Computed Tomographic Angiography Assessment of Epicardial Coronary Vasoreactivity for Early Detection of Doxorubicin-Induced Cardiotoxicity

Attila Feher; Nabil E Boutagy; John C Stendahl; Christi Hawley; Nicole Guerrera; Carmen J Booth; Eva Romito; Steven Wilson; Chi Liu; Albert J Sinusas

doi:10.1016/j.jaccao.2020.05.007

Computed Tomographic Angiography Assessment of Epicardial Coronary Vasoreactivity for Early Detection of Doxorubicin-Induced Cardiotoxicity

JACC CardioOncol. 2020 Jun 16;2(2):207-219. doi: 10.1016/j.jaccao.2020.05.007. eCollection 2020 Jun.

Authors

Attila Feher^{1

2}, Nabil E Boutagy^{1

2}, John C Stendahl^{1

2}, Christi Hawley², Nicole Guerrera², Carmen J Booth³, Eva Romito^{1

2}, Steven Wilson³, Chi Liu⁴, Albert J Sinusas^{1

2

4

5}

Affiliations

¹ Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
² Yale Translational Research Imaging Center, Yale University, New Haven, Connecticut, USA.
³ Department of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
⁴ Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, Connecticut, USA.
⁵ Department of Biomedical Engineering, Yale University School of Medicine, New Haven, Connecticut, USA.

Abstract

Background: The vascular endothelium is a novel target for the detection, management, and prevention of doxorubicin (DOX)-induced cardiotoxicity.

Objectives: The study aimed to: 1) develop a methodology by computed tomography angiography (CTA) to evaluate stress-induced changes in epicardial coronary diameter; and 2) apply this to a chronic canine model of DOX-induced cardiotoxicity to assess vascular toxicity.

Methods: To develop and validate quantitative methods, sequential retrospectively gated coronary CTAs were performed in 16 canines. Coronary diameters were measured at prespecified distances during rest, adenosine (ADE) (280 μg/kg/min), rest 30 min post-ADE, and dobutamine (DOB) (5 μg/kg/min). A subgroup of 8 canines received weekly intravenous DOX (1 mg/kg) for 12 to 15 weeks, followed by rest-stress CTA at cumulative doses of ∼4-mg/kg (3 to 5 mg/kg), ∼8-mg/kg (7 to 9 mg/kg), and ∼12-mg/kg (12 to 15 mg/kg) of DOX. Echocardiograms were performed at these timepoints to assess left ventricular ejection fraction and global longitudinal strain.

Results: Under normal conditions, epicardial coronary arteries reproducibly dilated in response to ADE (left anterior descending coronary artery [LAD]: 12 ± 2%, left circumflex coronary artery [LCx]: 13 ± 2%, right coronary artery [RCA]: 14 ± 2%) and DOB (LAD: 17 ± 3%, LCx: 18 ± 2%, RCA: 15 ± 3%). With DOX, ADE vasodilator responses were impaired after ∼4-mg/kg (LAD: -3 ± 1%, LCx: 0 ± 2%, RCA: -5 ± 2%) and ∼8-mg/kg (LAD: -3 ± 1%, LCx: 0 ± 1%, RCA: -2 ± 2%). The DOB dilation response was preserved at ∼4-mg/kg of DOX (LAD: 18 ± 4%, LCx: 11 ± 3%, RCA: 11 ± 2%) but tended to decrease at ∼8-mg/kg of DOX (LAD: 4 ± 2%, LCx: 8 ± 3%, RCA: 3 ± 2%). A significant left ventricular ejection fraction reduction was observed only at 12 to 15 mg/kg DOX (baseline: 63 ± 2%, 12-mg/kg: 45 ± 3%). Global longitudinal strain was abnormal at ∼4-mg/kg of DOX (p = 0.011).

Conclusions: CTA can reliably assess epicardial coronary diameter in response to pharmacological stressors, providing a noninvasive functional index of coronary vasoreactivity. Impaired epicardial vasodilation occurs early in DOX-induced cardiotoxicity.

Keywords: ADE, adenosine; CAD, coronary artery disease; CT angiography; CTA, computed tomography angiography; DOB, dobutamine; DOX, doxorubicin; GLS, global longitudinal strain; HR, heart rate; LAD, left anterior descending coronary artery; LCx, left circumflex coronary artery; LV, left ventricular; LVEF, left ventricular ejection fraction; MAP, mean arterial pressure; RCA, right coronary artery; TTE, transthoracic echocardiography; anthracycline; cardiomyopathy; diagnosis; imaging; preclinical study.

Abstract

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