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家族性自主神经功能异常中尽管存在器官灌注不足但终末血管灌注过多

Terminal vessel hyperperfusion despite organ hypoperfusion in familial dysautonomia.

作者信息

Stemper Brigitte, Axelrod Felicia B, Marthol Harald, Brown Clive, Brys Miroslav, Welsch Goetz, Hilz Max J

机构信息

Department of Neurology, New York University, New York, NY, USA.

出版信息

Clin Sci (Lond). 2003 Sep;105(3):295-301. doi: 10.1042/CS20030046.

Abstract

Patients with familial dysautonomia (FD) exhibit orthostatic hypotension as well as recumbent hypertension. In addition, during dysautonomic crises, patients have hypertensive blood pressure that is presumed to be secondary to episodic vasoconstriction, as well as swollen hands that are presumed to be secondary to vasodilatation. This discrepancy in vascular control is poorly understood, yet may provide insight into the pathophysiology of autonomic crises. To evaluate the pathological mechanisms of overall blood flow and end-organ perfusion, we assessed resting and post-ischaemic limb and skin blood flow in FD patients. In groups of 15 FD patients and 15 controls, we measured resting and post-ischaemic forearm blood flow using venous occlusion plethysmography, and superficial skin blood flow using laser Doppler flowmetry. At rest, arterial inflow was averaged from eight venous occlusion measurements and expressed as percentage volume change/min. Post-ischaemic plethysmographic inflow was determined from the peak influx during the first venous occlusion following 3 min of ischaemia. Transcutaneous forearm partial pressures of oxygen and carbon dioxide were monitored continuously. At rest, plethysmographic limb perfusion was lower in FD patients than in controls, while skin blood flow did not differ between the two groups. After ischaemia, hyperperfusion of the forearm and hand was less pronounced in FD patients than in controls, while skin blood flow was significantly higher in patients than in controls. Partial pressures of O(2) and CO(2) did not differ between the two groups. We conclude that the reduced overall limb perfusion in patients with FD is due to hypertension-induced structural changes to vessel walls, with an increase in resistance vessel rigidity. The exaggerated post-ischaemic skin perfusion in FD patients seems to be due to deficient sympathetic innervation of precapillary vessels and arteriovenous shunts and to denervation hypersensitivity of intradermal small nerve fibres. Both the reduced limb perfusion and the dysfunctional end-organ blood supply in FD patients are likely to be major contributors to the vasomotor instability observed in these subjects, particularly during periods of stress.

摘要

家族性自主神经功能障碍(FD)患者表现出直立性低血压以及卧位高血压。此外,在自主神经功能障碍危象期间,患者会出现高血压,推测这是由间歇性血管收缩继发引起的,同时还会出现手部肿胀,推测这是由血管扩张继发引起的。这种血管控制方面的差异目前了解甚少,但可能有助于深入了解自主神经危象的病理生理学。为了评估整体血流和终末器官灌注的病理机制,我们评估了FD患者静息和缺血后肢体及皮肤的血流情况。在15名FD患者和15名对照组成的小组中,我们使用静脉阻断体积描记法测量静息和缺血后前臂血流,使用激光多普勒血流仪测量浅表皮肤血流。静息时,通过八次静脉阻断测量来平均动脉流入量,并表示为每分钟体积变化百分比。缺血后体积描记法的流入量是根据缺血3分钟后第一次静脉阻断期间的峰值流入量来确定的。连续监测经皮前臂氧分压和二氧化碳分压。静息时,FD患者的体积描记法肢体灌注低于对照组,而两组之间的皮肤血流没有差异。缺血后,FD患者前臂和手部的过度灌注不如对照组明显,而患者的皮肤血流明显高于对照组。两组之间的氧分压和二氧化碳分压没有差异。我们得出结论,FD患者整体肢体灌注减少是由于高血压导致血管壁结构改变,阻力血管僵硬度增加。FD患者缺血后皮肤灌注过度似乎是由于毛细血管前血管和动静脉分流的交感神经支配不足以及真皮内小神经纤维的去神经超敏反应。FD患者肢体灌注减少和终末器官血液供应功能障碍都可能是这些受试者出现血管运动不稳定的主要原因,尤其是在应激期间。

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