Carsten Skarke, Wei Yang, Daohang Sha, Nicholas F Lahens, Tamara Isakova, Mark Unruh, Rajat Deo, Eunice Carmona-Powell, John H Holmes, Elaine Ficarra, Jing Chen, Jiang He, Hernan Rincon-Choles, Vallabh Shah, Chi-Yuan Hsu, Amanda H Anderson, James P Lash, Mahboob Rahman
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Multivariable linear regression revealed that participants without proteinuria (uPCR<0.2) had a 5.15 ms higher SDNN compared to participants with proteinuria (uPCR≥0.2, <i>p</i>=0.027). Cosinor modeling suggested differences in SDNN acrophase quartiles for diabetes (<i>p</i>=0.02), history of cardiovascular disease (<i>p</i>=0.003), eGFR (<i>p</i>=0.04), systolic blood pressure (<i>p</i>=0.04), and beta blocker use (<i>p</i>=0.0002). In the spline analysis, the SDNN curve differed between participants with and without cardiovascular disease (<i>p</i>=0.0005). This study assembled the largest dataset to date of SDNN as an index for heart rate variability from wearable digital health technology in the CRIC. The study demonstrates that several clinical and demographic factors are associated with SDNN in participants with CKD. 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引用次数: 0
摘要
对于慢性肾脏疾病(CKD)的临床外心血管功能生物监测的预后价值知之甚少。采用现实世界的抽样策略,从7个慢性肾功能不全队列(CRIC)中心的458名参与者中收集了来自可穿戴式BioPatch ECG设备的平均(+/-SD) 50.3+/-9.3小时的ECG记录。与非糖尿病参与者相比,糖尿病患者的神经网络间隔标准差(SDNN)降低7.4 ms (p=0.001)。多变量线性回归显示,无蛋白尿(uPCR)的参与者
A multi-center study to discern the diurnal variation of wearable device-based heart rate variability (HRV) in the Chronic Renal Insufficiency Cohort (CRIC) Study.
Little is known about the prognostic value of out-of-clinic biometric monitoring of cardiovascular function in chronic kidney disease (CKD). Using real-world sampling strategies, a mean (±SD) of 50.3±9.3 hours of ECG recordings from wearable BioPatch ECG devices was collected in a cohort consisting of 458 participants from seven Chronic Renal Insufficiency Cohort (CRIC) centers. The presence of diabetes was associated with a 7.4 ms lower Standard Deviation of NN Intervals (SDNN) compared to non-diabetic participants (p=0.001). Multivariable linear regression revealed that participants without proteinuria (uPCR<0.2) had a 5.15 ms higher SDNN compared to participants with proteinuria (uPCR≥0.2, p=0.027). Cosinor modeling suggested differences in SDNN acrophase quartiles for diabetes (p=0.02), history of cardiovascular disease (p=0.003), eGFR (p=0.04), systolic blood pressure (p=0.04), and beta blocker use (p=0.0002). In the spline analysis, the SDNN curve differed between participants with and without cardiovascular disease (p=0.0005). This study assembled the largest dataset to date of SDNN as an index for heart rate variability from wearable digital health technology in the CRIC. The study demonstrates that several clinical and demographic factors are associated with SDNN in participants with CKD. This sets the stage to determine the predictiveness of time-specific HRV metrics for future clinical outcomes.