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 - Funding Information:
Funding Sources: Dr. de Bruyn was funded for clinical research fellowship by European Union grant, FP7-Health-2013-Innovation-1: European Project - “EPISTOP.” Dr. Tousseyn received grant support for postdoctoral research from the Belgian American Educational Foundation. Tuberous Sclerosis Complex Natural History Database is funded by Tuberous Sclerosis Alliance.We thank the TSC consortium and all the contributors to the TSC Natural History Database. This database received support from private donors and the Pediatric Epilepsy Research Foundation. TS Alliance TSC Natural History Database Consortium: Minnesota Epilepsy Group, P.A. St. Paul, MN (Michael Frost, MD); Texas Scottish Rite Hospital for Children, Dallas, TX (Steven Sparagana, MD); New York University School of Medicine, New York, NY (Josiane LaJoie, MD 2007 to 2011; James Riviello, Jr MD 2011 to 2013; Orrin Devinsky, MD 2013-2015; Josiane LaJoie, MD); Massachusetts General Hospital, Boston, MA (Elizabeth Thiele, MD, PhD); Children's Research Institute, Washington, DC (William McClintock, MD); The University of Chicago, Chicago, IL (Michael Kohrman, MD); UCSF Benioff Children's Hospital Oakland, Oakland, CA (Candida Brown, MD 2007 to 2010, Rachel Kuperman, MD); University of California Los Angeles, Los Angeles, CA (Joyce Wu, MD); The University of Texas Health Science Center at Houston, Houston, TX (Hope Northrup, MD); University of Alabama at Birmingham, Birmingham, AL (E. Martina Bebin, MD, MPA & Bruce Korf, MD, PhD); Cleveland Clinic, Cleveland, OH (Ajay Gupta, MD); Children's Hospital Colorado, Aurora, CO (Paul Levisohn, MD 2008 to 2011; Susan Koh, MD); Nicklaus Children's Hospital Miami, Miami, FL (Ian O'Neil Miller, MD & Michael Duchowny, MD); Loma Linda University, Loma Linda, CA (Stephen Ashwal, MD); UZ Brussels, Belgium (Anna Jansen, MD, PhD); University of Pennsylvania, Philadelphia, PA (Peter Crino, MD, PhD 2009 to 2012; John Pollard, MD 2012 to 2013; Kate Nathanson, MD); Boston Children's Hospital, Boston, MA (Mustafa Sahin, MD, PhD); Cincinnati Children's Hospital Medical Center, Cincinnati, OH (Darcy A. Krueger, MD, PhD); Washington University St. Louis, St. Louis, MO (Michael Wong, MD, PhD and Anna Jeong, MD). We also acknowledge the EPISTOP project. Declaration of interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Funding Information:
We thank the TSC consortium and all the contributors to the TSC Natural History Database. This database received support from private donors and the Pediatric Epilepsy Research Foundation .
Funding Information:
Funding Sources: Dr. de Bruyn was funded for clinical research fellowship by European Union grant, FP7-Health-2013-Innovation-1: European Project - “EPISTOP.” Dr. Tousseyn received grant support for postdoctoral research from the Belgian American Educational Foundation . Tuberous Sclerosis Complex Natural History Database is funded by Tuberous Sclerosis Alliance .
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
UR - http://www.scopus.com/inward/record.url?scp=85080916450&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85080916450&partnerID=8YFLogxK
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 -