Literature DB >> 22489040

COL1A1 association and otosclerosis: a meta-analysis.

Isabelle Schrauwen1, Ayda Khalfallah, Megan Ealy, Erik Fransen, Charlotte Claes, Alex Huber, Laura Rodriguez Murillo, Saber Masmoudi, Richard J H Smith, Guy Van Camp.   

Abstract

Otosclerosis is a disease of abnormal bone remodeling in the human otic capsule that can lead to progressive hearing loss. Little of the underlying disease etiology has been elucidated thus far, although several studies have suggested that COL1A1 may play a role based on its importance in bone metabolism and other diseases like osteoporosis and osteogenesis imperfecta. Genetic association studies between COL1A1 and otosclerosis, however, have been contradictory. To resolve this issue, we studied a large Belgian-Dutch and a Swiss population for a genetic association between COL1A1 and otosclerosis and additionally performed a meta-analysis to investigate the overall genetic effect of COL1A1 on all otosclerosis populations studied to date. We found a significant association both in the Belgian-Dutch population and in the meta-analysis. In aggregate, our analysis supports evidence for an association between COL1A1 and otosclerosis although effect sizes of the variants reported in the initial studies are likely to be an overestimate of true effect sizes.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22489040     DOI: 10.1002/ajmg.a.35276

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  Stapedotomy and its effect on hearing - our experience with 54 cases.

Authors:  Taiwo Olugbemiga Adedeji; Shabbir Indorewala; Abuzar Indorewala; Gaurav Nemade
Journal:  Afr Health Sci       Date:  2016-03       Impact factor: 0.927

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

Authors:  Allan Thomas Højland; Lisse J M Tavernier; Guy Van Camp; Erik Fransen; Isabelle Schrauwen; Manou Sommen; Vedat Topsakal; Isabelle Schatteman; Ingeborg Dhooge; Alex Huber; Diego Zanetti; Henricus P M Kunst; Alexander Hoischen; Michael B Petersen
Journal:  Hum Genet       Date:  2021-08-19       Impact factor: 4.132

Review 3.  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

4.  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

5.  Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling.

Authors:  Megan Ealy; Nicole C Meyer; Johnny Cruz Corchado; Isabelle Schrauwen; Andreas Bress; Markus Pfister; Guy Van Camp; Richard J H Smith
Journal:  Otol Neurotol       Date:  2014-03       Impact factor: 2.311

6.  Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis.

Authors:  Alexia Hawkey-Noble; Justin A Pater; Roshni Kollipara; Meriel Fitzgerald; Alexandre S Maekawa; Christopher S Kovacs; Terry-Lynn Young; Curtis R French
Journal:  Genes (Basel)       Date:  2022-06-21       Impact factor: 4.141

  6 in total

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