Targeted assessment of lower motor neuron burden is associated with survival in amyotrophic lateral sclerosis

Abstract

Estimating survival in amyotrophic lateral sclerosis (ALS) is challenging due to heterogeneity in clinical features of disease and a lack of suitable markers that predict survival. Our aim was to determine whether scoring of upper or lower motor neuron weakness is associated with survival.

With this objective, 161 ALS subjects were recruited from two tertiary referral centres. Scoring of upper (UMN) and lower motor neuron (LMN) signs was performed, in addition to a brief questionnaire. Subjects were then followed until the censorship date. Univariate analysis was performed to identify variables associated with survival to either non-invasive ventilation (NIV) or death, which were then further characterized using Cox regression. Results showed that factors associated with reduced survival included older age, bulbar and respiratory involvement and shorter diagnostic delay (all p < 0.05). Whole body LMN score was strongly associated with time to NIV or death (p ≤0.001) whereas UMN scores were poorly associated with survival. In conclusion, our results suggest that, early in disease assessment and in the context of other factors (age, bulbar, respiratory status), the burden of LMN weakness provides an accurate estimate of outcome. Such a scoring system could predict prognosis, and thereby aid in selection of patients for clinical trials.

Key words:

• Biomarker
• survival
• prognostic
• amyotrophic lateral sclerosis
• clinical phenotype

Acknowledgements

We acknowledge the assistance of Nicole Hutchinson, Helen Woodhouse, Susan Heggie and Kate Thorpe (RBWH) and Eleanor Ramsey (POWH). This study was funded by the MND Research Fund, held with the Royal Brisbane and Women’s Hospital Foundation.

Declaration of interest

The authors have no competing interests to disclose.