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Structural and functional abnormality of systemic microvessels in cardiac syndrome X
A L Pasqui1, L Puccetti, M Di Renzo
1Department of Clinical Medicine and Immunology, Internal Medicine Division, University of Siena, Italy. pasquian@unisi.it
Insights
Patients with cardiac syndrome X show systemic microvascular damage, indicating an inflammatory vascular lesion. These findings suggest similar inflammatory processes may affect coronary microvessels in these patients.
Area of Science:
- Cardiology
- Vascular Biology
- Internal Medicine
Background:
- Cardiac syndrome X is linked to coronary microvascular damage.
- Peripheral vascular dysfunction is suggested in syndrome X.
- A generalized microvascular disturbance hypothesis was explored.
Purpose of the Study:
- To investigate systemic microcirculation in cardiac syndrome X patients.
- To compare microvascular structure and function with healthy controls.
- To test the hypothesis of generalized microvascular disturbance.
Main Methods:
- Intravital videocapillaroscopy (VCP) of peripheral and conjunctival microvessels.
- Biohumoral analysis including inflammation, endothelial function, coagulation, and lipid markers.
- Morphologic and quantitative assessment of microvascular alterations.
Main Results:
- Significant morphologic and quantitative microvascular changes observed in syndrome X patients.
- Alterations included capillary density, vessel profile, and diameter.
- Humoral study revealed changes in endothelial (vWF, ICAM-1, E-sel, PAI-1), inflammatory (CRP, fibrinogen), and metabolic (HDL-chol) factors.
Conclusions:
- Cardiac syndrome X patients exhibit systemic microvascular structural and functional alterations.
- The observed pattern resembles vascular lesions in systemic inflammatory diseases.
- These inflammatory microvascular changes may also affect coronary vessels in syndrome X.
Background And Aim:
Microvascular damage of coronary bed has been considered the main pathogenetic factor of cardiac syndrome X (chest pain, exercise-induced ischemic ST-segment changes and angiographically normal coronary arteries). Previous studies have demonstrated that vascular abnormalities are not confined to the heart, suggesting a peripheral vascular dysfunction. On the hypothesis of a generalized microvascular disturbance in cardiac syndrome X, we performed a morphologic and functional study of systemic microcirculation in patients with syndrome X compared to normal subjects.
Methods And Results:
Microvessels were evaluated with intravital videocapillaroscopy (VCP) executed in peripheral and conjunctival observation sites which explore micro and paramicrocirculation; biohumoral study included markers of inflammation and of endothelial function, coagulative-fibrinolytic system and lipid metabolism. Videocapillaroscopy showed several morphologic changes (present in high percent of patients with syndrome X and not in controls) and significant quantitative alterations (capillary density, granular flow score, alterations of vessel profile, length of capillary loop branches and of arteriole/venule diameter) which indicated a severe alteration of whole vessel structure and an important rearrangement of microvascular disposition. In a similar way, the humoral study showed some significant changes of endothelial (vWF, ICAM-1, E-sel, PAI-1), inflammatory (C-reactive protein (CRP), fibrinogen) and metabolic factors (HDL-chol) which are commonly associated with inflammatory response.
Conclusions:
We conclude that patients with cardiac syndrome X exhibited some structural and functional alterations of systemic microvasculature; the pattern is similar to that detected in systemic inflammatory diseases and suggests a vascular lesion of inflammatory type. The same changes could be operating also in coronary microvessels of patients with syndrome X.
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