Literature DB >> 15303007

Relief of gastrointestinal symptoms under enzyme replacement therapy [corrected] in patients with Fabry disease.

F Dehout1, D Roland, S Treille de Granseigne, B Guillaume, L Van Maldergem.   

Abstract

Gastrointestinal symptoms, including diarrhoea and abdominal pain, are one of the earliest and most frequently reported signs of Fabry disease, a rare X-linked lipid storage disorder. As the disease progresses, renal, cardiac and cerebrovascular complications develop, resulting in more serious symptoms and early mortality. The present study evaluated the effects of enzyme replacement therapy (ERT) with agalsidase alfa on the gastrointestinal symptoms of Fabry disease. Following 6 months of treatment, both the severity ( p < 0.02) and frequency ( p < 0.02) of abdominal pain decreased. For those patients who had received agalsidase alfa for more than 6 months, the observed improvement was generally maintained. This is the first study indicating a significant beneficial effect of ERT on gastrointestinal symptoms in a group of patients treated for Fabry disease.

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Year:  2004        PMID: 15303007     DOI: 10.1023/B:BOLI.0000037342.59612.69

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


  14 in total

1.  Gastrointestinal symptoms and delayed gastric emptying in Fabry's disease: response to metoclopramide.

Authors:  C E Argoff; N W Barton; R O Brady; H A Ziessman
Journal:  Nucl Med Commun       Date:  1998-09       Impact factor: 1.690

2.  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

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

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Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

4.  Gastrointestinal structure and function in Fabry's disease.

Authors:  K J Sheth; S L Werlin; M E Freeman; A E Hodach
Journal:  Am J Gastroenterol       Date:  1981-09       Impact factor: 10.864

5.  Jejunal diverticulosis with perforation as a complication of Fabry's disease.

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Journal:  Gastroenterology       Date:  1984-03       Impact factor: 22.682

6.  Intestinal manifestations of Fabry's disease.

Authors:  J W Rowe; J I Gilliam; T A Warthin
Journal:  Ann Intern Med       Date:  1974-11       Impact factor: 25.391

7.  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

Review 8.  [Fabry's disease: diagnosis in the pediatric age group].

Authors:  G Pintos Morell
Journal:  An Esp Pediatr       Date:  2002-07

9.  Quality of life of patients with Fabry disease.

Authors:  K F Gold; G M Pastores; M F Botteman; J M Yeh; S Sweeney; W Aliski; C L Pashos
Journal:  Qual Life Res       Date:  2002-06       Impact factor: 4.147

10.  Small bowel ischaemia in Fabry's disease.

Authors:  D L Jardine; M A Fitzpatrick; W D Troughton; A B Tie
Journal:  J Gastroenterol Hepatol       Date:  1994 Mar-Apr       Impact factor: 4.029

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  15 in total

1.  Exocrine pancreatic insufficiency is not a cause of abdominal complaints in patients with Fabry disease.

Authors:  Miroslav Vujasinovic; Bojan Tepes; Bojan Vujkovac; Andreja Cokan Vujkovac; Martin Tretjak; Vesna Korat
Journal:  Wien Klin Wochenschr       Date:  2015-04-03       Impact factor: 1.704

Review 2.  Effects of Enzyme Replacement Therapy and Antidrug Antibodies in Patients with Fabry Disease.

Authors:  Malte Lenders; Eva Brand
Journal:  J Am Soc Nephrol       Date:  2018-08-09       Impact factor: 10.121

3.  Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing.

Authors:  Raphael Schiffmann; Hasan Askari; Margaret Timmons; Chevalia Robinson; William Benko; Roscoe O Brady; Markus Ries
Journal:  J Am Soc Nephrol       Date:  2007-04-04       Impact factor: 10.121

Review 4.  Enzyme replacement therapy of Fabry disease.

Authors:  Joe T R Clarke; R Mark Iwanochko
Journal:  Mol Neurobiol       Date:  2005-08       Impact factor: 5.590

5.  Enzyme replacement therapy for Fabry disease: some answers but more questions.

Authors:  Majid Alfadhel; Sandra Sirrs
Journal:  Ther Clin Risk Manag       Date:  2011-02-25       Impact factor: 2.423

Review 6.  Update on role of agalsidase alfa in management of Fabry disease.

Authors:  Uma Ramaswami
Journal:  Drug Des Devel Ther       Date:  2011-03-14       Impact factor: 4.162

Review 7.  Enzyme replacement therapy for Anderson-Fabry disease: A complementary overview of a Cochrane publication through a linear regression and a pooled analysis of proportions from cohort studies.

Authors:  Regina El Dib; Huda Gomaa; Alberto Ortiz; Juan Politei; Anil Kapoor; Fellype Barreto
Journal:  PLoS One       Date:  2017-03-15       Impact factor: 3.240

8.  Chronic intestinal pseudo-obstruction. Did you search for lysosomal storage diseases?

Authors:  J Politei; C Durand; A B Schenone; A Torres; J Mukdsi; B L Thurberg
Journal:  Mol Genet Metab Rep       Date:  2017-03-25

9.  Clinical-Pathological Conference Series from the Medical University of Graz : Case No 153: A 55-year-old woman with atypical multiple sclerosis and irritable bowel syndrome.

Authors:  Elisabeth Fabian; Dietmar Schiller; Hermann Toplak; Michaela Brunner-Krainz; Franz Fazekas; Rainer Schoefl; Guenter J Krejs
Journal:  Wien Klin Wochenschr       Date:  2017-11-21       Impact factor: 1.704

10.  Gastrointestinal Symptoms of Patients with Fabry Disease.

Authors:  Licia Pensabene; Simona Sestito; Angela Nicoletti; Francesca Graziano; Pietro Strisciuglio; Daniela Concolino
Journal:  Gastroenterol Res Pract       Date:  2015-12-31       Impact factor: 2.260

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