31P NMR spectroscopy detects metabolic abnormalities in asymptomatic patients with hypertrophic cardiomyopathy

被引:150
作者
Jung, WI
Sieverding, L
Breuer, J
Hoess, T
Widmaier, S
Schmidt, O
Bunse, M
van Erckelens, F
Apitz, J
Lutz, O
Dietze, GJ [1 ]
机构
[1] Max Grundig Clin, Hypertens & Diabet Res Unit, D-77815 Buhl, Germany
[2] Univ Tubingen, Div Pediat Cardiol, D-72074 Tubingen, Germany
[3] Univ Tubingen, Inst Phys, D-72074 Tubingen, Germany
关键词
cardiomyopathy; ischemia; metabolism;
D O I
10.1161/01.CIR.97.25.2536
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Hypertrophic cardiomyopathy (HCM) often causes sudden, unexpected death in adolescents and young adults. Alterations in myocardial metabolism are considered to be causes for contractile dysfunction. We examined the question of whether metabolic abnormalities antedate the manifestation of symptoms in patients with HCM. Methods and Results-Proton-decoupled P-31 NMR spectroscopy of the anterior left ventricular wall of the heart of 14 young, asymptomatic patients with HCM was performed with a 1.5-T whole-body imager. Spectra of the phosphate metabolites were compared with those of normal control subjects. The patients exhibited a significantly reduced (P<0.02) ratio of phosphocreatine (PCr) to ATP of 1.98 +/- 0.37 (mean +/- SD), compared with 2.46 +/- 0.53 obtained in 11 normal control subjects. In addition, the group of patients with severe hypertrophy of the interventricular septum (n=8) showed a significantly increased (P<0.05) P-i-to-PCr ratio, with a P-i x 100/PCr of 20.0 +/- 8.3 versus 9.7 +/- 7.2 in control subjects. Both abnormalities are similar to those found in ischemic myocardium. This view is also supported by a significantly increased (P<0.01) phosphomonoester (PME)-to-PCr ratio, with a PME x 100/PCr of 20.7 +/- 11.2 compared with 8,4 +/- 6.7 in control subjects, indicating altered glucose metabolism. Conclusions-P-31 NMR spectroscopy detects alterations of myocardial metabolism in asymptomatic patients with HCM. These alterations may contribute to the understanding of the pathophysiology and natural history of the disease.
引用
收藏
页码:2536 / 2542
页数:7
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