Aspects of autism spectrum disorder and correlation with neuroimaging findings in tuberous sclerosis complex

被引:1
作者
Dedeoglu, Ozge [1 ]
Cetinkaya, Miray [2 ]
Derinkuyu, Betul Emine [3 ]
Aksoy, Erhan [4 ]
Oztoprak, Ulkuhan [4 ]
Sel, Cigdem Genc [4 ]
Ozcan, Hatice Nursun [5 ]
Aksoy, Ayse [6 ]
Yuksel, Deniz [4 ]
机构
[1] Ankara City Hosp, Dept Pediat Neurol, Pediat Neurol, Ankara, Turkey
[2] Univ Hlth Sci, Sami Ulus Child Hlth & Dis Training & Res Hosp, Dept Child & Adolescent Physciatry, Child & Adolescent Physciatry, Ankara, Turkey
[3] Univ Hlth Sci, Sami Ulus Child Hlth & Dis Training & Res Hosp, Dept Pediat Radiol, Pediat Radiol, Ankara, Turkey
[4] Univ Hlth Sci, Sami Ulus Child Hlth & Dis Training & Res Hosp, Dept Pediat Neurol, Pediat Neurol, Ankara, Turkey
[5] Hacettepe Univ, Dept Pediat Radiol, Pediat Radiol, Ankara, Turkey
[6] 19 May Univ Hosp, Dept Pediat Neurol, Pediat Neurol, Samsun, Turkey
关键词
Tuberosclerosis Complex Disease; Autism Spectrum Disorder; Magnetic Resonance Imaging; EPILEPSY; CHILDREN; MANAGEMENT; SYMPTOMS; PATHWAYS;
D O I
10.1016/j.clineuro.2022.107550
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Tuberous sclerosis complex (TSC) patients may have different specific neuropsychological deficits related to the location of the tubers. Autism spectrum disorders (ASD) are common in TSC patients but the relationship between these diagnoses has not been formally explored. In this study we sought to examine brain Magnetic Resonance Imaging (MRI) findings in TSC patients with ASD.Methods: We evaluated 34 TSC patients on the basis of DSM-V diagnostic criteria for ASD, Wechsler Intelligence Scale for Children (WISC-R), psychiatrist's examination and also structured parent interviews. The number and localization of the tubers, postcontrast signal characteristics of the tubers, SWI findings, DWI findings on brain MRI were recorded. Demographic features, epilepsy histories, number of antiseizure medications, cognitive status were eveluated also. Patients were divided into two groups: ASD group, which represented group 1 and group 2 consisting of patients without any ASD symptoms.Results: In our study, the mean number of tuber count was 21.8 in patients with ASD patients (Group 1, n = 13) and 12.4 in other TSC patients without ASD (Group 2, n = 21). Rate of tubers in prefrontal cortex/whole tubers (0.51) in patients with ASD was determined to be higher in group 1 (p = 0.003). Also a significant difference was detected between generalize epileptiform activities on EEG and the rate of DRE (p = 0.002; p = 0.001) between groups. Cognitive disturbances and infantile spasm history were similar between groups. TSC2 mutations have been identified in 29 (86%) patients.Conclusion: The mean of total tuber count and the rate of the location in the prefrontal cortex were determined to be higher in TSC patients with ASD. Specific areas on brain MRI may help understanding the development of ASD in TSC patients.
引用
收藏
页数:5
相关论文
共 19 条
[1]   Longitudinal Changes in Diffusion Properties in White Matter Pathways of Children With Tuberous Sclerosis Complex [J].
Baumer, Fiona M. ;
Song, Jae W. ;
Mitchell, Paul D. ;
Pienaar, Rudolph ;
Sahin, Mustafa ;
Grant, P. Ellen ;
Takahashi, Emi .
PEDIATRIC NEUROLOGY, 2015, 52 (06) :615-623
[2]   Influence of seizures on early development in tuberous sclerosis complex [J].
Capal, Jamie K. ;
Bernardino-Cuesta, Beatriz ;
Horn, Paul S. ;
Murray, Donna ;
Byars, Anna Weber ;
Bing, Nicole M. ;
Kent, Bridget ;
Pearson, Deborah A. ;
Sahin, Mustafa ;
Krueger, Darcy A. .
EPILEPSY & BEHAVIOR, 2017, 70 :245-252
[3]   The natural history of epilepsy in tuberous sclerosis complex [J].
Chu-Shore, Catherine J. ;
Major, Philippe ;
Camposano, Susana ;
Muzykewicz, David ;
Thiele, Elizabeth A. .
EPILEPSIA, 2010, 51 (07) :1236-1241
[4]   Update on Drug Management of Refractory Epilepsy in Tuberous Sclerosis Complex [J].
Clement, Emma van der Poest ;
Jansen, Floor E. ;
Braun, Kees P. J. ;
Peters, Jurriaan M. .
PEDIATRIC DRUGS, 2020, 22 (01) :73-84
[5]   Neurological and neuropsychiatric aspects of tuberous sclerosis complex [J].
Curatolo, Paolo ;
Moavero, Romina ;
de Vries, Petrus J. .
LANCET NEUROLOGY, 2015, 14 (07) :733-745
[6]   A circuitry and biochemical basis for tuberous sclerosis symptoms: from epilepsy to neurocognitive deficits [J].
Feliciano, David M. ;
Lin, Tiffany V. ;
Hartman, Nathaniel W. ;
Bartley, Christopher M. ;
Kubera, Cathryn ;
Hsieh, Lawrence ;
Lafourcade, Carlos ;
O'Keefe, Rachel A. ;
Bordey, Angelique .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2013, 31 (07) :667-678
[7]   Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study [J].
Grau, Janina ;
Zollner, Johann Philipp ;
Schubert-Bast, Susanne ;
Kurlemann, Gerhard ;
Hertzberg, Christoph ;
Wiemer-Kruel, Adelheid ;
Bast, Thomas ;
Bertsche, Astrid ;
Bettendorf, Ulrich ;
Fiedler, Barbara ;
Hahn, Andreas ;
Hartmann, Hans ;
Hornemann, Frauke ;
Immisch, Ilka ;
Jacobs, Julia ;
Kieslich, Matthias ;
Klein, Karl Martin ;
Klotz, Kerstin A. ;
Kluger, Gerhard ;
Knuf, Markus ;
Mayer, Thomas ;
Marquard, Klaus ;
Meyer, Sascha ;
Muhle, Hiltrud ;
Muller-Schluter, Karen ;
Noda, Anna H. ;
Ruf, Susanne ;
Sauter, Matthias ;
Schlump, Jan-Ulrich ;
Syrbe, Steffen ;
Thiels, Charlotte ;
Trollmann, Regina ;
Wilken, Bernd ;
Willems, Laurent M. ;
Rosenow, Felix ;
Strzelczyk, Adam .
ORPHANET JOURNAL OF RARE DISEASES, 2021, 16 (01)
[8]   Cerebral tuber count and its impact on mental outcome of patients with tuberous sclerosis complex [J].
Kaczorowska, Magdalena ;
Jurkiewicz, Elzbieta ;
Domanska-Pakiela, Dorota ;
Syczewska, Malgorzata ;
Lojszczyk, Barbara ;
Chmielewski, Dariusz ;
Kotulska, Katarzyna ;
Kuczynski, Dariusz ;
Kmiec, Tomasz ;
Dunin-Wasowicz, Dorota ;
Kasprzyk-Obara, Jolanta ;
Jozwiak, Sergiusz .
EPILEPSIA, 2011, 52 (01) :22-27
[9]   Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference [J].
Krueger, Darcy A. ;
Northrup, Hope ;
Northrup, Hope ;
Krueger, Darcy A. ;
Roberds, Steven ;
Smith, Katie ;
Sampson, Julian ;
Korf, Bruce ;
Kwiatkowski, David J. ;
Mowat, David ;
Nellist, Mark ;
Northrup, Hope ;
Povey, Sue ;
de Vries, Petrus ;
Byars, Anna ;
Dunn, David ;
Ess, Kevin ;
Hook, Dena ;
Jansen, Anna ;
King, Bryan ;
Sahin, Mustafa ;
Whittemore, Vicky ;
Thiele, Elizabeth ;
Bebin, E. Martina ;
Chugani, Harry T. ;
Crino, Peter ;
Curatolo, Paolo ;
Holmes, Greg ;
Nabbout, Rima ;
O'Callaghan, Finbar ;
Wheless, James ;
Wu, Joyce ;
Darling, Thomas N. ;
Cowen, Edward W. ;
Gosnell, Elizabeth ;
Hebert, Adelaide ;
Mlynarczyk, Greg ;
Soltani, Keyomaurs ;
Teng, Joyce ;
Wataya-Kaneda, Mari ;
Witman, Patricia M. ;
Kingswood, Chris ;
Bissler, John ;
Budde, Klemens ;
Hulbert, John ;
Guay-Woodford, Lisa ;
Sampson, Julian ;
Sauter, Matthias ;
Zonneberg, Bernard ;
Jozwiak, Sergiusz .
PEDIATRIC NEUROLOGY, 2013, 49 (04) :255-265
[10]   Definition of drug resistant epilepsy: Consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies [J].
Kwan, Patrick ;
Arzimanoglou, Alexis ;
Berg, Anne T. ;
Brodie, Martin J. ;
Hauser, W. Allen ;
Mathern, Gary ;
Moshe, Solomon L. ;
Perucca, Emilio ;
Wiebe, Samuel ;
French, Jacqueline .
EPILEPSIA, 2010, 51 (06) :1069-1077