First-in-Human Experience With Peritoneal Direct Sodium Removal Using a Zero-Sodium Solution: A New Candidate Therapy for Volume Overload.
clinical trial [publication type]
heart failure
Journal
Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763
Informations de publication
Date de publication:
31 03 2020
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
1043-1053Subventions
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
Références
Blood Purif. 2016;42(4):279-281
pubmed: 27577583
J Hepatol. 2017 Nov;67(5):940-949
pubmed: 28645737
Circ Heart Fail. 2014 Sep;7(5):766-72
pubmed: 25037309
Circulation. 1990 Nov;82(5):1724-9
pubmed: 2146040
N Engl J Med. 1973 Oct 18;289(16):843-4
pubmed: 4763428
JAMA. 2007 Mar 28;297(12):1319-31
pubmed: 17384437
J Am Coll Cardiol. 2009 Feb 17;53(7):557-573
pubmed: 19215829
Am J Med. 1999 Apr;106(4):399-403
pubmed: 10225241
Cardiology. 2001;96(3-4):132-43
pubmed: 11805380
J Am Coll Cardiol. 2017 Mar 21;69(11):1409-1419
pubmed: 28302292
Am J Physiol Renal Physiol. 2003 May;284(5):F1115-9
pubmed: 12676739
Eur J Heart Fail. 2010 May;12(5):423-33
pubmed: 20354029
JAMA. 2007 Mar 28;297(12):1332-43
pubmed: 17384438
Ann Intern Med. 1985 Jul;103(1):1-6
pubmed: 2860833
J Am Soc Nephrol. 2001 Jul;12(7):1335-41
pubmed: 11423562
J Am Coll Cardiol. 2017 Mar 21;69(11):1399-1406
pubmed: 27654854
Physiol Rev. 2000 Jan;80(1):277-313
pubmed: 10617770
Circ Heart Fail. 2014 Mar 1;7(2):261-70
pubmed: 24379278
Am J Med. 2006 Dec;119(12 Suppl 1):S3-S10
pubmed: 17113398
JACC Heart Fail. 2019 May;7(5):383-391
pubmed: 31047017
JAMA. 2013 Dec 18;310(23):2533-43
pubmed: 24247300
Eur Heart J. 2014 May 14;35(19):1284-93
pubmed: 24585267
Circ Heart Fail. 2016 Aug;9(8):
pubmed: 27507113
J Clin Invest. 1989 Jan;83(1):113-26
pubmed: 2910903
Curr Heart Fail Rep. 2006 Apr;3(1):41-5
pubmed: 16684496
J Am Coll Cardiol. 2013 Jan 29;61(4):391-403
pubmed: 23219302
Am J Physiol. 1989 Jul;257(1 Pt 2):F1-10
pubmed: 2546443
Am J Physiol. 1985 Mar;248(3 Pt 2):F374-81
pubmed: 3976898
Circ Heart Fail. 2016 Jan;9(1):e002370
pubmed: 26721915