甘油三酯沉积性心肌病血液透析患者的肉毒碱给药和123I-BMIPP洗脱率

Annals of nuclear cardiology Pub Date : 2024-01-01 Epub Date: 2024-10-31 DOI:10.17996/anc.23-00014
Ken-Ichi Hirano, Keita Kodama, Hideyuki Miyauchi, Yasuyuki Nagasawa, Yusuke Nakano, Masaki Matsunaga, Tetsuya Amano, Kenichi Nakajima
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摘要

甘油三酯沉积性心肌病(TGCV)是一种新兴的高死亡率的罕见心脏病,其特征是细胞内甘油三酯(TG)的脂解缺陷。我们制定了TGCV的诊断标准,其中BMIPP- wr的低洗脱率是一个关键因素。日本核心脏病学会工作组最近发表了测量BMIPP-WR的实践建议。我们报道了患有TGCV的血液透析(HD)患者比没有TGCV的患者表现出明显更高的心血管风险。继发性肉碱缺乏在HD患者中很常见,因为肉碱从循环中被清除。然而,将肉毒碱水平与BMIPP-WR联系起来的临床证据有限。在此,我们报告了在一项回顾性队列研究中,左旋肉碱给药对9例合并TGCV的慢性HD患者BMIPP-WR的影响。TGCV诊断时的平均年龄为59岁。口服标准剂量左旋肉碱后,血浆游离左旋肉碱水平显著升高。然而,BMIPP-WR没有改变。在正常情况下,摄取的大部分BMIPP被酯化/纳入TG池,由细胞内脂肪酶水解,然后通过肉碱穿梭输送到线粒体。在TGCV中,细胞内TG脂解存在缺陷。在BMIPP的细胞内代谢过程中,肉碱穿梭发生在TG脂解的下游。因此,即使肉毒碱水平升高,TGCV患者慢性HD患者的BMIPP-WR也没有改变。TGCV的IIb/III期临床试验正在进行中(jRCT2051210177)。有必要提高对TGCV疾病概念的认识,以及使用BMIPP显像的诊断原则和程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carnitine Administration and 123I-BMIPP Washout Rate in Hemodialysis Patients with Triglyceride Deposit Cardiomyovasculopathy.

Triglyceride deposit cardiomyovasculopathy (TGCV) is an emerging rare heart disease with high mortality, characterized by defective intracellular lipolysis of triglycerides (TG). We developed diagnostic criteria for TGCV, in which low washout rate of BMIPP (BMIPP-WR) is a key factor. The working group of the Japan Society of Nuclear Cardiology recently published practice recommendations for measuring BMIPP-WR. We reported that hemodialysis (HD) patients with TGCV exhibited a markedly higher cardiovascular risk than those without TGCV. Secondary carnitine deficiency is common in patients undergoing HD, as carnitine is removed from the circulation. However, clinical evidence linking carnitine levels to BMIPP-WR is limited. Here we report the effect of L-carnitine administration on the BMIPP-WR in 9 chronic HD patients with TGCV in a retrospective cohort. The mean age at TGCV diagnosis was 59 years. Following standard doses of oral L-carnitine administration, plasma free carnitine levels significantly increased. However, BMIPP-WR was not changed. In normal condition, most BMIPP taken up were esterified/incorporated into TG pool, hydrolyzed by intracellular lipases, and then transported by carnitine shuttle to mitochondria. In TGCV, intracellular TG lipolysis is defective. During the intracellular metabolism of BMIPP, carnitine shuttling occurs downstream of TG lipolysis. Therefore, even when carnitine levels were increased, BMIPP-WR did not change in patients with TGCV who underwent chronic HD. A phase IIb/III clinical trial for TGCV, is underway (jRCT2051210177). Increased awareness of the disease concept of TGCV, along with its diagnostic principles and procedures using BMIPP scintigraphy, is warranted.

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