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Biomarkers and genetic determinants of cardiac sarcoidosis : current status, the unmet needs and future perspectives
ID Bajec, Tine (Avtor), ID Harlander, Matevž (Avtor), ID Koren Pucelj, Nadja (Avtor), ID Kassi, Mahwash (Avtor), ID Poglajen, Gregor (Avtor)

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URLURL - Izvorni URL, za dostop obiščite https://www.frontiersin.org/journals/cardiovascular-medicine/articles/10.3389/fcvm.2026.1754375/full Povezava se odpre v novem oknu

Izvleček
Sarcoidosis is a systemic disorder driven by genetic predisposition, environmental exposures, and immune dysregulation, resulting in the formation of noncaseating granulomas across multiple organs. In cardiac sarcoidosis (CS), immune cell infiltration of the myocardium, epicardium, and endocardium may lead to conduction disturbances, ventricular arrhythmias, and heart failure. While overt cardiac involvement was historically considered rare, affecting only 5% of sarcoidosis patients, the wider availability and improved sensitivity of contemporary cardiac imaging have revealed a substantially higher burden, with cardiac involvement reaching up to 55% in selected, systematically screened populations. Current diagnostic approaches for CS, including endomyocardial biopsy (EMB), cardiovascular magnetic resonance (CMR), and fluorine-18 fluorodeoxyglucose–positron emission tomography (FDG-PET), offer valuable insights but are restricted by high costs, invasiveness, and limited sensitivity and specificity. These challenges, together with the disproportionate contribution of cardiac involvement to sarcoidosis-related mortality, underscore the need for innovative, non-invasive, and widely accessible diagnostic strategies. Emerging evidence suggests that novel serum biomarkers and genomic studies hold promise for transforming the diagnostic landscape of CS. Biomarkers may provide accessible, cost-effective tools to complement established diagnostic methods, while genetic insights could identify individuals at higher risk for cardiac involvement and stratify patients based on disease phenotype. This review examines current evidence on serum biomarkers and genetic studies in CS diagnosis, identifies critical knowledge gaps, and proposes future directions aimed at advancing diagnostic precision and improving clinical outcomes.

Jezik:Angleški jezik
Ključne besede:biomarker, genetics, heart, sarcoidosis, therapy
Vrsta gradiva:Članek v reviji
Tipologija:1.02 - Pregledni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2026
Št. strani:10 str.
Številčenje:Vol. 13, art. 1754375
PID:20.500.12556/RUL-181249 Povezava se odpre v novem oknu
UDK:616.1
ISSN pri članku:2297-055X
DOI:10.3389/fcvm.2026.1754375 Povezava se odpre v novem oknu
COBISS.SI-ID:271877123 Povezava se odpre v novem oknu
Datum objave v RUL:01.04.2026
Število ogledov:275
Število prenosov:99
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Frontiers in cardiovascular medicine
Skrajšan naslov:Front. cardiovasc. med.
Založnik:Frontiers Media
ISSN:2297-055X
COBISS.SI-ID:523093273 Povezava se odpre v novem oknu

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:biološki označevalec, genetika, srce, sarkoidoza, terapija

Projekti

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0457
Naslov:Nove strategije diagnostike in zdravljenja srčnega popuščanja

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