Pre-morbid risk factors for amyotrophic lateral sclerosis.
Pre-morbid risk factors for amyotrophic lateral sclerosis.
Background As a neurodegenerative disorder with high case-fatality, there is a need to identify primary, modifiable risk factors for amyotrophic lateral sclerosis (ALS). Their detection has, however, proved elusive and this may be ascribed to the scarcity of well-characterised, sufficiently-powered cohort studies necessary to explore the aetiology of this rare condition.
Methods UK Biobank is an on-going, closed, prospective cohort study in which 502,524 participants (273,420 women) have been linked to national hospital and mortality registries. Baseline data collection took place between 2006 and 2010 when a range of psychosocial, physiological, and demographic data were captured.
Results Approximately 11 years of event surveillance gave rise to 301 hospitalisations and 279 deaths ascribed to ALS. After left censoring to account for reverse causality and adjustment for confounding factors, being older (hazard ratio per 10 year increase; 95% confidence interval: 1.92; 1.58, 2.33) and male (1.37; 1.00, 1.87) were associated with elevated rates of hospitalisation for ALS. Similar effects were apparent when death due to the disorder was the outcome of interest. Of the remaining 23 potential risk indices, however, there was only a suggestion that taller people experienced an increased risk of hospitalisation (per SD increase: 1.31; 1.09, 1.59).
Conclusions In the present study, a comprehensive array of potential risk indices were essentially unrelated to later ALS.
Batty, G. D.
b9f925eb-88c8-4f27-8148-8929fdb84149
Gale, Catharine
5bb2abb3-7b53-42d6-8aa7-817e193140c8
Batty, G. D.
b9f925eb-88c8-4f27-8148-8929fdb84149
Gale, Catharine
5bb2abb3-7b53-42d6-8aa7-817e193140c8
Batty, G. D. and Gale, Catharine
(2021)
Pre-morbid risk factors for amyotrophic lateral sclerosis.
Clinical Epidemiology.
(doi:10.1101/2021.07.01.21259861).
(In Press)
Abstract
Background As a neurodegenerative disorder with high case-fatality, there is a need to identify primary, modifiable risk factors for amyotrophic lateral sclerosis (ALS). Their detection has, however, proved elusive and this may be ascribed to the scarcity of well-characterised, sufficiently-powered cohort studies necessary to explore the aetiology of this rare condition.
Methods UK Biobank is an on-going, closed, prospective cohort study in which 502,524 participants (273,420 women) have been linked to national hospital and mortality registries. Baseline data collection took place between 2006 and 2010 when a range of psychosocial, physiological, and demographic data were captured.
Results Approximately 11 years of event surveillance gave rise to 301 hospitalisations and 279 deaths ascribed to ALS. After left censoring to account for reverse causality and adjustment for confounding factors, being older (hazard ratio per 10 year increase; 95% confidence interval: 1.92; 1.58, 2.33) and male (1.37; 1.00, 1.87) were associated with elevated rates of hospitalisation for ALS. Similar effects were apparent when death due to the disorder was the outcome of interest. Of the remaining 23 potential risk indices, however, there was only a suggestion that taller people experienced an increased risk of hospitalisation (per SD increase: 1.31; 1.09, 1.59).
Conclusions In the present study, a comprehensive array of potential risk indices were essentially unrelated to later ALS.
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Accepted/In Press date: 27 August 2021
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Local EPrints ID: 451207
URI: http://eprints.soton.ac.uk/id/eprint/451207
ISSN: 1179-1349
PURE UUID: 32ccd6e1-bff1-491a-8aee-99898ece91be
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Date deposited: 14 Sep 2021 16:35
Last modified: 17 Mar 2024 02:42
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Author:
G. D. Batty
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