Department of Neurology, NYU Grossman School of Medicine, 8714 5th Ave 2nd Floor, Brooklyn, NY, 11209, USA.
Center for Biostatistics and Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Clin Auton Res. 2022 Jun;32(3):175-184. doi: 10.1007/s10286-022-00865-2. Epub 2022 May 14.
Resting heart rate variability (HRV) is an important biomarker linking mental health to cardiovascular outcomes. However, resting HRV is also impaired in autonomic neuropathy, a common and underdiagnosed complication of common medical conditions which is detected by testing autonomic reflexes. We sought to describe the relationship between autonomic reflex abnormalities and resting HRV, taking into consideration medical comorbidities and demographic variables.
Participants (n = 209) underwent a standardized autonomic reflex screen which was summarized as the Composite Autonomic Severity Score (CASS) and included measures of reflexive HRV, e.g., heart rate with deep breathing (HRDB). Resting HRV measures were: pNN50 (percentage of NN intervals that differ by > 50 ms) and cvRMSSD (adjusted root mean square of successive differences).
In univariate analyses, lower resting HRV was associated with: older age, higher CASS, neuropathy on examination, hypertension, diabetes, chronic obstructive pulmonary disease, chronic kidney disease, and psychiatric disease. Adaptive regression spline analysis revealed that HRDB explained 27% of the variability in resting HRV for participants with values of HRDB in the normal range. Outside this range, there was no linear relationship because: (1) when HRDB was low (indicating autonomic neuropathy), resting HRV was also low with low variance; and (2) when HRDB was high, the variance in resting HRV was high. In multivariate models, only HRDB was significantly independently associated with cvRMSSD and pNN50.
Subclinical autonomic neuropathy, as evidenced by low HRDB and other autonomic reflexes, should be considered as a potential confounder of resting HRV in research involving medically and demographically diverse populations.
静息心率变异性(HRV)是将心理健康与心血管结果联系起来的重要生物标志物。然而,自主神经病变也会损害静息 HRV,这是常见医疗条件的常见且未被充分诊断的并发症,通过测试自主反射来检测。我们旨在描述自主反射异常与静息 HRV 之间的关系,同时考虑到医学合并症和人口统计学变量。
参与者(n=209)接受了标准化自主反射筛查,该筛查被总结为综合自主严重程度评分(CASS),并包括反射性 HRV 的测量,例如深呼吸时的心率(HRDB)。静息 HRV 测量值为:pNN50(NN 间期差异大于 50ms 的百分比)和 cvRMSSD(调整后的连续差异均方根)。
在单变量分析中,较低的静息 HRV 与:年龄较大、CASS 较高、检查时存在神经病变、高血压、糖尿病、慢性阻塞性肺疾病、慢性肾脏病和精神疾病有关。适应性回归样条分析显示,对于 HRDB 值处于正常范围内的参与者,HRDB 解释了静息 HRV 变异的 27%。在该范围之外,没有线性关系,因为:(1)当 HRDB 较低(表明自主神经病变)时,静息 HRV 也较低,且方差较小;(2)当 HRDB 较高时,静息 HRV 的方差较大。在多变量模型中,只有 HRDB 与 cvRMSSD 和 pNN50 显著独立相关。
以 HRDB 和其他自主反射降低为特征的亚临床自主神经病变,应被视为涉及医学和人口统计学上多样化人群的静息 HRV 研究中的潜在混杂因素。