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. 2021 Jun;10(3):215-221.
doi: 10.1159/000509775. Epub 2020 Sep 3.

High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism

Tal Almagor  1   2   3 , Shoshana Rath  1 , Dan Nachtigal  4 , Zohara Sharroni  4 , Ghadir Elias-Assad  1   3 , Ora Hess  1 , Gilad Havazelet  5 , Yoav Zehavi  2 , Ronen Spiegel  2   3 , Dani Bercovich  6   7 , Shlomo Almashanu  8 , Yardena Tenenbaum-Rakover  1   3
Affiliations

High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism

Tal Almagor et al. Eur Thyroid J. 2021 Jun.

Abstract

Background: An association between hearing impairment (HI) and congenital hypothyroidism (CH) has been reported previously. However, in general, studies were retrospective and had small sample sizes, and the results were variable and inconclusive. The aim of our study was to assess the prevalence of HI among patients with CH and to examine factors potentially predictive of HI including severity of CH, etiology of CH, and timing of treatment initiation.

Methods: Audiometry was undertaken prospectively in 66 patients aged 3-21 years diagnosed with primary CH and 49 healthy matched controls. All patients with HI underwent examination by an otolaryngologist, and in patients with sensorineural loss, brainstem evoked response audiometry was performed. A next-generation sequencing (NGS) panel for genes involved in deafness was performed in patients with sensorineural HI to exclude additional genetic etiologies.

Results: HI was found in 19 patients (28.7%). Among them, 5 (7.6%) had moderate to severe bilateral sensorineural impairment and 14 (21.2%) had mild conductive HI. Conductive HI was bilateral in 5 of these patients (36%). None of the controls had HI. No specific etiology was found in patients with HI, and no differences were identified in age at diagnosis, age at initiation of levothyroxine (LT4) therapy, gender, or ethnicity between patients with and without HI. A nonsignificant trend toward lower mean screening TT4 levels was found in patients with HI (compared to those without HI) (3.42 vs. 5.34 μg/dL, p = 0.095). No pathogenic variants in genes attributed to HI were identified by NGS in the 5 patients with sensorineural deafness, indicating that HI in these patients was likely attributable to CH rather than other genetic etiologies.

Conclusions: Our findings indicate a high prevalence of HI among patients with CH, predominantly of the conductive type. HI was not associated with the etiology of CH or with delayed initiation of LT4 therapy. Audiometry is recommended for children diagnosed with CH and repeat monitoring may be warranted to identify acquired HI and to prevent long-term sequelae of undiagnosed deafness.

Keywords: Conductive hearing impairment; Deafness; Hearing impairment; Primary congenital hypothyroidism; Sensorineural hearing impairment.

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Conflict of interest statement

All authors have nothing to disclose.

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