Book contents
- Imaging Biomarkers in Epilepsy
- Imaging Biomarkers in Epilepsy
- Copyright page
- Dedication
- Contents
- Preface
- Contributors
- Part I Imaging the Development and Early Phase of the Disease
- Chapter 1 Imaging Biomarkers for Febrile Status Epilepticus and Other Forms of Convulsive Status Epilepticus
- Chapter 2 Experimental MRI Approaches to Study Posttraumatic Epilepsy
- Chapter 3 Imaging Biomarkers of Acquired Epilepsies
- Chapter 4 Imaging and Cognition in Children with New-Onset Epilepsies
- Chapter 5 Imaging Genetics for Benign Mesial Temporal Lobe Epilepsy
- Part II Modeling Epileptogenic Lesions and Mapping Networks
- Part III Predicting the Response to Therapeutic Interventions
- Part IV Mapping Consequences of the Disease
- Index
- References
Chapter 5 - Imaging Genetics for Benign Mesial Temporal Lobe Epilepsy
from Part I - Imaging the Development and Early Phase of the Disease
Published online by Cambridge University Press: 07 January 2019
Book contents
- Imaging Biomarkers in Epilepsy
- Imaging Biomarkers in Epilepsy
- Copyright page
- Dedication
- Contents
- Preface
- Contributors
- Part I Imaging the Development and Early Phase of the Disease
- Chapter 1 Imaging Biomarkers for Febrile Status Epilepticus and Other Forms of Convulsive Status Epilepticus
- Chapter 2 Experimental MRI Approaches to Study Posttraumatic Epilepsy
- Chapter 3 Imaging Biomarkers of Acquired Epilepsies
- Chapter 4 Imaging and Cognition in Children with New-Onset Epilepsies
- Chapter 5 Imaging Genetics for Benign Mesial Temporal Lobe Epilepsy
- Part II Modeling Epileptogenic Lesions and Mapping Networks
- Part III Predicting the Response to Therapeutic Interventions
- Part IV Mapping Consequences of the Disease
- Index
- References
- Type
- Chapter
- Information
- Imaging Biomarkers in Epilepsy , pp. 48 - 54Publisher: Cambridge University PressPrint publication year: 2019
References
Manford, M, Hart, YM, Sander, JW, Shorvon, SD National General Practice Study of Epilepsy (NGPSE): partial seizure patterns in a general population. Neurology. 1992;42:1911–7.Google Scholar
Falconer, MA, Serafetinides, EA, Corsellis, JAN Etiology and pathogenesis of temporal lobe epilepsy. Arch Neurol. 1964;10:233–40.Google Scholar
de Tisi, J, Bell, GS, Peacock, JL, et al. The long-term outcome of adult epilepsy surgery, patterns of seizure remission, and relapse: a cohort study. Lancet. 2011;378:1388–95.Google Scholar
Semah, F, Picot, MC, Adam, C, et al. Is the underlying cause of epilepsy a major prognostic factor for recurrence? Neurology. 1998;51:1256–62.Google Scholar
Spooner, CG, Berkovic, SF, Mitchell, LA, Wrennall, JA, Harvey, AS New-onset temporal lobe epilepsy in children: lesion on MRI predicts poor seizure outcome. Neurology. 2006;67:2147–53.Google Scholar
Labate, A, Gambardella, A, Andermann, E, et al. Benign mesial temporal lobe epilepsy. Nat Rev Neurol. 2011;7:237–40.Google Scholar
Aguglia, U, Gambardella, A, Le Piane, E, et al. Mild non-lesional temporal lobe epilepsy. A common unrecognized disorder with onset in adulthood. Can J Neurol Sci. 1998;25:282–6.Google Scholar
Gambardella, A, Manna, I, Labate, A, et al. GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. Neurology. 2003;60:560–3.Google Scholar
Labate, A, Ventura, P, Gambardella, A, et al. MRI evidence of mesial temporal sclerosis in sporadic “benign” temporal lobe epilepsy. Neurology. 2006;66:562–5.Google Scholar
Labate, A, Aguglia, U, Tripepi, G, et al. Long-term outcome of mild mesial temporal lobe epilepsy: a prospective longitudinal cohort study. Neurology. 2016;86:1904–10.Google Scholar
Pitkänen, A, Löscher, W, Vezzani, A, et al. Advances in the development of biomarkers for epilepsy. Lancet Neurol. 2016;15:843–56.Google Scholar
Engel, J Jr, Pitkänen, A, Loeb, JA, et al. Epilepsy biomarkers. Epilepsia. 2013;54(S4):S61–9.Google Scholar
Berkovic, SF, McIntosh, A, Howell, RA, Mitchell, A, Sheffield, LJ, Hopper, JL Familial temporal lobe epilepsy: a common disorder identified in twins. Ann Neurol. 1996;40:227–35.Google Scholar
Crompton, DE, Scheffer, IE, Taylor, I, et al. Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. Brain. 2010;133:3221–31.CrossRefGoogle ScholarPubMed
Gambardella, A, Messina, D, Le Piane, E, et al. Familial temporal lobe epilepsy. Autosomal dominant inheritance in a large pedigree from southern Italy. Epilepsy Res. 2000;38:127–32.Google Scholar
Kobayashi, E, D’Agostino, MD, Lopes-Cendes, I, et al. Hippocampal atrophy and T2 weighted signal changes in familial mesial temporal lobe epilepsy. Neurology. 2003;60:405–9.Google Scholar
Hedera, P, Blair, MA, Andermann, E, et al. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Neurology. 2007;68:2107–12.Google Scholar
Dibbens, LM, de Vries, B, Donatello, S, et al. Mutations in DEPDC5 cause familial focal epilepsy with variable foci. Nat Genet. 2013;45:546–51.Google Scholar
Colosimo, E, Gambardella, A, Mantegazza, M, et al. Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation. Epilepsia. 2007;48:1691–6.Google Scholar
Scheffer, IE, Harkin, LA, Grinton, BE, et al. Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. Brain. 2007;130:100–9.Google Scholar
Al-Asmi, A, Jansen, AC, Badhwar, A, et al. Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis. Epilepsia. 2005;46:1256–63.Google Scholar
Gottesman, II, Gould, TD The endophenotype concept in psychiatry: etymology and strategic intentions. Am J Psychiatry. 2003;160:636–45.CrossRefGoogle ScholarPubMed
Hasler, G, Drevets, WC, Gould, TD, Gottesman, II, Manji, HK Toward constructing an endophenotype strategy for bipolar disorders. Biol Psychiatry. 2006;60:93–105.Google Scholar
Hashimoto, R, Ohi, K, Yamamori, H, et al. Imaging genetics and psychiatric disorders. Curr Mol Med. 2015;15:168–75.Google Scholar
Medland, SE, Jahanshad, N, Neale, BM, Thompson, PM Whole-genome analyses of whole-brain data: working within an expanded search space. Nat Neurosci. 2014;17:791–800.CrossRefGoogle ScholarPubMed
Thompson, PM, Cannon, TD, Narr, KL, et al. Genetic influences on brain structure. Nat Neurosci. 2001;4:1253–8.Google Scholar
Tsai, MH, Pardoe, HR, Perchyonok, Y, et al. Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomaly. Neurology. 2013;81:144–9.Google Scholar
Jackson, GD, McIntosh, AM, Briellmann, RS, Berkovic, SF Hippocampal sclerosis studied in identical twins. Neurology. 1998;51:78–84.Google Scholar
Fernández, G, Effenberger, O, Vinz, B, et al. Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis. Neurology. 1998;50:909–17.Google Scholar
Kobayashi, E, Li, LM, Lopes-Cendes, I, Cendes, F. Magnetic resonance imaging evidence of hippocampal sclerosis in asymptomatic, first-degree relatives of patients with familial mesial temporal lobe epilepsy. Arch Neurol. 2002;59:1891–4.Google Scholar
Sisodiya, SM, Ragge, NK, Cavalleri, GL, et al. Role of SOX2 mutations in human hippocampal malformations and epilepsy. Epilepsia. 2006;47:534–42.Google Scholar
Bernasconi, N, Kinay, D, Andermann, F, Antel, S, Bernasconi, A. Analysis of shape and positioning of the hippocampal formation: an MRI study in patients with partial epilepsy and healthy controls. Brain. 2005;128:2442–52.Google Scholar
Bernhardt, BC, Worsley, KJ, Kim, H, Evans, AC, Bernasconi, A, Bernasconi, N. Longitudinal and cross-sectional analysis of atrophy in pharmacoresistant temporal lobe epilepsy. Neurology. 2009;72:1747–54.Google Scholar
Bernhardt, BC, Bernasconi, N, Concha, L, Bernasconi, A. Cortical thickness analysis in temporal lobe epilepsy: reproducibility and relation to outcome. Neurology. 2010;74:1776–84.Google Scholar
Labate, A, Cerasa, A, Aguglia, U, Mumoli, L, Quattrone, A, Gambardella, A. Neocortical thinning in “benign” mesial temporal lobe epilepsy. Epilepsia. 2011;52:712–7.Google Scholar
Bast, T, Feldon, J. Hippocampal modulation of sensorimotor processes. Prog Neurobiol. 2003;70:319–45.CrossRefGoogle ScholarPubMed
Labate, A, Cerasa, A, Gambardella, A, Aguglia, U, Quattrone, A. Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study. Neurology. 2008;71:1094–101.Google Scholar
Alhusaini, S, Scanlon, C, Ronan, L, et al. Heritability of subcortical volumetric traits in mesial temporal lobe epilepsy. PLOS ONE. 2013;8:e61880.Google Scholar
Labate, A, Cherubini, A, Tripepi, G, et al. White matter abnormalities differentiate severe from benign temporal lobe epilepsy. Epilepsia. 2015;56:1109–16.Google Scholar
Caligiuri, ME, Labate, A, Cherubini, A, et al. Integrity of the corpus callosum in patients with benign temporal lobe epilepsy. Epilepsia 2016;57:590–6.Google Scholar
International League Against Epilepsy Consortium on Complex Epilepsies. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. Lancet Neurol. 2014;13:893–903.Google Scholar
Whelan, CD, Altmann, A, Botía, JA, et al. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study. Brain. 2018;141:391–408.Google Scholar
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