18. PET for Diagnosis of Mytochondrial Cardiomyopathy in Children

Litvinova I. , Litvinov M. , Leonteva I. , Sebeleva I.
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引用次数: 5

Abstract

Purpose: To study the capability of positron emission tomography for mitochondrial dysfunction diagnosis on basis of oxidative metabolism evaluation.

Methods: PET studies were carried out in 13 patients (pts.) aged from 2 to 13 years (7,5+3,1) with CMP: hypertopic (HCMP) – 4, dilated (DCMP) – 9.The dynamic study with [C-11]-acetate was performed for evaluation of Krebs cycle activity. Rate constant (kmono) and [C-11]-activity clearance half-time (t1/2) were calculated using myocardial time-activity curve (from 3 to 10 min.). Myocardial perfusion was assessed with [N-13]-ammonia, glucose metabolism - with [F-18]-fluorodeoxylucose (FDG).

Results: Perfusion was normal in hypertohic parts of left ventricle (LV) in patients with HCMP. Krebs cycle activity was reduced (kmono = 0,077 ± 0,013 min−1). Glucose utilisation was increased in comparison with norm. Thus, Krebs cycle activity reduction (mitochondrial dysfunction) was compensated by increasing glycolysis activity. Perfusion was normal in all children with DCMP. Krebs cycle activity was reduced in LV in 6 pts. (kmono = 0,065 ± 0,029 min−1), normal - in 3 (kmono = 0,104 ± 0,010 min−1). All children had normal oxidative metabolism in right ventricle (kmono = 0,129 ± 0,203 min−1).Focal perfusion defects were noted in 2 pts. with CMP. In this region the Krebs cycle activity was decreased more then another LV parts. It means that ischemic injuries were. Glucose utilisation reduction in this field means that injuries were irreversible.

Conclusion: PET study showed Krebs cycle activity reduction in children with cardiomyopathy was noted despite in normal perfusion (mitochondrial dysfunction) vs. ischemic injuries of myocardium.

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18. PET对儿童心肌性心肌病的诊断价值
目的:探讨基于氧化代谢评价的正电子发射断层扫描诊断线粒体功能障碍的能力。方法:对13例2 ~ 13岁(7,5+3,1)CMP患者进行PET检查,CMP:增生性(HCMP) - 4,扩张性(DCMP) - 9。用[C-11]-乙酸酯进行了动态研究,评价了克雷布斯循环活性。采用心肌时间-活动曲线(3 ~ 10 min)计算速率常数(kmono)和[C-11]-活性清除半衰期(t1/2)。心肌灌注用[N-13]-氨法测定,葡萄糖代谢用[F-18]-氟脱氧葡萄糖(FDG)测定。结果:HCMP患者左心室高渗部分灌注正常。克雷布斯循环活性降低(kmono = 0,077±0,013 min−1)。与正常相比,葡萄糖利用率增加。因此,克雷布斯循环活性降低(线粒体功能障碍)通过糖酵解活性的增加得到补偿。所有DCMP患儿灌注正常。6例左室克雷布斯循环活性降低。(kmono = 0,065±0,029 min - 1),正常- 3 (kmono = 0,104±0,010 min - 1)。所有患儿右心室氧化代谢正常(kmono = 0,129±0,203 min−1)。2例发现局灶性灌注缺损。CMP。该区域克雷布斯循环活性下降幅度大于其他左室部位。这意味着缺血性损伤。葡萄糖利用减少在这个领域意味着伤害是不可逆的。结论:PET研究显示,尽管灌注正常(线粒体功能障碍)与心肌缺血损伤相比,心肌病患儿的Krebs循环活性降低。
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