Literature DB >> 19797197

Screening for Fabry disease in high-risk populations: a systematic review.

G E Linthorst1, M G Bouwman, F A Wijburg, J M F G Aerts, B J H M Poorthuis, C E M Hollak.   

Abstract

INTRODUCTION: Fabry disease (FD) may present with left ventricular hypertrophy (LVH), renal insufficiency or stroke. Several studies investigated FD prevalence in populations expressing these symptoms. A systematic review was conducted to calculate the overall prevalence of FD in these cohorts.
METHODS: Online databases were searched for studies on screening for FD. Study population selection, screening methods and outcome of screening were recorded.
RESULTS: 20 studies were identified, 10 of which included both male and female patients. In all (n=19) studies with male and almost all (n=10) with female patients, alpha-galactosidase A (alpha-Gal A) activity was used as the screening method. In men on dialysis (10 studies), overall FD prevalence was 0.33% (95% CI 0.20% to 0.47%) and in women (6 studies) 0.10% (95% CI 0% to 0.19%). Combined prevalence of FD in patients with renal transplant was 0.38% in men (95% CI 0.07% to 0.69%) and 0% in women. In patients with LVH, selection of study population and differences in the method of screening hampered the calculation of an overall prevalence (ranging from 0.9% to 3.9% in men and 1.1% to 11.8% in women). In premature strokes (n=2 studies), overall FD prevalence was 4.2% (95% CI 2.4% to 6.0%) in men and 2.1% (95% CI 0.5% to 3.7%) in women. DISCUSSION: The prevalence of FD in dialysis patients is 0.33% for men and 0.10% for women. The prevalence of FD in LVH is at least 1% for both genders. In women, most studies were performed with alpha-Gal A activity measurements as the screening tool, although this method fails to detect one third of female patients with FD, underestimating the overall prevalence in women.

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Year:  2009        PMID: 19797197     DOI: 10.1136/jmg.2009.072116

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  48 in total

Review 1.  Fabry disease, enzyme replacement therapy and the significance of antibody responses.

Authors:  Patrick B Deegan
Journal:  J Inherit Metab Dis       Date:  2011-10-25       Impact factor: 4.982

2.  Fabry or not Fabry--a question of ascertainment.

Authors:  Gunnar Houge; Camilla Tøndel; Oyvind Kaarbøe; Asle Hirth; Leif Bostad; Einar Svarstad
Journal:  Eur J Hum Genet       Date:  2011-05-18       Impact factor: 4.246

3.  Considering Fabry, but Diagnosing MPS I: Difficulties in the Diagnostic Process.

Authors:  E J Langereis; I E T van den Berg; D J J Halley; B J H M Poorthuis; F M Vaz; J H J Wokke; G E Linthorst
Journal:  JIMD Rep       Date:  2012-10-30

4.  Lyso-Gb3 Indicates that the Alpha-Galactosidase A Mutation D313Y is not Clinically Relevant for Fabry Disease.

Authors:  Markus Niemann; Arndt Rolfs; Anne Giese; Hermann Mascher; Frank Breunig; Georg Ertl; Christoph Wanner; Frank Weidemann
Journal:  JIMD Rep       Date:  2012-07-01

5.  The Prevalence and Clinical Features of Fabry Disease in Hemodialysis Patients: Russian Nationwide Fabry Dialysis Screening Program.

Authors:  Sergey Moiseev; Victor Fomin; Kirill Savostyanov; Alexander Pushkov; Alexey Moiseev; Andrey Svistunov; Leyla Namazova-Baranova
Journal:  Nephron       Date:  2019-01-24       Impact factor: 2.847

6.  Fabry disease: incidence of the common later-onset α-galactosidase A IVS4+919G→A mutation in Taiwanese newborns--superiority of DNA-based to enzyme-based newborn screening for common mutations.

Authors:  Yin-Hsiu Chien; Ni-Chung Lee; Shu-Chuan Chiang; Robert J Desnick; Wuh-Liang Hwu
Journal:  Mol Med       Date:  2012-07-18       Impact factor: 6.354

Review 7.  Stroke and Fabry disease.

Authors:  Miguel Viana-Baptista
Journal:  J Neurol       Date:  2011-10-27       Impact factor: 4.849

8.  Newborn screening for lysosomal storage diseases: an ethical and policy analysis.

Authors:  Lainie Friedman Ross
Journal:  J Inherit Metab Dis       Date:  2011-12-22       Impact factor: 4.982

9.  A case of female Fabry disease revealed by renal biopsy.

Authors:  Sae Aratani; Hiroyuki Yamakawa; Shinya Suzuki; Tomoyuki Otsuka; Yukinao Sakai; Akira Shimizu; Shuichi Tsuruoka
Journal:  CEN Case Rep       Date:  2019-09-21

10.  Exploratory screening for Fabry's disease in young adults with cerebrovascular disorders in northern Sardinia.

Authors:  Laura Fancellu; Walter Borsini; Ilaria Romani; Angelo Pirisi; Giovanni Andrea Deiana; Elia Sechi; Pietro Emiliano Doneddu; Anna Laura Rassu; Rita Demurtas; Anna Scarabotto; Pamela Cassini; Eloisa Arbustini; GianPietro Sechi
Journal:  BMC Neurol       Date:  2015-12-12       Impact factor: 2.474

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