Coronary microvascular dysfunction is associated with impaired cognitive function: the Cerebral-Coronary Connection study (C3 study)

Author:

Mejia-Renteria Hernan1ORCID,Travieso Alejandro1ORCID,Matías-Guiu Jordi A2ORCID,Yus Miguel3ORCID,Espejo-Paeres Carolina1,Finocchiaro Francesca1,Fernández Sara1,Gomez-Escalonilla Carlos Ignacio2,Reneses-Prieto Blanca4,Gómez-Garré Maria Dulcenombre5ORCID,Delgado-Alvarez Alfonso2,Bustos Ana3,Perez de Isla Leopoldo6,de Diego Jose Juan Gomez6,Modrego-Martin Javier5ORCID,Ortega-Hernandez Adriana5ORCID,Papadopoulos Petros7,Arrazola-García Juan3,Matías-Guiu Jorge2,Escaned Javier1ORCID

Affiliation:

1. Interventional Cardiology Unit, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , c/ Profesor Martín Lagos, s/n. 28240 Madrid , Spain

2. Neurology Department, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , 28040 Madrid , Spain

3. Radiology Department, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , 28040 Madrid , Spain

4. Psychiatry Department, Hospital Clinico San Carlos IdISSC CIBERSAM, Universidad Complutense de Madrid , 28040 Madrid , Spain

5. Microbiota and Cardiovascular Risk Laboratory CIBER CV, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , 28040 Madrid , Spain

6. Cardiovascular Imaging Unit, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , 28040 Madrid , Spain

7. Hematology Department, Hospital Clinico San Carlos IdISSC, Universidad Complutense de Madrid , 28040 Madrid , Spain

Abstract

Abstract Background It remains unknown whether the presence of coronary microcirculatory dysfunction (CMD) correlates with its equivalent condition in the brain, cerebral small vessel disease (CSVD). The cerebral-coronary connection (C3), a prospective blinded study, investigated the prevalence of CMD in patients with coronary artery disease (CAD) and its association with CSVD and cognitive function. Methods and results Patients with documented CAD fulfilling inclusion criteria underwent physiological assessment of epicardial vessels and the microcirculation using intracoronary pressure and Doppler. Coronary microcirculation-related indices included coronary flow reserve (CFR) and hyperaemic microvascular resistance. Brain magnetic resonance imaging, transcranial Doppler (TCD), and neurocognitive examination were performed. Overall, 67 patients were included in the study (mean age 66 years, 73% female). Patients with abnormal CFR (<2.0) (55.2%) showed higher burden of white-matter hyperintensities: 43.2 vs. 20.0% (P = 0.044). After statistical adjustment, low CFR was associated with lower grey matter volume (P = 0.024) and with parameters of white-matter microstructural damage in diffusion-tensor imaging (lower fractional anisotropy and higher mean diffusivity, P = 0.029 and P = 0.032, respectively). Low CFR was associated with higher resistive (P = 0.027) and pulsatility (P = 0.043) values on TCD, and worse neurocognitive test scores (lower mini mental state examination, P = 0.025, and slower Trail Making Test A, P = 0.034). Conclusions Coronary microcirculatory dysfunction is frequent in patients with CAD and correlates with CSVD, abnormal cerebral flow haemodynamics, and significant cognitive impairment. These findings support the hypothesis that microvascular dysfunction in the heart and the brain are part of a single pathological process affecting microcirculation in patients with CAD. Clinical Trial Registration ClinicalTrials.gov NCT04131075.

Funder

Instituto Carlos III

FEDER

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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