A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Inflammatory proteomics profiling for prediction of incident atrial fibrillation (2023)


Börschel, C. S., Ortega-Alonso, A., Havulinna, A. S., Jousilahti, P., Salmi, M., Jalkanen, S., Salomaa, V., Niiranen, T., & Schnabel, R. B. (2023). Inflammatory proteomics profiling for prediction of incident atrial fibrillation. Heart, 109(13), 1000-1006. https://doi.org/10.1136/heartjnl-2022-321959


JYU-tekijät tai -toimittajat


Julkaisun tiedot

Julkaisun kaikki tekijät tai toimittajatBörschel, Christin S.; Ortega-Alonso, Alfredo; Havulinna, Aki S.; Jousilahti, Pekka; Salmi, Marko; Jalkanen, Sirpa; Salomaa, Veikko; Niiranen, Teemu; Schnabel, Renate B.

Lehti tai sarjaHeart

ISSN1355-6037

eISSN1468-201X

Julkaisuvuosi2023

Ilmestymispäivä17.02.2023

Volyymi109

Lehden numero13

Artikkelin sivunumerot1000-1006

KustantajaBMJ Publishing Group

JulkaisumaaBritannia

Julkaisun kielienglanti

DOIhttps://doi.org/10.1136/heartjnl-2022-321959

Julkaisun avoin saatavuusAvoimesti saatavilla

Julkaisukanavan avoin saatavuusOsittain avoin julkaisukanava

Julkaisu on rinnakkaistallennettu (JYX)https://jyx.jyu.fi/handle/123456789/85947


Tiivistelmä

Objective Atrial fibrillation (AF) has emerged as a common condition in older adults. Cardiovascular risk factors only explain about 50% of AF cases. Inflammatory biomarkers may help close this gap as inflammation can alter atrial electrophysiology and structure. This study aimed to determine a cytokine biomarker profile for this condition in the community using a proteomics approach.

Methods This study uses cytokine proteomics in participants of the Finnish population-based FINRISK cohort studies 1997/2002. Risk models for 46 cytokines were developed to predict incident AF using Cox regressions. Furthermore, the association of participants’ C reactive protein (CRP) and N-terminal pro B-type natriuretic peptide (NT-proBNP) concentrations with incident AF was examined.

Results In 10 744 participants (mean age of 50.9 years, 51.3% women), 1246 cases of incident AF were observed (40.5% women). The main analyses, adjusted for participants’ sex and age, suggested that higher concentrations of macrophage inflammatory protein-1β (HR=1.11; 95% CI 1.04, 1.17), hepatocyte growth factor (HR=1.12; 95% CI 1.05, 1.19), CRP (HR=1.17; 95% CI 1.10, 1.24) and NT-proBNP (HR=1.58; 95% CI 1.45, 1.71) were associated with increased risk of incident AF. In further clinical variable-adjusted models, only NT-proBNP remained statistically significant.

Conclusion Our study confirmed NT-proBNP as a strong predictor for AF. Observed associations of circulating inflammatory cytokines were primarily explained by clinical risk factors and did not improve risk prediction. The potential mechanistic role of inflammatory cytokines measured in a proteomics approach remains to be further elucidated.


YSO-asiasanatsydän- ja verisuonitauditeteisvärinäennusteetmatala-asteinen tulehdusbiomarkkeritproteomiikkasytokiinitc-reaktiivinen proteiini


Liittyvät organisaatiot


OKM-raportointiKyllä

VIRTA-lähetysvuosi2023

JUFO-taso2


Viimeisin päivitys 2024-12-10 klo 17:00