Clinical Perspective
What Is New?
- In a phenotypically homogeneous patient cohort, invasively characterized coronary flow reserve (CFR) identifies those who may respond to anti-ischemic therapy.
- The optimal threshold of CFR that identifies responders to therapy is the same as the one that is used to diagnose coronary microvascular disease.
What Are the Clinical Implications?
- CFR measurement should be considered in patients with limiting angina and nonobstructive coronary arteries to identify those who will derive benefit from anti-ischemic therapy.
- Patients with an abnormal CFR responded to therapy, whereas those with a normal CFR did not, suggesting that physiology-stratified therapy may be preferable to treating undifferentiated patients with angina and nonobstructive coronary arteries with empirical therapy.
- Among patients with an impaired CFR, measurement of minimal microvascular resistance may enable tailored, pathobiology-directed, therapy.
Angina with nonobstructive coronary arteries (ANOCA) is a common clinical condition, although this umbrella term covers several distinct pathophysiological entities. These include coronary microvascular disease (CMD), defined as an inability of the coronary vasculature to increase coronary blood flow in response to heightened myocardial oxygen demand despite the absence of epicardial coronary artery disease. CMD leads to impaired quality of life and a heightened risk of adverse cardiovascular outcomes. A diagnosis of CMD is traditionally made by invasive assessment in the cardiac catheter laboratory to delineate the hallmark of CMD, a diminished coronary flow reserve (CFR), representing the ratio of maximal achievable flow to resting flow. CFR<2.5 is associated with impaired coronary perfusion efficiency during exercise and myocardial ischemia on noninvasive assessment. It has recently been demonstrated that CMD itself may be a heterogeneous condition comprising 2 distinct endotypes termed functional and structural CMD, distinguished by elevated minimal microvascular resistance in the latter. Although the 2 endotypes are phenotypically similar, the underlying pathobiology is distinct.
Although the CorMicA study (Coronary Microvascular Angina) has previously demonstrated the value of coronary physiology-stratified therapy in enhancing angina-specific quality of life in patients with ANOCA (including patients with CMD, vasospastic angina, and noncardiac chest pain), uptake by physicians has been low; this is partly because of skepticism about the mechanistic link between coronary physiology parameters and response to therapy. Furthermore, it is not known whether physiology-stratified therapy leads to an improvement in exercise capacity, which is the reference standard for efficacy of anti-ischemic therapies.
The ChaMP-CMD trial (Characterising Mechanisms in Patients with Coronary Microvascular Disease to Stratify Therapy) aims to assess whether a diminished CFR relates to the effects of anti-ischemic therapy on exercise time in patients with ANOCA and, if it does, whether further endotyping, on the basis of minimal microvascular resistance, allows even more granular stratification of therapy.






