SGLT2 inhibition to target kidney aging.

SGLT2 inhibitors aging chronic kidney disease molecular pathways senescence

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
May 2024
Historique:
received: 09 02 2024
medline: 28 5 2024
pubmed: 28 5 2024
entrez: 28 5 2024
Statut: epublish

Résumé

Anti-aging therapy is the latest frontier in the world of medical science, especially for widespread diseases such as chronic kidney disease (CKD). Both renal aging and CKD are characterized by increased cellular senescence, inflammation and oxidative stress. A variety of cellular signalling mechanisms are involved in these processes, which provide new potential targets for therapeutic strategies aimed at counteracting the onset and progression of CKD. At the same time, sodium-glucose co-transporter 2 inhibitors (SGLT2is) continuously demonstrate large beneficial effects at all stages of the cardiorenal metabolic continuum. The broad-spectrum benefits of SGLT2is have led to changes in several treatment guidelines and to growing scientific interest in the underlying working principles. Multiple mechanisms have been studied to explain these great renal benefits, but many things remain to be solved. With this in mind, we provide an overview of the experimental evidence for the effects of SGLT2is on the molecular pathway's ability to modulate senescence, aging and parenchymal damage, especially at the kidney level. We propose to shed some light on the role of SGLT2is in kidney care by focusing on their potential to reduce the progression of kidney disease across the spectrum of aging and dysregulation of senescence.

Identifiants

pubmed: 38803397
doi: 10.1093/ckj/sfae133
pii: sfae133
pmc: PMC11129592
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

sfae133

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Déclaration de conflit d'intérêts

All authors and co-authors declare no conflicts of interest.

Auteurs

Elisa Russo (E)

Department of Internal Medicine, University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Valentina Zanetti (V)

Department of Internal Medicine, University of Genoa, Genoa, Italy.

Lucia Macciò (L)

Department of Internal Medicine, University of Genoa, Genoa, Italy.

Giulia Benizzelli (G)

Department of Internal Medicine, University of Genoa, Genoa, Italy.

Federico Carbone (F)

Department of Internal Medicine, University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Edoardo La Porta (E)

UO Nephrology Dialysis and Transplant, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
UOSD Dialysis IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Pasquale Esposito (P)

Department of Internal Medicine, University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Daniela Verzola (D)

Department of Internal Medicine, University of Genoa, Genoa, Italy.

Giacomo Garibotto (G)

Department of Internal Medicine, University of Genoa, Genoa, Italy.

Francesca Viazzi (F)

Department of Internal Medicine, University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Classifications MeSH