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[Study of cutaneous microcirculation using the laser-Doppler method in syndrome X]
P Pignocchino1, M R Conte, S Scarnato
1Cattedra di Angiologia, Università degli Studi, Torino.
Summary
Patients with Syndrome X exhibit altered microvascular circulation, including increased flow velocity and reduced vasodilatory reserve, suggesting basal arterovenous hyperstomia. This indicates a potential link between Syndrome X and generalized microangiopathy.
Area of Science:
- Cardiovascular Research
- Microcirculation Physiology
- Vascular Biology
Background:
- Syndrome X, characterized by chest pain despite normal coronary angiograms, remains incompletely understood.
- Generalized microangiopathy, a potential underlying cause, requires further investigation in this patient group.
Purpose of the Study:
- To investigate the relationship between Syndrome X and generalized microangiopathy.
- To assess microvascular circulation parameters in patients with typical and atypical chest pain compared to controls.
Main Methods:
- Laser Doppler Periflux PF3 used to measure microvascular blood flow velocity (FV/CMBC ratio), flux (FV), and concentration of moving blood cells (CMBC).
- Measurements taken at rest, during ischemia, and post-ischemic hyperemia on plantar and dorsal foot regions with varying arterovenous anastomoses.
- Comparison of parameters between 11 Syndrome X patients, 8 atypical chest pain patients, and 12 healthy controls.
Main Results:
- Syndrome X patients showed a significantly higher FV/CMBC ratio (indicating higher flow velocity) at rest and during hyperemia in both foot regions (p < 0.015).
- A significantly lower percent increase in FV and CMBC during hyperemia was observed in the plantar foot region of Syndrome X patients (p < 0.014).
- No significant differences in hyperemia response were noted on the foot dorsum.
Conclusions:
- Elevated microvascular flow velocity and reduced vasodilatory reserve in Syndrome X patients suggest basal arterovenous hyperstomia.
- These findings support a potential link between Syndrome X and generalized microangiopathy.
- Microvascular dysfunction may play a key role in the pathophysiology of Syndrome X.