Literature DB >> 26197777

Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST).

Osamu Saito1, Eiji Kusano2, Tetsu Akimoto1, Yasushi Asano3, Teruo Kitagawa4, Ken Suzuki4, Nobuyuki Ishige4, Takashi Akiba5, Akira Saito6, Eiji Ishimura7, Motoshi Hattori8, Akira Hishida9, Chu Guili10, Hiroki Maruyama10, Masahisa Kobayashi11, Touya Ohashi12, Ichiro Matsuda13, Yoshikatsu Eto14.   

Abstract

BACKGROUND: In Fabry disease, progressive glycolipid accumulation leads to damage in kidney and other organs. This study was designed to determine the prevalence rate of Fabry disease in Japanese dialysis patients.
METHODS: All dialysis patients agreeing to Japan Fabry disease screening study (J-FAST) with informed consent were selected except for Fabry disease. The screening was performed by a method of measuring plasma and/or leukocytes lysosomal α-galactosidase A protein level and α-galactosidase A activity. If positive, genetic analysis was carried out upon patient's agreement.
RESULTS: J-FAST dealt with 8547 patients (male 5408, female 3139). At the tertiary examination, 26 out of 8547 patients were found to be positive. Six out of 26 patients could not accept genetic analysis because of death. Remaining 20 patients agreed with genetic analysis; then 2 patients (male 2, female 0) had a variation of the α-Gal gene and 11 patients showed E66Q variations. Therefore, the frequency of Fabry disease in J-FAST was 0.04 % (2/5408) in males and 0 % (0/3139) in females, and then 0.02 % (2/8547) in all patients. The presumptive clinical diagnoses of end-stage kidney disease (ESKD) were 10 chronic glomerulonephritis, 7 diabetic nephropathy, 3 unknown etiology, 3 nephrosclerosis, 1 gouty nephropathy, 1 autosomal dominant polycystic kidney disease and 1 renal tuberculosis among 26 tertiary positive patients. Two male Fabry patients were initially diagnosed as nephrosclerosis and chronic glomerulonephritis.
CONCLUSIONS: The prevalence rate of Fabry disease in J-FAST was 0.02 %. Moreover, Fabry disease could not be ruled out as the clinical diagnosis of ESKD.

Entities:  

Keywords:  Dialysis patient; E66Q variation; Fabry disease; Screening; X-linked recessive inheritance; Α-galactosidase activity

Mesh:

Year:  2015        PMID: 26197777     DOI: 10.1007/s10157-015-1146-7

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  34 in total

Review 1.  The frequency of Fabry disease with the E66Q variant in the α-galactosidase A gene in Japanese dialysis patients: a case report and a literature review.

Authors:  Y Kikumoto; H Sugiyama; H Morinaga; T Inoue; K Takiue; M Kitagawa; D Saito; Y Takatori; M Kinomura; S Kitamura; S Akagi; K Sada; K Nakao; Y Maeshima; H Kitayama; H Makino
Journal:  Clin Nephrol       Date:  2012-09       Impact factor: 0.975

2.  Fabry disease peripheral blood immune cells release inflammatory cytokines: role of globotriaosylceramide.

Authors:  Pablo N De Francesco; Juan M Mucci; Romina Ceci; Carlos A Fossati; Paula A Rozenfeld
Journal:  Mol Genet Metab       Date:  2013-02-13       Impact factor: 4.797

3.  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

4.  A nationwide blood spot screening study for Fabry disease in the Czech Republic haemodialysis patient population.

Authors:  Miroslav Merta; Jana Reiterova; Jana Ledvinova; Helena Poupetová; Robert Dobrovolny; Romana Rysavá; Dita Maixnerová; Jan Bultas; Jirí Motán; Jitka Slivkova; Doris Sobotova; Jana Smrzova; Vladimir Tesar
Journal:  Nephrol Dial Transplant       Date:  2006-10-13       Impact factor: 5.992

5.  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

6.  Frequency of Fabry disease in male and female haemodialysis patients in Spain.

Authors:  Paulo Gaspar; Julio Herrera; Daniel Rodrigues; Sebastián Cerezo; Rodrigo Delgado; Carlos F Andrade; Ramón Forascepi; Juan Macias; Maria D del Pino; Maria D Prados; Pilar R de Alegria; Gerardo Torres; Pedro Vidau; Maria C Sá-Miranda
Journal:  BMC Med Genet       Date:  2010-02-01       Impact factor: 2.103

7.  Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot study.

Authors:  Takahito Inoue; Kiyoko Hattori; Kenji Ihara; Atsushi Ishii; Kimitoshi Nakamura; Shinichi Hirose
Journal:  J Hum Genet       Date:  2013-05-16       Impact factor: 3.172

8.  Fabry's disease: alpha-galactosidase deficiency.

Authors:  J A Kint
Journal:  Science       Date:  1970-02-27       Impact factor: 47.728

9.  Consequences of a global enzyme shortage of agalsidase beta in adult Dutch Fabry patients.

Authors:  Bouwien E Smid; Saskia M Rombach; Johannes M F G Aerts; Symen Kuiper; Mina Mirzaian; Hermen S Overkleeft; Ben J H M Poorthuis; Carla E M Hollak; Johanna E M Groener; Gabor E Linthorst
Journal:  Orphanet J Rare Dis       Date:  2011-10-31       Impact factor: 4.123

10.  Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications.

Authors:  F Weidemann; M Niemann; S Störk; F Breunig; M Beer; C Sommer; S Herrmann; G Ertl; C Wanner
Journal:  J Intern Med       Date:  2013-05-06       Impact factor: 8.989

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  18 in total

1.  High-risk screening for Anderson-Fabry disease in patients with cardiac, renal, or neurological manifestations.

Authors:  Naoki Nakagawa; Jun Sawada; Naka Sakamoto; Toshiharu Takeuchi; Fumihiko Takahashi; Jun-Ich Maruyama; Ken Momosaki; Kimitoshi Nakamura; Fumio Endo; Naoyuki Hasebe
Journal:  J Hum Genet       Date:  2019-06-19       Impact factor: 3.172

2.  Clinical course and pathological findings of two late-onset Fabry hemizygous patients including mulberry cell counts after enzyme replacement therapy.

Authors:  Homare Shimohata; Marina Yamashita; Kentaro Ohgi; Hiroshi Maruyama; Mamiko Takayasu; Kouichi Hirayama; Masaki Kobayashi
Journal:  CEN Case Rep       Date:  2020-03-18

3.  Screening for Fabry Disease in Patients With Juvenile Systemic Lupus Erythematosus.

Authors:  Ertugrul Kiykim; Sezgin Şahİn; Tanyel ZubarioĞlu; Kenan Barut; Amra Adrovic; Mehmet Şerif Cansever; Ayşe Çiğdem AktuĞlu Zeybek; Özgür KasapÇopur
Journal:  Arch Rheumatol       Date:  2020-02-07       Impact factor: 1.472

4.  Low frequency of Fabry disease in patients with common heart disease.

Authors:  Raphael Schiffmann; Caren Swift; Nathan McNeill; Elfrida R Benjamin; Jeffrey P Castelli; Jay Barth; Lawrence Sweetman; Xuan Wang; Xiaoyang Wu
Journal:  Genet Med       Date:  2017-10-26       Impact factor: 8.864

5.  p.R301X Mutation and Variable Phenotypic Appearance of Fabry Disease.

Authors:  Ruya Ozelsancak; Bulent Uyar
Journal:  Am J Case Rep       Date:  2016-05-09

6.  A Renal Variant of Fabry Disease Diagnosed by the Presence of Urinary Mulberry Cells.

Authors:  Homare Shimohata; Yujiro Ogawa; Hiroshi Maruyama; Kouichi Hirayama; Masaki Kobayashi
Journal:  Intern Med       Date:  2016-12-01       Impact factor: 1.271

7.  Fabry disease in children: a federal screening programme in Russia.

Authors:  Leyla Seymurovna Namazova-Baranova; Alexander Alexandrovich Baranov; Aleksander Alekseevich Pushkov; Kirill Victorovich Savostyanov
Journal:  Eur J Pediatr       Date:  2017-09-04       Impact factor: 3.183

8.  A prospective, observational study of patients with uncommon distal symmetric painful small-fiber neuropathy.

Authors:  Jung-Lung Hsu; Ming-Feng Liao; Hui-Ching Hsu; Yi-Ching Weng; Ai-Lun Lo; Kuo-Hsuan Chang; Hong-Shiu Chang; Hung-Chou Kuo; Chin-Chang Huang; Long-Sun Ro
Journal:  PLoS One       Date:  2017-09-28       Impact factor: 3.240

9.  Enhancing the diagnosis of fabry disease in cardiology with a targeted information: a before-after control-impact study.

Authors:  Anne-Louise Savary; Remy Morello; Carole Brasse-Lagnel; Paul Milliez; Soumeya Bekri; Fabien Labombarda
Journal:  Open Heart       Date:  2017-03-13

10.  Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype.

Authors:  Jin-Ho Choi; Beom Hee Lee; Sun Hee Heo; Gu-Hwan Kim; Yoo-Mi Kim; Dae-Seong Kim; Jung Min Ko; Young Bae Sohn; Yong Hee Hong; Dong-Hwan Lee; Hoon Kook; Han Hyuk Lim; Kyung Hee Kim; Woo-Shik Kim; Geu-Ru Hong; Su-Hyun Kim; Sang Hyun Park; Chan-Duck Kim; So Mi Kim; Jeong-Sook Seo; Han-Wook Yoo
Journal:  Medicine (Baltimore)       Date:  2017-07       Impact factor: 1.889

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