A novel locus for familial migraine on Xp22

Headache

Volumn 50, Issue 6, 2010, Pages 955-962

  Wieser, Thomas ^a,d   Pascual, Julio ^b   Oterino, Agusto ^b   Soso, Michael ^d   Barmada, Michael ^c   Gardner, Kathy L ^d  

^a Department of Neurology KH Göttlicher Heiland ^*  (Austria)

^b HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^c UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^d UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

Genetic linkage; Migraine; X chromosome

Indexed keywords

ARTICLE; CHROMOSOME XP; COMPUTER PROGRAM; FAMILY STUDY; FEMALE; GENE LOCUS; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; PEDIGREE; PRIORITY JOURNAL; SEX RATIO; X CHROMOSOME LINKED DISORDER; ALLELE; FAMILY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; X CHROMOSOME;

ALLELES; CHROMOSOMES, HUMAN, X; FAMILY; GENETIC LINKAGE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; LOD SCORE; MIGRAINE DISORDERS;

EID: 77953210083     PISSN: 00178748     EISSN: 15264610     Source Type: Journal    
DOI: 10.1111/j.1526-4610.2010.01673.x     Document Type: Article

References (40)

1. Rasmussen BK, Jensen R, Schroll M, Olesen J. Epidemiology of headache in a general population - A prevalence study. J Clin Epidemiol. 1991 44 : 1147 1157.
2. Stovner LJ, Hagen K. Prevalence, burden, and cost of headache disorders. Curr Opin Neurol. 2006 19 : 281 285.
3. Hu XH, Markson LE, Lipton RB, Stewart WF, Berger ML. Burden of migraine in the United States: Disability and economic costs. Arch Intern Med. 1999 159 : 813 818.
4. Ducros A, Denier C, Joutel A, et al. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med. 2001 345 : 17 24.
5. Kallela M, Wessman M, Havanka H, Palotie A, Farkkila M. Familial migraine with and without aura: Clinical characteristics and co-occurrence. Eur J Neurol. 2001 8 : 441 449.
6. Ligthart L, Boomsma DI, Martin NG, Stubbe JH, Nyholt DR. Migraine with aura and migraine without aura are not distinct entities: Further evidence from a large Dutch population study. Twin Res Hum Genet. 2006 9 : 54 63.
7. Nyholt DR, Gillespie NG, Heath AC, Merikangas KR, Duffy DL, Martin NG. Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities. Genet Epidemiol. 2004 26 : 231 244.
8. de Vries B, Frants RR, Ferrari MD, van den Maagdenberg AM. Molecular genetics of migraine. Hum Genet. 2009 126 : 115 132.
9. Gardner K, Barmada MM, Ptacek LJ, Hoffman EP. A new locus for hemiplegic migraine maps to chromosome 1q31. Neurology. 1997 49 : 1231 1238.
10. De Fusco M, Marconi R, Silvestri L, et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet. 2003 33 : 192 196.
11. Wessman M, Terwindt GM, Kaunisto MA, Palotie A, Ophoff RA. Migraine: A complex genetic disorder. Lancet Neurol. 2007 6 : 521 532.
12. Gervil M, Ulrich V, Kyvik KO, Olesen J, Russell MB. Migraine without aura: A population-based twin study. Ann Neurol. 1999 46 : 606 611.
13. Mulder EJ, Van Baal C, Gaist D, et al. Genetic and environmental influences on migraine: A twin study across six countries. Twin Res. 2003 6 : 422 431.
14. Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell. 1996 87 : 543 552.
15. Vanmolkot KR, Kors EE, Hottenga JJ, et al. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol. 2003 54 : 360 366.
16. Dichgans M, Freilinger T, Eckstein G, et al. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet. 2005 366 : 371 377.
17. May A, Ophoff RA, Terwindt GM, et al. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Hum Genet. 1995 96 : 604 608.
18. Lea RA, Shepherd AG, Curtain RP, et al. A typical migraine susceptibility region localizes to chromosome 1q31. Neurogenetics. 2002 4 : 17 22.
19. Ophoff RA, Terwindt GM, Ferrari MD, Sandkuijl L, Frants RR. Involvement of the P/Q-type Ca+2 channel alpha1A subunit (CACNL1A4) gene region on 19p13 in migraine with and without aura. Am J Hum Genet. 1997 61 : 1590.
20. Nyholt DR, Curtain RP, Griffiths LR. Familial typical migraine: Significant linkage and localization of a gene to Xq24-28. Hum Genet. 2000 107 : 18 23.
21. Todt U, Dichgans M, Jurkat-Rott K, et al. Rare missense variants in ATP1A2 in families with clustering of common forms of migraine. Hum Mutat. 2005 26 : 315 321.
22. Wieser T, Mueller CR, Evers S, Zierz S, Deufel T. Absence of FHM mutations in common forms of migraine. Clin Chem Lab Med. 2003 41 : 272 275.
23. Kim JS, Yue Q, Jen JC, Nelson SF, Baloh RW. Familial migraine with vertigo: No mutations found in CACNA1A. Am J Med Genet. 1998 79 : 148 151.
24. Ulrich V, Olesen J, Gervil M, Russell MB. Possible risk factors and precipitants for migraine with aura in discordant twin-pairs: A population-based study. Cephalalgia. 2000 20 : 821 825.
25. McCarthy LC, Hosford DA, Riley JH, et al. Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. Genomics. 2001 78 : 135 149.
26. Rasmussen BK. Migraine and tension-type headache in a general population: Precipitating factors, female hormones, sleep pattern and relation to lifestyle. Pain. 1993 53 : 65 72.
27. Russell BM, Olesen J. The genetics of migraine without aura and migraine with aura. Cephalalgia. 1993 13 : 245 248.
28. Stewart WF, Staffa J, Lipton RB, Ottman R. Familial risk of migraine: A population-based study. Ann Neurol. 1997 41 : 166 172.
29. Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders: 2nd edition. Cephalalgia. 2004 24 (Suppl. 1 9 160.
30. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988 16 : 7207 7221.
31. O'Connell JR, Weeks DE. PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet. 1998 63 : 259 266.
32. Wessman M, Kallela M, Kaunisto MA, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet. 2002 70 : 652 662.
33. Franco B, Guioli S, Pragliola A, et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature. 1991 353 : 529 536.
34. Ferrante MI, Giorgio G, Feather SA, et al. Identification of the gene for oral-facial-digital type I syndrome. Am J Hum Genet. 2001 68 : 569 576.
35. van Slegtenhorst MA, Bassi MT, Borsani G, et al. A gene from the Xp22.3 region shares homology with voltage-gated chloride channels. Hum Mol Genet. 1994 3 : 547 552.
36. Song KK, Feingold E, Weeks DE. Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees. Am J Hum Genet. 2002 70 : 181 191.
37. Lander E, Kruglyak L. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nat Genet. 1995 11 : 241 247.
38. Ulrich V, Gervil M, Kyvik KO, Olesen J, Russell MB. Evidence of a genetic factor in migraine with aura: A population-based Danish twin study. Ann Neurol. 1999 45 : 242 246.
39. Ferrari MD. Migraine. Lancet. 1998 351 : 1043 1051.
40. Bjornsson A, Gudmundsson G, Gudfinnsson E, et al. Localization of a gene for migraine without aura to chromosome 4q21. Am J Hum Genet. 2003 73 : 986 993.