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2020 (English)In: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol. 21, no 4, article id 1522Article in journal (Refereed) Published
Abstract [en]
Tryptophan is an essential dietary amino acid that originates uremic toxins that contribute to end-stage kidney disease (ESKD) patient outcomes. We evaluated serum levels and removal during haemodialysis and haemodiafiltration of tryptophan and tryptophan-derived uremic toxins, indoxyl sulfate (IS) and indole acetic acid (IAA), in ESKD patients in different dialysis treatment settings. This prospective multicentre study in four European dialysis centres enrolled 78 patients with ESKD. Blood and spent dialysate samples obtained during dialysis were analysed with high-performance liquid chromatography to assess uremic solutes, their reduction ratio (RR) and total removed solute (TRS). Mean free serum tryptophan and IS concentrations increased, and concentration of IAA decreased over pre-dialysis levels (67%, 49%, -0.8%, respectively) during the first hour of dialysis. While mean serum total urea, IS and IAA concentrations decreased during dialysis (-72%, -39%, -43%, respectively), serum tryptophan levels increased, resulting in negative RR (-8%) towards the end of the dialysis session (p < 0.001), despite remarkable Trp losses in dialysate. RR and TRS values based on serum (total, free) and dialysate solute concentrations were lower for conventional low-flux dialysis (p < 0.001). High-efficiency haemodiafiltration resulted in 80% higher Trp losses than conventional low-flux dialysis, despite similar neutral Trp RR values. In conclusion, serum Trp concentrations and RR behave differently from uremic solutes IS, IAA and urea and Trp RR did not reflect dialysis Trp losses. Conventional low-flux dialysis may not adequately clear Trp-related uremic toxins while high efficiency haemodiafiltration increased Trp losses.
Place, publisher, year, edition, pages
MDPI, 2020
Keywords
uremic toxins; tryptophan; tryptophan-derived uremic toxins; indoxyl sulfate; indole-3 acetic acid; end-stage kidney disease; chronic kidney disease; haemodialysis; haemodiafiltration
National Category
Clinical Medicine
Identifiers
urn:nbn:se:liu:diva-165195 (URN)10.3390/ijms21041522 (DOI)000522524400349 ()32102247 (PubMedID)2-s2.0-85079893233 (Scopus ID)
Note
Funding Agencies|European Union through the European Regional Development FundEuropean Union (EU) [H2020-SMEINST-2-2017]; Estonian Ministry of Education and ResearchMinistry of Education and Research, Estonia [IUT 19-2]; Estonian Centre of Excellence in IT (EXCITE) - European Regional Development Fund; Njurfonden (2017), Sweden; Njurfonden (2018), Sweden; Programa Rio Hortega ISCIII FEDER funds; ISCIII-RETIC REDinREN [RD016/0009]; Sociedad Espanola de Nefrologia; Fundacion Renal Inigo Alvarez de Toledo (FRIAT)Fonds de la Recherche Scientifique - FNRS; Comunidad de MadridComunidad de MadridInstituto de Salud Carlos III [CIFRA2 B2017/BMD-3686]; OLDIAS2-Online Dialysis Sensor Phase2 project [767572]; ERA-PerMed-JTC2018 [KIDNEY ATTACK AC18/00064, PERSTIGAN AC18/00071]; FEDER fundsEuropean Union (EU); [PI19/00588]; [PI19/00815]; [DTS18/00032]
2020-04-172020-04-172025-02-18Bibliographically approved