COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype–genotype study

Kyung Seok Oh, Daniel Walls, Sun Young Joo, Jung Ah Kim, Jee Eun Yoo, Young Ik Koh, Da Hye Kim, John Hoon Rim, Hye Ji Choi, Hye Youn Kim, Seyoung Yu, Richard J. Smith, Jae Young Choi, Heon Yung Gee, Jinsei Jung

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)


This phenotype–genotype study aimed to investigate the extent of audioprofile variability related to cochlin major domains and to identify potential ethnic-specific differences associated with COCH-related hearing loss. Eight Korean families (26 cases) were diagnosed with COCH-related hearing loss by exome sequencing. Audiometric test results were combined with those from nine published East Asian families (20 cases) and compared with those from 38 European-descent families (277 cases). Audioprofiles were created by grouping audiometric test results into age ranges by age at testing and then averaging hearing loss thresholds by frequency within age ranges. The functional impact of the identified variants was assessed in vitro by examining the intracellular trafficking, secretion, and cleavage of cochlin. In both East Asian and European-descent families segregating COCH-related hearing loss, deafness-associated variants in non-LCCL domains of cochlin were associated with hearing loss that was more severe earlier in life than hearing loss caused by variants in the LCCL domain. Consistent with this phenotypic difference, functional studies demonstrated distinct pathogenic mechanisms for COCH variants in a domain-dependent manner; specifically, a cytotoxic effect was observed for the p.Phe230Leu variant, which is located in the vWFA1 domain. No ethnic-specific differences in hearing loss progression were observed, except for those attributable to an overrepresentation of presymptomatic cases in the European-descent cohort.

Original languageEnglish
Pages (from-to)889-901
Number of pages13
JournalHuman Genetics
Issue number3-4
Publication statusPublished - 2022 Apr

Bibliographical note

Funding Information:
We thank the families that participated in the study. We also thank Yonsei Advanced Imaging Center for helping with the microscopy experiments.

Funding Information:
This study was supported by the National Biobank of Korea, Centers for Disease Control and Prevention, Republic of Korea (4845-301, 4851-302, and 4851-307); by the Team Science Award of Yonsei University College of Medicine (6-2021-0003 to HYG, and 6-2021-0002 to JJ); by the Basic Research Program of the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2019R1A2C1084033 to JJ, 2020R1A2C3005787 to JYC, and 2021R1A2C2003549 and 2018R1A5A2025079 to HYG); and by the National Institutes of Health, NIDCDs R01's DC002842, DC012049, and DC017955 to RJS.

Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)


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