Tirzepatide against obesity and insulin-resistance: pathophysiological aspects and clinical evidence.
GIP
GLP - 1
Tirzepatide
arterial hypertension
clinical trials
insulin-resistance
obesity
pathophysiology
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2024
2024
Historique:
received:
17
03
2024
accepted:
07
06
2024
medline:
9
7
2024
pubmed:
9
7
2024
entrez:
9
7
2024
Statut:
epublish
Résumé
Obesity is a chronic, multifactorial disease in which accumulated excess body fat has a negative impact on health. Obesity continues to rise among the general population, resulting in an epidemic that shows no significant signs of decline. It is directly involved in development of cardiometabolic diseases, ischemic coronary heart disease peripheral arterial disease, heart failure, and arterial hypertension, producing global morbidity and mortality. Mainly, abdominal obesity represents a crucial factor for cardiovascular illness and also the most frequent component of metabolic syndrome. Recent evidence showed that Tirzepatide (TZP), a new drug including both Glucagon Like Peptide 1 (GLP-1) and Glucose-dependent Insulinotropic Polypeptide (GIP) receptor agonism, is effective in subjects with type 2 diabetes (T2D), lowering body weight, fat mass and glycated hemoglobin (HbA
Identifiants
pubmed: 38978621
doi: 10.3389/fendo.2024.1402583
pmc: PMC11228148
doi:
Substances chimiques
tirzepatide
OYN3CCI6QE
Glucagon-Like Peptide-2 Receptor
0
Gastric Inhibitory Polypeptide
59392-49-3
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1402583Informations de copyright
Copyright © 2024 Corrao, Pollicino, Maggio, Torres and Argano.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.