National Heart, Lung, and Blood Institute and Boston University's Framingham Heart Study, Framingham, Massachusetts; Section of Cardiovascular Medicine, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Heart Rhythm. 2021 Sep;18(9):1500-1507. doi: 10.1016/j.hrthm.2021.05.009. Epub 2021 May 11.
P-wave signal-averaged electrocardiography (P-SAECG) quantifies atrial electrical activity. P-SAECG measures and their clinical correlates and heritability have had limited characterization in community-based cohorts.
The purpose of this study was to (1) establish reference values; (2) identify clinical risk factors associated with P-SAECG; and (3) estimate genetic heritability for P-SAECG traits.
We performed P-SAECG in 2 generations of Framingham Heart Study participants. We performed backward elimination regression models to assess associations of clinical factors with each SAECG trait (P-wave [PW] duration, root mean square voltage in terminal 40 ms [RMS40], terminal 30 ms RMS30, terminal 20 ms RMS20, RMS PW, and PW integral). We estimated the adjusted genetic heritability of P-SAECG measures using the Sequential Oligogenic Linkage Analysis Routines (SOLAR) program.
We included 4307 participants (age 55 ± 14 years; 56% female). The reference values were derived from 1752 participants without cardiovascular risk factors. Median (2.5th percentile; 97.5th percentile) total PW duration was 118 ms (93; 146) in women and 128 ms (104; 158) in men in the reference sample, and 121 ms (94; 151) in women and 129 ms (103; 159) in the entire study cohort (broad sample). In the broad sample, after adjusting for age and sex, total PW duration was positively associated with height, weight, prevalent heart failure, history of atrial fibrillation (AF), and atrioventricular node blockers, and negatively associated with smoking, waist circumference, heart rate, and diabetes. The estimated heritability of P-SAECG traits was moderate, ranging from 11.9% for RMS30 to 24.9% for PW integral.
P-SAECG traits are associated with multiple AF-related risk factors and are moderately heritable.
P 波信号平均心电图(P-SAECG)量化心房电活动。P-SAECG 测量及其临床相关性和遗传性在基于社区的队列中受到了有限的描述。
本研究的目的是:(1)建立参考值;(2)确定与 P-SAECG 相关的临床危险因素;(3)估计 P-SAECG 特征的遗传遗传性。
我们在 2 代弗雷明汉心脏研究参与者中进行了 P-SAECG。我们使用向后消除回归模型评估临床因素与每个 SAECG 特征(P 波[PW]持续时间、终末 40ms 均方根电压[RMS40]、终末 30ms RMS30、终末 20ms RMS20、RMS PW 和 PW 积分)之间的关联。我们使用序贯遗传连锁分析程序(SOLAR)程序估计 P-SAECG 测量的调整后遗传遗传性。
我们纳入了 4307 名参与者(年龄 55±14 岁;56%为女性)。参考值来自于 1752 名无心血管危险因素的参与者。在参考样本中,女性的总 PW 持续时间中位数(25%分位数;97.5%分位数)为 118ms(93;146),男性为 128ms(104;158),在整个研究队列(广泛样本)中,女性为 121ms(94;151),男性为 129ms(103;159)。在广泛的样本中,在调整年龄和性别后,总 PW 持续时间与身高、体重、现患心力衰竭、心房颤动(AF)病史和房室结阻滞剂呈正相关,与吸烟、腰围、心率和糖尿病呈负相关。P-SAECG 特征的遗传遗传性估计值适中,范围从 RMS30 的 11.9%到 PW 积分的 24.9%。
P-SAECG 特征与多种与 AF 相关的危险因素相关,具有中等程度的遗传性。