TY - JOUR
T1 - Epilepsy and Neurodevelopmental Comorbidities in Tuberous Sclerosis Complex
T2 - A Natural History Study
AU - The TSC Natural History Database Consortium
AU - Gupta, Ajay
AU - de Bruyn, Gwendolyn
AU - Tousseyn, Simon
AU - Krishnan, Balu
AU - Lagae, Lieven
AU - Agarwal, Nitin
AU - Minnesota Epilepsy Group, Epilepsy Group
AU - Frost, Michael
AU - Sparagana, Steven
AU - LaJoie, Josiane
AU - Riviello, James
AU - Devinsky, Orrin
AU - Thiele, Elizabeth
AU - McClintock, William
AU - Kohrman, Michael
AU - Brown, Candida
AU - Kuperman, Rachel
AU - Wu, Joyce
AU - Northrup, Hope
AU - Bebin, E. Martina
AU - Korf, Bruce
AU - Levisohn, Paul
AU - Koh, Susan
AU - O'Neil Miller, Ian
AU - Duchowny, Michael
AU - Ashwal, Stephen
AU - Jansen, Anna
AU - Crino, Peter
AU - Pollard, John
AU - Nathanson, Kate
AU - Sahin, Mustafa
AU - Krueger, Darcy A.
AU - Wong, Michael
AU - Jeong, Anna
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/5
Y1 - 2020/5
N2 - Background: We studied the natural history, genotype influence, and inter-relationship of epilepsy and neuropsychiatric disorders in tuberous sclerosis complex. Methods: Patients were identified using the TSC Natural History Database, the largest repository of longitudinally studied patients enrolled by the TSC Clinics Consortium. Results: A cohort of 1657 TSC Natural History Database patients was analyzed. Eighty-eight percent patients (91% TSC2 vs 82% TSC1; P = 0.002) had epilepsy; TSC2 was more frequent with epilepsy onset at age less than two years (TSC2 82% vs TSC1 54%; P < 0.001) and infantile spasms (TSC2 56% vs TSC1 27%; P < 0.001). Frequency of intellectual disability (intelligence quotient less than 70) was higher when epilepsy coexisted (P < 0.001), but was not impacted by genotype (P = 0.08). Severe intellectual disability (intelligence quotient less than 50) was associated with epilepsy onset at age less than two years (P = 0.007), but not with the epilepsy duration (P = 0.45). Autism was diagnosed in 23% and was associated with epilepsy (P < 0.001), particularly with epilepsy onset at age less than two years (P = 0.02) but not with genotype (P = 0.06). Attention-deficit/hyperactivity disorder (age greater than four years) was diagnosed in 18% and was associated with epilepsy (P < 0.001), but genotype made no difference. Nine percent had anxiety (age greater than seven years) and 6% had depression (age greater than nine years), but neither showed association with epilepsy or genotype. Conclusions: Epilepsy is associated with intellectual disability, and when epilepsy begins before age two years the frequency and severity of intellectual disability is much higher. Epilepsy is also associated with autism and attention-deficit/hyperactivity disorder but not with anxiety and depression. Additional trials, blinded, prospective, and adequately powered, will help clarify if early and effective treatment of epilepsy may also mitigate intellectual disability, autism, and attention-deficit/hyperactivity disorder.
AB - Background: We studied the natural history, genotype influence, and inter-relationship of epilepsy and neuropsychiatric disorders in tuberous sclerosis complex. Methods: Patients were identified using the TSC Natural History Database, the largest repository of longitudinally studied patients enrolled by the TSC Clinics Consortium. Results: A cohort of 1657 TSC Natural History Database patients was analyzed. Eighty-eight percent patients (91% TSC2 vs 82% TSC1; P = 0.002) had epilepsy; TSC2 was more frequent with epilepsy onset at age less than two years (TSC2 82% vs TSC1 54%; P < 0.001) and infantile spasms (TSC2 56% vs TSC1 27%; P < 0.001). Frequency of intellectual disability (intelligence quotient less than 70) was higher when epilepsy coexisted (P < 0.001), but was not impacted by genotype (P = 0.08). Severe intellectual disability (intelligence quotient less than 50) was associated with epilepsy onset at age less than two years (P = 0.007), but not with the epilepsy duration (P = 0.45). Autism was diagnosed in 23% and was associated with epilepsy (P < 0.001), particularly with epilepsy onset at age less than two years (P = 0.02) but not with genotype (P = 0.06). Attention-deficit/hyperactivity disorder (age greater than four years) was diagnosed in 18% and was associated with epilepsy (P < 0.001), but genotype made no difference. Nine percent had anxiety (age greater than seven years) and 6% had depression (age greater than nine years), but neither showed association with epilepsy or genotype. Conclusions: Epilepsy is associated with intellectual disability, and when epilepsy begins before age two years the frequency and severity of intellectual disability is much higher. Epilepsy is also associated with autism and attention-deficit/hyperactivity disorder but not with anxiety and depression. Additional trials, blinded, prospective, and adequately powered, will help clarify if early and effective treatment of epilepsy may also mitigate intellectual disability, autism, and attention-deficit/hyperactivity disorder.
KW - Autism
KW - Epilepsy
KW - Neurodevelopmental disorders
KW - Pediatric epilepsy
KW - TSC
KW - Tuberous sclerosis complex
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U2 - 10.1016/j.pediatrneurol.2019.12.016
DO - 10.1016/j.pediatrneurol.2019.12.016
M3 - Article
C2 - 32139167
AN - SCOPUS:85080916450
SN - 0887-8994
VL - 106
SP - 10
EP - 16
JO - Pediatric neurology
JF - Pediatric neurology
ER -