Genetics of migraine: An update

Headache

Volumn 46, Issue SUPPL. 1, 2006, Pages

  Gardner, Kathy L ^a  

^a UNIVERSITY OF PITTSBURGH MEDICAL CENTER   (United States)

Author keywords

Genetics; Headache; Migraine

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); APOLIPOPROTEIN E; CALCIUM CHANNEL; CYTOCHROME P450 2D6; DIPEPTIDYL CARBOXYPEPTIDASE; DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; DOPAMINE 3 RECEPTOR; DOPAMINE 4 RECEPTOR; DOPAMINE 5 RECEPTOR; DOPAMINE BETA MONOOXYGENASE; GLUTAMATE TRANSPORTER; GLUTAMIC ACID; GLUTATHIONE TRANSFERASE; GLUTATHIONE TRANSFERASE M1; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 6; LYMPHOTOXIN; SEROTONIN 1B RECEPTOR; SEROTONIN 2A RECEPTOR; SEROTONIN 2B RECEPTOR; SEROTONIN TRANSPORTER; VOLTAGE GATED SODIUM CHANNEL;

AUTOSOMAL DOMINANT INHERITANCE; CONFERENCE PAPER; ENVIRONMENTAL FACTOR; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY STUDY; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENETIC SUSCEPTIBILITY; GENOME; HERITABILITY; HUMAN; MIGRAINE; PHENOTYPE; PRIORITY JOURNAL; SPREADING CORTICAL DEPRESSION; TWINS;

CALCIUM CHANNELS; FEMALE; HUMANS; MALE; MIGRAINE DISORDERS; NA(+)-K(+)-EXCHANGING ATPASE; PEDIGREE; TWIN STUDIES;

EID: 33646926107     PISSN: 00178748     EISSN: 15264610     Source Type: Journal    
DOI: 10.1111/j.1526-4610.2006.00486.x     Document Type: Conference Paper

References (37)

1. Lipton RB, Stewart WF, Diamond S, Diamond ML, Reed M. Prevalence and burden of migraine in the United States: Data from the American Migraine Study II. Headache. 2001 41:646 657.
2. Wessman M, Kaunisto MA, Kallela M, Palotie A. The molecular genetics of migraine. Ann Med. 2004 36:462 473.
3. Gardner K. The genetic basis of migraine: How much do we know¿ Can J Neurol Sci. 1999 26 suppl 3 S37 S43.
4. Estevez M, Gardner KL. Update on the genetics of migraine. Hum Genet. 2004 114:225 235.
5. Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr., Hawkes R, Frankel WN, et al. Absence of epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 87:607 617.
6. Ayata C, Shimizu-Sasamata M, Lo EH, Noebels JL, Moskowitz MA. Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha-1A subunit of P/Q type calcium channels. Neuroscience. 2000 95:639 645.
7. Jen JC, Wan J, Palos TP, Howard BD, Baloh RW. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegic, and seizures. Neurology. 2005 65:529 534.
8. Dichgans M, Freilinger T, Eckstein G, Babini E, Lorenz-Depiereux B, Biskup S, et al. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet. 2005 366:371 377.
9. Bassoe P. Migraine. JAMA. 1933 101:599 605.
10. Selby G, Lance JW. Observations on 500 cases of migraine and allied vascular headache. N Neurol Neurosurg Psychiatr. 1960 23:23 32.
11. Bille B. Migraine in school children. A study of the incidence and short-term prognosis, and a clinical, psychological, and electroencephalographic comparison between children with migraine and matched controls. Acta Paediatr. 1962 51 suppl 136
12. Sorensen SA, Araki S. Genetics. In:Olesen J, Tfelt-Hansen P, Welch KMA, eds. The Headaches. New York:Raven Press Ltd, 1991 21 26.
13. Waters WE. Migraine: intelligence, social class, and familial prevalence. Br Med J. 1971 2:77 81.
14. Russell MB, Olesen J. Increased familial risk and evidence of genetic factor in migraine. Br Med J. 1995 311:541 544.
15. Russell MB, Iselius L, Olesen J. Inheritance of migraine investigated by complex segregation analysis. Hum Genet. 1995 96:726 730.
16. Merikangas KR, Tierney C, Martin NG, Heath AC. The genetics of migraine in the Australian Twin Registry. In:Rose F, ed. New Advances in Headache Research. London:Smith Gordon & Co., 1994 27.
17. Larsson B, Bille B, Pederson NL. Genetic influence in headaches: A Swedish twin study. Headache. 1995 35:513 519.
18. Honkasalo ML, Kaprio J, Winter T, Heikkila K, Sillanpaa M, Kaskenvuo M. Migraine and concomitant symptoms among 8167 adult twin pairs. Headache. 1995 35:70 78.
19. Gervil M, Ulrich V, Kaprio J, Olesen J, Russell MB. The relative role of genetic and environmental factors in migraine without aura. Neurology. 1999 53:995 999.
20. 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.
21. Lucas RN. Migraine in twins. J Psychosom Res. 1977 20:147 156.
22. Harvald B, Hauge M. A catamnestic investigation of Danish twins. Danish Med Bull. 1956 3:150 158.
23. Mulder EJ, Van Baal C, Gaist D, Kallela M, Raprio J, Svensson DA, et al. Genetic and environmental influences on migraine: A twin study across six countries. Twin Res. 2003 6:422 431.
24. Ziegler DK, Hur YM, Bouchard TJ Jr., Hassanein RS, Barter R. Migraine in twins raised together and apart. Headache. 1998 38:417 422.
25. Svensson DA, Larsson B, Waldenlind E, Pedersen NL. Shared rearing environment in migraine: Results from twins reared apart and twins reared together. Headache. 2003 43:235 244.
26. Wessman M, Kallela M, Kaunisto MA, Marttile P, Sobel E, Hortiala J, et al. A susceptibility locus for migraine with aura, on chromosome 4924. Am J Hum Genet. 2002 70:652 662.
27. Carlsson A, Forsgren L, Nylander PO, Hellman U, Forsman-Semb K, Holmgren G, et al. Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1. Neurology. 2002 59:1804 1807.
28. Soragna D, Vettori A, Carraro G, Marchioni E, Vazza G, Bellini S, et al. A locus for migraine without aura maps on chromosome 14q21.2-q22.3. Am J Hum Genet. 2003 72:161 167.
29. Cader ZM, Noble-Topham SE, Dyment DA, Cherny SS, Brown JD, Rice GP, et al. Significant linkage to migraine with aura on chromosome 11q24. Hum Mol Genet. 2003 12: 2511 2517.
30. Bjornsson A, Gudmundsson G, Gudfinnsson E, Hrafnsdottir M, Benedikz J, Skuladottir S, et al. Localization of a gene for migraine without aura to chromosome 4q21. Am J Hum Genet. 2003 73: 986 993.
31. May A, Ophoff RA, Terwindt GM, Urban C, van Eijk R, Haan J, 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.
32. Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR. Familial typical migraine: Linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology. 1998 50: 1428 1432.
33. Terwindt GM, Ophoff RA, van Eijk R, Vergouwe MN, Haan J, Frants RR, et al. Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology. 2001 56:1028 1032.
34. Hovatta I, Kallela M, Farkkila M, Peltonen L. Familial migraine: Exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p. Genomics. 1994 23:707 709.
35. Lea RA, Curtain RP, Hutchins C, Brimage PJ, Griffiths LR. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. Am J Med Genet. 2001 105:707 712.
36. Noble-Topham SE, Dyment DA, Cader MZ, Ganapathy R, Brown JD, Rice GP, et al. Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13. Neurology. 2002 59:1099 1101.
37. McCarthy LC, Hosford DA, Riley JH, Bird MI, White NJ, Hewett DR, et al. Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. Genomics. 2001 78:135 149.