TY - JOUR
T1 - Fractional flow reserve (FFR) and index of microcirculatory resistance (IMR) relationship in patients with chronic or stabilized acute coronary syndromes
AU - Galante, Domenico
AU - Viceré, Andrea
AU - Marrone, Andrea
AU - Verardi, Filippo Maria
AU - Viccaro, Vincenzo
AU - Giuliana, Chiara
AU - Pollio Benvenuto, Ciro
AU - Todisco, Simona
AU - Biscaglia, Simone
AU - Aurigemma, Cristina
AU - Romagnoli, Enrico
AU - Capalbo, Gennaro
AU - Trani, Carlo
AU - Burzotta, Francesco
AU - Crea, Filippo
AU - Campo, Gianluca
AU - Leone, Antonio Maria
PY - 2025
Y1 - 2025
N2 - Aims: To investigate the influence of index of microcirculatory resistance (IMR) on fractional flow reserve (FFR) and adenosine-induced hyperemia (ΔPd/Pa-FFR) in patients with chronic (CCS) or stabilized acute coronary syndromes (ACS), utilizing various IMR threshold values. Methods: Data were extracted from two ongoing Italian registries involving patients with CCS or stabilized ACS who underwent a #FullPhysiology approach [Pd/Pa, FFR, IMR, coronary flow reserve (CFR)] by bolus thermodilution technique in the left anterior descending artery. Correlations between IMR and both FFR and ΔPd/Pa-FFR were analyzed both globally and within three IMR-defined groups: Group 1 (IMR <25), Group 2 (25 ≤ IMR <40), and Group 3 (IMR ≥40). A multiple linear regression was employed to adjust for confounding factors. Results: Of 275 patients, 163 were in Group 1, 60 in Group 2, and 52 in Group 3. Globally, a weak but significant correlation was observed between IMR and both FFR (r = 0.170, p < 0.01) and ΔPd/Pa-FFR (r = −0.159, p < 0.01). After stratification only patients in Group 3 exhibited a significant and more pronounced, though still weak, correlation between FFR and IMR (r = 0.387, p < 0.01) coupled with a reduction of ΔPd/Pa-FFR as IMR values increased (r = −0.411, p < 0.01). After adjustment, a significant increase of 0.01 in FFR values was observed for every 14-unit rise in IMR (p < 0.01) in Group 3. Conclusions: FFR appears particularly influenced by elevated IMR values (≥40) highlighting the importance of the #FullPhysiology approach in understanding epicardial and microvascular contribution of myocardial ischemia.
AB - Aims: To investigate the influence of index of microcirculatory resistance (IMR) on fractional flow reserve (FFR) and adenosine-induced hyperemia (ΔPd/Pa-FFR) in patients with chronic (CCS) or stabilized acute coronary syndromes (ACS), utilizing various IMR threshold values. Methods: Data were extracted from two ongoing Italian registries involving patients with CCS or stabilized ACS who underwent a #FullPhysiology approach [Pd/Pa, FFR, IMR, coronary flow reserve (CFR)] by bolus thermodilution technique in the left anterior descending artery. Correlations between IMR and both FFR and ΔPd/Pa-FFR were analyzed both globally and within three IMR-defined groups: Group 1 (IMR <25), Group 2 (25 ≤ IMR <40), and Group 3 (IMR ≥40). A multiple linear regression was employed to adjust for confounding factors. Results: Of 275 patients, 163 were in Group 1, 60 in Group 2, and 52 in Group 3. Globally, a weak but significant correlation was observed between IMR and both FFR (r = 0.170, p < 0.01) and ΔPd/Pa-FFR (r = −0.159, p < 0.01). After stratification only patients in Group 3 exhibited a significant and more pronounced, though still weak, correlation between FFR and IMR (r = 0.387, p < 0.01) coupled with a reduction of ΔPd/Pa-FFR as IMR values increased (r = −0.411, p < 0.01). After adjustment, a significant increase of 0.01 in FFR values was observed for every 14-unit rise in IMR (p < 0.01) in Group 3. Conclusions: FFR appears particularly influenced by elevated IMR values (≥40) highlighting the importance of the #FullPhysiology approach in understanding epicardial and microvascular contribution of myocardial ischemia.
KW - #FullPhysiology
KW - Fractional flow reserve
KW - Index of microcirculatory resistance
KW - #FullPhysiology
KW - Fractional flow reserve
KW - Index of microcirculatory resistance
UR - http://hdl.handle.net/10807/306680
U2 - 10.1016/j.ijcard.2025.132978
DO - 10.1016/j.ijcard.2025.132978
M3 - Article
SN - 0167-5273
VL - 422
SP - N/A-N/A
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -