4.4 Article

Episodic Ataxia Type 1: Natural History and Effect on Quality of Life

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CEREBELLUM
卷 22, 期 4, 页码 578-586

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SPRINGER
DOI: 10.1007/s12311-021-01360-6

关键词

Episodic ataxia type 1; EA1; KCNA1; Natural history; SF-36

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Episodic ataxia type 1 (EA1) is a rare autosomal potassium channelopathy that causes intermittent attacks of ataxia in patients. A multi-centre study was conducted to understand the natural history of EA1. The study found that the disability and impairment caused by EA1 did not accumulate significantly over a 2-year period. The quality of life of EA1 patients was lower compared to controls, especially in the physical domain. The study also discovered stable attack duration and frequency in EA1 patients. This prospective study provides valuable data for future clinical trials and outcome measures development.
Episodic ataxia type 1 (EA1) is a rare autosomal potassium channelopathy, due to mutations in KCNA1. Patients have childhood onset of intermittent attacks of ataxia, dizziness or imbalance. In order to quantify the natural history of EA1, its effect on quality of life and in preparation for future clinical trials, we set up an international multi-centre study of EA1. We recruited thirty-three participants with EA1: twenty-three completed 1-year follow-up and eighteen completed 2-year follow-up. There was very little accumulation of disability or impairment over the course of the 2 years of the study. The outcome measures of ataxia (SARA and functional rating of ataxia) and the activities of daily living scale were largely stable over time. Self-reported health-related quality of life (SF-36) scores were lower across all domains than controls, in keeping with a chronic condition. Physical subdomain scores appeared to deteriorate over time, which seems to be driven by the female participants in the study. This is an interesting finding and warrants further study. Attacks of EA1 reported by participants in real time via an interactive voice response system showed that symptoms were not stereotyped; however, attack duration and frequency was stable between individuals. This large prospective study is the first ever completed in subjects with EA1. We document the natural history of the disorder over 2 years. These data will enable the development of outcome measures for clinical trials of treatment.

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