Literature DB >> 15149877

Correlation of surrogate markers of Gaucher disease. Implications for long-term follow up of enzyme replacement therapy.

Mario A Cabrera-Salazar1, Erin O'Rourke, Nadene Henderson, Howard Wessel, John A Barranger.   

Abstract

BACKGROUND: The excessive storage of cellular debris in the lysosomal storage disorders triggers a variety of cellular responses. Some of these responses are maladaptative and result in the pathology of these diseases. To some extent, cellular responses are specific to the stored material, which influences the pathophysiology of the disease and results in some of its characteristic features.
METHODS: A large body of data has been collected for three biochemical (surrogate) markers of Gaucher Disease: angiotensin converting enzyme (ACE), tartrate-resistant acid phosphatase (TRAP) and chitotriosidase (CHITO) using currently available enzyme analysis. Follow up data was gathered in a group of 18 patients.
RESULTS: The three markers are correlated between each other and are useful indicators of the disease progress and its response to enzyme replacement therapy (ERT). Retrospective analysis of clinical records and comparison of chitotriosidase values with the baseline Severity Score Index (SSI) allowed prediction of the response patterns for this marker when long-term ERT (>24 months) was evaluated.
CONCLUSIONS: The less severely affected patients are more likely to normalize their chitotriosidase activities after long term ERT. Copyright 2004 Elsevier B.V.

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Year:  2004        PMID: 15149877     DOI: 10.1016/j.cccn.2004.02.018

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  15 in total

1.  Successful screening for Gaucher disease in a high-prevalence population in tabuleiro do Norte (northeastern Brazil): a cross-sectional study.

Authors:  Rigoberto Gadelha Chaves; Janice Carneiro Coelho; Kristiane Michelin-Tirelli; Tibelle Freitas Maurício; Edineide de Freitas Maia Chaves; Paulo César de Almeida; Carlos Rômulo Filgueira Maurício; Geraldo Barroso Cavalcanti
Journal:  JIMD Rep       Date:  2011-06-22

2.  Allele frequency of a 24 bp duplication in exon 10 of the CHIT1 gene in the general Korean population and in Korean patients with Gaucher disease.

Authors:  Kyu Ha Woo; Beom Hee Lee; Sun Hee Heo; Jae-Min Kim; Gu-Hwan Kim; Yoo-Mi Kim; Ja Hye Kim; In-Hee Choi; Song Hyun Yang; Han-Wook Yoo
Journal:  J Hum Genet       Date:  2014-03-13       Impact factor: 3.172

3.  Substrate reduction therapy of glycosphingolipid storage disorders.

Authors:  Johannes M F G Aerts; Carla E M Hollak; Rolf G Boot; Johanna E M Groener; Mario Maas
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

Review 4.  Laboratory and genetic evaluation of Gaucher disease.

Authors:  Olaf A Bodamer; Christina Hung
Journal:  Wien Med Wochenschr       Date:  2010-08-16

5.  Thirty-year clinical outcomes after haematopoietic stem cell transplantation in neuronopathic Gaucher disease.

Authors:  Aimee Donald; Cecilia Kämpe Björkvall; Ashok Vellodi; Timothy M Cox; Derralyn Hughes; Simon A Jones; Robert Wynn; Maciej Machaczka
Journal:  Orphanet J Rare Dis       Date:  2022-06-18       Impact factor: 4.303

6.  Bone events and evolution of biologic markers in Gaucher disease before and during treatment.

Authors:  Jérôme Stirnemann; Nadia Belmatoug; Corine Vincent; Olivier Fain; Bruno Fantin; France Mentré
Journal:  Arthritis Res Ther       Date:  2010-08-09       Impact factor: 5.156

7.  Evaluation of estimation methods and power of tests of discrete covariates in repeated time-to-event parametric models: application to Gaucher patients treated by imiglucerase.

Authors:  Marie Vigan; Jérôme Stirnemann; France Mentré
Journal:  AAPS J       Date:  2014-02-26       Impact factor: 4.009

Review 8.  Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring.

Authors:  T M Cox; J M F G Aerts; N Belmatoug; M D Cappellini; S vom Dahl; J Goldblatt; G A Grabowski; C E M Hollak; P Hwu; M Maas; A M Martins; P K Mistry; G M Pastores; A Tylki-Szymanska; J Yee; N Weinreb
Journal:  J Inherit Metab Dis       Date:  2008-05-23       Impact factor: 4.982

9.  Clinical and genetic characteristics of Gaucher disease according to phenotypic subgroups.

Authors:  Ju-Young Lee; Beom Hee Lee; Gu-Hwan Kim; Chang-Woo Jung; Jin Lee; Jin-Ho Choi; Han-Wook Yoo
Journal:  Korean J Pediatr       Date:  2012-02-14

10.  Increased tartrate-resistant acid phosphatase (TRAP) expression in malignant breast, ovarian and melanoma tissue: an investigational study.

Authors:  A Honig; L Rieger; M Kapp; M Krockenberger; M Eck; J Dietl; U Kämmerer
Journal:  BMC Cancer       Date:  2006-07-25       Impact factor: 4.430

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