Atriumfibrilleren

AF-screening naar genetisch risico: LOOP subanalyse

LOOP subanalyse onderzocht of genetisch risico de opbrengst van AF-screening beïnvloedt. Hogere genetische risicoscores waren geassocieerd met meer AF-detectie, wat gerichte screening kan informeren.

Abstract (original)

BACKGROUND: Polygenic risk scores (PRS) hold promise in risk stratification and screening for cardiovascular diseases, including atrial fibrillation (AF). OBJECTIVES: This study investigated the efficacy of AF screening for stroke prevention based on a PRS for AF. METHODS: This prespecified post hoc analysis of the randomized LOOP (Atrial Fibrillation Detected by Continuous ECG Monitoring Using Implantable Loop Recorder to Prevent Stroke in High-Risk Individuals) study included 5,656 AF-naive individuals aged ≥70 years with stroke risk factors and available genetic data. The participants were randomized 1:3 for screening with an implantable loop recorder (ILR) vs usual care. Genetic risk of AF was assessed using a PRS for AF (PRSAF). The primary outcome was a composite of stroke and systemic embolism (SE). Interaction between the randomization arm and PRSAF was assessed in cause-specific Cox regressions for the full cohort and across the observed range of polygenic risk using a continuous prediction grid. Secondary analyses included models stratified by PRS level, gene-screening interactions for major bleeding events, and associations between PRSAF and AF burden (≥1 episode lasting ≥24 hours among participants with ILR-detected AF). RESULTS: Over a median follow-up period of 5.4 years, 969 participants (17.1%) received a diagnosis of AF, 296 (5.2%) had stroke/SE, and 206 (3.6%) had major bleeding. PRSAF was associated with higher rates of AF (HR per SD increase: 1.20; 95% CI: 1.13-1.28; P < 0.001). A significant interaction was observed between ILR screening and PRSAF for stroke/SE (Pinteraction = 0.006). ILR screening was associated with lower rates of stroke/SE in individuals with PRSAF ≥median (HR: 0.65; 95% CI: 0.43-0.97; P = 0.036) but not in those with PRSAF <median (HR: 1.06; 95% CI: 0.72-1.57; P = 0.75). ILR screening was associated with higher rates of major bleeding at lower levels of PRSAF (Pinteraction = 0.036), corresponding to a HR of 1.71 (95% CI: 1.12-2.64; P = 0.011) in those with PRSAF <median. A 1-SD increase in PRSAF was associated with an OR of 1.35 (95% CI: 1.02-1.78; P = 0.037) for having ≥1 AF episode lasting ≥24 hours. CONCLUSIONS: ILR screening for AF was associated with a significant reduction in stroke/SE in individuals with higher genetic risk of AF but not in those with lower genetic risk. These hypothesis-generating findings indicate that genetic predisposition may aid in selecting individuals who benefit from AF screening.

Dit artikel is een samenvatting van een publicatie in Journal of the American College of Cardiology. Voor het volledige artikel, alle details en referenties verwijzen wij u naar de oorspronkelijke bron.

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DOI: 10.1016/j.jacc.2025.09.024