Otological Features of Patients with Musculocontractural Ehlers–Danlos Syndrome Caused by Pathogenic Variants in CHST14 (mcEDS-CHST14)

Author:

Kawakita Masayuki1,Iwasaki Satoshi23,Moteki Hideaki24,Nishio Shin-ya2ORCID,Kosho Tomoki5678ORCID,Usami Shin-ichi2ORCID

Affiliation:

1. Asama General Hospital, Saku 385-8558, Japan

2. Department of Hearing Implant Sciences, Shinshu University School of Medicine, Matsumoto 390-8621, Japan

3. Department of Otolaryngology, International University of Health and Welfare, Mita Hospital, Tokyo 108-8329, Japan

4. Department of Otolaryngology, Aizawa Hospital, Matsumoto 390-8621, Japan

5. Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto 390-8621, Japan

6. Center for Medical Genetics, Shinshu University Hospital, Matsumoto 390-8621, Japan

7. Division of Clinical Sequencing, Shinshu University School of Medicine, Matsumoto 390-8621, Japan

8. Research Center for Supports to Advanced Science, Shinshu University, Matsumoto 390-8621, Japan

Abstract

Musculocontractural Ehlers–Danlos syndrome (EDS) caused by pathogenic variants in CHST14 (mcEDS-CHST14) is a subtype of EDS characterized by multisystem malformations and progressive fragility-related manifestations. A recent international collaborative study showed that 55% of mcEDS-CHST14 patients had hearing loss (HL), more commonly of the high-frequency type. Here, we report the first systemic investigation of the otological features of patients with this disorder based on the world’s largest cohort at Shinshu University Hospital. Nine patients [18 ears; four male and five female patients; mean age, 18 years old (range, 10–28)] underwent comprehensive otological evaluation: audiogram, distortion product otoacoustic emission (DPOAE) test, and tympanometry. The audiogram, available in all 18 ears, showed HL in eight patients (8/9, 89%) and in 14 ears (14/18, 78%): bilateral in six patients (6/9, 67%) and unilateral in two (2/9, 22%); mild in eight ears (8/18, 44%) and moderate in six (6/18, 33%); and high-frequency HL in five (5/18, 28%) and low-frequency HL in five (5/18, 28%). An air-bone gap was detected in one ear (1/18, 6%). DPOAE was available in 13 ears, with the presence of a response in five (5/13, 38%) and the absence in eight (8/13, 62%), including in three ears of normal hearing. Tympanometry results were available in 12 ears: Ad type in nine (9/12, 75%) and As type in one (1/12, 8.3%). Patients with mcEDS-CHST14 had a high prevalence of HL, typically sensorineural and bilateral, with mild to moderate severity, of high-frequency or low-frequency type, and sometimes with no DPOAE response. The pathophysiology underlying HL might be complex, presumably related to alterations of the tectorial membrane and/or the basilar membrane of Corti associated with disorganized collagen fibril networks. Regular and careful check-ups of hearing using multiple modalities are recommended for mcEDS-CHST14 patients.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Agency for Medical Research and Development

Ministry of Health, Labour and Welfare, Japan

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference16 articles.

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