Literature DB >> 18003767

Screening for Fabry disease in patients with chronic kidney disease: limitations of plasma alpha-galactosidase assay as a screening test.

Jason Andrade1, Paula J Waters, R Suneet Singh, Adeera Levin, Bee-Chin Toh, Hilary D Vallance, Sandra Sirrs.   

Abstract

BACKGROUND AND OBJECTIVES: Fabry disease is a progressive X-linked disorder of glycosphingolipid metabolism that typically presents in childhood and progresses to heart failure and renal failure in adulthood. This study sought to determine the prevalence of Fabry disease in a multiethnic male chronic kidney disease population, involving dialysis-dependent, non-dialysis-dependent, and transplant patients. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A total of 499 patients were screened with assay of alpha-galactosidase activity using fluorometric enzyme assay on plasma prepared from fresh heparinized blood, followed by leukocyte alpha-galactosidase activity in the subset of patients with plasma alpha-galactosidase activity below the second percentile (corresponding to a value <3.0 nmol/h per ml plasma).
RESULTS: This study did not identify any new cases of Fabry disease; however, repeat testing of some of the study patients identified three limitations of the plasma enzyme assay that is commonly used as a high throughput screening method for Fabry disease: (1) False-negative results can occur; (2) these false-negative results are not prevented by use of inhibitors of alpha-galactosidase B activity; and (3) considerable intraindividual variation in plasma alpha-galactosidase levels reduces the discriminatory power of the screening test.
CONCLUSION: Clinicians need to be aware that screening using plasma will fail to detect some patients with Fabry disease.

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Year:  2007        PMID: 18003767      PMCID: PMC2390977          DOI: 10.2215/CJN.02490607

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  20 in total

1.  Natural history of Fabry disease in females in the Fabry Outcome Survey.

Authors:  P B Deegan; A F Baehner; M-A Barba Romero; D A Hughes; C Kampmann; M Beck
Journal:  J Med Genet       Date:  2005-10-14       Impact factor: 6.318

2.  Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase A.

Authors:  Y Nagao; H Nakashima; Y Fukuhara; M Shimmoto; A Oshima; Y Ikari; Y Mori; H Sakuraba; Y Suzuki
Journal:  Clin Genet       Date:  1991-03       Impact factor: 4.438

3.  An atypical variant of Fabry's disease with manifestations confined to the myocardium.

Authors:  W von Scheidt; C M Eng; T F Fitzmaurice; E Erdmann; G Hübner; E G Olsen; H Christomanou; R Kandolf; D F Bishop; R J Desnick
Journal:  N Engl J Med       Date:  1991-02-07       Impact factor: 91.245

4.  Significance of screening for Fabry disease among male dialysis patients.

Authors:  Mayuri Ichinose; Masaaki Nakayama; Toya Ohashi; Yasunori Utsunomiya; Masahisa Kobayashi; Yoshikatsu Eto
Journal:  Clin Exp Nephrol       Date:  2005-09       Impact factor: 2.801

5.  High incidence of later-onset fabry disease revealed by newborn screening.

Authors:  Marco Spada; Severo Pagliardini; Makiko Yasuda; Turgut Tukel; Geetha Thiagarajan; Hitoshi Sakuraba; Alberto Ponzone; Robert J Desnick
Journal:  Am J Hum Genet       Date:  2006-04-28       Impact factor: 11.025

6.  Fabry disease in patients with end-stage renal failure: the potential benefits of screening.

Authors:  Soumeya Bekri; Adrian Enica; Thomas Ghafari; Gisèle Plaza; Isabelle Champenois; Gabriel Choukroun; Robert Unwin; Philippe Jaeger
Journal:  Nephron Clin Pract       Date:  2005-05-09

Review 7.  Chronic renal failure, dialysis, and renal transplantation in Anderson-Fabry disease.

Authors:  Adalberto Sessa; Mietta Meroni; Graziana Battini; Marco Righetti; Renzo Mignani
Journal:  Semin Nephrol       Date:  2004-09       Impact factor: 5.299

8.  An atypical variant of Fabry's disease in men with left ventricular hypertrophy.

Authors:  S Nakao; T Takenaka; M Maeda; C Kodama; A Tanaka; M Tahara; A Yoshida; M Kuriyama; H Hayashibe; H Sakuraba
Journal:  N Engl J Med       Date:  1995-08-03       Impact factor: 91.245

9.  Enzyme replacement therapy administered during hemodialysis in patients with Fabry disease.

Authors:  Markus Kosch; Hans-Georg Koch; Joao Paulo Oliveira; Carlos Soares; Francesco Bianco; Frank Breuning; Ase Krogh Rasmussen; Roland M Schaefer
Journal:  Kidney Int       Date:  2004-09       Impact factor: 10.612

10.  Prevalence of lysosomal storage disorders.

Authors:  P J Meikle; J J Hopwood; A E Clague; W F Carey
Journal:  JAMA       Date:  1999-01-20       Impact factor: 56.272

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  13 in total

Review 1.  Fabry's disease: an example of cardiorenal syndrome type 5.

Authors:  Aashish Sharma; Marco Sartori; Jose J Zaragoza; Gianluca Villa; Renhua Lu; Elena Faggiana; Alessandra Brocca; Luca Di Lullo; Sandro Feriozzi; Claudio Ronco
Journal:  Heart Fail Rev       Date:  2015-11       Impact factor: 4.214

2.  Screening of male dialysis patients for fabry disease by plasma globotriaosylsphingosine.

Authors:  Hiroki Maruyama; Takuma Takata; Yutaka Tsubata; Ryushi Tazawa; Kiyoe Goto; Jun Tohyama; Ichiei Narita; Hidekatsu Yoshioka; Satoshi Ishii
Journal:  Clin J Am Soc Nephrol       Date:  2013-01-10       Impact factor: 8.237

Review 3.  Fabry disease.

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

4.  A distinct urinary biomarker pattern characteristic of female Fabry patients that mirrors response to enzyme replacement therapy.

Authors:  Andreas D Kistler; Justyna Siwy; Frank Breunig; Praveen Jeevaratnam; Alexander Scherl; William Mullen; David G Warnock; Christoph Wanner; Derralynn A Hughes; Harald Mischak; Rudolf P Wüthrich; Andreas L Serra
Journal:  PLoS One       Date:  2011-06-15       Impact factor: 3.240

5.  Importance of Echocardiography and Clinical "Red Flags" in Guiding Genetic Screening for Fabry Disease.

Authors:  Rodolfo Citro; Costantina Prota; Donatella Ferraioli; Giuseppe Iuliano; Michele Bellino; Ilaria Radano; Angelo Silverio; Serena Migliarino; Maria Vincenza Polito; Artemisia Ruggiero; Rosa Napoletano; Vincenzo Bellizzi; Michele Ciccarelli; Gennaro Galasso; Carmine Vecchione
Journal:  Front Cardiovasc Med       Date:  2022-04-25

6.  Organ manifestations and long-term outcome of Fabry disease in patients with the GLA haplotype D313Y.

Authors:  Daniel Oder; Nurcan Üçeyler; Dan Liu; Kai Hu; Bernhard Petritsch; Claudia Sommer; Georg Ertl; Christoph Wanner; Peter Nordbeck
Journal:  BMJ Open       Date:  2016-04-08       Impact factor: 2.692

7.  Plasma mutant α-galactosidase A protein and globotriaosylsphingosine level in Fabry disease.

Authors:  Takahiro Tsukimura; Sachie Nakano; Tadayasu Togawa; Toshie Tanaka; Seiji Saito; Kazuki Ohno; Futoshi Shibasaki; Hitoshi Sakuraba
Journal:  Mol Genet Metab Rep       Date:  2014-08-02

8.  Glycosphingolipid storage in Fabry mice extends beyond globotriaosylceramide and is affected by ABCB1 depletion.

Authors:  Mustafa A Kamani; Philippe Provençal; Michel Boutin; Natalia Pacienza; Xin Fan; Anton Novak; Tonny C Huang; Beth Binnington; Bryan C Au; Christiane Auray-Blais; Clifford A Lingwood; Jeffrey A Medin
Journal:  Future Sci OA       Date:  2016-10-13

9.  Screening Fabry's disease in chronic kidney disease patients not on dialysis: a multicenter study.

Authors:  Yavuz Yeniçerioğlu; Hakan Akdam; Belda Dursun; Alper Alp; Funda Sağlam Eyiler; Davut Akın; Yelda Gün; Bülent Hüddam; Mehmet Batmazoğlu; Dilek Gibyeli Genek; Serhat Pirinççi; İsmail Rıfkı Ersoy; Atilla Üzüm; Zeki Soypaçacı; Mehmet Tanrısev; Hülya Çolak; Sibel Demiral Sezer; Gökay Bozkurt; Utku Oğan Akyıldız; Ayşe İpek Akyüz Ünsal; Mustafa Ünübol; Meltem Uslu; Ufuk Eryılmaz; Ceren Günel; İbrahim Meteoğlu; İrfan Yavaşoğlu; Alparslan Ünsal; Harun Akar; Pınar Okyay
Journal:  Ren Fail       Date:  2016-11-10       Impact factor: 2.606

10.  Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study.

Authors:  Sadia Jahan; Subashini Sarathchandran; Shamina Akhter; Jack Goldblatt; Samantha Stark; Douglas Crawford; Andrew Mallett; Mark Thomas
Journal:  Orphanet J Rare Dis       Date:  2020-01-13       Impact factor: 4.123

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