Quality of Life in Multiple Sclerosis Compared to Amyotrophic Lateral Sclerosis: Fatigue and Fast Disease Progression Interferes with the Ability to Psychosocially Adjust
Luisa T. Balz, Ingo Uttner, Jochen Weishaupt, Albert C. Ludolph, Daniela Taranu, Ioannis Vardakas, Stefanie Jung, Tanja Fangerau, Deborah K. Erhart, Makbule Senel, Hayrettin Tumani, Dorothée E. Lulé

TL;DR
This study compares how people with multiple sclerosis and amyotrophic lateral sclerosis adjust to their conditions, finding that fatigue and disease progression affect quality of life and mental health.
Contribution
The study identifies fatigue as a key predictor of psychosocial adjustment in MS and compares adjustment between MS and ALS.
Findings
Cognitive and motor fatigue significantly predict psychosocial adjustment in MS patients.
MS patients showed higher physical and subjective quality of life and lower depression than ALS patients.
Both MS and ALS patients had similar mental quality of life despite differing disease progression rates.
Abstract
Background/Objectives: Multiple sclerosis (MS) is a complex neurological disease that is associated with a broad spectrum of physical and psychological symptoms. Psychosocial adjustment (PSA) refers to the ability to cope with these challenges, which influence quality of life (QoL) and depressiveness in ways not yet fully understood. This study explores the relationship of PSA and disease-specific symptoms in MS, including fatigue, a prominent MS symptom. Additionally, PSA was compared to Amyotrophic Lateral Sclerosis (ALS) to disentangle the impact of disease trajectory on PSA. Methods: We interviewed 77 MS patients using patient-reported outcome measures on QoL and depression and compared them to 30 ALS patients. Confirmatory factor analysis and regression analysis were used to identify PSA indicators and predictors in MS, while t-tests assessed PSA differences across diseases.…
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Taxonomy
TopicsMultiple Sclerosis Research Studies · Fibromyalgia and Chronic Fatigue Syndrome Research · Amyotrophic Lateral Sclerosis Research
