Key result
Cardiac Syndrome X is linked to higher IMR and lower CFR versus matched controls.
Why the study?
Is coronary microvascular resistance associated with endothelial dysfunction and inflammation in patients with Cardiac Syndrome X?
Case-Control (n=40)
Is coronary microvascular resistance associated with endothelial dysfunction and inflammation in patients with Cardiac Syndrome X?
p-value: p=<0.001
In patients with Cardiac Syndrome X, impaired exercise tolerance is significantly associated with increased inflammation and systemic endothelial dysfunction.
Supports microvascular dysfunction in Cardiac Syndrome X; hypothesis-generating for targeted therapies pending prospective trials.
BACKGROUND: Although a proportion of CSX patients have impaired brachial artery flow-mediated dilatation (FMD) in response to hyperemia, suggesting that endothelial dysfunction in these patients may be systemic and not just confined to the coronary circulation; the underlying mechanisms triggering endothelial dysfunction in these patients are still incompletely understood. OBJECTIVES: To assess the association of the index of Microcirculatory Resistance (IMR) with endothelial dysfunction and inflammation in patients with CSX. METHODS: We studied 20 CSX patients and 20 age and gender-matched control subjects. Thermodilution-derived coronary flow reserve (CFR) and IMR were measured using a pressure-temperature sensor-tipped guidewire. Brachial artery FMD was measured using high-resolution, two-dimensional ultrasound images obtained with a Doppler ultrasound device (HDI-ATL 5000, USA) with a 5 MHz to 12 MHz linear-array transducer. RESULTS: Compared with in control subjects, CFR was significantly lower (2.42 ± 0.78 vs. 3.59 ± 0.79, p < 0.001); IMR was higher (32.2 ± 8.0 vs. 19.5 ± 5.5, p < 0.001); the concentration of hs-CRP and FMD was higher (4.75 ± 1.62 vs. 2.75 ± 1.50; 5.24 ± 2.41 vs. 8.57 ± 2.46, p < 0.001) in CSX patients. The Duke treadmill score (DTS) was correlated positively to CFR and FMD (0.489 and 0.661, p < 0.001), it was negative to IMR and hsCRP (-0.761 and -0.087, p < 0.001) in CSX patients. CONCLUSIONS: The main finding in this study is that the DTS measured in patients with CSX was associated to hsCRP and FMD. Moreover, the independent effects of exercise tolerance can significantly impair FMD and hsCRP in CSX patients; especially it is particularly important to whom where FMD was associated negatively with IMR.
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Long et al. (2017) conducted a case-control in Cardiac Syndrome X (n=40). Cardiac Syndrome X vs. Healthy controls was evaluated on Coronary flow reserve (CFR) and Index of Microcirculatory Resistance (IMR) (p=<0.001). Cardiac Syndrome X was associated with higher index of microcirculatory resistance (32.2 vs 19.5) and lower coronary flow reserve (2.42 vs 3.59) compared to matched controls (p<0.001).
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