Abstract

BackgroundThe study aimed to appraise the health-related quality of life (HRQoL) measured by the five-level EuroQol-5 dimensions (EQ-5D-5L) in amyotrophic lateral sclerosis (ALS), and to explore the associations between non-motor symptoms (mood changes, cognitive disturbances and sleep disturbances).MethodsEQ-5D-5L descriptive scores were converted into a single aggregated “health utility” score. A calibrated visual analog scale (EQ-VAS) was used for self-rating of current health status. Multiple logistic regression analysis was used to explore the factors associated with HRQoL.ResultsAmong the 547 enrolled ALS patients who were assessed using EQ-5D-5L, the highest frequency of reported problems was with usual activities (76.7%), followed by self-care (68.8%) and anxiety/depression (62.0%). The median health utility score was 0.78 and the median EQ-VAS score was 70. Clinical factors corresponding to differences in the EQ-5D-5L health utility score included age of onset, onset region, the ALS Functional Rating Scale-Revised (ALSFRS-R) score, and King’s College stages. Patients with depression, anxiety, and poor sleep had lower health utility scores. Patients with excessive daytime sleepiness and rapid eye movement sleep behavior disorder had lower EQ-VAS scores. Multivariate logistic analysis indicated that ALSFRS-R scores, depression, and anxiety were associated with health utility scores. After adjusting other parameters, ALSFRS-R score, stages, and depression were significantly associated with EQ-VAS scores (P < 0.05).ConclusionThis study examined HRQoL in ALS patients using the Chinese version of the EQ-5D-5L scale across different stages of the disease. We found that HRQoL is related to disease severity and to mood disturbances. Management of non-motor symptoms may help improve HRQoL in ALS patients.

Highlights

  • The study aimed to appraise the health-related quality of life (HRQoL) measured by the five-level EuroQol-5 dimensions (EQ-5D-5L) in amyotrophic lateral sclerosis (ALS), and to explore the associations between nonmotor symptoms

  • Two hundred and seventy-three patients (49.9%) had upper limb onset, 37.7% of patients had lower limb onset, and 12.4% had bulbar onset form. 224 (41.0%) patients were at stage 1, 193 (35.3%) patients were at stage 2, 86 (15.7%) patients were at stage 3, and 44 (8.0%) patients were at stage 4 according to the King’s College staging system

  • We found that ALSFRS-R scores, depression, and anxiety were associated with healthy utility scores in all ALS patients from multivariate logistic regression analyses

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Summary

Introduction

The study aimed to appraise the health-related quality of life (HRQoL) measured by the five-level EuroQol-5 dimensions (EQ-5D-5L) in amyotrophic lateral sclerosis (ALS), and to explore the associations between nonmotor symptoms (mood changes, cognitive disturbances and sleep disturbances). Amyotrophic lateral sclerosis (ALS) is a fatal disease caused by progressive degeneration of both upper and lower motor neurons in the brain and spinal cord [1]. In the ALS functional rating scales and health-related quality of life (HRQoL) questionnaires were adopted as the primary or secondary endpoints in many clinical trials [4]. HRQoL declines as the disease progress, and the rate of change correlates with physical, psychological, existential, and support factors [5, 6]. It is possible to calculate the varied health utility scores when different aggregated EQ-5D-5L value sets are applied

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