Department of Neurology, Dysautonomia Center, New York University School of Medicine, New York, NY.
Departments of Medicine and Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
Ann Neurol. 2018 Mar;83(3):522-531. doi: 10.1002/ana.25170. Epub 2018 Mar 10.
Blunted tachycardia during hypotension is a characteristic feature of patients with autonomic failure, but the range has not been defined. This study reports the range of orthostatic heart rate (HR) changes in patients with autonomic failure caused by neurodegenerative synucleinopathies.
Patients evaluated at sites of the U.S. Autonomic Consortium (NCT01799915) underwent standardized autonomic function tests and full neurological evaluation.
We identified 402 patients with orthostatic hypotension (OH) who had normal sinus rhythm. Of these, 378 had impaired sympathetic activation (ie, neurogenic OH) and based on their neurological examination were diagnosed with Parkinson disease, dementia with Lewy bodies, pure autonomic failure, or multiple system atrophy. The remaining 24 patients had preserved sympathetic activation and their OH was classified as nonneurogenic, due to volume depletion, anemia, or polypharmacy. Patients with neurogenic OH had twice the fall in systolic blood pressure (SBP; -44 ± 25 vs -21 ± 14 mmHg [mean ± standard deviation], p < 0.0001) but only one-third of the increase in HR of those with nonneurogenic OH (8 ± 8 vs 25 ± 11 beats per minute [bpm], p < 0.0001). A ΔHR/ΔSBP ratio of 0.492 bpm/mmHg had excellent sensitivity (91.3%) and specificity (88.4%) to distinguish between patients with neurogenic from nonneurogenic OH (area under the curve = 0.96, p < 0.0001). Within patients with neurogenic OH, HR increased more in those with multiple system atrophy (p = 0.0003), but there was considerable overlap with patients with Lewy body disorders.
A blunted HR increase during hypotension suggests a neurogenic cause. A ΔHR/ΔSBP ratio < 0.5 bpm/mmHg is diagnostic of neurogenic OH. Ann Neurol 2018;83:522-531.
低血压时心动过缓减弱是自主神经衰竭患者的特征,但范围尚未确定。本研究报告了神经退行性突触核蛋白病引起的自主神经衰竭患者直立性心率(HR)变化范围。
在美国自主神经联合体(NCT01799915)评估的患者接受了标准化自主功能测试和全面的神经评估。
我们确定了 402 名患有直立性低血压(OH)的窦性心律患者。其中,378 名患者交感神经激活受损(即神经源性 OH),根据他们的神经系统检查,被诊断为帕金森病、路易体痴呆、单纯自主神经衰竭或多系统萎缩。其余 24 名患者交感神经激活正常,其 OH 由于容量不足、贫血或多药治疗被归类为非神经源性。神经源性 OH 患者的收缩压(SBP)下降幅度是后者的两倍(-44±25 与-21±14 mmHg[平均值±标准差],p<0.0001),但 HR 增加幅度仅是后者的三分之一(8±8 与 25±11 次/分钟[bpm],p<0.0001)。ΔHR/ΔSBP 比值 0.492 bpm/mmHg 对区分神经源性与非神经源性 OH 患者具有出色的敏感性(91.3%)和特异性(88.4%)(曲线下面积=0.96,p<0.0001)。在神经源性 OH 患者中,多系统萎缩患者的 HR 增加更多(p=0.0003),但与路易体障碍患者有相当大的重叠。
低血压时 HR 增加减弱提示神经源性原因。ΔHR/ΔSBP 比值<0.5 bpm/mmHg 是神经源性 OH 的诊断标准。Ann Neurol 2018;83:522-531.