Literature DB >> 22426290

Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.

Naoki Nishio1, Masaaki Teranishi, Yasue Uchida, Saiko Sugiura, Fujiko Ando, Hiroshi Shimokata, Michihiko Sone, Hironao Otake, Ken Kato, Tadao Yoshida, Mitsuhiko Tagaya, Tatsuya Hibi, Tsutomu Nakashima.   

Abstract

Sudden sensorineural hearing loss (SSNHL) is one of the most common diseases encountered by otolaryngologists; however, the etiology is unclear. The aim of this study was to assess the association between SSNHL and polymorphism of complement factor H (CFH) Y402H, which is implicated in age-related macular degeneration. We conducted a case-control study, in which the cases were 72 SSNHL patients and the controls were 2161 residents selected randomly from the resident register. The odds ratio (OR) for SSNHL risk was determined using the additive-genetic model of CFH Y402H polymorphism. The OR for SSNHL risk was 1.788 (95% confidence interval [CI]: 1.008-3.172) with no adjustments and 1.820 (CI: 1.025-3.232) after adjusting for age and sex. Of the three lifestyle-related diseases hypertension, dyslipidemia, and diabetes, only diabetes was significantly associated with SSNHL risk. We classified both the controls and SSNHL patients into those with or without diabetes, and the OR for SSNHL risk was 6.326 (CI: 1.885-21.225) in diabetic subjects and 1.214 (CI: 0.581-2.538) in nondiabetic subjects. We conclude that CFH Y402H polymorphism and SSNHL risk are significantly related, and that diabetic CFH Y402H minor allele carriers may be susceptible to SSNHL.
Copyright © 2012 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22426290     DOI: 10.1016/j.gene.2012.02.027

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  4 in total

1.  Complement factor H genotypes impact risk of age-related macular degeneration by interaction with oxidized phospholipids.

Authors:  Peter X Shaw; Li Zhang; Ming Zhang; Hongjun Du; Ling Zhao; Clara Lee; Seanna Grob; Siok Lam Lim; Guy Hughes; Janet Lee; Matthew Bedell; Mark H Nelson; Fang Lu; Martin Krupa; Jing Luo; Hong Ouyang; Zhidan Tu; Zhiguang Su; Jin Zhu; Xinran Wei; Zishan Feng; Yaou Duan; Zhenglin Yang; Henry Ferreyra; Dirk-Uwe Bartsch; Igor Kozak; Liangfang Zhang; Feng Lin; Hui Sun; Hong Feng; Kang Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-08       Impact factor: 11.205

2.  A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiency.

Authors:  Jing Zou; Xiangqiang Duan; Guiliang Zheng; Zhen Zhao; Shiyue Chen; Pu Dai; Hongliang Zheng
Journal:  J Otol       Date:  2016-06-08

Review 3.  Therapeutic Lessons to be Learned From the Role of Complement Regulators as Double-Edged Sword in Health and Disease.

Authors:  Esther C W de Boer; Anouk G van Mourik; Ilse Jongerius
Journal:  Front Immunol       Date:  2020-12-10       Impact factor: 7.561

4.  Nutritional Mushroom Treatment in Meniere's Disease with Coriolus versicolor: A Rationale for Therapeutic Intervention in Neuroinflammation and Antineurodegeneration.

Authors:  Maria Scuto; Paola Di Mauro; Maria Laura Ontario; Chiara Amato; Sergio Modafferi; Domenico Ciavardelli; Angela Trovato Salinaro; Luigi Maiolino; Vittorio Calabrese
Journal:  Int J Mol Sci       Date:  2019-12-31       Impact factor: 5.923

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.