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Erschienen in: Journal of Inherited Metabolic Disease 2/2015

01.03.2015 | Original Article

Hearing loss in adult patients with Fabry disease treated with enzyme replacement therapy

verfasst von: Eefje B. Suntjens, Bouwien E. Smid, Marieke Biegstraaten, Wouter A. Dreschler, Carla E. M. Hollak, Gabor E. Linthorst

Erschienen in: Journal of Inherited Metabolic Disease | Ausgabe 2/2015

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Abstract

Introduction

Data on prevalence, natural history, and effect of enzyme replacement therapy (ERT) on hearing loss (HL) in Fabry disease (FD) are scarce.

Methods

This is a retrospective study with cross-sectional and longitudinal analyses. Low and high-frequency HL in the Dutch FD cohort was studied in four groups: classical and non-classical FD patients with or without ERT. To study effects of ERT, longitudinal data, corrected for age and gender according to ISO-1999 guidelines, were analyzed with mixed models.

Results

In the cross-sectional analysis, 107 FD patients (41 males), median age 47.6 years (18.8–80.6) were analyzed. At baseline, i.e., before start of ERT, HL was present in 18 patients (16.8 %), of whom four had bilateral sensorineural HL. HL was more often present in patients with the classical phenotype than non-classical patients (p < 0.01). Likewise, males had more often HL than females. Compared to the general population, FD patients show a median HL of 8.2 dB at low frequencies (p < 0.01) and 29.5 dB at ultra-high frequencies (p < 0.01). Longitudinal analyses (n = 91) revealed that ERT treated patients show a similar rate of decline, not significantly different from healthy controls.

Conclusion

Adult FD patients, especially classical affected males, show impaired hearing. Longitudinal analyses during ERT in these patients demonstrates a decline of HL similar to healthy controls, but HL present before initiation of therapy cannot be reversed. Whether early therapy can prevent hearing loss is unknown.
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Literatur
Zurück zum Zitat Aerts JM, Groener JE, Kuiper S et al (2008) Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci U S A 105(8):2812–2817CrossRefPubMedCentralPubMed Aerts JM, Groener JE, Kuiper S et al (2008) Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci U S A 105(8):2812–2817CrossRefPubMedCentralPubMed
Zurück zum Zitat Altarescu GM, Goldfarb LG, Park KY et al (2001) Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease. Clin Genet 60(1):46–51CrossRefPubMed Altarescu GM, Goldfarb LG, Park KY et al (2001) Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease. Clin Genet 60(1):46–51CrossRefPubMed
Zurück zum Zitat Biegstraaten M, Hollak CE, Bakkers M, Faber CG, Aerts JM, van Schaik IN (2012) Small fiber neuropathy in Fabry disease. Mol Genet Metab 106(2):135–141CrossRefPubMed Biegstraaten M, Hollak CE, Bakkers M, Faber CG, Aerts JM, van Schaik IN (2012) Small fiber neuropathy in Fabry disease. Mol Genet Metab 106(2):135–141CrossRefPubMed
Zurück zum Zitat Brady RO, Schiffmann R (2000) Clinical features of and recent advances in therapy for Fabry disease. JAMA J Am Med Assoc 284(21):2771–2775CrossRef Brady RO, Schiffmann R (2000) Clinical features of and recent advances in therapy for Fabry disease. JAMA J Am Med Assoc 284(21):2771–2775CrossRef
Zurück zum Zitat Brady RO, Gal AE, Bradley RM, Martensson E, Warshaw AL, Laster L (1967) Enzymatic defect in Fabry’s disease. Ceramidetrihexosidase deficiency. N Engl J Med 276(21):1163–1167CrossRefPubMed Brady RO, Gal AE, Bradley RM, Martensson E, Warshaw AL, Laster L (1967) Enzymatic defect in Fabry’s disease. Ceramidetrihexosidase deficiency. N Engl J Med 276(21):1163–1167CrossRefPubMed
Zurück zum Zitat Conti G, Sergi B (2003) Auditory and vestibular findings in Fabry disease: a study of hemizygous males and heterozygous females. Acta Paediatr (Oslo, Norway: 1992) 92(Supplement443):33–37, discussion 27 Conti G, Sergi B (2003) Auditory and vestibular findings in Fabry disease: a study of hemizygous males and heterozygous females. Acta Paediatr (Oslo, Norway: 1992) 92(Supplement443):33–37, discussion 27
Zurück zum Zitat Dreschler WA, vd Hulst RJ, Tange RA, Urbanus NA (1985) The role of high-frequency audiometry in early detection of ototoxicity. Audiol Off Organ Int Soc Audiol 24(6):387–395CrossRef Dreschler WA, vd Hulst RJ, Tange RA, Urbanus NA (1985) The role of high-frequency audiometry in early detection of ototoxicity. Audiol Off Organ Int Soc Audiol 24(6):387–395CrossRef
Zurück zum Zitat Germain DP (2002) Fabry’s disease (alpha-galactosidase-A deficiency): physiopathology, clinical signs, and genetic aspects. J Soc Biol 196(2):161–173PubMed Germain DP (2002) Fabry’s disease (alpha-galactosidase-A deficiency): physiopathology, clinical signs, and genetic aspects. J Soc Biol 196(2):161–173PubMed
Zurück zum Zitat Germain DP, Avan P, Chassaing A, Bonfils P (2002) Patients affected with Fabry disease have an increased incidence of progressive hearing loss and sudden deafness: an investigation of 22 hemizygous male patients. BMC Med Genet 3:10CrossRefPubMedCentralPubMed Germain DP, Avan P, Chassaing A, Bonfils P (2002) Patients affected with Fabry disease have an increased incidence of progressive hearing loss and sudden deafness: an investigation of 22 hemizygous male patients. BMC Med Genet 3:10CrossRefPubMedCentralPubMed
Zurück zum Zitat Hajioff D, Enever Y, Quiney R, Zuckerman J, Mackermot K, Mehta A (2003a) Hearing loss in Fabry disease: the effect of agalsidase alfa replacement therapy. J Inherit Metab Dis 26(8):787–794CrossRefPubMed Hajioff D, Enever Y, Quiney R, Zuckerman J, Mackermot K, Mehta A (2003a) Hearing loss in Fabry disease: the effect of agalsidase alfa replacement therapy. J Inherit Metab Dis 26(8):787–794CrossRefPubMed
Zurück zum Zitat Hajioff D, Goodwin S, Quiney R, Zuckerman J, MacDermot KD, Mehta A (2003b) Hearing improvement in patients with Fabry disease treated with agalsidase alfa. Acta Paediatr (Oslo, Norway : 1992) 92(Supplement 443):28–30, discussion 27 Hajioff D, Goodwin S, Quiney R, Zuckerman J, MacDermot KD, Mehta A (2003b) Hearing improvement in patients with Fabry disease treated with agalsidase alfa. Acta Paediatr (Oslo, Norway : 1992) 92(Supplement 443):28–30, discussion 27
Zurück zum Zitat Hajioff D, Hegemann S, Conti G et al (2006) Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey. Eur J Clin Investig 36(9):663–667CrossRef Hajioff D, Hegemann S, Conti G et al (2006) Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey. Eur J Clin Investig 36(9):663–667CrossRef
Zurück zum Zitat Hegemann S, Hajioff D, Conti G et al (2006) Hearing loss in Fabry disease: data from the Fabry Outcome Survey. Eur J Clin Investig 36(9):654–662CrossRef Hegemann S, Hajioff D, Conti G et al (2006) Hearing loss in Fabry disease: data from the Fabry Outcome Survey. Eur J Clin Investig 36(9):654–662CrossRef
Zurück zum Zitat Johansson MS, Arlinger SD (2002) Hearing threshold levels for an otologically unscreened, non-occupationally noise-exposed population in Sweden. Int J Audiol 41(3):180–194CrossRefPubMed Johansson MS, Arlinger SD (2002) Hearing threshold levels for an otologically unscreened, non-occupationally noise-exposed population in Sweden. Int J Audiol 41(3):180–194CrossRefPubMed
Zurück zum Zitat Kaminsky P, Noel E, Jaussaud R et al (2013) Multidimensional analysis of clinical symptoms in patients with Fabry’s disease. Int J Clin Pract 67(2):120–127CrossRefPubMed Kaminsky P, Noel E, Jaussaud R et al (2013) Multidimensional analysis of clinical symptoms in patients with Fabry’s disease. Int J Clin Pract 67(2):120–127CrossRefPubMed
Zurück zum Zitat MacDermot KD, Holmes A, Miners AH (2001) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet 38(11):750–760CrossRefPubMedCentralPubMed MacDermot KD, Holmes A, Miners AH (2001) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet 38(11):750–760CrossRefPubMedCentralPubMed
Zurück zum Zitat Mehta A, Beck M, Elliott P et al (2009) Enzyme replacement therapy with agalsidase alfa in patients with Fabry’s disease: an analysis of registry data. Lancet 374(9706):1986–1996CrossRefPubMed Mehta A, Beck M, Elliott P et al (2009) Enzyme replacement therapy with agalsidase alfa in patients with Fabry’s disease: an analysis of registry data. Lancet 374(9706):1986–1996CrossRefPubMed
Zurück zum Zitat Narozny W, Gromnicki M, Majkowicz M, Kuczkowski J, Sochaczewska A (2014) Quality of life patients with sudden sensorineural hearing loss. Otolaryngol Polska Polish Otolaryngol 68(2):69–76CrossRef Narozny W, Gromnicki M, Majkowicz M, Kuczkowski J, Sochaczewska A (2014) Quality of life patients with sudden sensorineural hearing loss. Otolaryngol Polska Polish Otolaryngol 68(2):69–76CrossRef
Zurück zum Zitat Palla A, Hegemann S, Widmer U, Straumann D (2007) Vestibular and auditory deficits in Fabry disease and their response to enzyme replacement therapy. J Neurol 254(10):1433–1442CrossRefPubMed Palla A, Hegemann S, Widmer U, Straumann D (2007) Vestibular and auditory deficits in Fabry disease and their response to enzyme replacement therapy. J Neurol 254(10):1433–1442CrossRefPubMed
Zurück zum Zitat Ries M, Kim HJ, Zalewski CK et al (2007) Neuropathic and cerebrovascular correlates of hearing loss in Fabry disease. Brain J Neurol 130(Pt 1):143–150 Ries M, Kim HJ, Zalewski CK et al (2007) Neuropathic and cerebrovascular correlates of hearing loss in Fabry disease. Brain J Neurol 130(Pt 1):143–150
Zurück zum Zitat Rombach SM, Dekker N, Bouwman MG et al (2010a) Plasma globotriaosylsphingosine: diagnostic value and relation to clinical manifestations of Fabry disease. Biochim Biophys Acta 1802(9):741–748CrossRefPubMed Rombach SM, Dekker N, Bouwman MG et al (2010a) Plasma globotriaosylsphingosine: diagnostic value and relation to clinical manifestations of Fabry disease. Biochim Biophys Acta 1802(9):741–748CrossRefPubMed
Zurück zum Zitat Rombach SM, Twickler TB, Aerts JM, Linthorst GE, Wijburg FA, Hollak CE (2010b) Vasculopathy in patients with Fabry disease: current controversies and research directions. Mol Genet Metab 99(2):99–108CrossRefPubMed Rombach SM, Twickler TB, Aerts JM, Linthorst GE, Wijburg FA, Hollak CE (2010b) Vasculopathy in patients with Fabry disease: current controversies and research directions. Mol Genet Metab 99(2):99–108CrossRefPubMed
Zurück zum Zitat Rombach SM, Smid BE, Bouwman MG, Linthorst GE, Dijkgraaf MG, Hollak CE (2013) Long term enzyme replacement therapy for Fabry disease: effectiveness on kidney, heart and brain. Orphanet J Rare Dis 8:47CrossRefPubMedCentralPubMed Rombach SM, Smid BE, Bouwman MG, Linthorst GE, Dijkgraaf MG, Hollak CE (2013) Long term enzyme replacement therapy for Fabry disease: effectiveness on kidney, heart and brain. Orphanet J Rare Dis 8:47CrossRefPubMedCentralPubMed
Zurück zum Zitat Sakurai Y, Kojima H, Shiwa M, Ohashi T, Eto Y, Moriyama H (2009) The hearing status in 12 female and 15 male Japanese Fabry patients. Auris Nasus Larynx 36(6):627–632CrossRefPubMed Sakurai Y, Kojima H, Shiwa M, Ohashi T, Eto Y, Moriyama H (2009) The hearing status in 12 female and 15 male Japanese Fabry patients. Auris Nasus Larynx 36(6):627–632CrossRefPubMed
Zurück zum Zitat Sakurai Y, Suzuki R, Yoshida R et al (2010) Inner ear pathology of alpha-galactosidase A deficient mice, a model of Fabry disease. Auris Nasus Larynx 37(3):274–280CrossRefPubMed Sakurai Y, Suzuki R, Yoshida R et al (2010) Inner ear pathology of alpha-galactosidase A deficient mice, a model of Fabry disease. Auris Nasus Larynx 37(3):274–280CrossRefPubMed
Zurück zum Zitat Schachern PA, Shea DA, Paparella MM, Yoon TH (1989) Otologic histopathology of Fabry’s disease. Ann Otol Rhinol Laryngol 98(5 Pt 1):359–363CrossRefPubMed Schachern PA, Shea DA, Paparella MM, Yoon TH (1989) Otologic histopathology of Fabry’s disease. Ann Otol Rhinol Laryngol 98(5 Pt 1):359–363CrossRefPubMed
Zurück zum Zitat Sergi B, Conti G, Paludetti G, Interdisciplinary Study Group On Fabry D (2010) Inner ear involvement in Anderson-Fabry disease: long-term follow-up during enzyme replacement therapy. Acta Otorhinolaryngol Ital organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 30(2):87–93 Sergi B, Conti G, Paludetti G, Interdisciplinary Study Group On Fabry D (2010) Inner ear involvement in Anderson-Fabry disease: long-term follow-up during enzyme replacement therapy. Acta Otorhinolaryngol Ital organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 30(2):87–93
Zurück zum Zitat Sirrs SM, Bichet DG, Casey R et al (2014) Outcomes of patients treated through the Canadian Fabry disease initiative. Mol Genet Metab 111(4):499–506CrossRefPubMed Sirrs SM, Bichet DG, Casey R et al (2014) Outcomes of patients treated through the Canadian Fabry disease initiative. Mol Genet Metab 111(4):499–506CrossRefPubMed
Zurück zum Zitat Standardization IOo (1990) Acoustics — determination of occupational noise exposure and estimation of noise-induced hearing impairment 1990REP. No. ISO 1999 Standardization IOo (1990) Acoustics — determination of occupational noise exposure and estimation of noise-induced hearing impairment 1990REP. No. ISO 1999
Zurück zum Zitat van der Tol L, Smid BE, Poorthuis BJ, et al (2014) A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance. J Med Genet 5(11):1–9 van der Tol L, Smid BE, Poorthuis BJ, et al (2014) A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance. J Med Genet 5(11):1–9
Zurück zum Zitat Vedder AC, Linthorst GE, Houge G et al (2007) Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2 mg/kg. PLoS One 2(7):e598CrossRefPubMedCentralPubMed Vedder AC, Linthorst GE, Houge G et al (2007) Treatment of Fabry disease: outcome of a comparative trial with agalsidase alfa or beta at a dose of 0.2 mg/kg. PLoS One 2(7):e598CrossRefPubMedCentralPubMed
Zurück zum Zitat Watt T, Burlina AP, Cazzorla C et al (2010) Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry. Genet Med Off J Am Coll Med Genet 12(11):703–712 Watt T, Burlina AP, Cazzorla C et al (2010) Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry. Genet Med Off J Am Coll Med Genet 12(11):703–712
Zurück zum Zitat Weidemann F, Niemann M, Stork S et al (2013) Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications. J Intern Med 274(4):331–341CrossRefPubMedCentralPubMed Weidemann F, Niemann M, Stork S et al (2013) Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications. J Intern Med 274(4):331–341CrossRefPubMedCentralPubMed
Zurück zum Zitat Whybra C, Kampmann C, Krummenauer F et al (2004) The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy. Clin Genet 65(4):299–307CrossRefPubMed Whybra C, Kampmann C, Krummenauer F et al (2004) The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy. Clin Genet 65(4):299–307CrossRefPubMed
Metadaten
Titel
Hearing loss in adult patients with Fabry disease treated with enzyme replacement therapy
verfasst von
Eefje B. Suntjens
Bouwien E. Smid
Marieke Biegstraaten
Wouter A. Dreschler
Carla E. M. Hollak
Gabor E. Linthorst
Publikationsdatum
01.03.2015
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe 2/2015
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-014-9783-7

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