HEMODYNAMICS IN NAILFOLD CAPILLARIES OF PATIENTS WITH SYSTEMIC SCLERODERMA - SYNCHRONOUS MEASUREMENTS OF CAPILLARY BLOOD-PRESSURE AND RED-BLOOD-CELL VELOCITY
M. Hahn et al., HEMODYNAMICS IN NAILFOLD CAPILLARIES OF PATIENTS WITH SYSTEMIC SCLERODERMA - SYNCHRONOUS MEASUREMENTS OF CAPILLARY BLOOD-PRESSURE AND RED-BLOOD-CELL VELOCITY, Journal of investigative dermatology, 110(6), 1998, pp. 982-985
There is increasing evidence that endothelial damage occurs at a very
early stage during the course of systemic scleroderma. Endothelial dam
age is accompanied by impaired microvascular function, which has clear
ly failed in patients with systemic scleroderma, as evidenced by necro
sis of the fingertips in severe cases. We investigated two important d
eterminants of microvascular function, namely capillary blood pressure
and capillary red blood cell velocity, simultaneously in the same cap
illary. In patients with systemic scleroderma and in healthy volunteer
s matched for age and sex, capillary blood pressure was measured by di
rect cannulation and capillary red blood cell velocity by video micros
copy, Capillary blood pressure and capillary red blood cell velocity w
ere significantly lower in patients (14.27 +/- 4.34 mmHg, 230 +/- 310
mu m per a) than in healthy controls (19.06 +/- 3.69 mmHg, p < 0.008,
and 910 +/- 240 mu m per s, p < 0.003) at an ambient temperature of 22
degrees C, whereas no significant difference in skin temperature was
observed (23.7 +/- 0.9 degrees C vs 24.7 +/- 1.9 degrees C) and no occ
lusion of finger arteries was detected. Capillary blood pressure in en
larged capillaries did not differ from that in normal-shaped capillari
es in the patients (correlation of diameter and capillary blood pressu
re, R-2 = 0.04), which was also the case with capillary red blood cell
velocity (R-2 = 0.13), Capillary pulse pressure amplitude and capilla
ry red blood cell velocity showed a strong correlation (R-2 = 0.81), s
uggesting that the pressure gradient across the capillary loop, which
is the driving force for capillary red blood cell velocity, was mainly
dependent on precapillary resistance. These observations reflect the
inadequate microvascular function in systemic scleroderma, which may b
e due mainly to a pathophysiologic functional increase in precapillary
resistance, even at comfortable ambient temperatures.