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Published on: June 28, 2019
Reduced coronary flow reserve and parasympathetic dysfunction in patients with cardiovascular syndrome X
Roberto Cemin1, Andrea Erlicher, Bruno Fattor
1Department of Cardiology, San Maurizio Regional Hospital of Bolzano, Bolzano, Italy. roberto.cemin@asbz.it
Insights
Cardiovascular syndrome X patients with vagal dysfunction show reduced coronary flow reserve. This suggests parasympathetic impairment contributes to the condition, highlighting syndrome X heterogeneity.
Area of Science:
- Cardiology
- Autonomic Nervous System Function
Background:
- Cardiovascular syndrome X, also known as cardiac syndrome X, is a condition characterized by chest pain despite normal coronary angiograms.
- The underlying causes of syndrome X remain unclear, with research exploring autonomic dysfunction and coronary flow reserve.
- Investigating the link between parasympathetic dysfunction and impaired coronary flow reserve is crucial for understanding syndrome X pathophysiology.
Purpose of the Study:
- To investigate the correlation between parasympathetic nervous system dysfunction and reduced coronary flow reserve in women with cardiovascular syndrome X.
- To determine if vagal impairment is associated with diminished coronary blood flow in these patients.
Main Methods:
- Eleven women diagnosed with cardiovascular syndrome X were evaluated.
- Autonomic function was assessed using heart rate and blood pressure variability analysis and the cold face test.
- Coronary flow reserve was noninvasively measured using transthoracic echocardiography.
- Patients were compared with healthy volunteers.
Main Results:
- Over half of the patients (64%) exhibited vagal impairment, indicated by heart rate/blood pressure variability and cold face test results.
- Patients with vagal impairment showed significantly reduced mean and maximal diastolic coronary velocity reserves compared to controls and syndrome X patients without vagal impairment.
- A significant difference in coronary velocity reserves was observed across groups (P=0.0005 for mean, P=0.0047 for maximal).
Conclusions:
- Cardiovascular syndrome X patients are a heterogeneous group.
- Vagal dysfunction is present in a significant proportion of syndrome X patients.
- Impaired coronary flow reserve is associated with vagal dysfunction in syndrome X, suggesting a role for parasympathetic impairment in the condition's development.
Objective:
Although cardiovascular syndrome X was described many years ago, its causes are still unclear. Many studies have addressed the autonomic function, whereas others have investigated the coronary reserve. The purpose of this study was to investigate the correlations between parasympathetic dysfunction and coronary flow reserve deficiency.
Basic Methods:
Eleven consecutive women suffering from cardiovascular syndrome X were enrolled in the study. All the patients underwent the analysis of heart rate and blood pressure variability, the cold face test and noninvasive evaluation of the coronary flow reserve by transthoracic echocardiography. Comparison was made with healthy volunteers.
Results:
Seven patients (64%) showed vagal impairment in the analysis of heart rate and blood pressure variability and a pathological response to the cold face test, whereas four patients (36%) did not show significant differences from the control group. In these three groups, patients with and without vagal impairment and controls, there was a difference in the mean diastolic coronary velocity reserve (1.94+/-0.48; 3.73+/-0.95, 2.88+/-0.55, P=0.0005) and in maximal diastolic velocity reserve (2.00+/-0.48, 3.26+/-0.64, 2.65+/-0.57, P=0.0047). Post-hoc analysis demonstrated that the mean and maximal diastolic velocity reserves of the patients with vagal impairment seemed to be reduced compared with those of the other groups (P<0.05), which were similar.
Conclusions:
This study confirmed that syndrome X patients represent a heterogeneous group. More than half of the patients exhibited vagal dysfunction. In these patients, coronary flow reserve was abnormal compared with controls and other syndrome X patients without vagal impairment.
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