Hibernating myocardium: morphological correlates of inotropic stimulation and glucose uptake

被引:52
作者
Pagano, D
Townend, JN
Parums, DV
Bonser, RS
Camici, PG
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, MRC,Cyclotron Unit, Hammersmith Hosp, London W14 0NN, England
[2] Univ Birmingham, Cardiothorac Surg Unit, Queen Elizabeth Hosp, Dept Cardiovasc Med, Birmingham B15 2TH, W Midlands, England
[3] Papworth Hosp, Dept Histopathol, Cambridge CB3 8RE, England
关键词
coronary artery disease; heart failure; myocardial viability; myocardial blood flow; positron emission tomography;
D O I
10.1136/heart.83.4.456
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-In patients with postischaemic left ventricular dysfunction, segments recovering function after revascularisation (hibernating myocardium) may not respond during dobutamine echocardiography, despite preserved [F-18] 2-fluoro-2-deoxy-D-glucose (FDG) uptake at position emission tomography. Objective-To investigate whether this lack of response might reflect the degree of ultrastructural change in hibernating myocardium. Methods-Transmural biopsies were obtained from 22 dysfunctional segments in 22 patients during coronary artery bypass grafting and examined by light and electron microscopy. Wall motion scores and coronary vasodilator reserve were assessed before and after coronary artery bypass grafting (CABG). Results-Mean (SD) wall motion score improved in all segments following CABG (from 2.24 (0.4) to 1.55 (0.4); p < 0.0001), confirming hibernating myocardium. In these segments myocardial blood flow (positron emission tomography with (H2O)-O-15) before CABG was similar to that in normal volunteers (1.02 (0.24) v 1.02 (0.23) ml/min/g), while the coronary vasodilator reserve was blunted (1.26 (0.7) v 3.2 (1.6); p < 0.0001). Myocardial blood flow was unchanged after CABG, whereas coronary vasodilator reserve increased to 2.10 (0.90) (p < 0.0007). In hibernating myocardium myofibrillar loss, interstitial fibrosis, and glycogen-rich myocytes were more marked than in control donor hearts. On the basis of the response to dobutamine before CABG, two functional groups were identified: group A, segments with inotropic reserve (n = 15); group B, segments without inotropic reserve (n = 7). FDG uptake was similar in group A and group B (0.40 (0.1) v 0.44 (0.1) mu mol/min/g). In group B there was more myofibrillar loss (26 (8)% v 11 (5)%; p = 0.0009) and glycogen-rich myocytes (28 (11)% v 17 (10)%; p = 0.02), whereas interstitial fibrosis, myocardial blood flow, and coronary vasodilator reserve were similar in the two groups. Myofibrillar loss was the only independent predictor of inotropic reserve (p = 0.01). Conclusions-Hibernating myocardium is characterised by a reduced coronary vasodilator reserve which improves on revascularisation and shows a spectrum of ultrastructural changes that influence the response to dobutamine, while FDG uptake is invariably preserved.
引用
收藏
页码:456 / 461
页数:6
相关论文
共 38 条
  • [1] NONINVASIVE QUANTIFICATION OF REGIONAL MYOCARDIAL BLOOD-FLOW IN CORONARY-ARTERY DISEASE WITH OXYGEN-15-LABELED CARBON-DIOXIDE INHALATION AND POSITRON EMISSION TOMOGRAPHY
    ARAUJO, LI
    LAMMERTSMA, AA
    RHODES, CG
    MCFALLS, EO
    IIDA, H
    RECHAVIA, E
    GALASSI, A
    DESILVA, R
    JONES, T
    MASERI, A
    [J]. CIRCULATION, 1991, 83 (03) : 875 - 885
  • [2] CHRONIC HIBERNATING MYOCARDIUM - INTERSTITIAL CHANGES
    AUSMA, J
    CLEUTJENS, J
    THONE, F
    FLAMENG, W
    RAMAEKERS, F
    BORGERS, M
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 147 (1-2) : 35 - 42
  • [3] AUSMA J, 1995, J MOL CELL CARDIOL, V27, P1202
  • [5] Identification of viable myocardium
    Bonow, RO
    [J]. CIRCULATION, 1996, 94 (11) : 2674 - 2680
  • [6] STRUCTURAL CORRELATES OF REGIONAL MYOCARDIAL DYSFUNCTION IN PATIENTS WITH CRITICAL CORONARY-ARTERY STENOSIS - CHRONIC HIBERNATION
    BORGERS, M
    THONE, F
    WOUTERS, L
    AUSMA, J
    SHIVALKAR, B
    FLAMENG, W
    [J]. CARDIOVASCULAR PATHOLOGY, 1993, 2 (04) : 237 - 245
  • [7] Increased sarcolemmal glucose transporter abundance in myocardial ischemia
    Brosius, FC
    Nguyen, N
    Egert, S
    Lin, ZW
    Deeb, GM
    Haas, F
    Schwaiger, M
    Sun, DQ
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1997, 80 (3A) : A77 - A84
  • [8] MYOCARDIAL-METABOLISM IN ISCHEMIC HEART-DISEASE - BASIC PRINCIPLES AND APPLICATION TO IMAGING BY POSITRON EMISSION TOMOGRAPHY
    CAMICI, P
    FERRANNINI, E
    OPIE, LH
    [J]. PROGRESS IN CARDIOVASCULAR DISEASES, 1989, 32 (03) : 217 - 238
  • [9] Camici P G, 1999, Cardiol Rev, V7, P39, DOI 10.1097/00045415-199901000-00013
  • [10] Pathophysiological mechanisms of chronic reversible left ventricular dysfunction due to coronary artery disease (hibernating myocardium)
    Camici, PG
    Wijns, W
    Borgers, M
    DeSilva, R
    Ferrari, R
    Knuuti, J
    Lammertsma, AA
    Liedtke, AJ
    Paternostro, G
    Vatner, SF
    [J]. CIRCULATION, 1997, 96 (09) : 3205 - 3214