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左心室心肌致密化不全:不断演变的概念

Left Ventricular Non-Compaction: Evolving Concepts.

作者信息

Pittorru Raimondo, De Lazzari Manuel, Migliore Federico, Frasson Enrica, Zorzi Alessandro, Cipriani Alberto, Brunetti Giulia, De Conti Giorgio, Motta Raffaella, Perazzolo Marra Martina, Corrado Domenico

机构信息

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova, 35128 Padua, Italy.

Radiology Unit, University of Padua-Azienda Ospedaliera, 35128 Padua, Italy.

出版信息

J Clin Med. 2024 Sep 24;13(19):5674. doi: 10.3390/jcm13195674.

Abstract

Left ventricular non-compaction (LVNC) is a rare heart muscle disease defined by the presence of prominent left ventricular trabeculation, deep intertrabecular recesses, and a thin compact layer. Several hypotheses have been proposed regarding its pathogenesis, with the most recently accepted one being that compact layer and trabeculated layers develop independently according to an "allometric growth". The current gold-standard diagnostic criteria (in particular, the Petersen index non-compaction/compaction ratio > 2.3) reflect an excess of myocardial trabeculation, which is not a specific morpho-functional feature of LVNC cardiomyopathy but merely a "phenotypic trait", even described in association with other myocardial disease and over-loading conditions. Accordingly, the European Society of Cardiology (ESC) guidelines have definitively abolished the term 'LVNC cardiomyopathy'. Recently, evolving perspectives led to the restoration of LVNC cardiomyopathy by distinguishing "hypertrabeculation phenotype" and "non-compaction phenotype". It has been proposed that the disease-specific pathophysiologic mechanism is a congenitally underdevelopment of the compact layer accounting for an impairment of the left ventricular systolic function. Future prospective research should focus on the clinical and prognostic relevance of compact layer thinning rather than excessive trabeculation, which could significantly influence the management of patients with LVNC. The review aims to update current knowledge on the pathogenesis, genetics, and diagnostic criteria of LVNC, offering modern insights for future perspectives.

摘要

左心室心肌致密化不全(LVNC)是一种罕见的心肌疾病,其特征为左心室肌小梁显著、肌小梁间深陷凹以及致密层薄。关于其发病机制已提出多种假说,目前最被认可的假说是致密层和肌小梁层根据“异速生长”独立发育。当前的金标准诊断标准(特别是彼得森指数,即非致密化/致密化比率>2.3)反映了心肌肌小梁过多,这并非LVNC心肌病的特定形态功能特征,而仅仅是一种“表型特征”,甚至在其他心肌疾病和负荷过重情况下也有描述。因此,欧洲心脏病学会(ESC)指南已明确废除“LVNC心肌病”这一术语。最近,随着观点的演变,通过区分“过度肌小梁化表型”和“非致密化表型”,LVNC心肌病得以恢复。有人提出,该疾病特异性的病理生理机制是致密层先天性发育不全,导致左心室收缩功能受损。未来的前瞻性研究应关注致密层变薄而非过度肌小梁化的临床和预后相关性,这可能会显著影响LVNC患者的管理。本综述旨在更新关于LVNC发病机制、遗传学和诊断标准的现有知识,为未来展望提供现代见解。

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