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Gadolinium enhanced magnetic resonance mean voxel signal intensity within the left ventricular myocardium changes prior to ejection fraction drop after receipt of cardiotoxic chemotherapy

Year: 2009
Type: article
Abstract: To determine if serial measures of gadolinium (GD) signal intensity acquired with cardiac magnetic resonance (CMR) during receipt of cardiotoxic doxorubicin (DOX) chemotherapy are associated with left ventricular ejection fraction (LVEF). 40 Sprague-Dawley rats were divided into 3 groups receiving weekly doses of: normal saline [NS] (n = 7), 1.5 mg/kg DOX (n = 19), or 2.5 mg/kg DOX (n = 14). 1.5 T CMR images of LVEF and myocardial GD signal were acquired before and at 2 and 4 weeks after DOX treatment. LVEF was determined from a multi-slice short axis cine acquisition; signal intensity was obtained from an inversion recovery (IR) mid-LV slice. Analysis of variance models were fit with group or LVEF drop status (>10% drop in LVEF from baseline yes/no, or NS) as factors. RESULTS: LVEF was similar among the 3 groups at baseline (p = 0.27), and at 2 weeks, (73+5%, NS; 74+5%,1.5 mg/kg DOX; 71+6%,2.5 mg/kg DOX). At 4 weeks, LVEF after NS was unchanged (77 ± 7%, p = 0.93), but there was a >10% drop in LVEF in 3/19 in the 1.5 mg/kg DOX, and 10/14 in the 2.5 mg/kg DOX groups: LVEF was 77 ± 7% in non-dropped and 64 ± 8% in dropped groups at 4 weeks (p < 0.001). LVEF remained ≥70% in all animals at 2 weeks. In animals dropping their LVEF at 4 weeks, the GD signal within the LV myocardium was elevated relative to baseline at week 2 (2 weeks prior to LVEF drop – Figure 1 ); in animals receiving NS or DOX without LVEF drop, GD was not elevated at 2 weeks. Figure 1 These data suggest gadolinium CMR may be useful to monitor for doxorubicin chemotherapy cardiotoxicity: low serial measures of GD intensity forecast no LVEF drop, whereas an increase in GD signal intensity forecasts a clinically important drop in LVEF.
Language: English
Field: Medicine
Open Access status: gold
Estimated APC paid: $3,000
OpenAlex ID: W2080546064
FWCI:
Cites: 14
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Related to: 10