2012 Fiscal Year Final Research Report
Disruption of the blood-labyrinthine barrier and related genes in sudden sensorineural hearing loss
Project/Area Number |
21390460
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Otorhinolaryngology
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Research Institution | Nagoya University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
NAGANAWA Shinji 名古屋大学, 大学院・医学系研究科, 教授 (50242863)
SHIMOKATA Hiroshi 国立長寿医療センター, 国立長寿医療センター研究所, 疫学研究部長 (10226269)
TERANISHI Masaaki 名古屋大学, 大学院・医学系研究科, 講師 (20335037)
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Co-Investigator(Renkei-kenkyūsha) |
UCHIDA Yasue 愛知医科大学, 医学部, 講師 (80313998)
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Project Period (FY) |
2009 – 2012
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Keywords | 突発性難聴 / 血液迷路関門 / MRI / 遺伝子多型 |
Research Abstract |
Disruption of the blood-labyrinthine barrier was evaluated by the degree of Gd contrast enhancement of the inner ear in suddensensorineural hearing loss. There were ears with significant Gd enhancenment but there were also ears without Gd enhancement. Disruption of the blood-labyrinthine barrier may be associated with impairment of the blood vessels, inflammation and oxidative stress. The relevant gene polymorphisms were investigated in patients with sudden sensorineural hearing loss and in controls. Polymorphisms of interleukin-1A (rs1800587), interleukin-6 (rs1061170), complement factor H (rs1061170), aquaporin5 (rs3736309) and NO synthase 3 (rs1799983) seemed to be related to onset of sudden sensorineural hearing loss.交付決定額
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Research Products
(16 results)
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[Journal Article] Polymorhisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Meniere's disease.2013
Author(s)
Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.
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Journal Title
Free Radic Res
Volume: (Epub ahead of print)
Peer Reviewed
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[Journal Article] Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Meniere's disease and sudden sensorineural hearing loss.2013
Author(s)
Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, Sone M, Otake H,Kato K, Yoshida T, Tagaya M, Hibi T, Nakashima T.
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Journal Title
Life Sci
Volume: 92
Pages: 541-546
Peer Reviewed
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[Journal Article] Polymorphisms in Genes Involved in Oxidative Stress Response in Patients with Sudden Sensorineural Hearing Loss and Meniere's Disease in a Japanese Population.2012
Author(s)
Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.
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Journal Title
DNA Cell Biol
Volume: 31
Pages: 1555-1562
Peer Reviewed
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[Journal Article] Polymorphisms in Genes Involved in Inflammatory Pathways in Patients with Sudden Sensorineural Hearing Loss.2012
Author(s)
Hiramatsu M, Teranishi M, Uchida Y, Nishio N, Suzuki H, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.
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Journal Title
J Neurogenet.
Volume: 26
Pages: 387-396
Peer Reviewed
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[Journal Article] Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.2012
Author(s)
Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, Sone M, Otake H, Kato K, Yoshida T, Tagaya M, Hibi T, Nakashima T.
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Journal Title
Gene
Volume: 499(1)
Pages: 226-230
Peer Reviewed
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[Journal Article] Association of interleukin-1 gene polymorphisms with sudden sensirineral hearing loss and Meniere's disease2011
Author(s)
Furuta T, Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sugiura M, Sone M, Hiramatsu M, Sugiura S, Ando F, Shimokata H, Nakashima T.
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Journal Title
Int Journal Immunogenet
Volume: 38
Pages: 249-254
Peer Reviewed
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[Presentation] Polymorphic analysis in patients with Meniere's disease and sudden sensorineural hearing loss2012
Author(s)
Teranishi M, Uchida Y, Nishio N, Kao K, Otake H, Yoshida T, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.
Organizer
49th Inner Ear Bioloby Workshop
Place of Presentation
Tubingen, Germany
Year and Date
20120930-1002
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[Presentation] Polymorphisms in genes involved in inflammatory pathways in patients with sudden sensorineural hearing loss2011
Author(s)
Teranishi M, Hiramatsu M, Uchida Y, Nishio N, Suzuki H, Kato K, Otake H, Yoshida T, Tagaya M, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T.
Organizer
48th Inner Ear Biology Workshop
Place of Presentation
Lisbon, Portugal
Year and Date
20110918-21
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[Presentation] Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes2011
Author(s)
Nishio N, Teranishi M, Uchida Y, Sugiura S, Ando F, Shimokata H, Sone M, Otake H, Kato K, Yoshida T, Tagaya M, Hibi T, Nakashima T.
Organizer
11th Japan-Taiwan Conference on Otolaryngology-Head and Neck Surgery
Place of Presentation
Kobe, Japan
Year and Date
2011-12-08
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