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Volumn 11, Issue 5, 2006, Pages 287-293

Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing loss

Author keywords

Methionine synthase; Methylenetetrahydrofolate reductase; Sudden sensorineural hearing loss; Vascular impairment

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); DNA FRAGMENT; HOMOCYSTEINE; METHIONINE SYNTHASE; RESTRICTION ENDONUCLEASE;

EID: 33749364356     PISSN: 14203030     EISSN: 14219700     Source Type: Journal    
DOI: 10.1159/000093957     Document Type: Article
Times cited : (23)

References (29)
  • 1
    • 0029066299 scopus 로고
    • A quantitative assessment of plasma homocysteine as a risk factor for vascular disease - Probable benefits of increasing folic acid intakes
    • Boushey CJ, Shirley A, Beresford A, Omenn GS, Motulsky AG: A quantitative assessment of plasma homocysteine as a risk factor for vascular disease - probable benefits of increasing folic acid intakes. JAMA 1995;274:1049-1057.
    • (1995) JAMA , vol.274 , pp. 1049-1057
    • Boushey, C.J.1    Shirley, A.2    Beresford, A.3    Omenn, G.S.4    Motulsky, A.G.5
  • 2
    • 3042822499 scopus 로고    scopus 로고
    • Low folate levels: A risk factor for sudden sensorineural hearing loss?
    • Cadoni G, Agostino S, Scipione S, Galli J: Low folate levels: a risk factor for sudden sensorineural hearing loss? Acta Otolaryngol 2004;124:608-611.
    • (2004) Acta Otolaryngol , vol.124 , pp. 608-611
    • Cadoni, G.1    Agostino, S.2    Scipione, S.3    Galli, J.4
  • 4
    • 0023688444 scopus 로고
    • Sudden hearing loss: An update
    • Cole RR, Jahrsdoerfer RA: Sudden hearing loss: an update. Am J Otol 1988;9:211-215.
    • (1988) Am J Otol , vol.9 , pp. 211-215
    • Cole, R.R.1    Jahrsdoerfer, R.A.2
  • 5
    • 0034168107 scopus 로고    scopus 로고
    • The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events
    • D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM: The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events. Thromb Haemost 2000;83:563-570.
    • (2000) Thromb Haemost , vol.83 , pp. 563-570
    • D'Angelo, A.1    Coppola, A.2    Madonna, P.3    Fermo, I.4    Pagano, A.5    Mazzola, G.6    Galli, L.7    Cerbone, A.M.8
  • 7
    • 0034747726 scopus 로고    scopus 로고
    • Increased prevalence of combined MTR and MTHFR genotypes among individuals with severely elevated total homocysteine plasma levels
    • Feix A, Fritsche-Polanz R, Kletzmayr J, Vychytil A, Horl WH, Sunder-Plassmann G, Fodinger M: Increased prevalence of combined MTR and MTHFR genotypes among individuals with severely elevated total homocysteine plasma levels. Am J Kidney Dis 2001;38:956-964.
    • (2001) Am J Kidney Dis , vol.38 , pp. 956-964
    • Feix, A.1    Fritsche-Polanz, R.2    Kletzmayr, J.3    Vychytil, A.4    Horl, W.H.5    Sunder-Plassmann, G.6    Fodinger, M.7
  • 8
    • 0032865186 scopus 로고    scopus 로고
    • A common mutation A1298C in human methylenetetrahydrofolate reductase gene: Association with plasma total homocysteine and folate concentrations
    • Friedman G, Goldschmidt N, Friedlander Y, Ben-Yehuda A, Selhub J, Babaey S, Mendel M, Kidron M, Bar-On H: A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations. J Nutr 1999;129:1656-1661.
    • (1999) J Nutr , vol.129 , pp. 1656-1661
    • Friedman, G.1    Goldschmidt, N.2    Friedlander, Y.3    Ben-Yehuda, A.4    Selhub, J.5    Babaey, S.6    Mendel, M.7    Kidron, M.8    Bar-On, H.9
  • 11
    • 0034670081 scopus 로고    scopus 로고
    • Effect of heterozygosity for the methionine synthase 2756 A->G mutation on the risk for recurrent cardiovascular events
    • Hyndman ME, Bridge PJ, Warnica JW, Fick G, Parsons HG: Effect of heterozygosity for the methionine synthase 2756 A->G mutation on the risk for recurrent cardiovascular events. Am J Cardiol 2000;86:1144-1146.
    • (2000) Am J Cardiol , vol.86 , pp. 1144-1146
    • Hyndman, M.E.1    Bridge, P.J.2    Warnica, J.W.3    Fick, G.4    Parsons, H.G.5
  • 12
    • 0142196591 scopus 로고    scopus 로고
    • The 2756A>G variant in the gene encoding methionine synthase: Its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study
    • Klerk M, Lievers KJ, Kluijtmans LA, Blom HJ, den Heijer M, Schouten EG, Kok FJ, Verhoef P: The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study. Thromb Res 2003;110:87-91.
    • (2003) Thromb Res , vol.110 , pp. 87-91
    • Klerk, M.1    Lievers, K.J.2    Kluijtmans, L.A.3    Blom, H.J.4    Den Heijer, M.5    Schouten, E.G.6    Kok, F.J.7    Verhoef, P.8
  • 15
    • 0032966833 scopus 로고    scopus 로고
    • Polymorphism of the methionine synthase gene: Association with homocysteine metabolism and late-onset vascular diseases in the Japanese population
    • Morita H, Kurihara H, Sugiyama T, Hamada C, Kurihara Y, Shindo T, Oh-hashi Y, Yazaki Y: Polymorphism of the methionine synthase gene: association with homocysteine metabolism and late-onset vascular diseases in the Japanese population. Arterioscler Thromb Vasc Biol 1999;19:298-302.
    • (1999) Arterioscler Thromb Vasc Biol , vol.19 , pp. 298-302
    • Morita, H.1    Kurihara, H.2    Sugiyama, T.3    Hamada, C.4    Kurihara, Y.5    Shindo, T.6    Oh-hashi, Y.7    Yazaki, Y.8
  • 16
    • 0020521338 scopus 로고
    • Perilymph oxygenationin sudden and progressive sensorineural hearing loss
    • Nagahara K, Fisch U, Yagi N: Perilymph oxygenationin sudden and progressive sensorineural hearing loss. Acta Otolaryngol 1983;96:57-68.
    • (1983) Acta Otolaryngol , vol.96 , pp. 57-68
    • Nagahara, K.1    Fisch, U.2    Yagi, N.3
  • 18
    • 1942453413 scopus 로고    scopus 로고
    • Platelet GPIaC807T polymorphism is associated with negative outcome of sudden hearing loss
    • Rudack C, Langer C, Junker R: Platelet GPIaC807T polymorphism is associated with negative outcome of sudden hearing loss. Hear Res 2004;191:41-48.
    • (2004) Hear Res , vol.191 , pp. 41-48
    • Rudack, C.1    Langer, C.2    Junker, R.3
  • 19
    • 0035072876 scopus 로고    scopus 로고
    • Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism
    • Salomon O, Rosenberg N, Zivelin A, Steinberg DM, Kornbrot N, Dardik R, Inbal A, Seligsohn U: Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism. Hematol J 2001;2:38-41.
    • (2001) Hematol J , vol.2 , pp. 38-41
    • Salomon, O.1    Rosenberg, N.2    Zivelin, A.3    Steinberg, D.M.4    Kornbrot, N.5    Dardik, R.6    Inbal, A.7    Seligsohn, U.8
  • 21
    • 0029035643 scopus 로고
    • Rapid, fully automated measurement of plasma homocysteine with the Abbott IMx analyzer
    • Shipchandler MT, Moore EG: Rapid, fully automated measurement of plasma homocysteine with the Abbott IMx analyzer. Clin Chem 1995;41:991-994.
    • (1995) Clin Chem , vol.41 , pp. 991-994
    • Shipchandler, M.T.1    Moore, E.G.2
  • 22
    • 0035973145 scopus 로고    scopus 로고
    • Homozygous V/V (677C to T) and D/D (2756G to A) variants in the methylene-tetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age
    • Song KS, Song JW, Choi JR, Kim HK, Shin JS, Kim JH: Homozygous V/V (677C to T) and D/D (2756G to A) variants in the methylene-tetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age. Exp Mol Med 2001;33:106-109.
    • (2001) Exp Mol Med , vol.33 , pp. 106-109
    • Song, K.S.1    Song, J.W.2    Choi, J.R.3    Kim, H.K.4    Shin, J.S.5    Kim, J.H.6
  • 23
    • 0037038824 scopus 로고    scopus 로고
    • Fibrinogen and LDL apheresis in treatment of sudden hearing loss: A randomised multicentre trial
    • Suckfüll M: Fibrinogen and LDL apheresis in treatment of sudden hearing loss: a randomised multicentre trial. Lancet 2002;360:1811-1817.
    • (2002) Lancet , vol.360 , pp. 1811-1817
    • Suckfüll, M.1
  • 24
    • 0033380439 scopus 로고    scopus 로고
    • Clinical utility of LDL-apheresis in the treatment of sudden hearing loss: A prospective, randomized study
    • Suckfüll M, Thiery J, Schorn K, Kastenbauer E, Seidel D: Clinical utility of LDL-apheresis in the treatment of sudden hearing loss: a prospective, randomized study. Acta Otolaryngol 1999;119:763-766.
    • (1999) Acta Otolaryngol , vol.119 , pp. 763-766
    • Suckfüll, M.1    Thiery, J.2    Schorn, K.3    Kastenbauer, E.4    Seidel, D.5
  • 28
    • 0032415394 scopus 로고    scopus 로고
    • The frequency of a common mutation of the methionine synthase gene in the Australian population and its relation to smoking and coronary artery disease
    • Wang XL, Cai H, Cranney G, Wilcken DEL: The frequency of a common mutation of the methionine synthase gene in the Australian population and its relation to smoking and coronary artery disease. J Cardiovasc Risk 1998;5:289-295.
    • (1998) J Cardiovasc Risk , vol.5 , pp. 289-295
    • Wang, X.L.1    Cai, H.2    Cranney, G.3    Wilcken, D.E.L.4
  • 29
    • 0032773207 scopus 로고    scopus 로고
    • Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population
    • Wang XL, Duarte N, Cai H, Adachi T, Sim AS, Cranney G, Wilcken DE: Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population. Atherosclerosis 1999;146:133-140.
    • (1999) Atherosclerosis , vol.146 , pp. 133-140
    • Wang, X.L.1    Duarte, N.2    Cai, H.3    Adachi, T.4    Sim, A.S.5    Cranney, G.6    Wilcken, D.E.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.