甘油三酯沉积性心肌病诊断标准 2020》。

Annals of nuclear cardiology Pub Date : 2020-01-01 Epub Date: 2020-08-31 DOI:10.17996/anc.20-00131
Kunihisa Kobayashi, Yasuhiko Sakata, Hideyuki Miyauchi, Yoshihiko Ikeda, Yasuyuki Nagasawa, Kenichi Nakajima, Kazunori Shimada, Junji Kozawa, Hiroyuki Hao, Tetsuya Amano, Hiroshi Yoshida, Tohru Inaba, Chikako Hashimoto, Ken-Ichi Hirano
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引用次数: 0

摘要

甘油三酯沉积性心肌病(TGCV)是一种新发现的疾病,2008 年在日本需要进行心脏移植的患者中被发现。细胞内脂肪分解缺陷会导致甘油三酯(TG)在心肌和冠状动脉血管平滑肌细胞内积聚,从而导致严重的心力衰竭和冠状动脉疾病,且预后不良。TGCV 的一个已知病因是脂肪甘油三酯脂肪酶(ATGL)的遗传缺陷,ATGL 是细胞内水解 TG 的限速酶。TGCV 可分为 ATGL 基因突变的原发性 TGCV 和无 ATGL 基因突变的特发性 TGCV。自发现以来,日本 TGCV 研究小组一直试图阐明其病理生理学,开发诊断程序和特定治疗方法。使用碘-123-β-甲基碘苯基十五烷酸(123I-BMIPP)进行心肌闪烁成像是一种独特的成像模式,可用于评估体内心肌脂肪溶解情况。123I-BMIPP 的洗脱率是诊断 TGCV 的重要指标。随着我们对这一疾病概念的认识和深入了解,我们发现临床诊断患者的累计人数已超过 200 人,病例分布在日本全国各地。此外,我们还成功完成了三项由研究者发起的 TGCV 潜在治疗药物(CNT-01)的临床试验,并于 2020 年 6 月获得日本厚生劳动省根据 "榊岳指定系统 "指定的治疗药物。在此,我们提供了 TGCV 的 2020 诊断标准,以进一步推动这一 "罕见难治疾病 "项目。
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The Diagnostic Criteria 2020 for Triglyceride Deposit Cardiomyovasculopathy.

Triglyceride deposit cardiomyovasculopathy (TGCV) is a newly identified disease that was discovered in individuals who required cardiac transplantation in Japan in 2008. Defective intracellular lipolysis causes triglyceride (TG) accumulation in the myocardium and coronary artery vascular smooth muscle cells, which results in severe heart failure and coronary artery disease with poor prognosis. A known cause of TGCV is a genetic deficiency of adipose triglyceride lipase (ATGL), a rate-limiting enzyme in the intracellular hydrolysis of TG. TGCV is classified into primary TGCV with ATGL mutations and idiopathic TGCV without ATGL mutations. Since its discovery, the Japan TGCV Study Group has attempted to elucidate its pathophysiology, develop diagnostic procedures, and specific treatment. Myocardial scintigraphy with iodine-123-β-methyl iodophenyl-pentadecanoic acid (123I-BMIPP) is a unique imaging modality for evaluating myocardial lipolysis in vivo. The washout rate of 123I-BMIPP is an essential indicator for the diagnosis of TGCV. Along with our efforts to provide awareness of and insights into this disease concept, we found that the cumulative number of clinically diagnosed patients has reached >200 and the cases are distributed throughout Japan. In addition, we successfully completed three investigator-initiated clinical trials of a potential therapeutic agent (CNT-01) for TGCV, which was assigned by the Ministry of Health, Labour, and Welfare, Japan, under the SAKIGAKE Designation System in June 2020. Here, we provide the Diagnostic Criteria 2020 for TGCV in order to further promote this "rare and intractable disease" project.

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