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ABSTRACT: Objective
To examine the relative risk of suicide mortality in patients with Huntington's disease (HD).Methods
A case-control study design was used. We used linked electronic records from primary care, secondary care and Office for National Statistics from England from 2001 through 2019. Controls were matched to cases by general practice and suicide date. Odds ratios (ORs) were adjusted for gender and age at suicide/index date.Results
Data were available for 594,674 individuals. Patients with HD who died from suicide were significantly younger at time of death than patients with HD who died from causes other than suicide (p < 0.001). The adjusted OR for HD was 9.2 (95% confidence intervals, CI 4.9-17.4) compared to those without HD. The increase in risk was higher amongst the younger age group who were ≤ 45.8 years at suicide/index date (OR 54.5, 95% CI 10.8-276.1).Conclusion
The markedly elevated suicide risk in patients with HD suggests that implementation of suicide risk assessment may improve survival in individuals with these diseases, especially in younger patients.
SUBMITTER: Alothman D
PROVIDER: S-EPMC9293836 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
Alothman Danah D Marshall Charles R CR Tyrrell Edward E Lewis Sarah S Card Timothy T Fogarty Andrew A
Journal of neurology 20220327 8
<h4>Objective</h4>To examine the relative risk of suicide mortality in patients with Huntington's disease (HD).<h4>Methods</h4>A case-control study design was used. We used linked electronic records from primary care, secondary care and Office for National Statistics from England from 2001 through 2019. Controls were matched to cases by general practice and suicide date. Odds ratios (ORs) were adjusted for gender and age at suicide/index date.<h4>Results</h4>Data were available for 594,674 indiv ...[more]