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Published on: August 17, 2022
Relation between cardiovascular risk factors and coronary microvascular dysfunction in cardiac syndrome X
Alfonso Sestito1, Gaetano A Lanza, Antonio Di Monaco
1Institute of Cardiology, Catholic University of the Sacred Heart, Rome, Italy.
Insights
Cardiovascular risk factors and inflammation do not predict coronary microvascular dysfunction (CMVD) in cardiac syndrome X (CSX) patients. Further research is needed to understand the causes of CMVD in CSX.
Area of Science:
- Cardiology
- Vascular Biology
- Internal Medicine
Background:
- The etiology of coronary microvascular dysfunction (CMVD) in cardiac syndrome X (CSX) remains unclear.
- While cardiovascular risk factors (CVRFs) and inflammation markers are implicated in CMVD, their specific role in CSX is poorly understood.
Purpose of the Study:
- To investigate the association between CVRFs, inflammation, and CMVD in CSX patients.
- To determine if CVRFs and C-reactive protein (CRP) levels predict CMVD in CSX.
Main Methods:
- Transthoracic Doppler echocardiography assessed coronary microvascular vasodilator function in 71 CSX patients and 20 controls.
- Coronary blood flow (CBF) velocity responses to adenosine and cold pressor test (CPT) were measured.
- Analysis included adjustment for common CVRFs and serum CRP levels.
Main Results:
- CSX patients exhibited significantly lower CBF responses to both adenosine and CPT compared to controls.
- CSX patients had higher C-reactive protein (CRP) levels.
- These differences persisted even after adjusting for CVRFs and CRP levels.
Conclusions:
- CVRFs and CRP levels do not reliably predict endothelium-dependent or endothelium-independent CMVD in CSX patients.
- The underlying mechanisms of CMVD in CSX require further investigation beyond traditional risk factors.
Background:
The causes of coronary microvascular dysfunction (CMVD) in patients with cardiac syndrome X (CSX) are largely unknown. Common cardiovascular risk factors (CVRFs) and increased markers of inflammation have been associated with CMVD in some studies, but their role in determining CMVD in CSX patients remains poorly known.
Methods And Results:
We studied 71 CSX patients (56 ± 9 years, 23 men) and 20 healthy volunteers (52 ± 7 years, nine men). Using transthoracic Doppler echocardiography, coronary microvascular vasodilator function was assessed in the left anterior descending coronary artery as the ratio of diastolic coronary blood flow (CBF) velocity at peak intravenous adenosine administration and during cold pressor test (CPT) to the respective basal CBF velocity values. Common CVRFs tended to be more frequent and C-reactive protein (CRP) levels were higher (P < 0.001) in CSX patients than in controls. Both CBF responses to adenosine (2.05 ± 0.6 vs. 2.92 ± 0.9, P < 0.001) and to CPT (1.71 ± 0.6 vs. 2.42 ± 0.7, P < 0.001) were lower in CSX patients than in controls. The differences between the two groups in CBF response to adenosine and in CBF response to CPT remained highly significant (P < 0.01 for both) after adjustment for all CVRFs, including serum CRP levels.
Conclusion:
In CSX patients, both endothelium-dependent and endothelium-independent CMVD cannot be reliably predicted by CVRFs (including serum CRP levels), alone or in combination.
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