Literature DB >> 34410490

A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis.

Allan Thomas Højland1,2, Lisse J M Tavernier3, Guy Van Camp4, Erik Fransen5,6, Isabelle Schrauwen7, Manou Sommen3, Vedat Topsakal8, Isabelle Schatteman9, Ingeborg Dhooge10, Alex Huber11, Diego Zanetti12, Henricus P M Kunst13,14, Alexander Hoischen15,16,17, Michael B Petersen1,2.   

Abstract

In this study, we investigated the association of ACAN variants with otosclerosis, a frequent cause of hearing loss among young adults. We sequenced the coding, 5'-UTR and 3'-UTR regions of ACAN in 1497 unrelated otosclerosis cases and 1437 matched controls from six different subpopulations. The association between variants in ACAN and the disease risk was tested through single variant and gene-based association tests. After correction for multiple testing, 14 variants were significantly associated with otosclerosis, ten of which represented independent association signals. Eight variants showed a consistent association across all subpopulations. Allelic odds ratios of the variants identified four predisposing and ten protective variants. Gene-based tests showed an association of very rare variants in the 3'-UTR with the phenotype. The associated exonic variants are all located in the CS domain of ACAN and include both protective and predisposing variants with a broad spectrum of effect sizes and population frequencies. This includes variants with strong effect size and low frequency, typical for monogenic diseases, to low effect size variants with high frequency, characteristic for common complex traits. This single-gene allelic spectrum with both protective and predisposing alleles is unique in the field of complex diseases. In conclusion, these findings are a significant advancement to the understanding of the etiology of otosclerosis.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34410490     DOI: 10.1007/s00439-021-02334-8

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  44 in total

1.  Analysis of genes from inner ear developmental-stage cDNA subtraction reveals molecular regionalization of the otic capsule.

Authors:  Michael Ficker; Nicola Powles; Nick Warr; Ulla Pirvola; Mark Maconochie
Journal:  Dev Biol       Date:  2004-04-01       Impact factor: 3.582

Review 2.  The different roles of aggrecan interaction domains.

Authors:  Anders Aspberg
Journal:  J Histochem Cytochem       Date:  2012-09-26       Impact factor: 2.479

3.  Single molecule molecular inversion probes for targeted, high-accuracy detection of low-frequency variation.

Authors:  Joseph B Hiatt; Colin C Pritchard; Stephen J Salipante; Brian J O'Roak; Jay Shendure
Journal:  Genome Res       Date:  2013-02-04       Impact factor: 9.043

4.  Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus.

Authors:  Zippora Brownstein; Abraham Goldfarb; Haya Levi; Moshe Frydman; Karen B Avraham
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2006-04

5.  Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis.

Authors:  W Chen; N C Meyer; M J McKenna; M Pfister; D J McBride; K Fukushima; M Thys; G V Camp; R J H Smith
Journal:  Clin Genet       Date:  2007-05       Impact factor: 4.438

6.  Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3.

Authors:  W Chen; C A Campbell; G E Green; K Van Den Bogaert; C Komodikis; L S Manolidis; E Aconomou; Y Kyamides; K Christodoulou; C Faghel; C M Giguére; R L Alford; S Manolidis; G Van Camp; R J H Smith
Journal:  J Med Genet       Date:  2002-07       Impact factor: 6.318

Review 7.  The genetics of otosclerosis: a review.

Authors:  M A Gordon
Journal:  Am J Otol       Date:  1989-11

8.  Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin.

Authors:  David J Brown; Theresa B Kim; Elizabeth M Petty; Catherine A Downs; Donna M Martin; Peter J Strouse; Sayoko E Moroi; Jeff M Milunsky; Marci M Lesperance
Journal:  Am J Hum Genet       Date:  2002-06-27       Impact factor: 11.025

9.  A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

Authors:  Insaf Bel Hadj Ali; Melissa Thys; Najeh Beltaief; Isabelle Schrauwen; Nele Hilgert; Kathleen Vanderstraeten; Nele Dieltjens; Emna Mnif; Slah Hachicha; Ghazi Besbes; Saïda Ben Arab; Guy Van Camp
Journal:  Hum Genet       Date:  2008-01-26       Impact factor: 4.132

10.  The second report on spondyloepimetaphyseal dysplasia, aggrecan type: a milder phenotype than originally reported.

Authors:  Yasuyuki Fukuhara; Sung Y Cho; Osamu Miyazaki; Atsushi Hattori; Joo-Hyun Seo; Ryuichi Mashima; Motomichi Kosuga; Maki Fukami; Dong-Kyu Jin; Torayuki Okuyama; Gen Nishimura
Journal:  Clin Dysmorphol       Date:  2019-01       Impact factor: 0.816

View more
  2 in total

Review 1.  Genetics of otosclerosis: finally catching up with other complex traits?

Authors:  Lisse J M Tavernier; Erik Fransen; Hanne Valgaeren; Guy Van Camp
Journal:  Hum Genet       Date:  2021-09-09       Impact factor: 4.132

2.  The risks of RELN polymorphisms and its expression in the development of otosclerosis.

Authors:  Saurabh Priyadarshi; Kirtal Hansdah; Neha Singh; Amal Bouzid; Chinmay Sundar Ray; Khirod Chandra Panda; Narayan Chandra Biswal; Ashim Desai; Jyotish Chandra Choudhury; Adel Tekari; Saber Masmoudi; Puppala Venkat Ramchander
Journal:  PLoS One       Date:  2022-06-03       Impact factor: 3.752

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.