Physiologic Assessment of Coronary Artery Disease: Focus on Fractional Flow Reserve.

The presence of myocardial ischemia is the most important prognostic factor in patients with ischemic heart disease. Fractional flow reserve (FFR) is a gold standard invasive method used to detect the stenosis-specific myocardial ischemia. FFR-guided revascularization strategy is superior to angiography-guided strategy. The recently developed hyperemia-free index, instantaneous wave free ratio is being actively investigated. A non-invasive FFR derived from coronary CT angiography is now used in clinical practice. Due to rapid expansion of invasive and non-invasive physiologic assessment, comprehensive understanding of the role and potential pitfalls of each modality are required for its application. In this review, we focus on the basic and clinical aspects of physiologic assessment in ischemic heart disease.

INTRODUCTION

Myocardial ischemia can occur when myocardial perfusion cannot meet the demands of the myocardium and is a key prognostic factor in patients with coronary artery disease (12). Numerous efforts are made to detect the presence of myocardial ischemia. Despite many available non-invasive tests, it is reported that about 60% of patients referred 320for invasive coronary angiography on suspicion of coronary artery disease from positive non-invasive tests do not have obstructive disease (3).

Current advances in the concept of physiologic assessment, and several newly developed invasive and non-invasive indices are being applied in clinical practice. Fractional flow reserve (FFR) is an invasive physiologic index that can be easily measured in the cardiac catheterization laboratory. In this review, we discuss the clinical aspects of coronary physiology through the concept, physiological background and clinical data of FFR. In addition, we further discuss resting physiologic indices, non-invasive FFR and comprehensive physiologic assessment in patients with ischemic heart disease.

Concept and Rationale of Fractional Flow Reserve

Fractional flow reserve is defined as the ratio of maximal coronary blood flow in a diseased artery to maximal coronary blood flow in the same artery without stenosis (456). Flow is proportional to pressure in the case of minimal and constant resistance, thus pressure can be a surrogate of flow during maximal hyperemia (Fig. 1). As distal coronary artery pressure (Pd) in a normal coronary artery is almost the same as the aortic pressure (Pa), normal perfusion pressure can be replaced by Pa. As venous pressures are generally negligible compared to arterial pressure, FFR can be simply calculated as the ratio of Pd to Pa during maximal hyperemia (456). The definition and an example of FFR measurement are shown in Figure 2. FFR of 0.80 indicates that the diseased coronary artery supplies 80% of the normal maximal flow due to the stenosis. The strength of FFR is that it can assess the degree and presence of epicardial lesion-specific inducible myocardial ischemia, not only in cases with negative or ambiguous results of non-invasive functional tests, but also in the presence of multivessel disease (Figs. 3, 4). FFR also has excellent reproducibility, regardless of changes in hemodynamics or myocardial contractility (789).

Fig. 1

Relationship between pressure and flow during resting and hyperemic states.

In resting state, coronary artery is under autoregulation to maintain adequate coronary flow according to oxygen demand. Pressure and flow are in linear correlation when microvascular resistance is minimal and constant.

Fig. 2

Concept of fractional flow reserve.

Fractional flow reserve (FFR) is defined as ratio of maximal coronary blood flow in diseased artery () to normal maximal coronary blood flow in same artery (). As venous pressure (Pv) is negligible compared to aortic (Pa) and distal coronary pressure (Pd), FFR can be calculated as ratio of Pd and Pa.

Fig. 3

Case with discrepancy between exercise stress test and fractional flow reserve (FFR).

76-year-old man with stable angina who underwent coronary CT angiography (A) and exercise stress test (B). There was intermediate stenosis in proximal left anterior descending coronary artery (LAD) and exercise stress test was negative. Invasive angiography revealed similar stenosis in LAD (C) and FFR measured in LAD was 0.70, which suggests presence of myocardial ischemia (D). Red arrows in (A) and (C) show same intermediate lesion in proximal LAD.

Fig. 4

Case with discrepancy between myocardial perfusion imaging and fractional flow reserve.

A. 72-year-old woman with stable angina who underwent myocardial SPECT. Reversible perfusion defect was absent. B. Invasive coronary angiography revealed severe 3-vessel disease (arrows). C. FFR was 0.69 in left anterior descending coronary artery and 0.73 in left circumflex artery, respectively. FFR = fractional flow reserve, LAD = left anterior descending coronary artery, LCX = left circumflex artery, SPECT = single photon emission computed tomography

As previously mentioned, a linear relationship between coronary flow and pressure is the fundamental assumption in the concept of FFR. As coronary blood flow and resistance are auto-regulated based on the myocardial demand, within the physiological range (10), induction of maximal hyperemia or minimizing microvascular resistance is mandatory for FFR measurement (56). Continuous intravenous infusion of adenosine (140 µg/kg/min) is considered as a gold standard method to orgachieve maximal hyperemia for FFR measurement (11). Intravenous infusion of adenosine can cause chest discomfort, atrioventricular conduction delay and bronchial hyper-reactivity, although their incidences and clinical significance are low. Intracoronary bolus administration of adenosine is a simple method for hyperemia induction, and injection of 50–200 µg of adenosine is considered adequate for FFR measurement (12). However, due to its short action time, steady state hyperemia for pressure pullback tracing cannot be maintained with a single bolus administration of adenosine. Besides adenosine, nicorandil and regadenoson are recently introduced as novel hyperemic agents. Nicorandil (Sigmart®, Chugai Pharmaceutical, Tokyo, Japan) is a nicotinamide ester with dual mechanisms of action on both macro- and microvascular systems (1314). Jang et al. (13) report similar hyperemic efficacy between intracoronary nicorandil injection (2 mg) and intravenous infusion of adenosine. Compared with adenosine, nicorandil causes less frequent adverse effects (pressure change, heart rate change, chest discomfort). The excellent diagnostic efficacy and safety of intracoronary bolus administration of nicorandil are confirmed at the patient-level pooled data from 429 patients with 480 coronary arteries (r = 0.941, intra-class correlation coefficient 0.980, classification agreement 90.8%, kappa = 0.814, area under curve of nicorandil 0.980, all p < 0.001) (15). Regadenoson is a direct A2A adenosine receptor agonist that can be administered as a single bolus intravenous injection. It has rapid onset but longer duration of action and fewer adverse effects, as compared with adenosine (1617). Lim et al. (18) compared intravenous infusion of adenosine, intracoronary bolus injection of adenosine, intracoronary bolus injection of nicorandil and regadenoson and reported that FFR values were not significantly different among the different hyperemic agents. The study results on the currently available hyperemic agents are summarized in Table 1.

Table 1

Summary of Clinical Studies on Hyperemic Agents

Study	Test (Vasodilator)		Reference Method	Results		P
	Route	Dose		Test	Reference
Adenosine
Jeremias et al. (82)	IC bolus	15–20 ug (RCA), 18–24 ug (LCA)	IV AD 140 ug/kg/min	0.78 ± 0.15	0.78 ± 0.15	NS
De Bruyne et al. (83)	IC bolus	20, 40 ug	IV AD 140 ug/kg/min	0.62 ± 0.20/0.60 ± 0.19	0.61 ± 0.19	NS
Koo et al. (84)	IC bolus	40, 80 ug	IV AD 140 ug/kg/min	0.83 ± 0.06	0.79 ± 0.07	< 0.01
	IC infusion	240 ug/min	IV AD 140 ug/kg/min	0.78 ± 0.09	0.79 ± 0.07	0.40
Yoon et al. (85)	IC bolus	36–60 ug (RCA), 48–80 ug (LCA)	IV AD 140 ug/kg/min	0.77 ± 0.10	0.80 ± 0.08	< 0.05
Seo et al. (86)	IC bolus	40 ug (RCA), 80 ug (LCA)	IV AD 140 ug/kg/min	0.81 ± 0.10	0.80 ± 0.10	NS
Lim et al. (18)	IC bolus	40 ug (RCA), 80 ug (LCA)	IV AD 140 ug/kg/min	Overall agreement = 92.9%, Cohen's kappa = 0.887, p < 0.001
Nicorandil
Jang et al. (13)	IC bolus	2 mg	IV AD 140 ug/kg/min	0.82 ± 0.09	0.82 ± 0.10	0.180
Kang et al. (15)	IC bolus	2 mg	IV AD 140 ug/kg/min	Overall agreement = 90.8%, Cohen's kappa = 0.814, p < 0.001
Lim et al. (18)	IC bolus	2 mg	IV AD 140 ug/kg/min	Overall agreement = 91.2%, Cohen's kappa = 0.817, p < 0.001
Regadenoson
Arumugham et al. (87)	IV bolus	400 ug	IV AD 140 ug/kg/min	ΔFFR = 0.0040, r2 = 0.933
Prasad et al. (88)	IV bolus	400 ug	IV AD 140 ug/kg/min	0.79 ± 0.09	0.79 ± 0.09	NS
Lim et al. (18)	IV bolus	400 ug	IV AD 140 ug/kg/min	Overall agreement = 100%, Cohen's kappa = 1.000, p < 0.001
van Nunen et al. (89)	IV bolus	400 ug	IV AD 140 ug/kg/min	ΔFFR = 0.00 ± 0.01, r = 0.994, p < 0.001

AD = adenosine, FFR = fractional flow reserve, IC = intracoronary, IV = intravenous, LCA = left coronary artery, NS = not significant, RCA = right coronary artery

Clinical Evidence of FFR-Guided Revascularization

Landmark Studies of FFR-Guided Strategy

The optimal cut-off value of FFR for defining inducible myocardial ischemia is extensively investigated using non-invasive stress tests. Pioneer work of Pijls et al. (6) proposed a cut-off value of 0.75, based on the comparison of invasive FFR and the results of sequential tests of exercise-stressed tests, thallium scintigraphy, and dobutamine-stress echocardiography (sensitivity 88%, specificity 100%, positive predictive value 100%, negative predictive value 88%, and accuracy 93%). Using the ischemic cut-off value of FFR, the first randomized study of FFR-guided percutaneous coronary intervention (PCI), the DEFER trial, tested the safety of deferral of functionally insignificant stenosis (19). The DEFER trial randomly assigned patients with functionally insignificant intermediate lesions (FFR ≥ 0.75) into the Perform group (n = 90) and the Defer group (n = 91). Patients with FFR < 0.75 were allocated into the Reference group and underwent PCI (n = 144). The 2- and 5-year follow-up data show that both the Defer and Perform groups have no difference in the incidence of mortality, myocardial infarction (MI), or revascularization (1920). Recently published, 15 year follow-up data further support the concept that the deferral of functionally insignificant lesions is safe, and stent implantation for these lesions cannot reduce the incidence of clinical events (21). In recent clinical practice, FFR binary cut-off value of 0.80 is in use, in order to minimize the chance of leaving an untreated functionally significant stenosis.

The Fractional Flow Reserve versus Angiography for Multivessel Evaluation (FAME) trial enrolled 1005 patients with multivessel disease and randomly assigned them to angiography-guided PCI group (n = 496) and FFR-guided PCI group (n = 509). In the FFR-guided group, stents were placed only for stenoses with FFR ≤ 0.80. The primary end-point was major adverse cardiac event (MACE, a composite of death, MI and any revascularization) at 1-year. At 1-year, the FFR-guided PCI group showed significantly lower rates of MACE (13.2% vs. 18.3%, p = 0.02) and combined death and MI (7.3% vs. 11%, p = 0.04), compared with the angiography-guided PCI group. Furthermore, the FFR-guided PCI group significantly enhanced the process-of-care index, including fewer stents per patient (1.9 ± 1.3 vs. 2.7 ± 1.2, p < 0.001), less contrast (272 mL vs. 302 mL, p < 0.001), lower procedural cost, and shorter hospital stay (22). FAME 2-year data shows similar benefit of FFR-guided PCI (23). Recently published 5-year results show that the MACE rate was similar between FFR-guided and angiography-guided groups (28% vs. 31%, relative risk 0.91, 95% confidential interval [CI] 0.75–1.10, p = 0.31) with significantly less number of stents at index procedure in the FFR-guided group (24).

The Fractional Flow Reserve versus Angiography for Multivessel Evaluation 2 (FAME 2) trial compared FFR-guided PCI plus optimal medical therapy with optimal medical therapy alone in patients with functionally significant stenosis (FFR ≤ 0.80) (2526). In this study, patients with a functionally significant lesion (FFR ≤ 0.80) were randomly assigned to FFR-guided PCI plus optimal medical therapy group and only optimal medical therapy group, whereas patients with FFR > 0.80 in all stenoses received optimal medical therapy and were assigned as a registry group. The study was halted prematurely because of the significant difference of composite of death, MI or urgent revascularization (4.3% for FFR-guided PCI group vs. 12.7% for optimal medical therapy group, p < 0.001) (2526). Accordingly, European guidelines recommend FFR-guided revascularization with Class I (level of evidence A) in stable patients when evidence of ischemia is not available (27).

Further Evidences for FFR-Guided Revascularization Strategy

Recently, 5-year results of the Proper Fractional Flow Reserve Criteria for Intermediate Lesions in the Era of Drug-Eluting Stent (DEFER-DES) trial demonstrated the clinical relevance of the FFR-guided strategy in the drug-eluting stent era.

Routine DES group underwent DES implantation without FFR measurement. At 5-year follow-up, routine DES implantation could not reduce the incidence of MACE compared to FFR-guided DES implantation group. Comparison of the 3 groups shows that 5-year MACE rate was higher in the FFR-DES (low FFR and DES implantation) group (24%) than the Routine-DES group (14%, p = 0.193) and FFR-Defer (high FFR and medical treatment) group (7%, p = 0.012) (28). The clinical benefit of FFR-guided strategy over angiography-only guided strategy is also well established by the large scale registry data (293031). Park et al. (30) report clinical outcomes before (2008–2009) and after (2010–2011) the adoption of the routine use of FFR from the single-center ASAN PCI registry. Comparison of primary endpoint (a composite of any death, MI, or any revascularization at 1-year) was performed in propensity-score matched population (2178 pairs). The risk of primary endpoint was significantly lower in patients treated by FFR-guided strategy, compared with those who were managed before the adoption of routine FFR-guided strategy (4.8% vs. 8.6%, hazard ratio [HR] 0.55, 95% CI 0.43–0.70, p < 0.001). The significant reduction of the risk of primary endpoint was mainly due to a reduction in MI and revascularization. The number of stents per patient was also significantly decreased with the adoption of FFR-guided strategy. In addition, Li et al. (29) compared long-term 7-year clinical outcomes between FFR-guided strategy and angiography-guided strategy from 7358 consecutive patients in the Mayo Clinic registry (2002–2009). The Kaplan-Meier fraction of MACE at 7 years was 57.0% in the angiography-guided group vs. 50.0% in the FFR-guided group (p = 0.016). In addition to those clinical data, cost-effectiveness of FFR-guided strategy over angiography-guided strategy is also demonstrated (3233). These investigations collectively support the safety and effectiveness of an FFR-guided strategy, which reduces unnecessary stent implantation and enhances patient's clinical outcome.

In addition to the robust data supporting the FFR-guided decision making process, recent investigations increase our understanding of coronary physiology and FFR. In meta-analysis at the study-level (n = 9173) as well as individual patient-level (n = 6961), Johnson et al. (34) provide new insight on the prognostic importance of FFR value in terms of a continuous variable. Study-level meta-regression analysis showed the significant inverse relationship between FFR values and normalized 1-year rate of MACE, and this inverse relationship was also repeated with Cox regression analysis of patient-level pooled data. When the regression lines according to treatment modality (revascularization vs. medical treatment) were plotted, 2 regression lines crossed at the point FFR value 0.75 in the study-level analysis and 0.67 in the patients-level analysis. Thus, patients with low-normal range of FFR value (0.81–0.85) had higher risk of future events than those with higher or near normal FFR values. In addition, FFR measured after PCI also had an inverse relationship with prognosis (HR 0.86, 95% CI 0.80–0.93, p < 0.001).

Resting Physiologic Index without Hyperemia

The concept of instantaneous wave free ratio (iFR) was originally derived from wave-intensity analysis using both intracoronary pressure and flow velocity data. Davies et al. (35) report a certain period in the cardiac cycle when the resistance is low and stable (36). iFR is calculated by Pd/Pa ratio at the wave-free period during resting state and does not require hyperemia (Fig. 5). The ADenosine Vasodilator Independent Stenosis Evaluation (ADVISE) is the first study to evaluate the concept of iFR (37). In this study, iFR was closely correlated with FFR (r = 0.9, p < 0.001) and showed excellent diagnostic performance (C-statistics 0.93) to predict low FFR. In the ADVISE study, the optimal cut-off value of iFR to predict FFR < 0.80 was 0.83 with sensitivity, specificity, positive predictive value, and negative predictive value of 85%, 91%, 91%, and 85%, respectively (37). Subsequent to the introduction of iFR, its diagnostic accuracy and validity during resting period have been under debate (383940). In this regard, the large scale RESOLVE study was designed to investigated the data of 1768 patients from 15 international centers. In this study, iFR was measured using a uniform calculation algorithm in the independent physiologic core laboratory (41). As a result, the optimal cut-off value of iFR was 0.90 for FFR ≤ 0.80 and C-statistics was 0.81 (95% CI: 0.79 to 0.84). The optimal cut-off value of resting Pd/Pa was 0.92 for FFR ≤ 0.80 and C-statistics was 0.82 (95% CI: 0.80 to 0.84). There was no significant difference in diagnostic performance between resting Pd/Pa and iFR (41). Despite its convenience, more evidence is needed to support the routine use of resting index, such as iFR, in daily clinical practice. The currently ongoing randomized controlled trials, which compare the clinical outcomes between iFR- and FFR-guided strategy, will clarify the clinical relevance of an iFR-guided strategy (DEFINE-FLAIR NCT02053038, SWEDEHEART NCT02166736) (42).

Fig. 5

Wave intensity analysis and concept of instantaneous wave-free ratio (iFR).

Upper panel shows example of wave intensity analysis. Different types of waves originating from proximal and distal (from microcirculatory beds) sites during entire cardiac cycle are presented. After beginning of diastole and before start of systole, there is wave free period in which microvascular resistance is minimized and constant. iFR is calculated by ratio of proximal and distal pressures during this period (lower panel).

Non-Invasive Assessment for FFR: CT-Derived FFR

Coronary CT angiography (cCTA) provides accurate anatomical information. However, the discrepancy between anatomical severity and functional significance is well-known (84344454647484950). With the advancement of computational fluid dynamics (CFD) technology, CT-derived FFR (FFRCT) has been developed to provide a non-invasive estimate of FFR (Fig. 6). The FFRCT technology possesses a robust scientific basis that is well described in previous reviews (515253). Briefly, a three-dimensional patient specific anatomic model of coronary artery is first constructed from the cCTA data. For assigning boundary conditions of CFD simulation, the basal coronary outlet resistances at resting state are determined from the principle of an allometric scaling law, which allows the estimation of total coronary flow from myocardial mass; and a morphometry law, which relates the resistance of the downstream vessel to the vessel size at each outlet. A mathematical model of hyperemic condition is derived from the effect of adenosine on reducing the resistance of the coronary microcirculation. Lastly, on the basis of discretized model of patient-specific geometry and boundary conditions, CFD analysis is performed to numerically solve the governing equations of fluid dynamics, i.e., Navier Stokes equations, as a Newtonian fluid. The numerical solutions of coronary flow and pressure fields are used to compute a complete spatial distribution of FFRCT.

Fig. 6

Non-invasive hemodynamic assessment using coronary CT angiography and computational fluid dynamics.

With recent advancement of computational fluid dynamics, non-invasive hemodynamic assessment has become feasible. Adding physiological modeling to coronary CT angiography-derived 3-dimensional coronary artery geometry enables assessment of several hemodynamic parameters, such as wall shear stress (A), pressure gradient (B), and fractional flow reserve (FFRCT) (C).

Table 2 summarizes the previous studies that evaluate the clinical relevance of FFRCT technology. Three prospective trials (DISCOVER-FLOW, DeFACTO, NXT) validate the efficacy of FFRCT technology and establish a role of FFRCT as a novel gate-keeper for patients with suspected coronary artery disease (545556). The obvious benefit in cost-effectiveness of a FFRCT-guided clinical decision making process is also presented using the previous trial populations, as compared with traditional clinical decision making process (5758).

Table 2

Summary of Clinical Studies on cCTA-Derived FFR

Study	Number of Lesions	Sensitivity (%)		Specificity (%)		PPV (%)		NPV (%)		Diagnostic Accuracy (%)
		FFRCT	cCTA	FFRCT	cCTA	FFRCT	cCTA	FFRCT	cCTA	FFRCT	cCTA
DISCOVER-FLOW (54)	103	93	94	82	25	85	58	91	80	84	61
DeFACTO (55)	252	90	84	54	42	67	61	84	72	73	64
NXT (56)	254	86	94	79	34	65	40	93	92	81	53
PLATFORM (59)	584	Study about impact of FFRCT on clinical practice
		FFRCT guided group showed significantly lower portion of no obstructive CAD than usual group in ICA (12% vs. 73%)
		Also, cCTA/FFRCT guided strategy decreased ICA about 61%
		Early adverse events for 90 days were similar between cCTA/FFRCT guided group and usual group

CAD = coronary artery disease, cCTA = coronary computed tomography angiography, FFRCT = computed tomography derived fractional flow reserve, ICA = invasive coronary angiography, NPV = negative predictive value, PPV = positive predictive value

Furthermore, the recently published Prospective LongitudinAl Trial of FFRCT: Outcome an Resource Impacts (PLATFORM) trial evaluates clinical outcomes of FFRCT-guided diagnostic strategy, compared with usual care of patients with suspected coronary artery disease in real-world practice (59). Among those with intended invasive coronary angiography (FFRCT-guided = 193; usual care = 187), no obstructive coronary artery disease was found at the time of invasive angiography in 24 (12%) in the cCTA/FFRCT arm and 137 (73%) in the usual care arm (risk difference 61%, 95% CI 53–69, p < 0.0001), with similar mean cumulative radiation exposure (9.9 mSv vs. 9.4 mSv, p = 0.20). In addition, invasive coronary angiography was ruled out in 61% after FFRCT (59). These results suggest the potential of FFRCT as a non-invasive diagnostic modality in the clinical decision-making process.

The investigators in DISCOVER-FLOW evaluate the potential of FFRCT technology in planning the treatment strategy using the so-called "Virtual PCI technology" (60). Modification of the computational model to restore the area of the target lesion according to the proximal and distal reference areas (i.e., virtual stenting), allows for estimation of post-interventional FFRCT values (60). Kim et al. (60) evaluated this novel strategy in 44 patients who had functionally significant coronary stenoses with available pre-intervention coronary cCTA and pre- and post-intervention FFR values. Both pre- and post-interventional values of invasive FFR and FFRCT showed an excellent correlation. The mean difference between FFRCT and FFR was 0.006 for pre-intervention (95% limit of agreement: -0.27 to 0.28) and 0.024 for post-intervention (95% limit of agreement: -0.08 to 0.13). Diagnostic accuracy of FFRCT to predict ischemia (FFR ≤ 0.8) prior to stenting was 77% (sensitivity: 85.3%, specificity: 57.1%, PPV: 83%, and NPV: 62%) and after stenting was 96% (sensitivity: 100%, specificity: 96%, PPV: 50%, and NPV: 100%). The value of FFRCT as a "treatment planner" is still under development and needs further investigation.

In addition to FFRCT, several investigators are working with new methodologies for non-invasive estimation of FFR using cCTA or angiograms (616263). Furthermore, the clinical relevance of comprehensive hemodynamic assessment using cCTA and CFD is under active investigation (64). However, any non-invasive FFR from cCTA requires adequate anatomic geometries and physiologic boundary conditions for CFD analysis. Adherence to established best image acquisition practices, including heart rate control and use of pre-scan nitroglycerin, is essential to improve cCTA image quality. Further refinement of this technology is expected to improve its diagnostic accuracy and contribute to better patient care in clinical practice.

Microvascular Assessment and Comprehensive Physiologic Evaluation

Although FFR is now regarded as the gold-standard invasive method to assess the functional significance of coronary artery stenosis (65), there is still room for further improvement in the diagnosis and treatment of patients with high FFR. In the FAME 2 study, 14.6% of the registry arm (FFR > 0.80 and deferral of PCI) experienced persistent angina, and 9.0% of these patients had clinical events during a 2-year follow-up period (66). This observation suggests that the ischemic heart disease cannot be fully explained by epicardial stenosis alone. The coronary artery system has 3 components with different functions (conductive epicardial coronary arteries, arterioles, and capillaries), hence, failure of any one of these systems could result in myocardial ischemia. Thus, the presence of epicardial coronary artery stenosis is not the sole factor for ischemic heart disease (67).

In this regard, previous studies have suggested that the measurement of coronary flow reserve (CFR) could be helpful in risk stratification for patients with high FFR (> 0.80). Previous studies report that low CFR has worse clinical outcome than normal CFR in the setting of normal FFR patients, implying that dysfunction or disease in microvascular circulatory beds are also contributors to ischemic heart disease, especially in the case of functionally insignificant epicardial stenosis (686970). An index of microcirculatory resistance (IMR) is currently introduced, since CFR is largely influenced by variations in the resting coronary flow and not a microcirculatory bed-specific index. IMR is a pressure-temperature derived parameter for quantifying microcirculatory resistance (71). As distal coronary pressure is used in the calculation of IMR, this index can be used to interrogate selectively the microcirculation of vessels with a coronary stenosis, in contrast to CFR, which is a combined assessment of the macro- and microcirculation. Table 3 summarizes previous evidence regarding IMR (72737475767778798081). According to the evidence of CFR and IMR, high FFR, low CFR and high IMR suggest the presence of microvascular disease in the coronary circulatory bed. Figure 7 shows an example of a patient with microcirculatory disease.

Table 3

Clinical Evidences on IMR

Study (Year)	Study Population	Results
Studies about distribution of IMR
Melikian et al. (72)	101 patients vs. 15 controls	IMR values of controls were lower than 25 U
Luo et al. (74)	18 with CXS vs. 18 controls	IMR values of CXS were higher than controls (33.1 ± 7.9 vs. 18.8 ± 5.6, p < 0.001)
Echavarría-Pinto et al. (73)	79 patients with FFR, CFR, and IMR	75th percentile value of IMR was 29 U
Studies about clinical implication of IMR
Fearon et al. (76)	29 patients with STEMI	Patients with IMR > 32 U had worse echocardiographic wall motion score than those with IMR ≤ 32. IMR was only significant predictor of recovery of left ventricular function
Cuisset et al. (75)	50 patients with stable angina who underwent elective PCI	Patients with conventional stenting had significantly higher value of post-PCI IMR than direct stenting (24 ± 14 U vs. 13 ± 3 U, p < 0.01)
McGeoch et al. (77)	57 patients with STEMI who underwent CMR	Patients with microvascular obstruction had higher IMR values than those without microvascular obstruction (38 U vs. 27 U, p = 0.003)
Fujii et al. (78)	80 patients with stable angina with or without pravastatin therapy after PCI	Pravastatin therapy lowered IMR significantly after PCI (12.6 U vs. 17.6 U, p = 0.007)
Layland et al. (79)	50 patients with elective PCI	IMR before PCI was higher in patients with PPMI (21.2 ± 2.1 vs. 15.6 ± 1.8, p = 0.02) and strongest predictor of PPMI (beta 0.7, p = 0.02)
Ng et al. (80)	50 patients with elective PCI	IMR value of > 27 was independent predictor of PPMI (odds ratio, 22.7; 95% CI, 3.8–133.9)
Fearon et al. (81)	254 patients with STEMI	Rate of death or re-hospitalization was higher in patients with IMR of > 40 U than those with IMR of ≤ 40 (17.1% vs. 6.6%, p = 0.027)

CFR = coronary flow reserve, CMR = cardiac magnetic resonance imaging, CXS = cardiac X syndrome, FFR = fractional flow reserve, IMR = index of microcirculatory resistance, MACE = major adverse cardiovascular event, PCI = percutaneous coronary intervention, PPMI = peri-procedural myocardial infarction, STEMI = ST-elevation myocardial infarction

Fig. 7

Case example of microvascular disease.

69-year-old female patient presented with stable angina. Despite positive exercise stress test (ST segment depression in inferior and lateral leads) (A), there was no significant coronary artery stenosis (B). Invasive physiologic assessment was performed and fractional flow reserve, coronary flow reserve (CFR) and index of microcirculatory resistance (IMR) were 0.94, 1.4, and 39, respectively (C). As there was no significant epicardial disease (high fractional flow reserve), low CFR and high IMR indicate presence of microvascular disease.

Therefore, comprehensive evaluation using multiple physiologic indices should be regarded as a diagnostic approach to enhance the stratification of patients, according to major compartment(s) involved in the development of ischemic heart disease.

Conclusions and Future Perspectives

This review focuses on the invasive physiologic assessment of ischemic heart disease, and presents evidence for its clinical relevance and effectiveness in the enhancement of patient's clinical outcomes. Despite the low prevalence of invasive physiologic assessment in daily practice, recently developed novel indices and hyperemic agents are expected to reduce the current barriers. Furthermore, comprehensive assessment of both macro- and microvascular systems and practical application of cCTA-derived non-invasive FFR will further improve clinical outcomes of patients with ischemic heart disease.