Department of Cardiology Institute of Cardiovascular Diseases First Affiliated Hospital of Dalian Medical University Dalian Liaoning China.
J Am Heart Assoc. 2022 Jan 4;11(1):e021997. doi: 10.1161/JAHA.121.021997. Epub 2021 Dec 31.
Background Subclinical atrial fibrillation (SCAF) is often asymptomatic nonetheless harmful. In patients with cardiac implantable electronic devices, we evaluated the combined performance of homocysteine and uric acid (UA) biomarkers to discriminate high-risk patients for SCAF. Methods and Results We enrolled 1224 consecutive patients for evaluation of SCAF in patients with cardiac implantable electronic devices in Dalian, China, between January 2013 and December 2019. Clinical data and blood samples were obtained from patients selected according to the absence or presence of atrial high-rate episodes >6 minutes. Blood samples were obtained, and homocysteine and UA biomarkers were tested in all patients to distinguish their prognostic performance for SCAF. Homocysteine and UA biomarkers were significantly different in SCAF versus no SCAF. On multivariable Cox regression analysis with potential confounders, elevated homocysteine and UA biomarkers were significantly associated with an increased risk of SCAF. A rise of 1 SD in homocysteine (5.7 μmol/L) was associated with an increased risk of SCAF in men and women regardless of their UA levels. Similarly, a 1-SD increase in UA (91 μmol/L) was associated with an increased risk of SCAF among the patients with high levels of homocysteine in men (hazard ratio, 1.81; 95% CI, 1.43-2.30) and women (hazard ratio, 2.11; 95% CI, 1.69-2.62). The addition of homocysteine and UA to the atrial fibrillation risk factors recommended by the 2020 European Society of Cardiology Guidelines significantly improved risk discrimination for SCAF. Conclusions Homocysteine and UA biomarkers were strongly associated with SCAF. The prediction performance of the European Society of Cardiology model for SCAF was increased by the addition of the selected biomarkers. Registration URL: https://www.chictr.org.cn; Unique identifier: Chi-CTR200003837.
背景 亚临床心房颤动(SCAF)通常无症状,但却有害。我们在植入心脏电子设备的患者中评估了同型半胱氨酸和尿酸(UA)生物标志物联合用于区分 SCAF 高危患者的表现。
方法和结果 我们在中国大连连续纳入了 1224 例因植入心脏电子设备评估 SCAF 的患者,入选时间为 2013 年 1 月至 2019 年 12 月。根据是否存在持续时间>6 分钟的心房高频事件,选择患者获取临床数据和血样。对所有患者进行血液样本采集,并检测同型半胱氨酸和 UA 生物标志物,以区分其对 SCAF 的预后表现。SCAF 患者的同型半胱氨酸和 UA 生物标志物显著高于无 SCAF 患者。多变量 Cox 回归分析潜在混杂因素后,同型半胱氨酸和 UA 生物标志物升高与 SCAF 风险增加显著相关。同型半胱氨酸(5.7μmol/L)升高 1 个标准差与男性和女性 SCAF 风险增加相关,无论其 UA 水平如何。同样,男性高同型半胱氨酸患者(危险比,1.81;95%CI,1.43-2.30)和女性高同型半胱氨酸患者(危险比,2.11;95%CI,1.69-2.62)UA 升高 1 个标准差与 SCAF 风险增加相关。同型半胱氨酸和 UA 与 2020 年欧洲心脏病学会指南推荐的房颤危险因素联合后,可显著提高 SCAF 风险分层。
结论 同型半胱氨酸和 UA 生物标志物与 SCAF 密切相关。加入所选生物标志物后,欧洲心脏病学会 SCAF 模型的预测性能提高。