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Naslov:Incretin-based therapies, obesity-associated inflammation, and atherosclerotic cardiovascular risk
Avtorji:ID Kafol, Jan (Avtor)
ID Jug, Borut (Avtor)
ID Fras, Zlatko (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (2,72 MB)
MD5: 1E3433C3B9EF0AB00BCE967B4B792E5C
 
URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/2073-4409/15/14/1293
 
Jezik:Angleški jezik
Tipologija:1.02 - Pregledni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Cardiovascular disease remains a leading cause of mortality despite major advances in lipid lowering and risk-factor control, highlighting the importance of residual cardiovascular risk. Inflammation is a central driver of atherosclerosis, while obesity promotes chronic low-grade inflammation, adipose tissue dysfunction, ectopic fat accumulation, and vascular injury. This narrative review focuses on obesity-associated inflammation as an upstream contributor to residual atherosclerotic risk and evaluates whether incretin-based therapies modify this pathway through weight loss, metabolic improvement, and additional inflammatory or vascular mechanisms. Data from mechanistic studies, biomarker analyses, vascular imaging studies, and cardiovascular outcome trials are reviewed. Anti-inflammatory trials support inflammation as a modifiable therapeutic pathway, although clinical benefit depends on the therapeutic target, timing, and patient selection. Glucagon-like peptide-1 receptor agonists reduce inflammatory and oxidative stress biomarkers and show anti-atherosclerotic effects in experimental models, but human vascular imaging data remain inconclusive. Cardiovascular outcome trials establish benefit with several GLP-1 receptor agonists, including semaglutide in selected patients with overweight or obesity without diabetes. However, direct human evidence for receptor-mediated anti-inflammatory or anti-atherosclerotic effects remains limited, and the relative contributions of weight loss, metabolic improvement, and additional mechanisms remain uncertain.
Ključne besede:atherosclerosis, inflammation, residual inflammatory risk, obesity, glucagon-like peptide-1 receptor agonists, semaglutide, tirzepatide, incretin-based therapy, cardiovascular prevention, adipose tissue inflammation
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2026
Št. strani:str. 1-20
Številčenje:Vol. 15, iss. 14, [article no.] 1293
PID:20.500.12556/DiRROS-32340 Novo okno
UDK:616.1
ISSN pri članku:2073-4409
DOI:10.3390/cells15141293 Novo okno
COBISS.SI-ID:290234627 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 7. 9. 2026;
Datum objave v DiRROS:07.09.2026
Število ogledov:31
Število prenosov:18
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Cells
Skrajšan naslov:Cells
Založnik:MDPI
ISSN:2073-4409
COBISS.SI-ID:519958809 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0308-2019
Naslov:Ateroskleroza in tromboza

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:J3-4525-2022
Naslov:SINHRONIZIRANA KARDIORESPIRATORNA KORONARNA REHABILITACIJA

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:V3-24038-2024
Naslov:Strokovna izhodišča in priporočila za oblikovanje državnega programa obvladovanja bolezni srca in ožilja v Sloveniji

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:ateroskleroza, vnetje, debelost


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