Journal
CLINICAL RESEARCH IN CARDIOLOGY
Volume 108, Issue 12, Pages 1364-1370Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s00392-019-01472-4
Keywords
Coronary microvascular dysfunction; Acute coronary syndrome with no obstructive coronary artery disease; Microvascular spasm
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Background Between 10 and 15% of patients admitted for non-ST-segment elevation acute coronary syndrome (NSTE-ACS) show no obstructive coronary artery disease (NO-CAD) at angiography. Coronary microvascular spasm is a possible mechanism of the syndrome, but there are scarce data about coronary microvascular function in these patients. Objectives To assess coronary microvascular function in patients with NSTE-ACS and NO-CAD. Methods We studied 30 patients (67 +/- 10 years, 19 female) with NSTE-ACS and NO-CAD. Specific causes of NSTE-ACS presentation (e.g., variant angina, takotsubo disease, tachyarrhythmias, etc.) were excluded. Coronary blood flow (CBF) velocity response to IV ergonovine (6 mu g/kg up to a maximal dose of 400 mu g) was evaluated before discharge by transthoracic Doppler echocardiography. CBF response to IV adenosine (140 mu g/kg/min) and cold pressor test (CPT) was also assessed after 1 month. Ten age- and sex-matched patients with non-cardiac chest pain served as controls. Vasoactive tests were repeated after 12 months in 10 NSTE-ACS patients. Results The ergonovine/basal CBF velocity ratio was 0.79 +/- 0.09 and 0.99 +/- 0.01 in patients and controls, respectively (p < 0.001). The adenosine/basal CBF velocity ratio was 1.46 +/- 0.2 and 3.25 +/- 1.2 in patients and controls, respectively (p < 0.001), and the CPT/basal CBF velocity ratio was 1.36 +/- 0.2 and 2.43 +/- 0.3 in the 2 groups, respectively (p < 0.001). In 10 patients assessed after 12 months, CBF velocity responses to ergonovine, adenosine, and CPT were found to be unchanged. Conclusions Patients with NSTE-ACS and NO-CAD exhibit a significant coronary dysfunction, which seems to involve both an increased constrictor reactivity, likely mainly involving coronary microcirculation, and a reduced microvascular dilator function, both persisting at 12-month follow-up.
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