ORCID: https://orcid.org/0000-0002-6798-1320; Omarov, Murad
ORCID: https://orcid.org/0000-0001-6126-8631; Xu, Lingling; Goma, Emil de; Natarajan, Pradeep
ORCID: https://orcid.org/0000-0001-8402-7435 und Georgakis, Marios K.
ORCID: https://orcid.org/0000-0003-3507-3659
(2025):
IL6 genetic perturbation mimicking IL-6 inhibition is associated with lower cardiometabolic risk.
In: Nature Cardiovascular Research, Bd. 4: S. 1172-1186
[PDF, 6MB]
Abstract
Human genetics supports a causal involvement of IL-6 signaling in atherosclerotic cardiovascular disease, prompting the clinical development of anti-IL-6 therapies. Genetic evidence has historically focused on IL6R missense variants, but emerging cardiovascular treatments target IL-6, not its receptor, questioning the translatability of genetic findings. Here we develop a genetic instrument for IL-6 signaling downregulation comprising IL6 locus variants that mimic the effects of the anti-IL-6 antibody ziltivekimab and use it to predict the effects of IL-6 inhibition on cardiometabolic and safety endpoints. Similar to IL6R, we found that genetically downregulated IL-6 signaling via IL6 perturbation is associated with lower lifetime risks of coronary artery disease, peripheral artery disease and ischemic atherosclerotic stroke in individuals of European and East Asian ancestry. Unlike IL6R missense variants linked to bacterial infections, the IL6 instrument was associated with lower risk of pneumonia hospitalization. Our data suggest that IL-6 inhibition can reduce cardiovascular risk without major unexpected safety concerns.
| Dokumententyp: | Zeitschriftenartikel |
|---|---|
| Fakultät: | Medizin > Munich Cluster for Systems Neurology (SyNergy) |
| Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
| URN: | urn:nbn:de:bvb:19-epub-129827-1 |
| ISSN: | 2731-0590 |
| Sprache: | Englisch |
| Dokumenten ID: | 129827 |
| Datum der Veröffentlichung auf Open Access LMU: | 27. Nov. 2025 07:44 |
| Letzte Änderungen: | 27. Nov. 2025 07:44 |
| DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 390857198 |
| DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 512461526 |
