Emerging glucose-lowering therapies: a guide for cardiologists.
Biomarkers
/ blood
Blood Glucose
/ drug effects
Cardiovascular Diseases
/ diagnosis
Diabetes Mellitus, Type 2
/ blood
Down-Regulation
Glucagon-Like Peptide-1 Receptor
/ agonists
Humans
Incretins
/ adverse effects
Patient Safety
Risk Assessment
Risk Factors
Sodium-Glucose Transporter 2 Inhibitors
/ adverse effects
Treatment Outcome
Type 2 diabetes mellitus
glucagon-like peptide-1 receptor agonists
sodium glucose co-transporter-2 inhibitors
Journal
Heart (British Cardiac Society)
ISSN: 1468-201X
Titre abrégé: Heart
Pays: England
ID NLM: 9602087
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
29
07
2019
revised:
19
08
2019
accepted:
28
08
2019
pubmed:
26
9
2019
medline:
7
7
2020
entrez:
26
9
2019
Statut:
ppublish
Résumé
In recent large-scale cardiovascular outcome trials, two new classes of glucose-lowering medications-sodium glucose cotransporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1RAs)-demonstrated cardiovascular benefits in adults with type 2 diabetes mellitus (T2DM). These findings have prompted growing optimism among clinicians regarding the potential for these agents to reduce the burden of cardiovascular disease in people with T2DM. GLP-1RAs and SGLT2i are now advocated as second-line agents in European and US guidelines for management of both hyperglycaemia and for primary prevention of cardiovascular disease in people with T2DM. Given the high prevalence of T2DM in patients with cardiovascular disease, cardiologists will increasingly encounter these agents in routine clinical practice. In this review, we summarise evidence from cardiovascular outcome trials of GLP-1RAs and SGLT2i, give practical advice on prescribing and detail safety considerations associated with their use. We also highlight areas where further work is needed, giving details on active clinical trials. The review aims to familiarise cardiologists with these emerging treatments, which will be increasingly encountered in clinical practice, given the expanding representation of T2DM in patients with cardiovascular disease. Whether these drugs will be initiated by cardiologists remains to be determined.
Identifiants
pubmed: 31551292
pii: heartjnl-2019-315758
doi: 10.1136/heartjnl-2019-315758
doi:
Substances chimiques
Biomarkers
0
Blood Glucose
0
GLP1R protein, human
0
Glucagon-Like Peptide-1 Receptor
0
Incretins
0
Sodium-Glucose Transporter 2 Inhibitors
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
18-23Subventions
Organisme : British Heart Foundation
ID : FS/16/47/32190
Pays : United Kingdom
Organisme : Department of Health
ID : RP-2017-08-ST2-007
Pays : United Kingdom
Informations de copyright
© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.