Hp. Albrecht et al., MICROCIRCULATORY FUNCTIONS IN SYSTEMIC-SCLEROSIS - ADDITIONAL PARAMETERS FOR THERAPEUTIC CONCEPTS, Journal of investigative dermatology, 101(2), 1993, pp. 211-215
To study the functional reactivity of the cutaneous microcirculation i
n progressive systemic sclerosis (PSS), hyperemic responses after arte
rial occlusion (3 min) and during local heating (42-degrees-C) were in
vestigated with simultaneous measurements of red blood cell flux and c
utaneous oxygen tension (p(cu)O2) of the skin in female patients (n =
19) with PSS and in healthy female controls (n = 15). Additionally, se
rum levels of 6-keto-prostaglandin 1alpha (PGF1alpha), a stable metabo
lite of prostacyclin, were compared to the microcirculatory data, and
both were used to evaluate further a standardized therapy with 10-d in
travenous calcitonin (100 IU/d) infusion in six PSS patients. In PSS,
the initial mean p(cu)O2 value was significantly reduced and was inver
sely proportional to flux and to PGF1alpha levels, whereas the flux an
d p(cu)O2 responses to the above hyperemic stimuli showed significant
reductions, revealing a pattern of ''hyperemic hypoxia'' probably due
to exhausted functional reserves of cutaneous perfusion. During calcit
onin infusion significant rises in p(cu)O2 and temporarily in PGF1alph
a and flux were found. After 10 d of therapy, increased p(cu)O2 was as
sociated significantly with decreased flux, indicating a shifting of b
lood from deeper regulatory vessels to the subepidermal capillaries. B
oth clinical improvement and the results of microcirculatory measureme
nts demonstrate a beneficial effect of calcitonin on the cutaneous mic
rocirculation in PSS patients, possibly due in part to a short-term in
crease in release of endogenous prostacyclin from the vascular endothe
lium during the infusion. The disturbed reactivity of the dermal vesse
ls in PSS is important for the evaluation of therapeutic concepts and
stresses, together with the elevated PGF1alpha plasma levels, vascular
factors in the pathogenesis of PSS.