Department of Cardiology Amsterdam University Medical Center Amsterdam Cardiovascular Sciences Vrije Universiteit University Medical Center Amsterdam Amsterdam the Netherlands.
Department of Physiology Amsterdam University Medical Center Amsterdam Cardiovascular Sciences Vrije Universiteit University Medical Center Amsterdam Amsterdam the Netherlands.
J Am Heart Assoc. 2020 Apr 21;9(8):e015316. doi: 10.1161/JAHA.119.015316. Epub 2020 Apr 15.
Background Hypertrophic cardiomyopathy is caused by pathogenic sarcomere gene variants. Individuals with a thin-filament variant present with milder hypertrophy than carriers of thick-filament variants, although prognosis is poorer. Herein, we defined if decreased energetic status of the heart is an early pathomechanism in (troponin T gene) variant carriers. Methods and Results Fourteen individuals with variants (genotype positive), without left ventricular hypertrophy (G+/LVH-; n=6) and with LVH (G+/LVH+; n=8) and 14 healthy controls were included. All participants underwent cardiac magnetic resonance and [C]-acetate positron emission tomography imaging to assess LV myocardial oxygen consumption, contractile parameters and myocardial external efficiency. Cardiac efficiency was significantly reduced compared with controls in G+/LVH- and G+/LVH+. Lower myocardial external efficiency in G+/LVH- is explained by higher global and regional oxygen consumption compared with controls without changes in contractile parameters. Reduced myocardial external efficiency in G+/LVH+ is explained by the increase in LV mass and higher oxygen consumption. Septal oxygen consumption was significantly lower in G+/LVH+ compared with G+/LVH-. Although LV ejection fraction was higher in G+/LVH+, both systolic and diastolic strain parameters were lower compared with controls, which was most evident in the hypertrophied septal wall. Conclusions Using cardiac magnetic resonance and [C]-acetate positron emission tomography imaging, we show that G+/LVH- have an initial increase in oxygen consumption preceding contractile dysfunction and cardiac hypertrophy, followed by a decline in oxygen consumption in G+/LVH+. This suggests that high oxygen consumption and reduced myocardial external efficiency characterize the early gene variant-mediated disease mechanisms that may be used for early diagnosis and development of preventive treatments.
肥厚型心肌病是由肌节基因突变引起的。与厚丝变体携带者相比,细丝变体携带者的心肌肥厚程度较轻,但预后较差。在此,我们定义了心脏能量状态的降低是否是 (肌钙蛋白 T 基因)变体携带者的早期发病机制。
纳入 14 名携带 变体的个体(基因型阳性),无左心室肥厚(G+/LVH-;n=6)和有 LVH(G+/LVH+;n=8)和 14 名健康对照者。所有参与者均接受心脏磁共振和 [C]-乙酸正电子发射断层扫描成像,以评估 LV 心肌耗氧量、收缩参数和心肌外效率。与对照组相比,G+/LVH-和 G+/LVH+中的心脏效率明显降低。G+/LVH-中的心肌外效率较低是由于与对照组相比,整体和局部耗氧量较高,但收缩参数无变化所致。G+/LVH+中的心肌外效率降低是由于 LV 质量增加和耗氧量增加所致。与 G+/LVH+相比,G+/LVH+的室间隔耗氧量明显较低。尽管 G+/LVH+的左心室射血分数较高,但与对照组相比,收缩和舒张应变参数均较低,在肥厚的室间隔壁中最为明显。
使用心脏磁共振和 [C]-乙酸正电子发射断层扫描成像,我们发现 G+/LVH-在出现收缩功能障碍和心肌肥厚之前,耗氧量首先增加,随后 G+/LVH-的耗氧量下降。这表明高耗氧量和心肌外效率降低是早期基因变异介导的疾病机制的特征,可能用于早期诊断和开发预防治疗方法。