Jelani Qurat-Ul-Ain, Norcliffe-Kaufmann Lucy, Kaufmann Horacio, Katz Stuart D
Leon H. Charney Division of Cardiology, New York University School of Medicine, New York University Langone Medical Center, New York, New York;
Dysautonomia Center, New York University School of Medicine, New York University Langone Medical Center, New York, New York.
Am J Hypertens. 2015 Feb;28(2):166-72. doi: 10.1093/ajh/hpu144. Epub 2014 Aug 15.
Familial dysautonomia (FD) is a rare hereditary disease characterized by loss of afferent autonomic neural fiber signaling and consequent profound impairment of arterial baroreflex function and blood pressure regulation. Whether vascular endothelial dysfunction contributes to defective vasomotor control in this form of afferent autonomic failure is not known.
We assessed blood pressure response to orthostatic stress and vascular endothelial function with brachial artery reactivity testing in 34 FD subjects with afferent autonomic failure and 34 healthy control subjects.
Forty-four percent of the afferent autonomic failure subjects had uncontrolled hypertension at supine rest (median systolic blood pressure = 148mm Hg, interquartile range (IQR) = 144-155mm Hg; median diastolic blood pressure = 83mm Hg, IQR = 78-105mm Hg), and 88% had abnormal response to orthostatic stress (median decrease in systolic blood pressure after upright tilt = 48mm Hg, IQR = 29-61mm Hg). Flow-mediated brachial artery reactivity did not differ in subjects with afferent autonomic failure vs. healthy control subjects (median = 6.00%, IQR = 1.86-11.77%; vs. median = 6.27%, IQR = 4.65-9.34%; P = 0.75). In afferent autonomic failure subjects, brachial artery reactivity was not associated with resting blood pressure or the magnitude of orthostatic hypotension but was decreased in association with reduced glomerular filtration rate (r = 0.62; P < 0.001).
Brachial artery reactivity was preserved in subjects with afferent autonomic failure despite the presence of marked blood pressure dysregulation. Comorbid renal dysfunction was associated with reduced brachial artery reactivity.
家族性自主神经功能异常(FD)是一种罕见的遗传性疾病,其特征是传入自主神经纤维信号缺失,进而导致动脉压力反射功能和血压调节严重受损。目前尚不清楚血管内皮功能障碍是否导致这种传入性自主神经功能衰竭形式的血管舒缩控制缺陷。
我们通过肱动脉反应性测试评估了34名患有传入性自主神经功能衰竭的FD受试者和34名健康对照受试者对直立位应激的血压反应和血管内皮功能。
44%的传入性自主神经功能衰竭受试者在仰卧位休息时患有未控制的高血压(收缩压中位数 = 148mmHg,四分位间距(IQR) = 144 - 155mmHg;舒张压中位数 = 83mmHg,IQR = 78 - 105mmHg),88%的受试者对直立位应激反应异常(直立倾斜后收缩压中位数下降 = 48mmHg,IQR = 29 - 61mmHg)。患有传入性自主神经功能衰竭的受试者与健康对照受试者的血流介导的肱动脉反应性无差异(中位数 = 6.00%,IQR = 1.86 - 11.77%;相比之下,中位数 = 6.27%,IQR = 4.65 - 9.34%;P = 0.75)。在传入性自主神经功能衰竭受试者中,肱动脉反应性与静息血压或直立性低血压的程度无关,但与肾小球滤过率降低相关(r = 0.62;P < 0.001)。
尽管存在明显的血压失调,但患有传入性自主神经功能衰竭的受试者肱动脉反应性仍得以保留。合并肾功能不全与肱动脉反应性降低相关。