A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

Progression of Amyloid Accumulation in Late Adulthood Among People With Childhood-Onset Epilepsy




TekijätJoutsa, Juho; Rinne, Juha O.; Niemi, Kalle J.; Karrasch, Mira; Parkkola, Riitta K.; Saunavaara, Jani; Helin, Semi P.; Hermann, Bruce P.; Sillanpää, Matti

KustantajaLIPPINCOTT WILLIAMS & WILKINS

KustannuspaikkaPHILADELPHIA

Julkaisuvuosi2025

JournalNeurology

Tietokannassa oleva lehden nimiNEUROLOGY

Lehden akronyymiNEUROLOGY

Artikkelin numeroe210303

Vuosikerta104

Numero3

Sivujen määrä6

ISSN0028-3878

eISSN1526-632X

DOIhttps://doi.org/10.1212/WNL.0000000000210303

Verkko-osoitehttps://doi.org/10.1212/WNL.0000000000210303


Tiivistelmä

Background and objectives: Previous research has demonstrated increased brain amyloid plaque load in individuals with childhood-onset epilepsy in late middle age. However, the trajectory of this process is not yet known. The aim of this study was to determine whether individuals with a history of childhood-onset epilepsy show progressive brain aging in amyloid accumulation in late adulthood (Turku Adult Childhood-Onset Epilepsy study, TACOE).

Methods: Adults from a prospective population-based cohort of individuals with childhood-onset epilepsy, originally recruited 1961-1964, together with matched controls, were scanned with [11C]PIB PET twice: after at least 50 years (TACOE-50) and again after at least 55 years (TACOE-55) from the diagnosis.

Results: At TACOE-55, 31.4% (11/36, mean age 63.3 years, 52.8% female) of individuals from the epilepsy group and 11.4% (4/35, 63.1 year, 54.3%) of controls had a visually abnormal [11C]PIB scan (p = 0.039). At TACOE-55, cortical brain [11C]PIB uptakes were higher and increased more from TACOE-50 in the epilepsy compared with the control group (p < 0.05). In voxelwise whole-brain analyses, the epilepsy group showed significantly higher and more widespread brain amyloid accumulation (pFWE < 0.05).

Discussion: The results demonstrate that childhood-onset epilepsy is associated with an earlier age at onset of amyloidosis and greater progressive amyloid accumulation in late adulthood.


Julkaisussa olevat rahoitustiedot
This work was funded by CURE Epilepsy (Innovator Award, Epilepsy Award, and Epilepsy Research Continuity Fund Award) (B.H., M.S), National Governmental Research Grant (VTR), and Pro Humanitate Foundation, and Sigrid Juselius Foundation. J. Joutsa received funding from the Research Council of Finland, Finnish Medical Foundation, Sigrid Juselius Foundation, Finnish Foundation for Alcohol Studies, University of Turku (private donation), and Turku University Hospital (VTR). J.O. Rinne has received funding from the Academy of Finland (project #310962), Sigrid Juselius Foundation, and Finnish Governmental Research Funding (VTR) for Turku University Hospital.


Last updated on 2025-19-03 at 12:53