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Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

Sophie Boucher 1, 2, 3, 4 Fabienne Wong Jun Tai 1 Sedigheh Delmaghani 1 Andrea Lelli 1 Amrit Singh-Estivalet 1, 2 Typhaine Dupont 1 Magali Niasme-Grare 1, 5 Vincent Michel 1 Nicolas Wolff 6 Amel Bahloul 1 Yosra Bouyacoub 1 Didier Bouccara 7 Bernard Fraysse 8 Olivier Deguine 8 Lionel Collet 9 Hung Thai-Van 1, 10, 11 Eugen Ionescu 10 Jean-Louis Kemeny 12 Fabrice Giraudet 13 Jean-Pierre Lavieille 14 Arnaud Devèze 14 Anne-Laure Roudevitch-Pujol 15 Christophe Vincent 16 Christian Renard 17 Valérie Franco-Vidal 18 Claire Thibult-Apt 18 Vincent Darrouzet 18 Eric Bizaguet 19 Arnaud Coez 19, 20 Hugues Aschard 21 Nicolas Michalski 1 Gaëlle Lefevre 1 Anne Aubois 15 Paul Avan 1, 13, 22 Crystel Bonnet 1, 2 Christine Petit 1, 23, *
Abstract : Presbycusis, or age-related hearing loss (ARHL), is a major public health issue. About half the phenotypic variance has been attributed to genetic factors. Here, we assessed the contribution to presbycusis of ultrarare pathogenic variants, considered indicative of Mendelian forms. We focused on severe presbycusis without environmental or comorbidity risk factors and studied multiplex family age-related hearing loss (mARHL) and simplex/sporadic age-related hearing loss (sARHL) cases and controls with normal hearing by whole-exome sequencing. Ultrarare variants (allele frequency [AF] < 0.0001) of 35 genes responsible for autosomal dominant early-onset forms of deafness, predicted to be pathogenic, were detected in 25.7% of mARHL and 22.7% of sARHL cases vs. 7.5% of controls ( P = 0.001); half were previously unknown (AF < 0.000002). MYO6 , MYO7A , PTPRQ , and TECTA variants were present in 8.9% of ARHL cases but less than 1% of controls. Evidence for a causal role of variants in presbycusis was provided by pathogenicity prediction programs, documented haploinsufficiency, three-dimensional structure/function analyses, cell biology experiments, and reported early effects. We also established Tmc1 N321I/+ mice, carrying the TMC1 :p.(Asn327Ile) variant detected in an mARHL case, as a mouse model for a monogenic form of presbycusis. Deafness gene variants can thus result in a continuum of auditory phenotypes. Our findings demonstrate that the genetics of presbycusis is shaped by not only well-studied polygenic risk factors of small effect size revealed by common variants but also, ultrarare variants likely resulting in monogenic forms, thereby paving the way for treatment with emerging inner ear gene therapy.
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Submitted on : Monday, May 3, 2021 - 10:23:19 AM
Last modification on : Thursday, June 17, 2021 - 3:33:59 AM

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Sophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani, Andrea Lelli, Amrit Singh-Estivalet, et al.. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2020, 117 (49), pp.31278-31289. ⟨10.1073/pnas.2010782117⟩. ⟨pasteur-03215054⟩

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