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Volumn 5, Issue 2, 2010, Pages 80-85

MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE ε4 gene polymorphisms are not associated with spontaneous cervical artery dissection

Author keywords

Cervical artery dissection; Genetics; Prothrombotic gene mutations

Indexed keywords

ADENINE; APOLIPOPROTEIN E4; BLOOD CLOTTING FACTOR 5 LEIDEN; CYTOSINE; ENDOTHELIAL NITRIC OXIDE SYNTHASE; GUANINE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); THROMBOCYTE FACTOR 2; THYMINE;

EID: 77951251198     PISSN: 17474930     EISSN: 17474949     Source Type: Journal    
DOI: 10.1111/j.1747-4949.2010.00412.x     Document Type: Article
Times cited : (14)

References (33)
  • 1
    • 0035932521 scopus 로고    scopus 로고
    • Spontaneous dissection of the carotid and vertebral arteries
    • Schievink WI. Spontaneous dissection of the carotid and vertebral arteries. N Engl J Med 2001, 344:898-906.
    • (2001) N Engl J Med , vol.344 , pp. 898-906
    • Schievink, W.I.1
  • 2
    • 0030033134 scopus 로고    scopus 로고
    • Cerebral infarction in people under 40 years: etiologic analysis of 300 cases prospectively evaluated
    • Barinagarrementeria F, Figueroa T, Huebe J, Cantú C. Cerebral infarction in people under 40 years: etiologic analysis of 300 cases prospectively evaluated. Cerebrovasc Dis 1996, 6:75-9.
    • (1996) Cerebrovasc Dis , vol.6 , pp. 75-79
    • Barinagarrementeria, F.1    Figueroa, T.2    Huebe, J.3    Cantú, C.4
  • 4
    • 0036193109 scopus 로고    scopus 로고
    • Spontaneous cervical artery dissection. From risk factors toward pathogenesis
    • Brandt T, Grond-Ginsbach C. Spontaneous cervical artery dissection. From risk factors toward pathogenesis. Stroke 2002, 33:657-8.
    • (2002) Stroke , vol.33 , pp. 657-658
    • Brandt, T.1    Grond-Ginsbach, C.2
  • 5
    • 0036882851 scopus 로고    scopus 로고
    • Epidemiology and pathophysiology of spontaneous cervical artery dissection
    • Guillon B, Bousser MG. Epidemiology and pathophysiology of spontaneous cervical artery dissection. J Neuroradiol 2002, 29:241-9.
    • (2002) J Neuroradiol , vol.29 , pp. 241-249
    • Guillon, B.1    Bousser, M.G.2
  • 6
    • 34047272648 scopus 로고    scopus 로고
    • Genetic approaches in the study of risk factors for cervical artery dissection
    • Grond-Ginsbach C, Debette S, Pezzini A. Genetic approaches in the study of risk factors for cervical artery dissection. Front Neurol Neurosci 2005, 20:30-43.
    • (2005) Front Neurol Neurosci , vol.20 , pp. 30-43
    • Grond-Ginsbach, C.1    Debette, S.2    Pezzini, A.3
  • 7
    • 0034630125 scopus 로고    scopus 로고
    • Hyperhomocyst(e)inemia and the increased risk of venous thromboembolism: more evidence from a case-control study
    • Langman LJ, Ray JG, Evrovski J, Yeo E, Cole DE. Hyperhomocyst(e)inemia and the increased risk of venous thromboembolism: more evidence from a case-control study. Arch Intern Med 2000, 160:961-4.
    • (2000) Arch Intern Med , vol.160 , pp. 961-964
    • Langman, L.J.1    Ray, J.G.2    Evrovski, J.3    Yeo, E.4    Cole, D.E.5
  • 8
    • 0034745239 scopus 로고    scopus 로고
    • Mild hyperhomocyst(e)inemia: a possible risk factor for cervical artery dissection
    • Gallai V, Caso V, Paciaroni M. Mild hyperhomocyst(e)inemia: a possible risk factor for cervical artery dissection. Stroke 2001, 32:714-8.
    • (2001) Stroke , vol.32 , pp. 714-718
    • Gallai, V.1    Caso, V.2    Paciaroni, M.3    et al4
  • 9
    • 8744223089 scopus 로고    scopus 로고
    • Plasma homocysteine, MTHFR C677T, CBS 844ins68pb, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections
    • Konrad C, Müller GA, Langer C. Plasma homocysteine, MTHFR C677T, CBS 844ins68pb, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections. J Neurol 2004, 251:1242-8.
    • (2004) J Neurol , vol.251 , pp. 1242-1248
    • Konrad, C.1    Müller, G.A.2    Langer, C.3    et al4
  • 10
    • 18344364639 scopus 로고    scopus 로고
    • Plasma homocysteine concentration, C677T MTHFR genotype, and 844ins68bp CBS genotype in young adults with spontaneous cervical artery dissection and atherothrombotic stroke
    • Pezzini A, Del Zotto E, Archetti S. Plasma homocysteine concentration, C677T MTHFR genotype, and 844ins68bp CBS genotype in young adults with spontaneous cervical artery dissection and atherothrombotic stroke. Stroke 2002, 33:664-9.
    • (2002) Stroke , vol.33 , pp. 664-669
    • Pezzini, A.1    Del Zotto, E.2    Archetti, S.3    et al4
  • 11
    • 33746302811 scopus 로고    scopus 로고
    • MTHFR 677TT genotype increases the risk for cervical artery dissections
    • Kloss M, Wiest T, Hyrenbach S. MTHFR 677TT genotype increases the risk for cervical artery dissections. J Neurol Neurosurg Psychiatry 2006, 77:951-2.
    • (2006) J Neurol Neurosurg Psychiatry , vol.77 , pp. 951-952
    • Kloss, M.1    Wiest, T.2    Hyrenbach, S.3    et al4
  • 12
    • 34548094049 scopus 로고    scopus 로고
    • Mild hyperhomocysteinemia and low folate concentrations as risk factors for cervical arterial dissection
    • Arauz A, Hoyos L, Cantú C. Mild hyperhomocysteinemia and low folate concentrations as risk factors for cervical arterial dissection. Cerebrovasc Dis 2007, 24:210-4.
    • (2007) Cerebrovasc Dis , vol.24 , pp. 210-214
    • Arauz, A.1    Hoyos, L.2    Cantú, C.3    et al4
  • 13
    • 45549104526 scopus 로고    scopus 로고
    • The genetics of carotid dissection: meta-analysis of a MTHFR/C677T common molecular variant
    • McColgan P, Sharma P. The genetics of carotid dissection: meta-analysis of a MTHFR/C677T common molecular variant. Cerebrovascular Dis 2008, 25:561-5.
    • (2008) Cerebrovascular Dis , vol.25 , pp. 561-565
    • McColgan, P.1    Sharma, P.2
  • 14
    • 0037458240 scopus 로고    scopus 로고
    • Congenital thrombophilic states associated with venous thrombosis: a qualitative overview and proposed classification system
    • Crowther MA, Kelton JG. Congenital thrombophilic states associated with venous thrombosis: a qualitative overview and proposed classification system. Ann Inter Med 2003, 138:128-34.
    • (2003) Ann Inter Med , vol.138 , pp. 128-134
    • Crowther, M.A.1    Kelton, J.G.2
  • 15
    • 0345367477 scopus 로고    scopus 로고
    • Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: a case-control study of 55 patients
    • Lüdemann P, Nabavi DG, Junker R. Factor V Leiden mutation is a risk factor for cerebral venous thrombosis: a case-control study of 55 patients. Stroke 1998, 29:2507-10.
    • (1998) Stroke , vol.29 , pp. 2507-2510
    • Lüdemann, P.1    Nabavi, D.G.2    Junker, R.3    et al4
  • 17
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothombin levels and an increase in venous thrombosis
    • Poort SR, Rosendal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothombin levels and an increase in venous thrombosis. Blood 1996, 88:3698-703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 18
    • 0031595694 scopus 로고    scopus 로고
    • Prothrombin gene G20210→A transition is a risk factor for cerebral venous thrombosis
    • Reuner KH, Ruf A, Grau A. Prothrombin gene G20210→A transition is a risk factor for cerebral venous thrombosis. Stroke 1998, 29:1765-9.
    • (1998) Stroke , vol.29 , pp. 1765-1769
    • Reuner, K.H.1    Ruf, A.2    Grau, A.3    et al4
  • 19
    • 0028233602 scopus 로고
    • Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene
    • Nadaud S, Bonnardeaux A, Lathrop M, Soubrier F. Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene. Biochem Biophys Res Commun 1994, 198:1027-33.
    • (1994) Biochem Biophys Res Commun , vol.198 , pp. 1027-1033
    • Nadaud, S.1    Bonnardeaux, A.2    Lathrop, M.3    Soubrier, F.4
  • 20
    • 0032753416 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in non-diabetic renal diseases
    • Wang Y, Kikuchi S, Suzuki H, Nagase S, Koyama A. Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in non-diabetic renal diseases. Nephrol Dial Transplant 1999, 14:2898-902.
    • (1999) Nephrol Dial Transplant , vol.14 , pp. 2898-2902
    • Wang, Y.1    Kikuchi, S.2    Suzuki, H.3    Nagase, S.4    Koyama, A.5
  • 21
    • 0030048029 scopus 로고    scopus 로고
    • A smoking dependent risk of coronary artery disease associated with a polymorphism of the endothelial constitutive nitric oxide synthase gene
    • Wang XL, Sim AS, Badenhop RF, Mccredie RM, Wilcken DEL. A smoking dependent risk of coronary artery disease associated with a polymorphism of the endothelial constitutive nitric oxide synthase gene. Nature Med 1996, 2:41-5.
    • (1996) Nature Med , vol.2 , pp. 41-45
    • Wang, X.L.1    Sim, A.S.2    Badenhop, R.F.3    Mccredie, R.M.4    Wilcken, D.E.L.5
  • 22
    • 1442348272 scopus 로고    scopus 로고
    • Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease
    • Hassan A, Gormley K, O'Sullivan M. Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease. Stroke 2004, 35:654-9.
    • (2004) Stroke , vol.35 , pp. 654-659
    • Hassan, A.1    Gormley, K.2    O'Sullivan, M.3    et al4
  • 24
    • 0021824223 scopus 로고
    • Role of apolipoprotein E genetic polymorphism in determining normal plasma lipid and lipoprotein variation
    • Sing CF, Davignon J. Role of apolipoprotein E genetic polymorphism in determining normal plasma lipid and lipoprotein variation. Am J Hum Genet 1985, 37:268-85.
    • (1985) Am J Hum Genet , vol.37 , pp. 268-285
    • Sing, C.F.1    Davignon, J.2
  • 25
    • 0023860891 scopus 로고
    • Apolipoprotein E polymorphism and atherosclerosis
    • Davignon J, Gregg RE, Sing SF. Apolipoprotein E polymorphism and atherosclerosis. Arteriosclerosis 1988, 8:1-21.
    • (1988) Arteriosclerosis , vol.8 , pp. 1-21
    • Davignon, J.1    Gregg, R.E.2    Sing, S.F.3
  • 26
    • 33644857332 scopus 로고    scopus 로고
    • Does apolipoproteína E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17965 controls
    • Sudlow C, Martínez González NA, Kim J, Clark C. Does apolipoproteína E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17965 controls. Stroke 2006, 37:364-70.
    • (2006) Stroke , vol.37 , pp. 364-370
    • Sudlow, C.1    Martínez González, N.A.2    Kim, J.3    Clark, C.4
  • 27
    • 0036393435 scopus 로고    scopus 로고
    • Dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism
    • Orlandi G, Fanucchi S, Mancuso M. Dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism. Eur J Neurol 2002, 1:19-21.
    • (2002) Eur J Neurol , vol.1 , pp. 19-21
    • Orlandi, G.1    Fanucchi, S.2    Mancuso, M.3    et al4
  • 28
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R. 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. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    et al4
  • 29
    • 0031205597 scopus 로고    scopus 로고
    • (1997) Multiplex PCR-mediated site-directed mutagenesis for one-step determination of factor V Leiden and G20210A transition of the prothrombin gene
    • Ripoll L, Paulin D, Thomas S, Drouet O. (1997) Multiplex PCR-mediated site-directed mutagenesis for one-step determination of factor V Leiden and G20210A transition of the prothrombin gene. Thromb Haemost 1997, 78:960-1.
    • (1997) Thromb Haemost , vol.78 , pp. 960-961
    • Ripoll, L.1    Paulin, D.2    Thomas, S.3    Drouet, O.4
  • 30
    • 0025257612 scopus 로고
    • Restriction isotoping of human apolipoprotein E by gene amplification and cleavage with Hha I
    • Hixon JE, Vernier DT. Restriction isotoping of human apolipoprotein E by gene amplification and cleavage with Hha I. J Lipid Res 1990, 31:545-7.
    • (1990) J Lipid Res , vol.31 , pp. 545-547
    • Hixon, J.E.1    Vernier, D.T.2
  • 31
    • 0345633546 scopus 로고    scopus 로고
    • Lipoprotein (a) and genetic polymorphisms of clotting factor V, Prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood
    • Nowak-Göttl U, Sträter, Heinecke A. Lipoprotein (a) and genetic polymorphisms of clotting factor V, Prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood. Blood 1999, 94:3678-82.
    • (1999) Blood , vol.94 , pp. 3678-3682
    • Nowak-Göttl, U.1    Sträter2    Heinecke, A.3    et al4
  • 32
    • 0030714108 scopus 로고    scopus 로고
    • Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease
    • Arruda VR, Annichino-Bizzacchi JM, Goncalves MS, Costa FF. Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease. Thromb Haemost 1997, 78:1430-3.
    • (1997) Thromb Haemost , vol.78 , pp. 1430-1433
    • Arruda, V.R.1    Annichino-Bizzacchi, J.M.2    Goncalves, M.S.3    Costa, F.F.4
  • 33
    • 1542347120 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene polymorphisms predict susceptibility to aneurismal subarachnoid hemorrhage and cerebral vasospasm
    • Khurana VG, Sohni YR, Mangrum WI. Endothelial nitric oxide synthase gene polymorphisms predict susceptibility to aneurismal subarachnoid hemorrhage and cerebral vasospasm. J Cereb Blood Flow Metabol 2004, 24:291-7.
    • (2004) J Cereb Blood Flow Metabol , vol.24 , pp. 291-297
    • Khurana, V.G.1    Sohni, Y.R.2    Mangrum, W.I.3    et al4


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