The osmo-metabolic approach: a novel and tantalizing glucose-sparing strategy in peritoneal dialysis.


Journal

Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 01 03 2020
accepted: 09 07 2020
pubmed: 9 8 2020
medline: 19 8 2021
entrez: 9 8 2020
Statut: ppublish

Résumé

Peritoneal dialysis (PD) is a viable but under-prescribed treatment for uremic patients. Concerns about its use include the bio-incompatibility of PD fluids, due to their potential for altering the functional and anatomical integrity of the peritoneal membrane. Many of these effects are thought to be due to the high glucose content of these solutions, with attendant issues of products generated during heat treatment of glucose-containing solutions. Moreover, excessive intraperitoneal absorption of glucose from the dialysate has many potential systemic metabolic effects. This article reviews the efforts to develop alternative PD solutions that obviate some of these side effects, through the replacement of part of their glucose content with other osmolytes which are at least as efficient in removing fluids as glucose, but less impactful on patient metabolism. In particular, we will summarize clinical studies on the use of alternative osmotic ingredients that are commercially available (icodextrin and amino acids) and preclinical studies on alternative solutions under development (taurine, polyglycerol, carnitine and xylitol). In addition to the expected benefit of a glucose-sparing approach, we describe an 'osmo-metabolic' approach in formulating novel PD solutions, in which there is the possibility of exploiting the pharmaco-metabolic properties of some of the osmolytes to attenuate the systemic side effects due to glucose. This approach has the potential to ameliorate pre-existing co-morbidities, including insulin resistance and type-2 diabetes, which have a high prevalence in the dialysis population, including in PD patients.

Identifiants

pubmed: 32767274
doi: 10.1007/s40620-020-00804-2
pii: 10.1007/s40620-020-00804-2
pmc: PMC8036224
doi:

Substances chimiques

Dialysis Solutions 0
Icodextrin 2NX48Z0A9G
Glucose IY9XDZ35W2

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

503-519

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Auteurs

Mario Bonomini (M)

Department of Medicine, Section of Nephrology and Dialysis, G. d'Annunzio University, Chieti-Pescara, Chieti, Italy. mario.bonomini@unich.it.

Victor Zammit (V)

Warwick Medical School, University of Warwick, Clinical Sciences Research Institute, Coventry, England.

José C Divino-Filho (JC)

Division of Renal Medicine, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Simon J Davies (SJ)

Faculty of Medicine and Health Sciences, Keele University, Staffordshire, UK.

Lorenzo Di Liberato (L)

Department of Medicine, Section of Nephrology and Dialysis, G. d'Annunzio University, Chieti-Pescara, Chieti, Italy.

Arduino Arduini (A)

Department of Research and Development, CoreQuest Sagl, Tecnopolo, Bioggio, Switzerland.

Mark Lambie (M)

Faculty of Medicine and Health Sciences, Keele University, Staffordshire, UK.

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