Panel 3: Genetics and Precision Medicine of Otitis Media

Author:

Lin Jizhen1,Hafrén Hena2,Kerschner Joseph3,Li Jian-Dong4,Brown Steve5,Zheng Qing Y.6,Preciado Diego7,Nakamura Yoshihisa8,Huang Qiuhong9,Zhang Yan10

Affiliation:

1. Department of Otolaryngology–Head and Neck Surgery, University of Minnesota, Minneapolis, Minnesota, USA

2. Departments of Otorhinolaryngology–Head and Neck Surgery, Helsinki University Hospital, Helsinki, Finland

3. Department of Otorhinolaryngology and Communication Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA

4. Center for Inflammation, Immunity and Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA

5. Medical Research Council Harwell Institute, Oxfordshire, UK

6. Department of Otolaryngology–Head and Neck Surgery, Case Western University, Cleveland, Ohio, USA

7. Shiekh Zayed Institute for Pediatric Surgical Innovation, Pediatric Otolaryngology, Children’s National Health System, Washington, DC, USA

8. Department of Otolaryngology, Nagoya City University, Nagoya, Japan

9. Department of Otolaryngology, Sun Yat-sen University, Guangzhou, China

10. Department of Otolaryngology, Second Affiliated Hospital, Xi’an Jiaotong University, Xi’an, China

Abstract

Objective The objective is to perform a comprehensive review of the literature up to 2015 on the genetics and precision medicine relevant to otitis media. Data Sources PubMed database of the National Library of Medicine. Review Methods Two subpanels were formed comprising experts in the genetics and precision medicine of otitis media. Each of the panels reviewed the literature in their respective fields and wrote draft reviews. The reviews were shared with all panel members, and a merged draft was created. The entire panel met at the 18th International Symposium on Recent Advances in Otitis Media in June 2015 and discussed the review and refined the content. A final draft was made, circulated, and approved by the panel members. Conclusion Many genes relevant to otitis media have been identified in the last 4 years in advancing our knowledge regarding the predisposition of the middle ear mucosa to commensals and pathogens. Advances include mutant animal models and clinical studies. Many signaling pathways are involved in the predisposition of otitis media. Implications for Practice New knowledge on the genetic background relevant to otitis media forms a basis of novel potential interventions, including potential new ways to treat otitis media.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Surgery

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. DEGREE OF HEARING LOSS IN INACTIVE MUCOSAL CHRONIC OTITIS MEDIA AND ITS CORRELATION WITH SITE AND SIZE OF TYMPANIC MEMBRANE PERFORATION- AN OBSERVATIONAL STUDY;PARIPEX INDIAN JOURNAL OF RESEARCH;2022-09-15

2. Clinical perspectives on nasopharyngeal morphology in humans;The Anatomical Record;2022-04-06

3. gom1 Mutant Mice as a Model of Otitis Media;Journal of the Association for Research in Otolaryngology;2022-02-03

4. Innate Immunity in the Middle Ear Mucosa;Frontiers in Cellular and Infection Microbiology;2021-10-29

5. Current Understanding of Host Genetics of Otitis Media;Frontiers in Genetics;2020-02-07

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