V ariable degrees of coronary microvascular dysfunction occur at the time of ST-segment-elevation myocardial infarction (STEMI) correlating with infarct size and long-term prognosis. Angiographic methods for assessing microvascular dysfunction in the cardiac catheterization laboratory at the time of STEMI include thrombolysis in myocardial infarction flow grade, thrombolysis in myocardial infarction frame count, and thrombolysis in myocardial infarction myocardial perfusion grade.1 More recently, coronary wire-based methods measuring Doppler-derived parameters, such as the coronary flow velocity reserve (CFVR), or measuring thermodilutionderived parameters, such as the index of microcirculatory resistance, have been shown to be more powerful predictors of acute left ventricular dysfunction, myocardial viability, and subsequent adverse outcomes.
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Article see p 207Although it is widely accepted that the degree of microvascular dysfunction occurring in the myocardium subtended by the infarct-related vessel correlates with infarct size and prognosis, there has been some debate on whether more global microvascular dysfunction, involving myocardial regions not supplied by the infarct-related vessel, is present at the time of STEMI. For example, Uren et al 4 performed positron emission tomography imaging in 13 patients with STEMI and found a decreased coronary flow reserve in the noninfarct-related vessel, which improved at 6-month follow-up. However, Ntalianis et al 5 measured fractional flow reserve in a nonculprit vessel at the time of STEMI in 75 patients and again 1 month later and found no significant difference in fractional flow reserve or in index of microcirculatory resistance, which was measured in a subgroup, suggesting that the microvascular dysfunction resulting from STEMI is limited to the territory supplied by the infarct-related artery.In this issue of Circulation: Cardiovascular Interventions, van de Hoef et al 6 report long-term follow-up in 100 patients presenting with STEMI, in whom they measured Doppler wire-derived CFVR, diastolic deceleration time, and systolic flow reversal in both the infarct-related artery and a nonculprit reference vessel. They found that the mean CFVR value in the infarct-related vessel was 1.6±0.4 and in the nonculprit vessel, it was 2.4±0.5. A normal CFVR value is generally thought to be >2.0. Interestingly, they found that CFVR in the nonculprit reference artery was an independent predictor of long-term cardiac mortality (hazard ratio, 4.1; 95% confidence interval, 1.2-14.2). On the basis of receiver operator characteristic curve analysis, 2.1 was the best cutoff value, with 35% of patients having a CFVR value below this cut point in the nonculprit vessel. The diastolic deceleration time, presence or absence of systolic flow reversal, and the CFVR measured in the infarct-related artery surprisingly were not predictive of long-term cardiac mortality.The implications of the findings are that microvascular dysfunction in the setting of STEMI can be global, and may not on...