4.5 Article

Quantification of coronary flow reserve in patients with ischaemic and non-ischaemic cardiomyopathy and its association with clinical outcomes

Journal

EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING
Volume 16, Issue 8, Pages 900-909

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ehjci/jev012

Keywords

coronary flow reserve; cardiomyopathy; positron emission tomography; myocardial blood flow; coronary vascular dysfunction; clinical outcomes

Funding

  1. National Institutes of Health [K23HL092299]
  2. NIH [HL-094301-03]
  3. Gilead
  4. Astellas
  5. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL094301, K23HL092299] Funding Source: NIH RePORTER

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Aims Patients with left ventricular systolic dysfunction frequently show abnormal coronary vascular function, even in the absence of overt coronary artery disease. Moreover, the severity of vascular dysfunction might be related to the aetiology of cardiomyopathy. We sought to determine the incremental value of assessing coronary vascular dysfunction among patients with ischaemic (ICM) and non-ischaemic (NICM) cardiomyopathy at risk for adverse cardiovascular outcomes. Methods and results Coronary flow reserve (CFR, stress/rest myocardial blood flow) was quantified in 510 consecutive patients with rest left ventricular ejection fraction (LVEF) <= 45% referred for rest/stress myocardial perfusion PET imaging. The primary end point was a composite of major adverse cardiovascular events (MACE) including cardiac death, heart failure hospitalization, late revascularization, and aborted sudden cardiac death. Median follow-up was 8.2 months. Cox proportional hazards model was used to adjust for clinical variables. The annualized MACE rate was 26.3%. Patients in the lowest two tertiles of CFR (CFR <= 1.65) experienced higher MACE rates than those in the highest tertile (32.6 vs. 15.5% per year, respectively, P = 0.004), irrespective of aetiology of cardiomyopathy. Conclusion Impaired coronary vascular function, as assessed by reduced CFR by PET imaging, is common in patients with both ischaemic and non-ischaemic cardiomyopathy and is associated with MACE.

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