Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
NT/12246-5
Internal Grant Agency, Ministry of Health of the Czech Republic
PubMed
30344259
PubMed Central
PMC6037260
DOI
10.3390/medicina54020028
PII: medicina54020028
Knihovny.cz E-zdroje
- Klíčová slova
- genetics, hearing loss, nonsyndromic, sensorineural,
- MeSH
- aktiny genetika MeSH
- dítě MeSH
- dospělí MeSH
- draslíkové kanály KCNQ genetika MeSH
- extracelulární matrix - proteiny genetika MeSH
- hluchota genetika MeSH
- kojenec MeSH
- konexin 26 MeSH
- konexiny genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- membránové proteiny genetika MeSH
- mikrofilamentové proteiny genetika MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mutace genetika MeSH
- mutační analýza DNA metody MeSH
- percepční nedoslýchavost genetika MeSH
- předškolní dítě MeSH
- serpiny genetika MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- kojenec MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- ACTG1 protein, human MeSH Prohlížeč
- aktiny MeSH
- COCH protein, human MeSH Prohlížeč
- draslíkové kanály KCNQ MeSH
- ESPN protein, human MeSH Prohlížeč
- extracelulární matrix - proteiny MeSH
- GJB2 protein, human MeSH Prohlížeč
- GJB3 protein, human MeSH Prohlížeč
- KCNQ4 protein, human MeSH Prohlížeč
- konexin 26 MeSH
- konexiny MeSH
- membránové proteiny MeSH
- mikrofilamentové proteiny MeSH
- serpin B6 MeSH Prohlížeč
- serpiny MeSH
- TMIE protein, human MeSH Prohlížeč
BACKGROUND AND OBJECTIVE: Hearing loss is the most common sensory deficit in humans. The aim of this study was to clarify the genetic aetiology of nonsyndromic hearing loss in the Moravian-Silesian population of the Czech Republic. PATIENTS AND METHODS: This study included 200 patients (93 males, 107 females, mean age 16.9 years, ranging from 4 months to 62 years) with nonsyndromic sensorineural hearing loss. We screened all patients for mutations in GJB2 and the large deletion del(GJB6-D13S1830). We performed further screening for additional genes (SERPINB6, TMIE, COCH, ESPN, ACTG1, KCNQ4, and GJB3) with Sanger sequencing on a subset of patients that were negative for GJB2 mutations. RESULTS: We detected biallelic GJB2 mutations in 44 patients (22%). Among these patients, 63.6%, 9.1% and 2.3% exhibited homozygous c.35delG, p.Trp24*, and p.Met34Thr mutations, respectively. The remaining 25% of these patients exhibited compound heterozygous c.35delG, c.-23+1G>A, p.Trp24*, p.Val37Ile, p.Met34Thr, p.Leu90Pro, c.235delC, c.313_326del14, p.Ser139Asn, and p.Gly147Leu mutations. We found a monoallelic GJB2 mutation in 12 patients (6.6%). We found no pathogenic mutations in the other tested genes. Conclusions: One fifth of our cohort had deafness related to GJB2 mutations. The del(GJB6-D13S1830), SERPINB6, TMIE, COCH, ESPN, ACTG1, GJB3, and KCNQ4 mutations were infrequently associated with deafness in the Moravian-Silesian population. Therefore, we suggest that del(GJB6-D13S1830) testing should be performed only when patients with deafness carry the monoallelic GJB2 mutation.
Department of Otorhinolaryngology Hospital of Havířov Dělnická 1132 24 736 01 Havířov Czech Republic
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Snoeckx R.L., Huygen P.L., Feldmann D., Marlin S., Denoyelle F., Waligora J., Mueller-Malesinska M., Pollak A., Ploski R., Murgia A., et al. GJB2 mutations and degree of hearing loss: A multicenter study. Am. J. Hum. Genet. 2005;77:945–947. doi: 10.1086/497996. PubMed DOI PMC
Kelsell D.P., Di W.L., Houseman M.J. Connexin mutations in skin disease and hearing loss. Am. J. Hum. Genet. 2001;68:559–568. doi: 10.1086/318803. PubMed DOI PMC
Kelley P.M., Harris D.J., Comer B.C., Askew J.W., Fowler T., Smith S.D., Kimberling W.J. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Am. J. Hum. Genet. 1998;62:792–799. doi: 10.1086/301807. PubMed DOI PMC
Janecke A.R., Hirst-Stadlmann A., Günther B., Utermann B., Müller T., Löffler J., Utermann G., Nekahm-Heis D. Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations—phenotypic spectrum and frequencies of GJB2 mutations in Austria. Hum. Genet. 2002;111:145–153. doi: 10.1007/s00439-002-0762-y. PubMed DOI
Del Castillo I., Villamar M., Moreno-Pelayo M.A., del Castillo F.J., Alvarez A., Tellería D., Menéndez I., Moreno F. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. N. Engl. J. Med. 2002;346:243–249. doi: 10.1056/NEJMoa012052. PubMed DOI
Denoyelle F., Marlin S., Weil D., Moatti L., Chauvin P., Garabédian E.N., Petit C. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: Implications for genetic counselling. Lancet. 1999;353:1298–1303. doi: 10.1016/S0140-6736(98)11071-1. PubMed DOI
Murgia A., Orzan E., Polli R., Martella M., Vinanzi C., Leonardi E., Arslan E., Zacchello F. Cx26 deafness: Mutation analysis and clinical variability. J. Med. Genet. 1999;36:829–832. PubMed PMC
Sansović I., Knezević J., Musani V., Seeman P., Barisić I., Pavelić J. GJB2 mutations in patients with nonsyndromic hearing loss from Croatia. Genet. Test. Mol. Biomark. 2009;13:693–699. doi: 10.1089/gtmb.2009.0073. PubMed DOI
Cryns K., Orzan E., Murgia A., Huygen P.L., Moreno F., del Castillo I., Chamberlin G.P., Azaiez H., Prasad S., Cucci R.A., et al. A genotype-phenotype correlation for GJB2 (connexin 26) deafness. J. Med. Genet. 2004;41:147–154. doi: 10.1136/jmg.2003.013896. PubMed DOI PMC
Zelante L., Gasparini P., Estivill X., Melchionda S., D’Agruma L., Govea N., Milá M., Monica M.D., Lutfi J., Shohat M., et al. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum. Mol. Genet. 1997;6:1605–1609. doi: 10.1093/hmg/6.9.1605. PubMed DOI
Seeman P., Malíková M., Rasková D., Bendová O., Groh D., Kubálková M., Sakmaryová I., Seemanová E., Kabelka Z. Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness. Clin. Genet. 2004;66:152–157. doi: 10.1111/j.1399-0004.2004.00283.x. PubMed DOI
Seeman P., Sakmaryová I. High prevalence of the IVS 1 + 1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB2. Clin. Genet. 2006;69:410–413. doi: 10.1111/j.1399-0004.2006.00602.x. PubMed DOI
Sirmaci A., Akcayoz-Duman D., Tekin M. The c.IVS1+1G>A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population. J. Genet. 2006;85:213–216. doi: 10.1007/BF02935334. PubMed DOI
Tóth T., Kupka S., Haack B., Riemann K., Braun S., Fazakas F., Zenner H.P., Muszbek L., Blin N., Pfister M., Sziklai I. GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Hum. Mutat. 2004;23:631–632. doi: 10.1002/humu.9250. PubMed DOI
Del Castillo I., Moreno-Pelayo M.A., Del Castillo F.J., Brownstein Z., Marlin S., Adina Q., Cockburn D.J., Pandya A., Siemering K.R., Chamberlin G.P., et al. Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: A multicenter study. Am. J. Hum. Genet. 2003;73:1452–1458. doi: 10.1086/380205. PubMed DOI PMC
Del Castillo F.J., Del Castillo I. DFNB1 non-syndromic hearing impairment: Diversity of mutations and associated phenotypes. Front. Mol. Neurosci. 2017;10:428. doi: 10.3389/fnmol.2017.00428. PubMed DOI PMC
Seeman P., Bendová O., Rasková D., Malíková M., Groh D., Kabelka Z. Double heterozygosity with mutations involving both the GJB2 and GJB6 genes is a possible, but very rare, cause of congenital deafness in the Czech population. Ann. Hum. Genet. 2005;69:9–14. doi: 10.1046/j.1529-8817.2003.00120.x. PubMed DOI
Demographics of the Czech Republic Wikipedia. [(accessed on 8 March 2018)]; Available online: https://en.wikipedia.org/wiki/Demographics_of_the_Czech_Republic.
Šveráková H., Kořínek R. The Immigrants and Ethnic Minorities in the Czech Republic. [(accessed on 8 March 2018)]; Available online: Ec.europa.eu/social/BlobServlet?docId=8190&langId=en.
RamShankar M., Girirajan S., Dagan O., Ravi Shankar H.M., Jalvi R., Rangasayee R., Avraham K.B., Anand A. Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India. J. Med. Genet. 2003;40:e68. doi: 10.1136/jmg.40.5.e68. PubMed DOI PMC
Minarik G., Ferakova E., Ficek A., Polakova H., Kadasi L. GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: Spectrum, frequencies and SNP analysis. Clin. Genet. 2005;68:554–557. PubMed
Alvarez A., del Castillo I., Villamar M., Aguirre L.A., González-Neira A., López-Nevot A., Moreno-Pelayo M.A., Moreno F. High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss. Am. J. Med. Genet. A. 2005;137A:255–258. doi: 10.1002/ajmg.a.30884. PubMed DOI
Bicego M., Beltramello M., Melchionda S., Carella M., Piazza V., Zelante L., Bukauskas F.F., Arslan E., Cama E., Pantano S., et al. Pathogenetic role of the deafness-related M34T mutation of Cx26. Hum. Mol. Genet. 2006;15:2569–2587. doi: 10.1093/hmg/ddl184. PubMed DOI PMC
Gallant E., Francey L., Tsai E.A., Berman M., Zhao Y., Fetting H., Kaur M., Deardorff M.A., Wilkens A., Clark D., et al. Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations. Am. J. Med. Genet. A. 2013;161A:2148–2157. doi: 10.1002/ajmg.a.36042. PubMed DOI PMC
D’Andrea P., Veronesi V., Bicego M., Melchionda S., Zelante L., Di Iorio E., Bruzzone R., Gasparini P. Hearing loss: Frequency and functional studies of the most common connexin26 alleles. Biochem. Biophys. Res. Commun. 2002;296:685–691. doi: 10.1016/S0006-291X(02)00891-4. PubMed DOI
Markova S., Safka Brozkova D., Meszarosova A., Neupauerova J., Groh D., Kreckova G., Lassuthova P., Seeman P. Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients. Int. J. Pediatr. Otorhinolaryngol. 2016;86:27–33. doi: 10.1016/j.ijporl.2016.04.005. PubMed DOI
Aken B.L., Achuthan P., Akanni W., Amode M.R., Bernsdorff F., Bhai J., Billis K., Carvalho-Silva D., Cummins C., Clapham P., et al. Ensembl 2017. Nucleic Acids Res. 2017;45:D635–D642. doi: 10.1093/nar/gkw1104. PubMed DOI PMC