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1.
J Cardiovasc Magn Reson ; 17: 15, 2015 Feb 12.
Article in English | MEDLINE | ID: mdl-25827220

ABSTRACT

BACKGROUND: Risk scores for cardiovascular disease (CVD) are in common use to integrate multiple cardiovascular risk factors in order to identify individuals at greatest risk for disease. The purpose of this study was to determine if individuals at greater cardiovascular risk have T1 mapping indices by cardiovascular magnetic resonance (CMR) indicative of greater myocardial fibrosis. METHODS: CVD risk scores for 1208 subjects (men, 50.8%) ages 55-94 years old were evaluated in the Multiethnic Study of Atherosclerosis (MESA) at six centers. T1 times were determined at 1.5Tesla before and after gadolinium administration (0.15 mmol/kg) using a modified Look-Locker pulse sequence. The relationship between CMR measures (native T1, 12 and 25 minute post-gadolinium T1, partition coefficient and extracellular volume fraction) and 14 established different cardiovascular risk scores were determined using regression analysis. Bootstrapping analysis with analysis of variance was used to compare different CMR measures. CVD risk scores were significantly different for men and women (p < 0.001). RESULTS: 25 minute post gadolinium T1 time showed more statistically significant associations with risk scores (10/14 scores, 71%) compared to other CMR indices (e.g. native T1 (7/14 scores, 50%) and partition coefficient (7/14, 50%) in men. Risk scores, particularly the new 2013 AHA/ASCVD risk score, did not correlate with any CMR fibrosis index. CONCLUSIONS: Men with greater CVD risk had greater CMR indices of myocardial fibrosis. T1 times at greater delay time (25 minutes) showed better agreement with commonly used risk score indices compared to ECV and native T1 time. CLINICAL TRIAL REGISTRATION: http://www.mesa-nhlbi.org/, NCT00005487.


Subject(s)
Heart Diseases/diagnosis , Magnetic Resonance Imaging , Myocardium/pathology , Age Factors , Aged , Aged, 80 and over , Analysis of Variance , Comorbidity , Contrast Media , Female , Fibrosis , Gadolinium , Heart Diseases/ethnology , Heart Diseases/mortality , Heart Diseases/pathology , Humans , Linear Models , Male , Middle Aged , Predictive Value of Tests , Prognosis , Risk Assessment , Risk Factors , Sex Factors , Time Factors , United States/epidemiology
2.
Int J Cardiovasc Imaging ; 30(7): 1339-46, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24903343

ABSTRACT

To evaluate long-term changes in diffuse myocardial fibrosis using cardiac magnetic resonance (CMR) with late gadolinium enhancement (LGE) and T1 mapping. Patients with chronic stable cardiomyopathy and stable clinical status (n = 52) underwent repeat CMR at a 6 month or greater follow up interval and had LGE and left ventricular (LV) T1 mapping CMR. Diffuse myocardial fibrosis (excluding areas of focal myocardial scar) was assessed by post gadolinium myocardial T1 times. Mean baseline age of 52 patients (66 % male) was 35 ± 19 years with a mean interval between CMR examinations of 2.0 ± 0.8 years. CMR parameters, including LV mass and ejection fraction, showed no change at follow-up CMR (p > 0.05). LVT1 times (excluding focal scar) decreased over the study interval (from 468 ± 106 to 434 ± 82 ms, p = 0.049). 38 Patients had no visual LGE-, while 14 were LGE+. For LGE- patients, greater change in LV mass and end systolic volume index were associated with change in T1 time (ß = -2.03 ms/g/m(2), p = 0.035 and ß = 2.1 ms/mL/m(2), p = 0.029, respectively). For LGE+ patients, scar size was stable between CMR1 and CMR2 (10.7 ± 13.8 and 11.5 ± 13.9 g, respectively, p = 0.32). These results suggest that diffuse myocardial fibrosis, as assessed by T1 mapping, progresses over time in patients with chronic stable cardiomyopathy.


Subject(s)
Cardiomyopathies/pathology , Magnetic Resonance Imaging , Myocardium/pathology , Adolescent , Adult , Cardiomyopathies/physiopathology , Chronic Disease , Disease Progression , Female , Fibrosis , Humans , Male , Middle Aged , Predictive Value of Tests , Stroke Volume , Time Factors , Ventricular Function, Left , Young Adult
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