Evidence for a shared genetic susceptibility to migraine and epilepsy

Epilepsia

Volumn 54, Issue 2, 2013, Pages 288-295

  Winawer, Melodie R ^a   Connors, Robert ^a,b  

^a Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^b Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

Comorbidity; Epilepsy; Genetic; Migraine; Seizure

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; FAMILY HISTORY; FEMALE; FOCAL EPILEPSY; GENERALIZED EPILEPSY; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MATHEMATICAL COMPUTING; MATHEMATICAL MODEL; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; PRIORITY JOURNAL; RELATIVE; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; DATA COLLECTION; DNA; ELECTROENCEPHALOGRAPHY; EPILEPSIES, PARTIAL; EPILEPSY; EPILEPSY, GENERALIZED; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME; HUMANS; MALE; MIDDLE AGED; MIGRAINE DISORDERS; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; NEUROIMAGING; PHENOTYPE; YOUNG ADULT;

EID: 84873405661     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/epi.12072     Document Type: Article

References (34)

1. Andermann E, Andermann F,. (1987) Migraine-epilepsy relationships: epidemiological and genetic aspects. In, Andermann F, Lugaresi E, (Eds) Migraine and epilepsy. Butterworths, Boston, MA, pp. 281-291.
2. Andermann F, Lugaresi E,. (1987) Migraine and epilepsy. Butterworths, Boston, MA.
3. Baca CB, Vickrey BG, Caplan R, Vassar SD, Berg AT,. (2011) Psychiatric and medical comorbidity and quality of life outcomes in childhood-onset epilepsy. Pediatrics 128: e1532-e1543.
4. Brodtkorb E, Bakken IJ, Sjaastad O,. (2008) Comorbidity of migraine and epilepsy in a Norwegian community. Eur J Neurol 15: 1421-1423.
5. Christensen J, Vestergaard M, Mortensen PB, Sidenius P, Agerbo E,. (2007) Epilepsy and risk of suicide: a population-based case-control study. Lancet Neurol 6: 693-698.
6. Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P,. (2001) De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet 68: 1327-1332.
7. Clarke T, Baskurt Z, Strug L, Pal D,. (2009) Evidence of shared genetic risk factors for migraine and rolandic epilepsy. Epilepsia 50: 2428-2433.
8. Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P,. (2007) Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q. Neurology 68: 1995-2002.
9. Deprez L, Weckhuysen S, Peeters K, Deconinck T, Claeys KG, Claes LR, Suls A, Van Dyck T, Palmini A, Matthijs G, Van Paesschen W, De Jonghe P,. (2008) Epilepsy as part of the phenotype associated with ATP1A2 mutations. Epilepsia 49: 500-508.
10. Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, Ferrari MD, Herzog J, van den Maagdenberg AM, Pusch M, Strom TM,. (2005) Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet 366: 371-377.
11. Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A,. (2000) Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet 24: 343-345.
12. Gilliam F, Hecimovic H, Sheline Y,. (2003) Psychiatric comorbidity, health, and function in epilepsy. Epilepsy Behav 4 (Suppl. 4): S26-S30.
13. Hitiris N, Mohanraj R, Norrie J, Sills GJ, Brodie MJ,. (2007) Predictors of pharmacoresistant epilepsy. Epilepsy Res 75: 192-196.
14. Imbrici P, Jaffe SL, Eunson LH, Davies NP, Herd C, Robertson R, Kullmann DM, Hanna MG,. (2004) Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia. Brain 127: 2682-2692.
15. Headache Classification Subcommittee of the International Headache Society. (2004) The International Classification of Headache Disorders: 2nd edition. Cephalalgia 24 (Suppl. 1): 9-160.
16. Jensen FE,. (2011) Epilepsy as a spectrum disorder: implications from novel clinical and basic neuroscience. Epilepsia 52 (Suppl. 1): 1-6.
17. Johnson MR, Shorvon SD,. (2011) Heredity in epilepsy: neurodevelopment, comorbidity, and the neurological trait. Epilepsy Behav 22: 421-427.
18. Kanner AM,. (2007) Epilepsy and mood disorders. Epilepsia 48: 20-22.
19. Kanner AM,. (2009) Psychiatric issues in epilepsy: the complex relation of mood, anxiety disorders, and epilepsy. Epilepsy Behav 15: 83-87.
20. Lipton RB, Stewart WF, Diamond S, Diamond ML, Reed M,. (2001) Prevalence and burden of migraine in the United States: data from the American Migraine Study II. Headache 41: 646-657.
21. Ludvigsson P, Hesdorffer D, Olafsson E, Kjartansson O, Hauser WA,. (2006) Migraine with aura is a risk factor for unprovoked seizures in children. Ann Neurol 59: 210-213.
22. Mula M,. (2012) Epilepsy: bidirectional link between epilepsy and psychiatric disorders. Nat Rev Neurol 8: 252-253.
23. Nesbitt G, McKenna K, Mays V, Carpenter A, Miller K, Williams M, The EPGP Investigators. (2012) The Epilepsy Phenome/Genome Project (EPGP) informatics platform. Int J Med Inform May 10 [Epub ahead of print].
24. Ottman R, Lipton RB,. (1994) Comorbidity of migraine and epilepsy. Neurology 44: 2105-2110.
25. Ottman R, Lipton RB,. (1996) Is the comorbidity of epilepsy and migraine due to a shared genetic susceptibility? Neurology 47: 918-924.
26. Ottman R, Hauser WA, Stallone L,. (1990) Semistructured interview for seizure classification: agreement with physicians' diagnoses. Epilepsia 31: 110-115.
27. Ottman R, Hong S, Lipton RB,. (1993a) Validity of family history data on severe headache and migraine. Neurology 43: 1954-1960.
28. Ottman R, Lee JH, Hauser WA, Hong S, Hesdorffer D, Schupf N, Pedley TA, Scheuer ML,. (1993b) Reliability of seizure classification using a semistructured interview. Neurology 43: 2526-2530.
29. Ottman R, Barker-Cummings C, Leibson CL, Vasoli VM, Hauser WA, Buchhalter JR,. (2011) Accuracy of family history information on epilepsy and other seizure disorders. Neurology 76: 390-396.
30. Panayiotopoulos CP, Michael M, Sanders S, Valeta T, Koutroumanidis M,. (2008) Benign childhood focal epilepsies: assessment of established and newly recognized syndromes. Brain 131: 2264-2286.
31. Polvi A, Siren A, Kallela M, Rantala H, Artto V, Sobel EM, Palotie A, Lehesjoki AE, Wessman M,. (2012) Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3. Neurology 78: 202-209.
32. Stewart WF, Wood C, Reed ML, Roy J, Lipton RB,. (2008) Cumulative lifetime migraine incidence in women and men. Cephalalgia 28: 1170-1178.
33. Tellez-Zenteno JF, Matijevic S, Wiebe S,. (2005) Somatic comorbidity of epilepsy in the general population in Canada. Epilepsia 46: 1955-1962.
34. Wirrell EC, Hamiwka LD,. (2006) Do children with benign rolandic epilepsy have a higher prevalence of migraine than those with other partial epilepsies or nonepilepsy controls? Epilepsia 47: 1674-1681.