Literature DB >> 19323351

Audiological findings in osteogenesis imperfecta.

Joseph P Pillion1, Jay Shapiro.   

Abstract

BACKGROUND: Osteogenesis imperfecta (OI) is an inherited bone and connective tissue disorder associated with the lifelong occurrence of frequent fractures following even mild trauma. Hearing loss is frequently reported in patients with OI.
PURPOSE: This investigation is a retrospective study of measurements of tympanometry, acoustic reflexes, and transient evoked otoacoustic emissions in a sample of patients with OI grouped according to age. The purpose of the study was to examine the relationship between the type of OI, age, and audiological findings in a sample of individuals with OI. RESEARCH
DESIGN: The study examined the correlation between audiometric measures, hearing loss of all types, and type of OI. STUDY SAMPLE: Forty-one patients with OI were included in the study. The patients were divided into two groups for analysis: one group less than 20 years of age (n=21) and the other group aged 20 and over (n=20).
RESULTS: Hearing loss of all etiologies was observed in 62% of ears. Sensorineural or mixed hearing loss was observed in 41% and conductive hearing loss in 21% of ears. Results indicate that the younger patients with OI were subject to a greater risk of middle ear dysfunction associated with otitis media than is typical for children of comparable age. Tympanometric abnormalities associated with ossicular dysfunction were more often found in the older age group of patients. Hearing loss of all types was more prevalent in the older group of patients (88%) than in the younger patient group (38%).
CONCLUSIONS: Hearing loss was not uncommon regardless of age. Therefore, close audiological monitoring of patients with OI is recommended across the age spectrum.

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Mesh:

Year:  2008        PMID: 19323351     DOI: 10.3766/jaaa.19.8.3

Source DB:  PubMed          Journal:  J Am Acad Audiol        ISSN: 1050-0545            Impact factor:   1.664


  12 in total

1.  Impact of fracture characteristics and disease-specific complications on health-related quality of life in osteogenesis imperfecta.

Authors:  Masaki Matsushita; Kenichi Mishima; Satoshi Yamashita; Nobuhiko Haga; Sayaka Fujiwara; Keiichi Ozono; Takuo Kubota; Taichi Kitaoka; Naoki Ishiguro; Hiroshi Kitoh
Journal:  J Bone Miner Metab       Date:  2019-08-13       Impact factor: 2.626

2.  Osteogenesis imperfecta and hearing loss: an analysis of patients attended at a benchmark treatment center in southern Brazil.

Authors:  Andressa Colares da Costa Otavio; Adriane Ribeiro Teixeira; Temis Maria Félix; Letícia Petersen Schimidt Rosito; Sady Selaimen da Costa
Journal:  Eur Arch Otorhinolaryngol       Date:  2020-01-31       Impact factor: 2.503

3.  Osteogenesis imperfecta and the teeth, eyes, and ears-a study of non-skeletal phenotypes in adults.

Authors:  J D Hald; L Folkestad; C Z Swan; J Wanscher; M Schmidt; H Gjørup; D Haubek; C-H Leonhard; D A Larsen; J Ø Hjortdal; T Harsløf; M Duno; A M Lund; J-E B Jensen; K Brixen; B Langdahl
Journal:  Osteoporos Int       Date:  2018-08-24       Impact factor: 4.507

4.  Prolyl 3-hydroxylase-1 null mice exhibit hearing impairment and abnormal morphology of the middle ear bone joints.

Authors:  Elena Pokidysheva; Sara Tufa; Chris Bresee; John V Brigande; Hans Peter Bächinger
Journal:  Matrix Biol       Date:  2012-11-24       Impact factor: 11.583

5.  Health-related quality of life in adults with osteogenesis imperfecta.

Authors:  Chaya N Murali; Brady Slater; Salma Musaad; David Cuthbertson; Dianne Nguyen; Alicia Turner; Mahshid Azamian; Laura Tosi; Frank Rauch; V Reid Sutton; Brendan Lee; Sandesh C S Nagamani
Journal:  Clin Genet       Date:  2021-02-22       Impact factor: 4.438

6.  Current and emerging treatments for the management of osteogenesis imperfecta.

Authors:  Elena Monti; Monica Mottes; Paolo Fraschini; Piercarlo Brunelli; Antonella Forlino; Giacomo Venturi; Francesco Doro; Silvia Perlini; Paolo Cavarzere; Franco Antoniazzi
Journal:  Ther Clin Risk Manag       Date:  2010-09-07       Impact factor: 2.423

7.  Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotype.

Authors:  Freya K R Swinnen; Paul J Coucke; Anne M De Paepe; Sofie Symoens; Fransiska Malfait; Filomena V Gentile; Luca Sangiorgi; Patrizia D'Eufemia; Mauro Celli; Ton J T M Garretsen; Cor W R J Cremers; Ingeborg J M Dhooge; Els M R De Leenheer
Journal:  Orphanet J Rare Dis       Date:  2011-12-29       Impact factor: 4.123

8.  Incorporating the patient perspective in the study of rare bone disease: insights from the osteogenesis imperfecta community.

Authors:  T Swezey; B B Reeve; T S Hart; M K Floor; C M Dollar; A P Gillies; L L Tosi
Journal:  Osteoporos Int       Date:  2018-09-06       Impact factor: 4.507

9.  Hearing loss in osteogenesis imperfecta: characteristics and treatment considerations.

Authors:  Joseph P Pillion; David Vernick; Jay Shapiro
Journal:  Genet Res Int       Date:  2011-12-14

10.  Initial report of the osteogenesis imperfecta adult natural history initiative.

Authors:  Laura L Tosi; Matthew E Oetgen; Marianne K Floor; Mary Beth Huber; Ann M Kennelly; Robert J McCarter; Melanie F Rak; Barbara J Simmonds; Melissa D Simpson; Carole A Tucker; Fergus E McKiernan
Journal:  Orphanet J Rare Dis       Date:  2015-11-14       Impact factor: 4.123

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