作者
Marie Ryan, Mark Heverin, Mark A Doherty, Nicola Davis, Emma M Corr, Alice Vajda, Niall Pender, Russell McLaughlin, Orla Hardiman
发表日期
2018/5/18
期刊
Neurology: Genetics
卷号
4
期号
3
页码范围
e239
出版商
Wolters Kluwer
简介
Objective
To assess temporal trends in familial amyotrophic lateral sclerosis (FALS) incidence rates in an Irish population and to determine factors influencing FALS ascertainment.
Methods
Population-based data collected over 23 years, using the Irish amyotrophic lateral sclerosis (ALS) register and DNA biobank, were analyzed and age-standardized rates of FALS and associated familial neuropsychiatric endophenotypes were identified.
Results
Between 1994 and 2016, 269 patients with a family history of ALS from 197 unique families were included on the register. Using stringent diagnostic criteria for FALS, the mean age-standardized FALS incidence rate for the study period was 11.1% (95% confidence interval [CI], 8.8–13.4). The FALS incidence rate increased steadily from 5.2% in 1994 to 19.1% in 2016, an annual increase of 0.7% (95% CI, 0.5–0.9, p < 0.0001). Inclusion of the presence of neuropsychiatric …
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