Literature DB >> 24594444

Assessment of hearing loss by pure-tone audiometry in patients with mucopolysaccharidoses.

Hsiang-Yu Lin1, Shou-Chuan Shih2, Chih-Kuang Chuang3, Kuo-Sheng Lee4, Ming-Ren Chen5, Hung-Ching Lin6, Pao Chin Chiu7, Dau-Ming Niu8, Shuan-Pei Lin9.   

Abstract

BACKGROUND: Patients with mucopolysaccharidoses (MPS) often have hearing loss. However, the characterization of hearing loss by pure-tone audiometry (PTA) in this rare disease population and its relationship to age and treatment is limited.
METHODS: PTA was performed in 39 patients with MPS (29 males and 10 females; 3 with MPS I, 21 with MPS II, 9 with MPS IVA, and 6 with MPS VI; median age, 11.9 years; age range, 4.4-34.2 years). The degree of hearing loss was classified by the age-independent World Health Organization (WHO) clinical guidelines.
RESULTS: Hearing loss by PTA was present in 85% (33/39) of patients and was categorized as mild (26-40 dB) in 18%, moderate (41-60 dB) in 36%, severe (61-80 dB) in 23%, and profound (≥81dB) in 5%. Among the patients with hearing loss, 33% were classified as mixed type (conductive and sensorineural), 30% as pure conductive type, 27% as pure sensorineural type, and 9% were undefined. The means of the right and left ear hearing thresholds at 2000 and 4000 Hz by air conduction (AC) and at 500, 1000, 2000, and 4000 Hz by bone conduction (BC) were all positively correlated with age (p<0.05). In the 6 patients with MPS II or VI who underwent follow-up PTA after ventilation tube insertion and enzyme replacement therapy for 1.9 to 8.5 years, all showed improvements in AC and BC of the better ear, as well as in the air-bone gap.
CONCLUSIONS: Hearing impairment is common in MPS. Early otolaryngological evaluation and intervention are recommended. These findings and the follow-up data can be used to develop quality of care strategies for patients with MPS.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Enzyme replacement therapy; Hearing loss; Mucopolysaccharidoses; Pure-tone audiometry

Mesh:

Year:  2014        PMID: 24594444     DOI: 10.1016/j.ymgme.2014.02.003

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  21 in total

Review 1.  Lysosomal Leukodystrophies Lysosomal Storage Diseases Associated With White Matter Abnormalities.

Authors:  Gustavo H B Maegawa
Journal:  J Child Neurol       Date:  2019-02-13       Impact factor: 1.987

2.  Hearing Loss in Patients With Morquio Syndrome: Protocol for a Scoping Review.

Authors:  Lorena Diaz-Ordoñez; Estephania Candelo; Katherine Silva-Cuero; Wilmar Saldarriaga; Lenka Murgašová; Martin Magner; Harry Pachajoa
Journal:  JMIR Res Protoc       Date:  2022-06-07

3.  Quantifying medical manifestations in Hurler syndrome with the infant physical symptom score: associations with long-term physical and adaptive outcomes.

Authors:  Alia Ahmed; Kyle Rudser; Kelly E King; Julie B Eisengart; Paul J Orchard; Elsa Shapiro; Chester B Whitley
Journal:  Mol Genet Metab       Date:  2022-03-10       Impact factor: 4.204

Review 4.  Molecular genetics and metabolism, special edition: Diagnosis, diagnosis and prognosis of Mucopolysaccharidosis IVA.

Authors:  Hira Peracha; Kazuki Sawamoto; Lauren Averill; Heidi Kecskemethy; Mary Theroux; Mihir Thacker; Kyoko Nagao; Christian Pizarro; William Mackenzie; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Toshiyuki Fukao; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2018-05-15       Impact factor: 4.797

5.  Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children.

Authors:  A Soni-Jaiswal; J Mercer; S A Jones; I A Bruce; P Callery
Journal:  Orphanet J Rare Dis       Date:  2016-07-12       Impact factor: 4.123

6.  Neurophysiology of hearing in patients with mucopolysaccharidosis type IV.

Authors:  Kyoko Nagao; Thierry Morlet; Elizabeth Haley; Jennifer Padilla; Julianne Nemith; Robert W Mason; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2018-02-08       Impact factor: 4.204

7.  A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses.

Authors:  Chih-Kuang Chuang; Hsiang-Yu Lin; Tuen-Jen Wang; Chia-Chen Tsai; Hsuan-Liang Liu; Shuan-Pei Lin
Journal:  Orphanet J Rare Dis       Date:  2014-09-02       Impact factor: 4.123

8.  Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series.

Authors:  Hsiang-Yu Lin; Chih-Kuang Chuang; Chung-Hsing Wang; Yin-Hsiu Chien; Yu-Mei Wang; Fuu-Jen Tsai; Yen-Yin Chou; Shio Jean Lin; Hui-Ping Pan; Dau-Ming Niu; Wuh-Liang Hwu; Yu-Yuan Ke; Shuan-Pei Lin
Journal:  Mol Genet Metab Rep       Date:  2016-04-18

9.  Hearing loss in children with Fabry disease.

Authors:  E Suntjens; W A Dreschler; J Hess-Erga; R Skrunes; F A Wijburg; G E Linthorst; C Tøndel; M Biegstraaten
Journal:  J Inherit Metab Dis       Date:  2017-05-31       Impact factor: 4.982

Review 10.  Mucopolysaccharidosis Type I: A Review of the Natural History and Molecular Pathology.

Authors:  Christiane S Hampe; Julie B Eisengart; Troy C Lund; Paul J Orchard; Monika Swietlicka; Jacob Wesley; R Scott McIvor
Journal:  Cells       Date:  2020-08-05       Impact factor: 6.600

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