Pastori Daniele, Antonucci Emilia, Milanese Alberto, Menichelli Danilo, Palareti Gualtiero, Farcomeni Alessio, Pignatelli Pasquale
Department of Clinical, Internal, Anesthesiological, and Cardiovascular Sciences, Sapienza University of Rome, 00185 Rome, Italy.
Arianna Anticoagulazione Foundation, 40138 Bologna, Italy.
J Pers Med. 2022 May 12;12(5):785. doi: 10.3390/jpm12050785.
Patients with atrial fibrillation (AF) still experience a high mortality rate despite optimal antithrombotic treatment. We aimed to identify clinical phenotypes of patients to stratify mortality risk in AF. Cluster analysis was performed on 5171 AF patients from the nationwide START registry. The risk of all-cause mortality in each cluster was analyzed. We identified four clusters. Cluster 1 was composed of the youngest patients, with low comorbidities; Cluster 2 of patients with low cardiovascular risk factors and high prevalence of cancer; Cluster 3 of men with diabetes and coronary disease and peripheral artery disease; Cluster 4 included the oldest patients, mainly women, with previous cerebrovascular events. During 9857 person-years of observation, 386 deaths (3.92%/year) occurred. Mortality rates increased across clusters: 0.42%/year (cluster 1, reference group), 2.12%/year (cluster 2, adjusted hazard ratio (aHR) 3.306, 95% confidence interval (CI) 1.204−9.077, p = 0.020), 4.41%/year (cluster 3, aHR 6.702, 95%CI 2.433−18.461, p < 0.001), and 8.71%/year (cluster 4, aHR 8.927, 95%CI 3.238−24.605, p < 0.001). We identified four clusters of AF patients with progressive mortality risk. The use of clinical phenotypes may help identify patients at a higher risk of mortality.
尽管接受了最佳抗栓治疗,房颤(AF)患者的死亡率仍然很高。我们旨在识别患者的临床表型,以对房颤患者的死亡风险进行分层。对来自全国START注册研究的5171例房颤患者进行了聚类分析。分析了每个聚类中全因死亡的风险。我们识别出了四个聚类。聚类1由最年轻、合并症少的患者组成;聚类2由心血管危险因素低、癌症患病率高的患者组成;聚类3由患有糖尿病、冠心病和外周动脉疾病的男性组成;聚类4包括年龄最大的患者,主要是女性,既往有脑血管事件。在9857人年的观察期内,发生了386例死亡(每年3.92%)。各聚类的死亡率逐渐升高:每年0.42%(聚类1,参照组)、每年2.12%(聚类2,调整后风险比(aHR)3.306,95%置信区间(CI)1.204−9.077,p = 0.020)、每年4.41%(聚类3,aHR 6.702,95%CI 2.433−18.461,p < 0.001)和每年8.71%(聚类4,aHR 8.927,95%CI 3.238−24.605,p < 0.001)。我们识别出了四组具有逐渐升高死亡风险的房颤患者。使用临床表型可能有助于识别死亡风险较高的患者。