Increased basal coronary blood flow as a cause of reduced coronary flow reserve in diabetic patients
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Updated: May 28, 2026

Evaluation of Coronary Flow Reserve After Myocardial Ischemia Reperfusion in Rats
Published on: June 28, 2019
Andrea Picchi1, Ugo Limbruno, Marta Focardi
1Department of Cardiology, Misericordia Hospital, Grosseto, Italy.
Insights
Coronary flow reserve (CFR) is reduced in diabetes due to increased basal coronary flow, not impaired hyperemic flow. This reduced CFR is linked to insulin resistance, highlighting cellular metabolism
Area of Science:
- Cardiology
- Diabetology
- Microvascular Function
Background:
- Reduced coronary flow reserve (CFR) is observed in diabetes mellitus.
- The underlying mechanisms contributing to this reduction remain unclear.
- Microvascular dysfunction is a potential contributor to impaired coronary blood flow in diabetic patients.
Purpose of the Study:
- To investigate the mechanisms behind reduced coronary flow reserve (CFR) in patients with diabetes.
- To assess the relationship between insulin resistance and coronary microvascular function.
- To differentiate between basal and hyperemic coronary flow in diabetic versus non-diabetic individuals.
Main Methods:
- Thermodilution-derived CFR was measured using a pressure-temperature sensor-tipped wire after adenosine infusion.
- Fractional flow reserve (FFR) was assessed to exclude significant epicardial coronary artery stenosis.
- Index of microvascular resistance (IMR) and basal/hyperemic mean transit times (Tmn) were calculated.
- Insulin resistance was quantified using the homeostasis model assessment (HOMA) index.
Main Results:
- FFR was normal in all patients, indicating no significant epicardial disease.
- CFR was significantly lower in diabetic patients compared to non-diabetic controls.
- Diabetic patients exhibited lower basal Tmn, suggesting increased basal coronary flow, while hyperemic Tmn and IMR were similar.
- LogCFR and basal Tmn showed significant correlations with the HOMA index.
Conclusions:
- Patients with diabetes have reduced CFR even without significant epicardial stenosis.
- The reduction in CFR is primarily driven by increased basal coronary flow, not impaired hyperemic response.
- Basal coronary flow is associated with insulin resistance, implicating cellular metabolism in coronary blood flow regulation.
Abstract:
A reduced coronary flow reserve (CFR) has been demonstrated in diabetes, but the underlying mechanisms are unknown. We assessed thermodilution-derived CFR after 5-min intravenous adenosine infusion through a pressure-temperature sensor-tipped wire in 30 coronary arteries without significant lumen reduction in 30 patients: 13 with and 17 without a history of diabetes. We determined CFR as the ratio of basal and hyperemic mean transit times (T(mn)); fractional flow reserve (FFR) as the ratio of distal and proximal pressures at maximal hyperemia to exclude local macrovascular disease; and an index of microvascular resistance (IMR) as the distal coronary pressure at maximal hyperemia divided by the inverse of the hyperemic T(mn). We also assessed insulin resistance by the homeostasis model assessment (HOMA) index. FFR was normal in all investigated arteries. CFR was significantly lower in diabetic vs. nondiabetic patients [median (interquartile range): 2.2 (1.4-3.2) vs. 4.1 (2.7-4.4); P = 0.02]. Basal T(mn) was lower in diabetic vs. nondiabetic subjects [median (interquartile range): 0.53 (0.25-0.71) vs. 0.64 (0.50-1.17); P = 0.04], while hyperemic T(mn) and IMR were similar. We found significant correlations at linear regression analysis between logCFR and the HOMA index (r(2) = 0.35; P = 0.0005) and between basal T(mn) and the HOMA index (r(2) = 0.44; P < 0.0001). In conclusion, compared with nondiabetic subjects, CFR is lower in patients with diabetes and epicardial coronary arteries free of severe stenosis, because of increased basal coronary flow, while hyperemic coronary flow is similar. Basal coronary flow relates to insulin resistance, suggesting a key role of cellular metabolism in the regulation of coronary blood flow.
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