Novak V, Novak P, Opfer-Gehrking T L, Low P A
Autonomic Disorders Research Center, Mayo Clinic, Rochester, MN 55905, USA.
J Auton Nerv Syst. 1996 Dec 14;61(3):313-20. doi: 10.1016/s0165-1838(96)00101-4.
Orthostatic tachycardia is common but its specificity remains uncertain. Our preliminary work suggested that using autonomic function testing in conjunction with time-frequency mapping (TFM), it might be possible to characterize a subset of the postural tachycardia syndrome (POTS), that is due to a restricted autonomic neuropathy. We describe 20 patients (17 women and 3 men, aged 14-43 years) with florid POTS and 20 controls (14 women and 6 men, aged 20-41 years). Autonomic failure was quantified by its distribution (cardiovagal, adrenergic and sudomotor) and severity, a symptom profile was generated, and spectral indices, based on modified Wigner distribution during rest and head-up tilt (80 degrees) were evaluated. During tilt-up POTS patients differed from controls by an excessive heart rate (> 130 bpm) (P < 0.001), and higher diastolic pressure (P < 0.01). During rest, cardiovagal oscillations (at respiratory frequencies [RF]) and slow rhythms at nonrespiratory frequencies (NONRF) (from 0.01 to 0.07 Hz) in R-R intervals (RRI) (P < 0.01) were reduced. Both RF and NONRF rhythms in RRI were further blunted with tilt-up (P < 0.001). Slow adrenergic vasomotor rhythms in blood pressure (BP) (approximately 0.07 Hz) surged with tilt-up and returned to normal levels afterwards. The index of sympatho-vagal balance (NONRF-Systolic BP (SBP)/RF-RRI) was dramatically increased in POTS (P < 0.001). Distal postganglionic sudomotor failure was observed, and impairment of the BP responses to the Valsalva maneuver (phase II) suggested peripheral adrenergic dysfunction. Persistent orthostatic dizziness, tiredness, gastrointestinal symptoms and palpitations were common in POTS patients. It is possible to identify a subset of POTS patients who have a length-dependent autonomic neuropathy, affecting the peripheral adrenergic and cardiovagal fibers, with relative preservation of cardiac adrenergic fibers.
直立性心动过速很常见,但其特异性仍不确定。我们的初步研究表明,结合自主神经功能测试和时频映射(TFM),有可能对姿势性心动过速综合征(POTS)的一个亚组进行特征描述,该亚组是由局限性自主神经病变引起的。我们描述了20例患有典型POTS的患者(17名女性和3名男性,年龄14 - 43岁)以及20名对照者(14名女性和6名男性,年龄20 - 41岁)。通过自主神经功能障碍的分布(心迷走神经、肾上腺素能和汗腺运动神经)及严重程度对自主神经功能衰竭进行量化,生成症状概况,并评估基于静息和头高位倾斜(80度)时改良维格纳分布的频谱指数。在倾斜过程中,POTS患者与对照者的区别在于心率过高(>130次/分钟)(P < 0.001)以及舒张压较高(P < 0.01)。在静息时,R - R间期(RRI)中心迷走神经振荡(在呼吸频率[RF])和非呼吸频率(NONRF)(0.01至0.07赫兹)的慢节律(P < 0.01)减少。随着倾斜,RRI中的RF和NONRF节律进一步减弱(P < 0.001)。血压(BP)中的慢肾上腺素能血管运动节律(约0.07赫兹)在倾斜时激增,随后恢复到正常水平。POTS患者的交感 - 迷走神经平衡指数(NONRF - 收缩压[SBP]/RF - RRI)显著升高(P < 0.001)。观察到节后远端汗腺运动神经功能衰竭,并且对瓦尔萨尔瓦动作(第二阶段)的血压反应受损提示外周肾上腺素能功能障碍。持续性直立性头晕、疲劳、胃肠道症状和心悸在POTS患者中很常见。有可能识别出一部分POTS患者,他们患有长度依赖性自主神经病变,影响外周肾上腺素能和心迷走神经纤维,而心脏肾上腺素能纤维相对保留。