Aim: We aim to determine whether individuals with adult-onset hydrocephalus have an increased risk of incident epilepsy over time. Methods: We analysed data from the UK Biobank cohort. Diagnoses of “hydrocephalus” and “epilepsy” were identified through ICD-10-coded health records, excluding congenital and secondary cases. The association between these two diseases was investigated using logistic regression (adjusted for age and sex); subsequently, we performed a sampled cohort study to evaluate the hazard ratio (HR) for incident epilepsy in people with adult-onset hydrocephalus using Cox proportional hazards models with a dedicated sensitivity analysis including different sets of covariates such as demographic, lifestyle, vascular, and genetic factors. Results: Our cohort included 483,790 controls, 5,028 individuals with epilepsy, and 320 with adult-onset hydrocephalus. Hydrocephalus and epilepsy were strongly associated (OR: 9.6, 95% CI: 6.4–13.8, p < 0.001). Adjusted Cox models demonstrated a markedly increased risk of incident epilepsy in people with adult-onset hydrocephalus, with HR values ranging from 14.62 (95% CI: 7.91–27.00, p < 0.001) to 23.80 (95% CI: 12.87–44.03, p < 0.001) across models, after adjusting for multiple covariates. Results were also consistent after excluding people with comorbid neurodegenerative dementias such as Alzheimer’s disease. Conclusions: We demonstrated a markedly increased risk of epilepsy in adult-onset hydrocephalus, independent of vascular and neurodegenerative comorbidities and not attributable to shunt-related complications. These findings underscore the importance of increased diagnostic vigilance, as seizures may be under-recognized in this population, and support further research to clarify mechanisms and optimize management strategies.

Risk of epilepsy in people with adult-onset hydrocephalus: insights from the UK Biobank

Buonocore, Jolanda;Fortunato, Francesco;Fratto, Enrico;Sammarra, Ilaria;Gambardella, Antonio;Quattrone, Aldo;Quattrone, Andrea
2026-01-01

Abstract

Aim: We aim to determine whether individuals with adult-onset hydrocephalus have an increased risk of incident epilepsy over time. Methods: We analysed data from the UK Biobank cohort. Diagnoses of “hydrocephalus” and “epilepsy” were identified through ICD-10-coded health records, excluding congenital and secondary cases. The association between these two diseases was investigated using logistic regression (adjusted for age and sex); subsequently, we performed a sampled cohort study to evaluate the hazard ratio (HR) for incident epilepsy in people with adult-onset hydrocephalus using Cox proportional hazards models with a dedicated sensitivity analysis including different sets of covariates such as demographic, lifestyle, vascular, and genetic factors. Results: Our cohort included 483,790 controls, 5,028 individuals with epilepsy, and 320 with adult-onset hydrocephalus. Hydrocephalus and epilepsy were strongly associated (OR: 9.6, 95% CI: 6.4–13.8, p < 0.001). Adjusted Cox models demonstrated a markedly increased risk of incident epilepsy in people with adult-onset hydrocephalus, with HR values ranging from 14.62 (95% CI: 7.91–27.00, p < 0.001) to 23.80 (95% CI: 12.87–44.03, p < 0.001) across models, after adjusting for multiple covariates. Results were also consistent after excluding people with comorbid neurodegenerative dementias such as Alzheimer’s disease. Conclusions: We demonstrated a markedly increased risk of epilepsy in adult-onset hydrocephalus, independent of vascular and neurodegenerative comorbidities and not attributable to shunt-related complications. These findings underscore the importance of increased diagnostic vigilance, as seizures may be under-recognized in this population, and support further research to clarify mechanisms and optimize management strategies.
2026
Adult-onset hydrocephalus
Epilepsy
Neurodegeneration
Seizures
UK Biobank
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12317/122809
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