Epidemiology of Fabry disease in patients in hemodialysis in the Madrid community

Elena Corchete Prats,Emilio Gonzalez-Parra,Almudena Vega,Nicolas Macias, Maria Delgado,Milagros Fernandez, Rafael Jesus Sanchez, Laura Alvarez, Ramon Jesus Miranda, Javier Vian, Virginia Lopez,Evangelina Merida,Monica Pereira, David Sapiencia, Natalia Andres,Patricia Munoz, Yohana Gil,Maria Sanchez, Clara Cases, Beatriz Gil,Alicia Garcia, Valeria Sainz,Simona Alexandru, Saul Pampa, Maria Lopez, Jose Carlos de la Flor, Patricia Nora Estrada, Jose Ramon Berlanga,Rocio Zamora, Rosa Sanchez, Laura Rodriguez-Osorio, Carmen Fraile,Fernando Caravaca-Fontan, Cristina Moratilla, Carmen Cabre,Karina Furaz, Luis Nieto, Maria Teresa Villaverde, Claudia Grisel Tapia,Santiago Cedeno, Sandra Castellano, Evaristo Valdes,Marta Ferreira, Pilar Martinez, Marta Sanz, Mercedes Sanchez,Francisco Rios, Sofia Palomo,Maria Luisa Serrano,Ana Blanco, Laura Espinel, Fernando Tornero,Jose Antonio Herrero

NEFROLOGIA(2023)

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摘要
This study screened for Fabry disease (FD) in patients in hemodialysis (HD) in the region of Madrid (CAM) with a cross-sectional design to evaluate HD-prevalent patients, followed by a three-year period prospective design to analyze HD-incident patients. Inclusion criteria: patients older than 18 years on HD in the CAM, excluding patients diag-nosed with any other hereditary disease with renal involvement different from FD, that sign the Informed Consent (IC). Exclusion criteria: underaged patients or not agreeing or not being capable of signing the IC. Results: 3470 patients were included, 63% males and with an average age of 67.9 +/- 9.7 years. 2357 were HD-prevalent patients and 1113 HD-incident patients. For HD-prevalent patients, average time in HD was 45.2 months (SD 51.3), in HD-incident patients proteinuria was present in 28.4%. There were no statistical differences in plasmatic alpha-galactosidase A (a-GAL-A) activity or Lyso-GL-3 values when comparing HD-prevalent and HD-incident populations and neither between males and females. A genetic study was performed in 87 patients (2.5% of patients): 60 male patients with decreased enzymatic activity and 27 female patients either with a decreased GLA activity, increased Lyso-Gl3 levels or both. The genetic variants identified were: p.Asp313Tyr (4 patients), p.Arg220Gln (3 patients) and M290I (1 patient). None of the identified variants is pathogenic. Conclusions: 76% of HD Centers of the CAM participated in the study. This is the first pub-lication to describe the prevalence of FD in the HD-population of a region of Spain as well as its average o-GAL-A-activity and plasmatic Lyso-Gl3 levels. It is also the first study that combines a cross-sectional design with a prospective follow-up design. This study has not identified any FD patient.(c) 2022 Sociedad Espanola de Nefrologia. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/ by-nc-nd/4.0/).
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关键词
Fabry disease,Hemodialysis,Screening,Lyso-Gl3,Madrid,Spain
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