Neurosonology and Cerebral Hemodynamics 10, 2014:38–42
|TITLE||Microvascular Disorders in Hand-Arm Vibration Syndrome|
|PUBL. DATE||May 2014|
|SOURCE||Neurosonology and Cerebral Hemodynamics 10, 2014:38–42|
|TYPE||Periodic scientific journal|
Objective: to assess microvascular morphological and functional changes in patients with hand-arm vibration syndrome (HAVS).
capillaroscopy, hand-arm vibration syndrome, laser Doppler flowmetry, microcirculation, thermography
Microvascular damages and dysfunctions are some of the morphological and functional markers of hand-arm vibration syndrome (HAVS), a specific occupational disease caused by exposure to vibration at work, characterized by peripheral vascular, nervous and musculoskeletal abnormalities in the upper limbs. The microvascular changes are characterized by spasm, Raynaud’s phenomenon, and thrombosis secondary to vibration exposure.
Many regulatory factors participate in pathophysiological mechanisms of vibration-induced microvascular changes. Autonomic dysbalance with increased sympathetic activity and/or parasympathetic depression, probably initiated by overstimulation of Pacinian corpuscles has been established [1, 9]. Mechanical damage to blood vessels, vasoregulatory nerve elements, especially sympathetic vasoconstrictor nerves and receptors in fingers and digital cutaneous perivascular nerves containing the neuropeptide with powerful vasodilator properties calcitonin gene-related peptide (CGRP) has been described [2, 3, 6, 10]. Pain-mediating nerve fibers and receptors, temperature nerve-endings, mechanoreceptors at the fingertips are affected by hand-arm vibration . The neural deficit in digital skin of patients with VRP has a functional counterpart with reduced ability to propagate an axon-reflex vasodilator response . Various degrees and forms of endothelial damage and dysfunctions may derive as a result of hand-arm vibration exposure .
The objective of the study is to assess noninvasively microvascular morphological and functional changes in patients with HAVS.
Material and Methods
Thirty HAVS patients and 30 healthy controls were included in the study. After acclimatization, all subjects underwent nailfold capillaroscopy, infrared thermography and fingertip laser Doppler flowmetry. The nailfold capillaroscopy was performed in the eponychium of the fingers with a microscope at 30× to 60× magnification. Skin blood flow of the volar part of the fingertips was measured in perfusion units (PU) using laser Doppler flowmeter Periflux4001 as initial values, at a temperature of 32°C with hands on the sternum (PUh) as a baseline and by lowering the arm from heart level hanging in dependency (PUd) to test skin venoarteriolar microcirculatory reflex responses (VAR). VAR indices were analyzed: delta VAR (ΔVAR) calculated as (PUd – PUh); percent change of perfusion (%change) – (ΔVAR/PUh).100; and venoarteriolar constriction response (VAC) – (PUd/PUh).
The spastic narrowed capillaries or capillary dilatation and tortuosity with aneurysms and pericapillary oedema prevailed in the HAVS patients (p<0.001) (fig. 1).
Fig. 1. Capillarographies in havs patients. Spastic capillaries, a single dilated one (A). Shortned, dilated capillary loops, decreased number, loss of capillaries (B). Capillary polymorphism – shortened, spastic, dilated, aneurysmal capillaries (C). Tortuous, dilated and aneurysmal capillaries (D).
The initial mean skin temperatures in HAVS patients were significantly lower compared to the healthy controls. Hypothermy of the hands and especially of the fingers in HAVS patients was established by infrared thermography, seen in fig. 2.
Fig. 2. Infrared thermography in HAVS. Thermoamputation of the distal phalanges of the fingers with temperature gradient wrist-fingers up to 4°C (A). Thermoamputation of the fingers and distal palms with temperature gradient wrist-fingers up to 4.5°C (B).
The fingertip skin perfusions were also significantly lower in patients than in healthy controls (fig. 3), but with wide overlap of the values in individual cases.
Fig. 3. Initial fingertip skin perfusion. PU – perfusion units; 1 – group of healthy controls, 2 – HAVS group.
Changes in bodily parts’ position related to the level of the heart cause local neural regulatory vasomotor responses. The dynamics of skin perfusion during venoarteriolar test is presented in figure 4. Venoarteriolar reflex responses to lowering the hands below heart’s level suppose a decrease of miscrovascular skin perfusion. In HAVS patients this reflex was quite abnormal. Significantly reduced sympathetically mediated axon-reflex response was established in HAVS patients without changes in skin blood flow values or even an increase instead of a decrease of skin perfusion.
Fig. 4. Dynamics of skin perfusion during venoarteriolar test. PU – perfusions units; PUi – initial PU; PUb –basal PU at 32°C; PUh – at heart level; PUd – in dependency; RP – Raynaud’s phenomenon; Ssc – scleroderma; *-p<0.05; **-p<0. 0001 compared to former perfusion value.
The venoarteriolar indices were significantly different between HAVS patients and healthy controls. The percent changes and delta perfusion indices were significantly higher in the control group compared to the HAVS group. The vasoconstriction indices between patients and controls differed, too, being higher in patients (p<0.0001). Loss of venoarteriolar reflex (ΔPU≥0) was established in 36.7% of HAVS patients.
Morphological changes of nutritional skin microvessels observed in vivo by nailfold capillaroscopy established both functional spastic and structural aneurismal and tortuous capillaries in HAVS patients. They corresponded to the decreased initial mean superficial skin temperatures and hypothermies of the hands and especially of the fingers in HAVS patients by infrared thermography, and lower initial mean skin perfusions of the fingertips. The significantly higher prevalence rate of impaired venoarteriolar reflex in HAVS patients proved local vasomotor dysfunction and reflected either postganglionar sympathetic insufficiency with vascular tone failure or altered vascular smooth muscle cells’ responses. Presented data confirm vibration-induced microcirculatory disorders established by many investigators [7, 8].
In conclusion, the assessment of nutritional capillary skin blood flow by capillaroscopy and global skin blood flow including thermoregulatory microcirculation by Doppler flowmetry and infrared thermography give thorough information about skin microvascular circulation and vasomotor function. Morphological and functional assessment of the cutaneous microvasculature has a crucial significance for diagnosis, prognosis and treatment of hand-arm vibration syndrome patients.
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