First-in-Human Experience With Peritoneal Direct Sodium Removal Using a Zero-Sodium Solution: A New Candidate Therapy for Volume Overload.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
31 03 2020
Historique:
pubmed: 9 1 2020
medline: 3 2 2021
entrez: 9 1 2020
Statut: ppublish

Résumé

Loop diuretics have well-described toxicities, and loss of response to these agents is common. Alternative strategies are needed for the maintenance of euvolemia in heart failure (HF). Nonrenal removal of sodium directly across the peritoneal membrane (direct sodium removal [DSR]) with a sodium-free osmotic solution should result in extraction of large quantities of sodium with limited off-target solute removal. This article describes the preclinical development and first-in-human proof of concept for DSR. Sodium-free 10% dextrose was used as the DSR solution. Porcine experiments were conducted to investigate the optimal dwell time, safety, and scalability and to determine the effect of experimental heart failure. In the human study, participants with end-stage renal disease on peritoneal dialysis (PD) underwent randomization and crossover to either a 2-hour dwell with 1 L DSR solution or standard PD solution (Dianeal 4.25% dextrose, Baxter). The primary end point was completion of the 2-hour dwell without significant discomfort or adverse events, and the secondary end point was difference in sodium removal between DSR and standard PD solution. Porcine experiments revealed that 1 L DSR solution removed 4.1±0.4 g sodium in 2 hours with negligible off-target solute removal and overall stable serum electrolytes. Increasing the volume of DSR solution cycled across the peritoneum increased sodium removal and substantially decreased plasma volume ( DSR was well tolerated in both animals and human subjects and produced substantially greater sodium removal than standard PD solution. Additional research evaluating the use of DSR as a method to prevent and treat hypervolemia in heart failure is warranted. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03801226.

Sections du résumé

BACKGROUND
Loop diuretics have well-described toxicities, and loss of response to these agents is common. Alternative strategies are needed for the maintenance of euvolemia in heart failure (HF). Nonrenal removal of sodium directly across the peritoneal membrane (direct sodium removal [DSR]) with a sodium-free osmotic solution should result in extraction of large quantities of sodium with limited off-target solute removal.
METHODS
This article describes the preclinical development and first-in-human proof of concept for DSR. Sodium-free 10% dextrose was used as the DSR solution. Porcine experiments were conducted to investigate the optimal dwell time, safety, and scalability and to determine the effect of experimental heart failure. In the human study, participants with end-stage renal disease on peritoneal dialysis (PD) underwent randomization and crossover to either a 2-hour dwell with 1 L DSR solution or standard PD solution (Dianeal 4.25% dextrose, Baxter). The primary end point was completion of the 2-hour dwell without significant discomfort or adverse events, and the secondary end point was difference in sodium removal between DSR and standard PD solution.
RESULTS
Porcine experiments revealed that 1 L DSR solution removed 4.1±0.4 g sodium in 2 hours with negligible off-target solute removal and overall stable serum electrolytes. Increasing the volume of DSR solution cycled across the peritoneum increased sodium removal and substantially decreased plasma volume (
CONCLUSIONS
DSR was well tolerated in both animals and human subjects and produced substantially greater sodium removal than standard PD solution. Additional research evaluating the use of DSR as a method to prevent and treat hypervolemia in heart failure is warranted. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03801226.

Identifiants

pubmed: 31910658
doi: 10.1161/CIRCULATIONAHA.119.043062
pmc: PMC7331276
mid: NIHMS1560173
doi:

Substances chimiques

Sodium 9NEZ333N27

Banques de données

ClinicalTrials.gov
['NCT03801226']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1043-1053

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL128973
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL139629
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL148354
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Veena S Rao (VS)

Department of Internal Medicine, Section of Cardiovascular Medicine (V.S.R., M.G., D.M., N.B., J.M. Testani), Yale University School of Medicine, New Haven, CT.

Jeffrey M Turner (JM)

Department of Medicine, Division of Nephrology (J.M. Turner, F.F.), Yale University School of Medicine, New Haven, CT.

Matthew Griffin (M)

Department of Internal Medicine, Section of Cardiovascular Medicine (V.S.R., M.G., D.M., N.B., J.M. Testani), Yale University School of Medicine, New Haven, CT.

Devin Mahoney (D)

Department of Internal Medicine, Section of Cardiovascular Medicine (V.S.R., M.G., D.M., N.B., J.M. Testani), Yale University School of Medicine, New Haven, CT.

Jennifer Asher (J)

Department of Comparative Medicine (J.A.), Yale University School of Medicine, New Haven, CT.

Sangchoon Jeon (S)

Yale School of Nursing, West Haven, CT (S.J.).

Peter S Yoo (PS)

Department of Surgery, Transplantation and Immunology (P.S.Y.), Yale University School of Medicine, New Haven, CT.

Nabil Boutagy (N)

Department of Internal Medicine, Section of Cardiovascular Medicine (V.S.R., M.G., D.M., N.B., J.M. Testani), Yale University School of Medicine, New Haven, CT.

Attila Feher (A)

Department of Internal Medicine (A.F.), Yale University School of Medicine, New Haven, CT.

Albert Sinusas (A)

Department of Medicine, Yale Translational Research Imaging Center, Section of Cardiovascular Medicine (A.S.), Yale University School of Medicine, New Haven, CT.

F Perry Wilson (FP)

Program of Applied Translational Research (F.P.W.), Yale University School of Medicine, New Haven, CT.

Fredric Finkelstein (F)

Department of Medicine, Division of Nephrology (J.M. Turner, F.F.), Yale University School of Medicine, New Haven, CT.

Jeffrey M Testani (JM)

Department of Internal Medicine, Section of Cardiovascular Medicine (V.S.R., M.G., D.M., N.B., J.M. Testani), Yale University School of Medicine, New Haven, CT.

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Classifications MeSH