Assessment of myocardial fibrosis in cardiomyopathic hamsters with gadolinium-DTPA enhanced magnetic resonance imaging

被引:53
作者
Aso, H
Takeda, K
Ito, T
Shiraishi, T
Matsumura, K
Nakagawa, T
机构
[1] Mie Univ, Sch Med, Dept Radiol, Tsu, Mie 514, Japan
[2] Mie Univ, Sch Med, Dept Pathol, Tsu, Mie 514, Japan
关键词
cardiomyopathy; magnetic resonance imaging; contrast media; myocardial fibrosis;
D O I
10.1097/00004424-199801000-00004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
RATIONALE AND OBJECTIVES. The authors investigated whether magnetic resonance (MR) imaging enhanced with gadolinium (Gd)-DTPA would be useful for assessment of myocardial fibrosis in cardiomyopathy. METHODS. The authors compared MR images of the excised heart after Gd-DTPA injection with histopathologic findings in 33 hamsters with cardiomyopathy of the Bio 14.6 strain and 26 healthy hamsters of various age groups and assessed localization of Gd-(14)-C-DTPA by autoradiography in the myocardium of three hamsters with cardiomyopathy. RESULTS. The mean signal intensity ratios for the entire myocardium in hamsters with cardiomyopathy relative to that in healthy hamsters was significantly higher in a younger age group than in an older age group (1.30 +/- 0.09 versus 1.03 +/- 0.08, P < 0.001, respectively). This myocardial enhancement was more obvious in areas containing massive fibrosis in the early and mid stages than in the late stage. Autoradiograms of hamsters with cardiomyopathy showed patchy or linear increases in uptake, corresponding to the areas of myocardial fibrosis. Gadolinium-C-14-DTPA radioactivity ratios of myocardial fibrosis to healthy myocardium were significantly higher in the early and mid stages than in the late state (P < 0.01). CONCLUSIONS. Myocardial fibrosis with high cellularity and proliferation of vessels was delineated as an area enhanced with Gd-DTPA on MR images, and its signal intensity decreased with the late stage of myocardial fibrosis.
引用
收藏
页码:22 / 32
页数:11
相关论文
共 25 条
[1]   DIAGNOSIS AND CLASSIFICATION OF MYOCARDITIS BY ENDOMYOCARDIAL BIOPSY [J].
FENOGLIO, JJ ;
URSELL, PC ;
KELLOGG, CF ;
DRUSIN, RE ;
WEISS, MB .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 308 (01) :12-18
[2]  
FUJIWARA H, 1985, Heart and Vessels, V1, P182, DOI 10.1007/BF02066416
[3]   PROGRESSION FROM HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY TO TYPICAL DILATED CARDIOMYOPATHY-LIKE FEATURES IN THE END STAGE [J].
FUJIWARA, H ;
ONODERA, T ;
TANAKA, M ;
SHIRANE, H ;
KATO, H ;
YOSHIKAWA, J ;
OSAKADA, G ;
SASAYAMA, S ;
KAWAI, C .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 1984, 48 (11) :1210-1214
[4]   DIASTOLIC FUNCTION AND MYOCARDIAL STRUCTURE IN PATIENTS WITH MYOCARDIAL HYPERTROPHY - SPECIAL REFERENCE TO NORMALIZED VISCOELASTIC DATA [J].
HESS, OM ;
SCHNEIDER, J ;
KOCH, R ;
BAMERT, C ;
GRIMM, J ;
KRAYENBUEHL, HP .
CIRCULATION, 1981, 63 (02) :360-371
[5]   SUBENDOMYOCARDIAL EXHAUSTION OF BLOOD-FLOW RESERVE AND INCREASED FIBROSIS IN CONSCIOUS DOGS WITH HEART-FAILURE [J].
HITTINGER, L ;
SHANNON, RP ;
BISHOP, SP ;
GELPI, RJ ;
VATNER, SF .
CIRCULATION RESEARCH, 1989, 65 (04) :971-980
[6]  
Homburger F, 1979, Ann N Y Acad Sci, V317, P1, DOI 10.1111/j.1749-6632.1979.tb37318.x
[7]   FIBRILLAR COLLAGEN AND MYOCARDIAL STIFFNESS IN THE INTACT HYPERTROPHIED RAT LEFT-VENTRICLE [J].
JALIL, JE ;
DOERING, CW ;
JANICKI, JS ;
PICK, R ;
SHROFF, SG ;
WEBER, KT .
CIRCULATION RESEARCH, 1989, 64 (06) :1041-1050
[8]  
JALIL JE, 1978, EXP MOL PATHOL, V29, P66
[9]   RELAXATION OF WATER PROTONS IN THE INTRACELLULAR AND EXTRACELLULAR REGIONS OF BLOOD CONTAINING GD(DTPA) [J].
KOENIG, SH ;
SPILLER, M ;
BROWN, RD ;
WOLF, GL .
MAGNETIC RESONANCE IN MEDICINE, 1986, 3 (05) :791-795
[10]   LEFT-VENTRICULAR MYOCARDIAL EDEMA - LYMPH-FLOW, INTERSTITIAL FIBROSIS, AND CARDIAC-FUNCTION [J].
LAINE, GA ;
ALLEN, SJ .
CIRCULATION RESEARCH, 1991, 68 (06) :1713-1721