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      Carnitine Administration and 123I-BMIPP Washout Rate in Hemodialysis Patients with Triglyceride Deposit Cardiomyovasculopathy

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      , MD, PhD 1) , , , MD 2) , , MD, PhD 3) , , MD, PhD 4) , , MD, PhD 5) , , MD, PhD 2) , , MD, PhD 5) , , MD, PhD 6) , for the Japan TGCV Study Group
      Annals of Nuclear Cardiology
      The Japanese Society of Nuclear Cardiology
      BMIPP, Carnitine, Hemodialysis, Triglyceride deposit cardiomyovasculopathy, Washout rate

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          Abstract

          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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          Most cited references20

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          The heart and vascular system in dialysis.

          The heart and the vascular tree undergo major structural and functional changes when kidney function declines and renal replacement therapy is required. The many cardiovascular risk factors and adaptive changes the heart undergoes include left ventricular hypertrophy and dilatation with concomitant systolic and diastolic dysfunction. Myocardial fibrosis is the consequence of impaired angio-adaptation, reduced capillary angiogenesis, myocyte-capillary mismatch, and myocardial micro-arteriopathy. The vascular tree can be affected by both atherosclerosis and arteriosclerosis with both lipid rich plaques and abundant media calcification. Development of cardiac and vascular disease is rapid, especially in young patients, and the phenotype resembles all aspects of an accelerated ageing process and latent cardiac failure. The major cause of left ventricular hypertrophy and failure and the most common problem directly affecting myocardial function is fluid overload and, usually, hypertension. In situations of stress, such as intradialytic hypotension and hypoxaemia, the hearts of these patients are more vulnerable to developing cardiac arrest, especially when such episodes occur frequently. As a result, cardiac and vascular mortality are several times higher in dialysis patients than in the general population. Trials investigating one pharmacological intervention (eg, statins) have shown limitations. Pragmatic designs for large trials on cardio-active interventions are mandatory for adequate cardioprotective renal replacement therapy.
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            Triglyceride deposit cardiomyovasculopathy.

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              Triglyceride deposit cardiomyovasculopathy: a rare cardiovascular disorder

              Triglyceride deposit cardiomyovasculopathy (TGCV) is a phenotype primarily reported in patients carrying genetic mutations in PNPLA2 encoding adipose triglyceride lipase (ATGL) which releases long chain fatty acid (LCFA) as a major energy source by the intracellular TG hydrolysis. These patients suffered from intractable heart failure requiring cardiac transplantation. Moreover, we identified TGCV patients without PNPLA2 mutations based on pathological and clinical studies. We provided the diagnostic criteria, in which TGCV with and without PNPLA2 mutations were designated as primary TGCV (P-TGCV) and idiopathic TGCV (I-TGCV), respectively. We hereby report clinical profiles of TGCV patients. Between 2014 and 2018, 7 P-TGCV and 18 I-TGCV Japanese patients have been registered in the International Registry. Patients with I-TGCV, of which etiologies and causes are not known yet, suffered from adult-onset severe heart disease, including heart failure and coronary artery disease, associated with a marked reduction in ATGL activity and myocardial washout rate of LCFA tracer, as similar to those with P-TGCV. The present first registry-based study showed that TGCV is an intractable, at least at the moment, and heterogeneous cardiovascular disorder.
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                Author and article information

                Journal
                Ann Nucl Cardiol
                Ann Nucl Cardiol
                anc
                anc
                Annals of Nuclear Cardiology
                The Japanese Society of Nuclear Cardiology
                2189-3926
                2424-1741
                2024
                31 October 2024
                22 December 2023
                : 10
                : 1
                : 38-42
                Affiliations
                [1) ]Department of Triglyceride Science, Graduate School of Medicine, Osaka University, Japan
                [2) ]Department of Cardiology, Iwata City Hospital, Japan
                [3) ]Department of Cardiovascular Medicine, Chiba University Graduate School of Medicine, Japan
                [4) ]Department of General Internal Medicine, Hyogo College of Medicine, Japan
                [5) ]Department of Cardiology, Aichi Medical University, Japan
                [6) ]Department of Functional Imaging and Artificial Intelligence, Kanazawa University, Japan
                Author notes
                Reprint requests and correspondence: Ken-ichi Hirano, MD, PhD / Laboratory of Cardiovascular Disease, Novel, Non-invasive, and Nutritional Therapeutics (CNT) and Triglyceride Research Center (TGRC), Department of Triglyceride Science, Graduate School of Medicine, Osaka University, 6-2-4, Furuedai, Suita, Osaka 565-0874, Japan / E-mail: khirano@ 123456cnt-osaka.com
                [*]

                These authors equally contributed to this work.

                Article
                10.17996/anc.23-00014
                11612398
                39635328
                bfd7303c-fd45-48ff-9aec-2a0fdf09101e
                © The Japanese Society of Nuclear Cardiology 2024

                This article is licensed under a Creative Commons [Attribution-NonCommercial-NoDerivatives 4.0 International] license. https://creativecommons.org/licenses/by-nc-nd/4.0/

                History
                : 24 November 2023
                : 5 December 2023
                : 6 December 2023
                Page count
                Figures: 2, Tables: 1, References: 20, Pages: 5
                Categories
                Letter to Editor

                bmipp,carnitine,hemodialysis,triglyceride deposit cardiomyovasculopathy,washout rate

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