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Volumn 31, Issue 10, 2012, Pages 1555-1562

Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population

Author keywords

[No Author keywords available]

Indexed keywords

ARYLDIALKYLPHOSPHATASE 1; ARYLDIALKYLPHOSPHATASE 2; GLUTATHIONE PEROXIDASE 1; MANGANESE SUPEROXIDE DISMUTASE;

EID: 84867031429     PISSN: 10445498     EISSN: 15577430     Source Type: Journal    
DOI: 10.1089/dna.2012.1631     Document Type: Article
Times cited : (30)

References (45)
  • 2
    • 0035283113 scopus 로고    scopus 로고
    • Paraoxonase 1 Met-Leu 54 polymorphism is associated with Parkinson's disease
    • Akhmedova, S.N., Yakimovsky, A.K., and Schwartz, E.I. (2001). Paraoxonase 1 Met-Leu 54 polymorphism is associated with Parkinson's disease. J Neurol Sci 184, 179-182.
    • (2001) J Neurol Sci , vol.184 , pp. 179-182
    • Akhmedova, S.N.1    Yakimovsky, A.K.2    Schwartz, E.I.3
  • 5
    • 78651268075 scopus 로고    scopus 로고
    • Oxidative stress, redox homeostasis and cellular stress response in Meniere's disease: Role of vitagenes
    • Calabrese, V., Cornelius, C., Maiolino, L., Luca, M., Chiaramonte, R., Toscano, M.A., and Serra, A. (2010). Oxidative stress, redox homeostasis and cellular stress response in Meniere's disease: role of vitagenes. Neurochem Res 35, 2208-2217.
    • (2010) Neurochem Res , vol.35 , pp. 2208-2217
    • Calabrese, V.1    Cornelius, C.2    Maiolino, L.3    Luca, M.4    Chiaramonte, R.5    Toscano, M.A.6    Serra, A.7
  • 7
    • 62449325160 scopus 로고    scopus 로고
    • Prothrombotic gene mutations in patients with sudden sensorineural hearing loss and cardiovascular thrombotic disease
    • Capaccio, P., Cuccarini, V., Ottaviani, F., Fracchiolla, N.S., Bossi, A., and Pignataro, L. (2009). Prothrombotic gene mutations in patients with sudden sensorineural hearing loss and cardiovascular thrombotic disease. Ann Otol Rhinol Laryngol 118, 205-210.
    • (2009) Ann Otol Rhinol Laryngol , vol.118 , pp. 205-210
    • Capaccio, P.1    Cuccarini, V.2    Ottaviani, F.3    Fracchiolla, N.S.4    Bossi, A.5    Pignataro, L.6
  • 12
    • 0036651220 scopus 로고    scopus 로고
    • Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease
    • Carmine, A., Buervenich, S., Sydow, O., Anvret, M., and Olson, L. (2002). Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease. Mov Disord 17, 764-766.
    • (2002) Mov Disord , vol.17 , pp. 764-766
    • Carmine, A.1    Buervenich, S.2    Sydow, O.3    Anvret, M.4    Olson, L.5
  • 13
    • 11944272254 scopus 로고
    • A power primer
    • Cohen, J. (1992). A power primer. Psychol Bull 112, 155-159.
    • (1992) Psychol Bull , vol.112 , pp. 155-159
    • Cohen, J.1
  • 16
    • 12244283743 scopus 로고    scopus 로고
    • A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women
    • Fortunato, G., Rubba, P., Panico, S., Trono, D., Tinto, N., Mazzaccara, C., DeMichele,M., Iannuzzi, A., Vitale, D.F., Salvatore, F., and Sacchetti, L. (2003). A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women. Atherosclerosis 167, 141-148.
    • (2003) Atherosclerosis , vol.167 , pp. 141-148
    • Fortunato, G.1    Rubba, P.2    Panico, S.3    Trono, D.4    Tinto, N.5    Demichelem, M.C.6    Iannuzzi, A.7    Vitale, D.F.8    Salvatore, F.9    Sacchetti, L.10
  • 18
    • 80053458900 scopus 로고    scopus 로고
    • Cerebral microvascular endothelium and the pathogenesis of neurodegenerative diseases
    • Grammas, P., Martinez, J., and Miller, B. (2011). Cerebral microvascular endothelium and the pathogenesis of neurodegenerative diseases. Expert Rev Mol Med 13, e19.
    • (2011) Expert Rev Mol Med , vol.13
    • Grammas, P.1    Martinez, J.2    Miller, B.3
  • 19
    • 84869664391 scopus 로고
    • Observations on the pathology of Meniere's syndrome
    • Hallpike, S.C., and Cairns, H. (1938). Observations on the pathology of Meniere's syndrome. J Laryngol Otol 53, 625-655.
    • (1938) J Laryngol Otol , vol.53 , pp. 625-655
    • Hallpike, S.C.1    Cairns, H.2
  • 20
  • 21
    • 34147098356 scopus 로고    scopus 로고
    • Lack of association of CPT1A polymorphisms or haplotypes on hepatic lipid content or insulin resistance in Japanese individuals with type 2 diabetes mellitus
    • Hirota, Y., Ohara, T., Zenibayashi, M., Kuno, S., Fukuyama, K., Teranishi, T., Kouyama, K., Miyake, K., Maeda, E., and Kasuga, M. (2007). Lack of association of CPT1A polymorphisms or haplotypes on hepatic lipid content or insulin resistance in Japanese individuals with type 2 diabetes mellitus. Metabolism 56, 656-661.
    • (2007) Metabolism , vol.56 , pp. 656-661
    • Hirota, Y.1    Ohara, T.2    Zenibayashi, M.3    Kuno, S.4    Fukuyama, K.5    Teranishi, T.6    Kouyama, K.7    Miyake, K.8    Maeda, E.9    Kasuga, M.10
  • 22
    • 85047699586 scopus 로고    scopus 로고
    • Codon 311 (Cys-> Ser) polymorphism of paraoxonase-2 gene is associated with apolipoprotein E4 allele in both Alzheimer's and vascular dementias
    • Janka, Z., Juhasz, A., Rimanoczy, A.A., Boda, K., Marki-Zay, J., and Kalman, J. (2002). Codon 311 (Cys-> Ser) polymorphism of paraoxonase-2 gene is associated with apolipoprotein E4 allele in both Alzheimer's and vascular dementias. Mol Psychiatry 7, 110-112.
    • (2002) Mol Psychiatry , vol.7 , pp. 110-112
    • Janka, Z.1    Juhasz, A.2    Rimanoczy, A.A.3    Boda, K.4    Marki-Zay, J.5    Kalman, J.6
  • 23
    • 0037727872 scopus 로고    scopus 로고
    • The signal sequence polymorphism of the MnSOD gene is associated with the degree of carotid atherosclerosis
    • Kakko, S., Paivansalo, M., Koistinen, P., Kesaniemi, Y.A., Kinnula, V.L., and Savolainen, M.J. (2003). The signal sequence polymorphism of the MnSOD gene is associated with the degree of carotid atherosclerosis. Atherosclerosis 168, 147-152.
    • (2003) Atherosclerosis , vol.168 , pp. 147-152
    • Kakko, S.1    Paivansalo, M.2    Koistinen, P.3    Kesaniemi, Y.A.4    Kinnula, V.L.5    Savolainen, M.J.6
  • 24
    • 54049155698 scopus 로고    scopus 로고
    • Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Meniere's disease
    • Kawaguchi, S., Hagiwara, A., and Suzuki, M. (2008). Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Meniere's disease. Acta Otolaryngol 128, 1173-1177.
    • (2008) Acta Otolaryngol , vol.128 , pp. 1173-1177
    • Kawaguchi, S.1    Hagiwara, A.2    Suzuki, M.3
  • 25
    • 0034533059 scopus 로고    scopus 로고
    • Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration
    • Kimura, K., Isashiki, Y., Sonoda, S., Kakiuchi-Matsumoto, T., and Ohba, N. (2000). Genetic association of manganese superoxide dismutase with exudative age-related macular degeneration. Am J Ophthalmol 130, 769-773.
    • (2000) Am J Ophthalmol , vol.130 , pp. 769-773
    • Kimura, K.1    Isashiki, Y.2    Sonoda, S.3    Kakiuchi-Matsumoto, T.4    Ohba, N.5
  • 26
    • 16444368333 scopus 로고    scopus 로고
    • Activation of caspase-3 is associated with oxidative stress in the hydropic guinea pig cochlea
    • Labbe, D., Teranishi, M.A., Hess, A., Bloch, W., and Michel, O. (2005). Activation of caspase-3 is associated with oxidative stress in the hydropic guinea pig cochlea. Hear Res 202, 21-27.
    • (2005) Hear Res , vol.202 , pp. 21-27
    • Labbe, D.1    Teranishi, M.A.2    Hess, A.3    Bloch, W.4    Michel, O.5
  • 28
    • 15744400003 scopus 로고    scopus 로고
    • Pathology and pathophysiology of idiopathic sudden sensorineural hearing loss
    • Merchant, S.N., Adams, J.C., and Nadol, J.B., Jr. (2005). Pathology and pathophysiology of idiopathic sudden sensorineural hearing loss. Otol Neurotol 26, 151-160.
    • (2005) Otol Neurotol , vol.26 , pp. 151-160
    • Merchant, S.N.1    Adams, J.C.2    Nadol Jr., J.B.3
  • 29
    • 0024558001 scopus 로고
    • Evaluation of prostaglandin E1 therapy for sudden deafness
    • Nakashima, T., Kuno, K., and Yanagita, N. (1989). Evaluation of prostaglandin E1 therapy for sudden deafness. Laryngoscope 99, 542-546.
    • (1989) Laryngoscope , vol.99 , pp. 542-546
    • Nakashima, T.1    Kuno, K.2    Yanagita, N.3
  • 31
    • 78651065963 scopus 로고    scopus 로고
    • A polymorphism at-1607 2G in the matrix metalloproteinase-1 (MMP-1) increased risk of sudden deafness in Korean population but not at-519A/G in MMP-1
    • Nam, S.I., Yu, G.I., Kim, H.J., Park, K.O., Chung, J.H., Ha, E., and Shin, D.H. (2011). A polymorphism at-1607 2G in the matrix metalloproteinase-1 (MMP-1) increased risk of sudden deafness in Korean population but not at-519A/G in MMP-1. Laryngoscope 121, 171-175.
    • (2011) Laryngoscope , vol.121 , pp. 171-175
    • Nam, S.I.1    Yu, G.I.2    Kim, H.J.3    Park, K.O.4    Chung, J.H.5    Ha, E.6    Shin, D.H.7
  • 32
    • 0034450206 scopus 로고    scopus 로고
    • Targeted mutation of the gene for cellular glutathione peroxidase (Gpx1) increases noise-induced hearing loss in mice
    • Ohlemiller, K.K., McFadden, S.L., Ding, D.L., Lear, P.M., and Ho, Y.S. (2000). Targeted mutation of the gene for cellular glutathione peroxidase (Gpx1) increases noise-induced hearing loss in mice. J Assoc Res Otolaryngol 1, 243-254.
    • (2000) J Assoc Res Otolaryngol , vol.1 , pp. 243-254
    • Ohlemiller, K.K.1    McFadden, S.L.2    Ding, D.L.3    Lear, P.M.4    Ho, Y.S.5
  • 33
    • 0029937118 scopus 로고    scopus 로고
    • The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family
    • Primo-Parmo, S.L., Sorenson, R.C., Teiber, J., and La Du, B.N. (1996). The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family. Genomics 33, 498-507.
    • (1996) Genomics , vol.33 , pp. 498-507
    • Primo-Parmo, S.L.1    Sorenson, R.C.2    Teiber, J.3    La Du, B.N.4
  • 35
    • 9144263553 scopus 로고    scopus 로고
    • Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese
    • Shi, J., Zhang, S., Tang, M., Liu, X., Li, T., Han, H., Wang, Y., Guo, Y., Zhao, J., Li, H., and Ma, C. (2004). Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer's disease in Chinese. Brain Res Mol Brain Res 120, 201-204.
    • (2004) Brain Res Mol Brain Res , vol.120 , pp. 201-204
    • Shi, J.1    Zhang, S.2    Tang, M.3    Liu, X.4    Li, T.5    Han, H.6    Wang, Y.7    Guo, Y.8    Zhao, J.9    Li, H.10    Ma, C.11
  • 36
    • 0037339203 scopus 로고    scopus 로고
    • The Ala 16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria
    • Sutton, A., Khoury, H., Prip-Buus, C., Cepanec, C., Pessayre, D., and Degoul, F. (2003). The Ala16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria. Pharmacogenetics 13, 145-157.
    • (2003) Pharmacogenetics , vol.13 , pp. 145-157
    • Sutton, A.1    Khoury, H.2    Prip-Buus, C.3    Cepanec, C.4    Pessayre, D.5    Degoul, F.6
  • 38
    • 62349109722 scopus 로고    scopus 로고
    • Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Meniere's syndrome
    • Teggi, R., Lanzani, C., Zagato, L., Delli Carpini, S., Manunta, P., Bianchi, G., and Bussi, M. (2008). Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Meniere's syndrome. Otol Neurotol 29, 824-828.
    • (2008) Otol Neurotol , vol.29 , pp. 824-828
    • Teggi, R.1    Lanzani, C.2    Zagato, L.3    Delli Carpini, S.4    Manunta, P.5    Bianchi, G.6    Bussi, M.7
  • 39
    • 18744393464 scopus 로고    scopus 로고
    • Is there a relevant effect of noise and smoking on hearing? A population-based aging study
    • Uchida, Y., Nakashimat, T., Ando, F., Niino, N., and Shimokata, H. (2005). Is there a relevant effect of noise and smoking on hearing? A population-based aging study. Int J Audiol 44, 86-91.
    • (2005) Int J Audiol , vol.44 , pp. 86-91
    • Uchida, Y.1    Nakashimat, T.2    Ando, F.3    Niino, N.4    Shimokata, H.5
  • 40
    • 77950820634 scopus 로고    scopus 로고
    • Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss
    • Uchida, Y., Sugiura, S., Ando, F., Shimokata, H., and Nakashima, T. (2010). Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss. Laryngoscope 120, 791-795.
    • (2010) Laryngoscope , vol.120 , pp. 791-795
    • Uchida, Y.1    Sugiura, S.2    Ando, F.3    Shimokata, H.4    Nakashima, T.5
  • 41
    • 80052768731 scopus 로고    scopus 로고
    • Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study
    • Uchida, Y., Sugiura, S., Nakashima, T., Ando, F., and Shimokata, H. (2011). Contribution of 1425G/A polymorphism in protein kinase C-Eta (PRKCH) gene and brain white matter lesions to the risk of sudden sensorineural hearing loss in a Japanese nested case-control study. J Neurogenet 25, 82-87.
    • (2011) J Neurogenet , vol.25 , pp. 82-87
    • Uchida, Y.1    Sugiura, S.2    Nakashima, T.3    Ando, F.4    Shimokata, H.5
  • 42
    • 79959973862 scopus 로고    scopus 로고
    • Steroid combination therapy and detoxification enzyme gene polymorphisms in sudden sensorineural hearing loss patients
    • Um, J.Y., Jang, C.H., Kim, S.J., Kim, H.L., Kim, S.Y., Cho, Y.B., and Hong, S.H. (2011). Steroid combination therapy and detoxification enzyme gene polymorphisms in sudden sensorineural hearing loss patients. Otol Neurotol 32, 872-876.
    • (2011) Otol Neurotol , vol.32 , pp. 872-876
    • Um, J.Y.1    Jang, C.H.2    Kim, S.J.3    Kim, H.L.4    Kim, S.Y.5    Cho, Y.B.6    Hong, S.H.7
  • 43
    • 0037960986 scopus 로고    scopus 로고
    • Association of polymorphisms of interleukin-6, osteocalcin, and vitamin D receptor genes, alone or in combination, with bone mineral density in community-dwelling Japanese women and men
    • Yamada, Y., Ando, F., Niino, N., and Shimokata, H. (2003). Association of polymorphisms of interleukin-6, osteocalcin, and vitamin D receptor genes, alone or in combination, with bone mineral density in community-dwelling Japanese women and men. J Clin Endocrinol Metab 88, 3372-3378.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 3372-3378
    • Yamada, Y.1    Ando, F.2    Niino, N.3    Shimokata, H.4
  • 44
    • 0000546788 scopus 로고
    • Uber die pathologisch Veranderung bei einem Meniere-Kranken
    • Yamakawa, K. (1938). Uber die pathologisch Veranderung bei einem Meniere-Kranken. J Otorhinolaryngol Soc Jpn 4, 2310-2312.
    • (1938) J Otorhinolaryngol Soc Jpn , vol.4 , pp. 2310-2312
    • Yamakawa, K.1
  • 45
    • 49649085627 scopus 로고    scopus 로고
    • Three-dimensional fluid-attenuated inversion recovery magnetic resonance imaging findings and prognosis in sudden sensorineural hearing loss
    • Yoshida, T., Sugiura, M., Naganawa, S., Teranishi, M., Nakata, S., and Nakashima, T. (2008). Three-dimensional fluid-attenuated inversion recovery magnetic resonance imaging findings and prognosis in sudden sensorineural hearing loss. Laryngoscope 118, 1433-1437.
    • (2008) Laryngoscope , vol.118 , pp. 1433-1437
    • Yoshida, T.1    Sugiura, M.2    Naganawa, S.3    Teranishi, M.4    Nakata, S.5    Nakashima, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.