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Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population

Mowat, AJ; Crompton, M; Ziff, JL; Aldren, CP; Lavy, JA; Saeed, SR; Dawson, SJ; (2018) Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Human Genetics , 137 (5) pp. 357-363. 10.1007/s00439-018-1889-9. Green open access

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Abstract

Otosclerosis is a common form of hearing loss which typically presents in young adults. The disease has a familial, monogenic form and a non-familial form with a more complex aetiology. A previous genome wide association study identified evidence that variants within RELN are associated with the condition. Other genes in which an association has been reported include BMP2, COL1A1, FGF2, PPP2R5B and TGFB1. However, follow up studies have often failed to replicate initial positive results. The aim of this study was to establish if an association exists between eight single nucleotide polymorphisms (SNPs) in these six previously implicated genes and otosclerosis in a British case-control cohort (n = 748). Evidence of an association between rs1800472 in TGFB1 and otosclerosis was found (p = 0.034), this association was strongest amongst non-familial cases (p = 0.011). No evidence of an association was detected with variants in COL1A1, FGF2, BMP2, and PPP2R5B. No association between variation in RELN and otosclerosis was observed in the whole cohort. However, a significant association (p = 0.0057) was detected between one RELN SNP (rs39399) and otosclerosis in familial patients. Additionally, we identify expression of one RELN transcript in 51 of 81 human stapes tested, clarifying previous conflicting data as to whether RELN is expressed in the affected tissue. Our findings strengthen the association of TGFB1 (rs1800472) with otosclerosis and support a relationship between RELN and familial otosclerosis only, which may explain previous variable replications.

Type: Article
Title: Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population
Open access status: An open access version is available from UCL Discovery
DOI: 10.1007/s00439-018-1889-9
Publisher version: http://dx.doi.org/10.1007/s00439-018-1889-9
Language: English
Additional information: © The Author(s) 2018. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > The Ear Institute
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10048569
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