Contribution of 'clinically negligible' residual kidney function to clearance of uremic solutes.


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 04 07 2018
accepted: 03 02 2019
pubmed: 18 3 2019
medline: 13 11 2020
entrez: 18 3 2019
Statut: ppublish

Résumé

Residual kidney function (RKF) is thought to exert beneficial effects through clearance of uremic toxins. However, the level of native kidney function where clearance becomes negligible is not known. We aimed to assess whether levels of nonurea solutes differed among patients with 'clinically negligible' RKF compared with those with no RKF. The hemodialysis study excluded patients with urinary urea clearance >1.5 mL/min, below which RKF was considered to be 'clinically negligible'. We measured eight nonurea solutes from 1280 patients participating in this study and calculated the relative difference in solute levels among patients with and without RKF based on measured urinary urea clearance. The mean age of the participants was 57 years and 57% were female. At baseline, 34% of the included participants had clinically negligible RKF (mean 0.7 ± 0.4 mL/min) and 66% had no RKF. Seven of the eight nonurea solute levels measured were significantly lower in patients with RKF than in those without RKF, ranging from -24% [95% confidence interval (CI) -31 to -16] for hippurate, -7% (-14 to -1) for trimethylamine-N-oxide and -4% (-6 to -1) for asymmetric dimethylarginine. The effect of RKF on plasma levels was comparable or more pronounced than that achieved with a 31% higher dialysis dose (spKt/Vurea 1.7 versus 1.3). Preserved RKF at 1-year follow-up was associated with a lower risk of cardiac death and first cardiovascular event. Even at very low levels, RKF is not 'negligible', as it continues to provide nonurea solute clearance. Management of patients with RKF should consider these differences.

Sections du résumé

BACKGROUND
Residual kidney function (RKF) is thought to exert beneficial effects through clearance of uremic toxins. However, the level of native kidney function where clearance becomes negligible is not known.
METHODS
We aimed to assess whether levels of nonurea solutes differed among patients with 'clinically negligible' RKF compared with those with no RKF. The hemodialysis study excluded patients with urinary urea clearance >1.5 mL/min, below which RKF was considered to be 'clinically negligible'. We measured eight nonurea solutes from 1280 patients participating in this study and calculated the relative difference in solute levels among patients with and without RKF based on measured urinary urea clearance.
RESULTS
The mean age of the participants was 57 years and 57% were female. At baseline, 34% of the included participants had clinically negligible RKF (mean 0.7 ± 0.4 mL/min) and 66% had no RKF. Seven of the eight nonurea solute levels measured were significantly lower in patients with RKF than in those without RKF, ranging from -24% [95% confidence interval (CI) -31 to -16] for hippurate, -7% (-14 to -1) for trimethylamine-N-oxide and -4% (-6 to -1) for asymmetric dimethylarginine. The effect of RKF on plasma levels was comparable or more pronounced than that achieved with a 31% higher dialysis dose (spKt/Vurea 1.7 versus 1.3). Preserved RKF at 1-year follow-up was associated with a lower risk of cardiac death and first cardiovascular event.
CONCLUSIONS
Even at very low levels, RKF is not 'negligible', as it continues to provide nonurea solute clearance. Management of patients with RKF should consider these differences.

Identifiants

pubmed: 30879076
pii: 5382105
doi: 10.1093/ndt/gfz042
pmc: PMC7203561
doi:

Substances chimiques

Urea 8W8T17847W

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

846-853

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK101674
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007732
Pays : United States
Organisme : NIA NIH HHS
ID : UH2 AG056933
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061022
Pays : United States
Organisme : CSRD VA
ID : IK2 CX001036
Pays : United States
Organisme : NIDDK NIH HHS
ID : R03 DK104012
Pays : United States
Organisme : NIA NIH HHS
ID : UH3 AG056933
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL132372
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK106965
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.

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Auteurs

Stephanie M Toth-Manikowski (SM)

Department of Medicine, Division of Nephrology, University of Illinois at Chicago, Chicago, IL, USA.

Tammy L Sirich (TL)

Department of Medicine, Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Timothy W Meyer (TW)

Department of Medicine, Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Thomas H Hostetter (TH)

Department of Medicine, Palo Alto Veterans Affairs Health Care System, Stanford University, Palo Alto, CA, USA.

Seungyoung Hwang (S)

Department of Medicine, Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Natalie S Plummer (NS)

Department of Medicine, Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Xin Hai (X)

Department of Medicine, Palo Alto Veterans Affairs Health Care System, Stanford University, Palo Alto, CA, USA.

Josef Coresh (J)

Department of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins University, Baltimore, MD, USA.

Neil R Powe (NR)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Tariq Shafi (T)

Department of Medicine, Division of Nephrology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Department of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Welch Center for Prevention, Epidemiology and Clinical Research, Johns Hopkins University, Baltimore, MD, USA.
Department of Medicine, Priscilla Chan and Mark Zuckerberg San Francisco General Hospital, University of California, San Francisco, San Francisco, CA, USA.

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