메뉴 건너뛰기




Volumn 26, Issue 6, 2006, Pages 731-737

Metabolic and genetic risk factors for migraine in children

Author keywords

Childhood; Folate metabolism; Migraine; Prothrombotic conditions; Risk factors

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; CYANOCOBALAMIN; FOLIC ACID; HOMOCYSTEINE; METHIONINE; PROTHROMBIN;

EID: 33745219611     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1111/j.1468-2982.2006.01107.x     Document Type: Article
Times cited : (53)

References (32)
  • 1
    • 0030903291 scopus 로고    scopus 로고
    • Association between migraine and stroke in a large-scale epidemiological study of the United States
    • Merikangas KR, Febton BT, Cheng SH, Stolar MJ, Risch N. Association between migraine and stroke in a large-scale epidemiological study of the United States. Arch Neurol 1997 54 : 362 8.
    • (1997) Arch Neurol , vol.54 , pp. 362-8
    • Merikangas, K.R.1    Febton, B.T.2    Cheng, S.H.3    Stolar, M.J.4    Risch, N.5
  • 3
    • 0029792843 scopus 로고    scopus 로고
    • Migraine and stroke: a possible complication of both migraine with and without aura
    • Narbone MC, Leggiadro N, La Spina P, Rao R, Grugno R, Musolino R. Migraine and stroke: a possible complication of both migraine with and without aura. Headache 1996 36 : 481 3.
    • (1996) Headache , vol.36 , pp. 481-3
    • Narbone, M.C.1    Leggiadro, N.2    La Spina, P.3    Rao, R.4    Grugno, R.5    Musolino, R.6
  • 4
    • 0022481380 scopus 로고
    • Stroke and migraine in the Oxfordshire Community Stroke Project
    • Henrich JB, Sandercock PA, Warlow CP, Jones LN. Stroke and migraine in the Oxfordshire Community Stroke Project. J Neurol 1986 233 : 257 62.
    • (1986) J Neurol , vol.233 , pp. 257-62
    • Henrich, J.B.1    Sandercock, P.A.2    Warlow, C.P.3    Jones, L.N.4
  • 5
    • 1442265540 scopus 로고    scopus 로고
    • The international classification of headache disorders
    • 2nd edition
    • Headache Classification Committee of the International Headache Society. The international classification of headache disorders, 2nd edition. Cephalalgia 2004 24 ( Suppl. 1 32 3.
    • (2004) Cephalalgia , vol.24 , Issue.1 , pp. 32-3
  • 6
    • 0032815149 scopus 로고    scopus 로고
    • Ischemic stroke and migraine in childhood: coincidence or causal relation?
    • Ebinger F, Boor R, Gawehn J, Reitter B. Ischemic stroke and migraine in childhood: coincidence or causal relation?. J Child Neurol 1999 14 : 451 5.
    • (1999) J Child Neurol , vol.14 , pp. 451-5
    • Ebinger, F.1    Boor, R.2    Gawehn, J.3    Reitter, B.4
  • 7
    • 33745213281 scopus 로고    scopus 로고
    • Relationship between migraine and stroke in paediatric age
    • Rossi LN. Relationship between migraine and stroke in paediatric age. J Headache Pain 2004 5 : 56.
    • (2004) J Headache Pain , vol.5 , pp. 56
    • Rossi, L.N.1
  • 8
    • 0025355959 scopus 로고
    • Migraine related stroke in the context of the International Headache Society Classification of Head Pain
    • Welch KM, Levine SR. Migraine related stroke in the context of the International Headache Society Classification of Head Pain. Arch Neurol 1990 47 : 458 62.
    • (1990) Arch Neurol , vol.47 , pp. 458-62
    • Welch, K.M.1    Levine, S.R.2
  • 10
    • 0031840850 scopus 로고    scopus 로고
    • Role of anticardiolipin antibodies in young persons with migraine and transient focal neurologic events. A prospective study
    • Tietjen GE, Day M, Norris L, Aurora S, Halvorsen A, Schultz LR, Levine SR. Role of anticardiolipin antibodies in young persons with migraine and transient focal neurologic events. A prospective study. Neurology 1998 50 : 1433 40.
    • (1998) Neurology , vol.50 , pp. 1433-40
    • Tietjen, G.E.1    Day, M.2    Norris, L.3    Aurora, S.4    Halvorsen, A.5    Schultz, L.R.6    Levine, S.R.7
  • 11
    • 0028988219 scopus 로고
    • Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction
    • Kontula K, Ylikorkala A, Miettinen H, Vuorio A, Kauppinen-Makelin R, Hamalainen L et al. Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction. Thromb Haemost 1995 73 : 558 60.
    • (1995) Thromb Haemost , vol.73 , pp. 558-60
    • Kontula, K.1    Ylikorkala, A.2    Miettinen, H.3    Vuorio, A.4    Kauppinen-Makelin, R.5    Hamalainen, L.6
  • 12
    • 0032525101 scopus 로고    scopus 로고
    • Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
    • De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998 91 : 3562 5.
    • (1998) Blood , vol.91 , pp. 3562-5
    • De Stefano, V.1    Chiusolo, P.2    Paciaroni, K.3    Casorelli, I.4    Rossi, E.5    Molinari, M.6
  • 13
    • 0034606262 scopus 로고    scopus 로고
    • The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine
    • Kowa H, Yasui K, Takeshima T, Urakami K, Sakai F, Nakashima K. The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine. Am J Med Genet 2000 96 : 762 4.
    • (2000) Am J Med Genet , vol.96 , pp. 762-4
    • Kowa, H.1    Yasui, K.2    Takeshima, T.3    Urakami, K.4    Sakai, F.5    Nakashima, K.6
  • 14
    • 4243070837 scopus 로고    scopus 로고
    • The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura
    • Lea RA, Ovcaric M, Sundholm J, MacMillan J, Griffiths LR. The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura. BMC Med 2004 2 : 3.
    • (2004) BMC Med , vol.2 , pp. 3
    • Lea, R.A.1    Ovcaric, M.2    Sundholm, J.3    MacMillan, J.4    Griffiths, L.R.5
  • 16
  • 17
    • 0347296358 scopus 로고    scopus 로고
    • Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk
    • Kara I, Sazci A, Ergul E, Kaya G, Kilic G. Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk. Brain Res Mol Brain Res 2003 111 : 84 0.
    • (2003) Brain Res Mol Brain Res , vol.111 , pp. 84-0
    • Kara, I.1    Sazci, A.2    Ergul, E.3    Kaya, G.4    Kilic, G.5
  • 18
    • 11844305001 scopus 로고    scopus 로고
    • Risk of ischaemic stroke in people with migraine: systematic review and meta-analysis of observational studies
    • Etminan M, Takkouche B, Isorna FC, Samii A. Risk of ischaemic stroke in people with migraine: systematic review and meta-analysis of observational studies. BMJ 2005 330 : 345.
    • (2005) BMJ , vol.330 , pp. 345
    • Etminan, M.1    Takkouche, B.2    Isorna, F.C.3    Samii, A.4
  • 19
    • 0002882576 scopus 로고
    • Diagnostic criteria for headache disorders, cranial neuralgias and facial pain
    • Headache Classification Committee of the International Headache Society.
    • Headache Classification Committee of the International Headache Society. Diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988 8 ( Suppl. 7 20.
    • (1988) Cephalalgia , vol.8 , Issue.7 SUPPL. , pp. 20
  • 20
    • 0028964549 scopus 로고
    • Applicability of the 1988 IHS criteria to headache patients under the age of 18 years attending 21 Italian headache clinics. Juvenile Headache Collaborative Study Group
    • Gallai V, Sarchielli P, Carboni F, Benedetti P, Mastropaolo C, Puca F. Applicability of the 1988 IHS criteria to headache patients under the age of 18 years attending 21 Italian headache clinics. Juvenile Headache Collaborative Study Group. Headache 1995 35 : 146 53.
    • (1995) Headache , vol.35 , pp. 146-53
    • Gallai, V.1    Sarchielli, P.2    Carboni, F.3    Benedetti, P.4    Mastropaolo, C.5    Puca, F.6
  • 21
    • 0034453037 scopus 로고    scopus 로고
    • Migraine without aura and migrainous disorder in children; International Headache Society (IHS) and revised IHS criteria
    • Cano A, Palomeras E, Alfonso S, Ortega D, Sanz P, Fossas P. Migraine without aura and migrainous disorder in children; International Headache Society (IHS) and revised IHS criteria. Cephalalgia 2000 20 : 617 20.
    • (2000) Cephalalgia , vol.20 , pp. 617-20
    • Cano, A.1    Palomeras, E.2    Alfonso, S.3    Ortega, D.4    Sanz, P.5    Fossas, P.6
  • 23
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995 10 : 111 3.
    • (1995) Nat Genet , vol.10 , pp. 111-3
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    Goyette, P.4    Sheppard, C.A.5    Matthews, R.G.6
  • 24
    • 0000453852 scopus 로고    scopus 로고
    • Reply to Donnelly
    • Letter to Editor
    • Van der Put NM, Blom HJ. Reply to Donnelly. Am J Hum Genet 2000 66 : 744 5 (Letter to Editor).
    • (2000) Am J Hum Genet , vol.66 , pp. 744-5
    • Van Der Put, N.M.1    Blom, H.J.2
  • 25
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996 88 : 3698 03.
    • (1996) Blood , vol.88 , pp. 3698-03
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 26
    • 0029050714 scopus 로고
    • Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in Factor V in 113 unrelated symptomatic protein C deficient patients. The French Network on the behalf of INSERM
    • Gandrille S, Greengard JS, Alhenc-Gelas M, Juhan-Vague I, Abgrall JF, Jude B et al. Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in Factor V in 113 unrelated symptomatic protein C deficient patients. The French Network on the behalf of INSERM. Blood 1995 86 : 219 24.
    • (1995) Blood , vol.86 , pp. 219-24
    • Gandrille, S.1    Greengard, J.S.2    Alhenc-Gelas, M.3    Juhan-Vague, I.4    Abgrall, J.F.5    Jude, B.6
  • 27
    • 0032545257 scopus 로고    scopus 로고
    • Determination of plasma and serum homocysteine by high-performance liquid chromatography with fluorescence detection
    • Minniti G, Piana A, Armani U, Cerone R. Determination of plasma and serum homocysteine by high-performance liquid chromatography with fluorescence detection. J Chromatogr A 1998 828 : 401 5.
    • (1998) J Chromatogr A , vol.828 , pp. 401-5
    • Minniti, G.1    Piana, A.2    Armani, U.3    Cerone, R.4
  • 28
    • 0035987006 scopus 로고    scopus 로고
    • Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
    • De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH et al. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet 2002 47 : 319 24.
    • (2002) J Hum Genet , vol.47 , pp. 319-24
    • De Marco, P.1    Calevo, M.G.2    Moroni, A.3    Arata, L.4    Merello, E.5    Finnell, R.H.6
  • 29
    • 0031687887 scopus 로고    scopus 로고
    • A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
    • Weisberg I, Tran P, Christensen B, Sibani S, Rozen R. A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 1998 64 : 169 72.
    • (1998) Mol Genet Metab , vol.64 , pp. 169-72
    • Weisberg, I.1    Tran, P.2    Christensen, B.3    Sibani, S.4    Rozen, R.5
  • 30
    • 0032822750 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population
    • Rady PL, Tyring SK, Hudnall SD, Vargas T, Kellner LH, Nitowsky H, Matalon RK. Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population. Am J Med Genet 1999 86 : 380 4.
    • (1999) Am J Med Genet , vol.86 , pp. 380-4
    • Rady, P.L.1    Tyring, S.K.2    Hudnall, S.D.3    Vargas, T.4    Kellner, L.H.5    Nitowsky, H.6    Matalon, R.K.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.