Literature DB >> 17619837

Natural history of the respiratory involvement in Anderson-Fabry disease.

S Magage1, J-C Lubanda, Z Susa, J Bultas, D Karetová, R Dobrovolný, M Hrebícek, D P Germain, A Linhart.   

Abstract

BACKGROUND: Anderson-Fabry disease (AFD) is an X-linked disorder caused by deficient activity of enzyme alpha-galactosidase A, resulting in the accumulation of glycosphingolipids within lysosomes. Pulmonary involvement in AFD has previously been documented, but until now has been studied only in a few series of patients without any longitudinal follow-up. The aim of this study was to compare spirometric changes in AFD patients with a matched control population and to follow the subsequent progression of the disease.
MATERIALS AND METHODS: Fifty individuals (27 women, 23 men, mean age 40 +/- 14 years) with AFD from 14 families underwent a static spirometric examination under standard conditions. A set of indices was compared with that of the control population. Out of this cohort, 39 individuals not receiving enzyme replacement therapy were longitudinally evaluated (median follow-up time 24 months).
RESULTS: A clinically significant reduction in spirometric parameters, corresponding to mild to severe airway obstruction, was observed in 26% of women and 61% of men. During the serial follow-up, a significant (p < 0.05) age-dependent reduction of predicted %FVC and %FEV1 values was observed in male patients, while the influence of age was not seen in female patients. The %FEF(25-75) values decreased by similar degrees in men and women and in older and younger patients, indicating that progressive bronchial disease affects the small airways first.
CONCLUSIONS: We have demonstrated a clinically relevant age- and sex-dependent progressive pulmonary involvement in AFD patients. The effects of enzyme replacement therapy on pulmonary involvement remain to be demonstrated.

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Year:  2007        PMID: 17619837     DOI: 10.1007/s10545-007-0616-9

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  17 in total

1.  Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females.

Authors:  K D MacDermot; A Holmes; A H Miners
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

3.  Pulmonary vasculature in Fabry's disease.

Authors:  P Smith; D Heath; B Rodgers; T Helliwell
Journal:  Histopathology       Date:  1991-12       Impact factor: 5.087

4.  Chronic airflow obstruction in Fabry's disease.

Authors:  D M Rosenberg; V J Ferrans; J D Fulmer; B R Line; J A Barranger; R O Brady; R G Crystal
Journal:  Am J Med       Date:  1980-06       Impact factor: 4.965

5.  Pulmonary involvement in Fabry's disease.

Authors:  K Kariman; W V Singletary; H O Sieker
Journal:  Am J Med       Date:  1978-05       Impact factor: 4.965

6.  Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy.

Authors:  M Elleder; V Bradová; F Smíd; M Budĕsínský; K Harzer; B Kustermann-Kuhn; J Ledvinová; V Král; V Dorazilová
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Review 7.  Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy.

Authors:  Robert J Desnick; Roscoe Brady; John Barranger; Allan J Collins; Dominique P Germain; Martin Goldman; Gregory Grabowski; Seymour Packman; William R Wilcox
Journal:  Ann Intern Med       Date:  2003-02-18       Impact factor: 25.391

8.  Enzyme replacement therapy in Fabry disease: a randomized controlled trial.

Authors:  R Schiffmann; J B Kopp; H A Austin; S Sabnis; D F Moore; T Weibel; J E Balow; R O Brady
Journal:  JAMA       Date:  2001-06-06       Impact factor: 56.272

9.  Pulmonary involvement in Fabry disease.

Authors:  L K Brown; A Miller; A Bhuptani; M F Sloane; M I Zimmerman; G Schilero; C M Eng; R J Desnick
Journal:  Am J Respir Crit Care Med       Date:  1997-03       Impact factor: 21.405

10.  Optimal assessment and management of chronic obstructive pulmonary disease (COPD). The European Respiratory Society Task Force.

Authors:  N M Siafakas; P Vermeire; N B Pride; P Paoletti; J Gibson; P Howard; J C Yernault; M Decramer; T Higenbottam; D S Postma
Journal:  Eur Respir J       Date:  1995-08       Impact factor: 16.671

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  12 in total

1.  Enzyme replacement therapy stabilizes obstructive pulmonary Fabry disease associated with respiratory globotriaosylceramide storage.

Authors:  R Y Wang; J T Abe; A H Cohen; W R Wilcox
Journal:  J Inherit Metab Dis       Date:  2008-10-21       Impact factor: 4.982

2.  Sleep Disturbance, Obstructive Sleep Apnoea and Abnormal Periodic Leg Movements: Very Common Problems in Fabry Disease.

Authors:  Andrew Talbot; Gary Hammerschlag; Jeremy Goldin; Kathy Nicholls
Journal:  JIMD Rep       Date:  2016-03-24

Review 3.  The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.

Authors:  Dominique P Germain; Sergey Moiseev; Fernando Suárez-Obando; Faisal Al Ismaili; Huda Al Khawaja; Gheona Altarescu; Fellype C Barreto; Farid Haddoum; Fatemeh Hadipour; Irina Maksimova; Mirelle Kramis; Sheela Nampoothiri; Khanh Ngoc Nguyen; Dau-Ming Niu; Juan Politei; Long-Sun Ro; Dung Vu Chi; Nan Chen; Sergey Kutsev
Journal:  Mol Genet Genomic Med       Date:  2021-04-09       Impact factor: 2.183

Review 4.  Fabry disease.

Authors:  Dominique P Germain
Journal:  Orphanet J Rare Dis       Date:  2010-11-22       Impact factor: 4.123

5.  Long-term follow-up of pulmonary function in Fabry disease: A bi-center observational study.

Authors:  Daniel P Franzen; Albina Nowak; Sarah R Haile; Dominique Mottet; Marco Bonani; Olivier Dormond; Malcolm Kohler; Pierre A Krayenbuehl; Frederic Barbey
Journal:  PLoS One       Date:  2017-07-25       Impact factor: 3.240

6.  Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients.

Authors:  Dominique P Germain; Alain Fouilhoux; Stéphane Decramer; Marine Tardieu; Pascal Pillet; Marc Fila; Serge Rivera; Georges Deschênes; Didier Lacombe
Journal:  Clin Genet       Date:  2019-06-06       Impact factor: 4.438

7.  Case Report: First Two Identified Cases of Fabry Disease in Central Asia.

Authors:  Francesca Cainelli; Dias Argandykov; Dauren Kaldarbekov; Murat Mukarov; Liên Tran Thi Phuong; Dominique P Germain
Journal:  Front Genet       Date:  2021-04-27       Impact factor: 4.599

8.  A single lung transplant in a patient with fabry disease: causality or far-fetched? A case report.

Authors:  Martina Gaggl; Renate Kain; Peter Jaksch; Dominik Haider; Gerald Mundigler; Till Voigtländer; Raute Sunder-Plassmann; Paulus Rommer; Walter Klepetko; Gere Sunder-Plassmann
Journal:  Case Rep Transplant       Date:  2013-04-07

Review 9.  Fabry disease, respiratory symptoms, and airway limitation - a systematic review.

Authors:  Camilla Kara Svensson; Ulla Feldt-Rasmussen; Vibeke Backer
Journal:  Eur Clin Respir J       Date:  2015-06-26

10.  Pulmonary involvement in Fabry disease: effect of plasma globotriaosylsphingosine and time to initiation of enzyme replacement therapy.

Authors:  Daniel Franzen; Sarah R Haile; David C Kasper; Thomas P Mechtler; Andreas J Flammer; Pierre A Krayenbühl; Albina Nowak
Journal:  BMJ Open Respir Res       Date:  2018-04-21
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