results revealed that discrete patterns of motor dysfunction based on ALSFRS-R subdomain scores were related to neuropathology. These findings support the use of ALSFRS-R subdomain scores to capture the heterogeneity of ALS and may help identify endophenotypes for separate assessment in clinical trials.
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.

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