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Effect of high-flux dialysis on circulating FGF-23 levels in end-stage renal disease patients: results from a randomized trial

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-148559
  • Background In patients undergoing maintenance hemodialysis (HD), increased levels of circulating fibroblast growth factor-23 (FGF-23) are independently associated with cardiovascular events and mortality. Interventional strategies aiming to reduce levels of FGF-23 in HD patients are of particular interest. The purpose of the current study was to compare the impact of high-flux versus low-flux HD on circulating FGF-23 levels. Methods We conducted a post-hoc analysis of the MINOXIS study, including 127 dialysis patients randomized toBackground In patients undergoing maintenance hemodialysis (HD), increased levels of circulating fibroblast growth factor-23 (FGF-23) are independently associated with cardiovascular events and mortality. Interventional strategies aiming to reduce levels of FGF-23 in HD patients are of particular interest. The purpose of the current study was to compare the impact of high-flux versus low-flux HD on circulating FGF-23 levels. Methods We conducted a post-hoc analysis of the MINOXIS study, including 127 dialysis patients randomized to low-flux (n = 62) and high-flux (n = 65) HD for 52 weeks. Patients with valid measures for FGF-23 investigated baseline and after 52 weeks were included. Results Compared to baseline, a significant increase in FGF-23 levels after one year of low-flux HD was observed (Delta plasma FGF-23: +4026 RU/ml; p < 0.001). In contrast, FGF-23 levels remained stable in the high flux group (Delta plasma FGF-23: +373 RU/ml, p = 0.70). The adjusted difference of the absolute change in FGF-23 levels between the two treatment groups was statistically significant (p < 0.01). Conclusions Over a period of 12 months, high-flux HD was associated with stable FGF-23 levels, whereas the low-flux HD group showed an increase of FGF-23. However, the implications of the different FGF 23 time-trends in patients on high flux dialysis, as compared to the control group, remain to be explored in specifically designed clinical trials.zeige mehrzeige weniger

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Metadaten
Autor(en): Andreas Schneider, Markus P. Schneider, Detlef H. Krieter, Bernd Genser, Hubert Scharnagl, Tatjana Stojakovic, Christoph Wanner, Christiane Drechsler
URN:urn:nbn:de:bvb:20-opus-148559
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Medizinische Klinik und Poliklinik I
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):PLoS ONE
Erscheinungsjahr:2015
Band / Jahrgang:10
Heft / Ausgabe:5
Seitenangabe:e0128079
Originalveröffentlichung / Quelle:PLoS ONE 10(5): e0128079 (2015). DOI: 10.1371/journal.pone.0128079
DOI:https://doi.org/10.1371/journal.pone.0128079
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):cardiovascular events; chronic kidney disease; fibroblast growth factor-23; hemodialysis; left ventricular hypertrophy; mineral metabolism; mortality; parathyroid hormone; phosphate homeostasis
Datum der Freischaltung:15.11.2018
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International