Ahn Hyo-Jeong, Rhee Tae-Min, Choi Eue-Keun, Lee Kyung-Yeon, Choi JungMin, Kim Jae-Hyun, Han Seokmoon, Kwon Soonil, Lee So-Ryoung, Oh Seil, Lip Gregory Y H
Department of Internal Medicine, Seoul National University Hospital, Republic of Korea.
Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Center, Republic of Korea.
Europace. 2025 Jul 1;27(7). doi: 10.1093/europace/euaf104.
Heart failure (HF) is the most concerning morbidity in atrial fibrillation (AF) through mutual influence on a poor prognosis. A polygenic risk score (PRS) has recently been proposed to improve the risk prediction for cardiovascular disease. The additive predictive role of PRS for incident HF in patients with AF who inherently carry a high risk of HF is unknown.
From the UK Biobank, we identified 21 167 White Caucasian participants with newly diagnosed AF without a prior history of HF. The PRS for HF was constructed using genetic instruments from previous genome-wide association studies. The primary outcome was the occurrence of incident HF. The prediction of incident HF was evaluated using the tertile categorization of PRS for HF (low vs. moderate-high PRS) across the entire AF cohort, as well as within age subgroups (young AF, age <60 years; old AF, age ≥60 years, respectively). The mean age was 69.0 ± 6.9 years in the total population (55.2 ± 3.9 years in age <60 years; 70.7 ± 5.0 years in age ≥60 years group). During a median follow-up of 3.8 (1.4-7.2) years, the incidence rate (1000-patient year) of HF was 29.9. In the total population, AF patients with moderate-high PRS for HF were associated with a higher risk of HF than those with low PRS for HF [adjusted hazard ratio (HR) 1.18 (95% confidence interval (CI), 1.05-1.32), P = 0.005]. The higher risk of HF in the moderate-high PRS group was particularly accentuated in young AF patients: adjusted HR, 2.14 (95% CI 1.29-3.57) in young AF, and 1.13 (95% CI 1.01-1.27) in old AF, P-for-interaction = 0.015. In young AF, the onset of incident HF was earlier in those with the moderate-high PRS group [median time from AF diagnosis to incident HF, 4.2 (0.8-7.1) years in low PRS vs. 1.5 (0.3-4.7) years in the moderate-high PRS group, P = 0.001]. The prediction of HF was significantly improved by adding PRS to the clinical risk factors for HF, especially in young AF patients, with a net reclassification improvement of 29.7% (P = 0.003).
PRS for HF can significantly improve the prediction of incident HF in patients with AF, especially in the young population, providing clinical utility of an individualized approach to integrated management of AF.
心力衰竭(HF)是心房颤动(AF)中最令人担忧的并发症,二者相互影响,预后较差。最近有人提出多基因风险评分(PRS)来改善心血管疾病的风险预测。对于固有HF风险较高的AF患者,PRS对新发HF的附加预测作用尚不清楚。
从英国生物银行中,我们识别出21167名新诊断为AF且无HF病史的白种人参与者。使用先前全基因组关联研究的基因工具构建HF的PRS。主要结局是新发HF的发生。在整个AF队列以及年龄亚组(年轻AF患者,年龄<60岁;老年AF患者,年龄≥60岁)中,使用HF的PRS三分位数分类(低与中高PRS)评估新发HF的预测情况。总体人群的平均年龄为69.0±6.9岁(年龄<60岁组为55.2±3.9岁;年龄≥60岁组为70.7±5.0岁)。在中位随访3.8(1.4 - 7.2)年期间,HF的发病率(每1000患者年)为29.9。在总体人群中,HF中高PRS的AF患者比低PRS的患者发生HF的风险更高[调整后风险比(HR)为1.18(95%置信区间(CI),1.05 - 1.32),P = 0.005]。中高PRS组HF风险较高在年轻AF患者中尤为明显:年轻AF患者调整后HR为2.14(95% CI 1.29 - 3.57),老年AF患者为1.13(95% CI 1.01 - 1.27),交互作用P值 = 0.015。在年轻AF患者中,中高PRS组新发HF的发病时间更早[从AF诊断到新发HF的中位时间,低PRS组为4.2(0.8 - 7.1)年,中高PRS组为1.5(0.3 - 4.7)年,P = 0.001]。将PRS添加到HF临床风险因素中可显著改善HF的预测,尤其是在年轻AF患者中,净重新分类改善率为29.7%(P = 0.003)。
HF的PRS可显著改善AF患者新发HF的预测,尤其是在年轻人群中,为AF综合管理的个体化方法提供了临床实用性。