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Gadolinium free cardiovascular magnetic resonance with 2-point Cine balanced steady state free precession
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نویسنده
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stromp t.a. ,leung s.w. ,andres k.n. ,jing l. ,fornwalt b.k. ,charnigo r.j. ,sorrell v.l. ,vandsburger m.h.
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منبع
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journal of cardiovascular magnetic resonance - 2015 - دوره : 17 - شماره : 1
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چکیده
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Background: cardiovascular magnetic resonance (cmr) of ventricular structure and function is widely performed using cine balanced steady state free precession (bssfp) mri. the bssfp signal of myocardium is weighted by magnetization transfer (mt) and t1/t2-relaxation times. in edematous and fibrotic tissues,increased t2 and reduced mt lead to increased signal intensity on images acquired with high excitation flip angles. we hypothesized that acquisition of two differentially mt-weighted bssfp images (termed 2-point bssfp) can identify tissue that would enhance with gadolinium similar to standard of care late gadolinium enhancement (lge). methods: cine bssfp images (flip angles of 5°and 45°) and native-t1 and t2 maps were acquired in one mid-ventricular slice in 47 patients referred for cmr and 10 healthy controls. afterwards,lge images and post-contrast t1 maps were acquired and gadolinium partition coefficient (gpc) was calculated. maps of δs/so were calculated as (s45-s5)/s5∗100 (%),where sflip-angle is the voxel signal intensity. results: twenty three patients demonstrated areas of myocardial hyper-enhancement with lge. in enhanced regions,δs/so,native-t1,t2,and gpc were heightened (p < 0.05 vs. non-enhanced tissues). δs/so,native-t1,and t2 all demonstrated association with gpc,however the association was strongest for δs/so. bland-altman analysis revealed a slight bias towards larger volume of enhancement with δs/so compared to lge,and similar transmurality. subjective analysis with 2-blinded expert readers revealed agreement between δs/so and lge of 73.4 %,with false positive detection of 16.7 % and false negative detection of 15.2 %. conclusions: gadolinium free 2-point bssfp identified tissue that enhances at lge with strong association to gpc. our results suggest that with further development,mt-weighted cmr could be used similar to lge for diagnostic imaging. © 2015 stromp et al.
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کلیدواژه
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Cardiomyopathy; Cardiovascular magnetic resonance; Infarction; Myocardium; Remodeling
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آدرس
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department of physiology,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States, gill heart institute,university of kentucky healthcare usa,lexington,ky,united states,saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States, saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States, saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536,united states,department of pediatrics,university of kentucky healthcare usa,lexington,ky, United States, department of physiology,university of kentucky usa,741 south limestone street,lexington,ky 40536,united states,saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536,united states,department of pediatrics,university of kentucky healthcare usa,lexington,ky,united states,department of biomedical engineering,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States, departments of statistics and biostatistics,university of kentucky usa,lexington,ky, United States, gill heart institute,university of kentucky healthcare usa,lexington,ky,united states,saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States, department of physiology,university of kentucky usa,741 south limestone street,lexington,ky 40536,united states,saha cardiovascular research center,university of kentucky usa,741 south limestone street,lexington,ky 40536,united states,department of biomedical engineering,university of kentucky usa,741 south limestone street,lexington,ky 40536, United States
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