Cardio-renal interaction - Clinical trials update 2022.
Chlorthalidone
/ therapeutic use
Clinical Trials as Topic
Diabetes Mellitus, Type 2
/ drug therapy
Glucose
Humans
Kidney
Mineralocorticoid Receptor Antagonists
/ therapeutic use
Renal Insufficiency, Chronic
/ diagnosis
Sodium
Sodium-Glucose Transporter 2
Sodium-Glucose Transporter 2 Inhibitors
Thiazides
/ therapeutic use
Chlorthalidone
Chronic kidney disease
Endocarditis
Finerenone
Hemodialysis
SGLT2-inhibitor
Journal
Nutrition, metabolism, and cardiovascular diseases : NMCD
ISSN: 1590-3729
Titre abrégé: Nutr Metab Cardiovasc Dis
Pays: Netherlands
ID NLM: 9111474
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
received:
13
06
2022
revised:
05
07
2022
accepted:
07
07
2022
pubmed:
6
9
2022
medline:
19
10
2022
entrez:
5
9
2022
Statut:
ppublish
Résumé
Chronic kidney disease is a common cardiovascular risk indicator and strongly associated with increased morbidity and mortality. The heart and kidneys are pathophysiologically closely connected, which becomes particularly obvious in patients with cardiorenal syndrome. This review summarizes clinically relevant studies on the cardio-renal interaction published in 2021 and 2022. Selected trials published in high-impact journals were chosen from the database Pubmed and included in this review. New evidence about the selective mineralocorticoid receptor antagonist finerenone and the renoprotective sodium-glucose co-transporter-2-inhibitors (SGLT2-Inhibitors) are discussed and we update on novel insights about the treatment of arterial hypertension in patients with severe chronic kidney disease with the thiazide-like diuretic chlorthalidone. Finally, data on infective endocarditis in patients on chronic hemodialysis and the treatment of secondary hyperparathyroidism with the calcimimetic drug etelcalcetide in patients with end stage kidney disease are critically reviewed. Several important studies investigating cardio-renal interactions were recently published may affect clinical practice. The graphical abstract (Fig. 1) depicts the most relevant clinical studies investigating cardio-renal interactions.
Identifiants
pubmed: 36064690
pii: S0939-4753(22)00290-3
doi: 10.1016/j.numecd.2022.07.002
pii:
doi:
Substances chimiques
Mineralocorticoid Receptor Antagonists
0
Sodium-Glucose Transporter 2
0
Sodium-Glucose Transporter 2 Inhibitors
0
Thiazides
0
Sodium
9NEZ333N27
Glucose
IY9XDZ35W2
Chlorthalidone
Q0MQD1073Q
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2451-2458Informations de copyright
Copyright © 2022 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest FM is supported by Deutsche Gesellschaft für Kardiologie (DGK), Deutsche Forschungsgemeinschaft (SFB TRR219), and Deutsche Herzstiftung and has received scientific support and/or speaker honoraria from Astra-Zeneca, Bayer, Boehringer Ingelheim, Medtronic, Merck, and ReCor Medical. IE has received speaker honoraria from Pharmacosmos and Astellas. VS has received speaker honoraria from Astra Zeneca and Novartis. MB is supported by the Deutsche Forschungsgemeinschaft (German Research Foundation; TTR 219, project number 322900939) and reports personal fees from Abbott, Amgen, Astra Zeneca, Bayer, Boehringer-Ingelheim, Cytokinetic, Edwards, Medtronic, Novartis, Recor, Servier and Vifor. FG and MK do not have conflicts of interest.