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代谢性心肌病:利用人干细胞衍生模型解析临床异质性

Metabolic cardiomyopathies: untangling clinical heterogeneity with human stem-cell derived models.

作者信息

Passadouro Adriana S, Balfoort Berith M, Langeveld Mirjam, van Karnebeek Clara D M, van der Velden Jolanda, Houtkooper Riekelt H, Mosegaard Signe

机构信息

Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Location University of Amsterdam, Amsterdam, The Netherlands.

Department of Physiology, Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

出版信息

EMBO Mol Med. 2025 Sep 22. doi: 10.1038/s44321-025-00313-4.

Abstract

Inherited metabolic diseases are rare monogenic conditions that disrupt biochemical pathways, affecting energy production and homeostasis, often leading to damaging metabolite accumulation. These disorders are clinically heterogeneous and can impact all organs, including the heart. Metabolic cardiomyopathies present with varying severity and unpredictable prognosis, complicating patient care. Pre-clinical research aims to model these cardiomyopathies to understand their pathophysiological mechanisms and develop personalised treatments. Animal models have provided insights into cardiac pathology and treatment, but species differences limit data translation. Human induced pluripotent stem cells (hiPSC) offer a valuable tool for establishing disease models using reprogrammed somatic cells from patients and healthy donors, differentiated into disease-relevant cell types. Cardiomyocytes generated in significant numbers are crucial for investigating cardiac mechanisms and assessing patient-specific drug responses. This review summarises literature on metabolic cardiomyopathies, focusing on long-chain fatty acid oxidation disorders and Barth syndrome. We highlight cardiac readouts from various models and discuss the potential of hiPSC technologies as clinically relevant disease models.

摘要

遗传性代谢疾病是罕见的单基因疾病,会扰乱生化途径,影响能量产生和体内平衡,常常导致有害代谢物积累。这些疾病在临床上具有异质性,可影响包括心脏在内的所有器官。代谢性心肌病的严重程度各不相同,预后不可预测,给患者护理带来复杂性。临床前研究旨在建立这些心肌病的模型,以了解其病理生理机制并开发个性化治疗方法。动物模型为心脏病理学和治疗提供了见解,但物种差异限制了数据的转化。人类诱导多能干细胞(hiPSC)为利用患者和健康供体的重编程体细胞建立疾病模型提供了一种有价值的工具,这些体细胞可分化为与疾病相关的细胞类型。大量生成的心肌细胞对于研究心脏机制和评估患者特异性药物反应至关重要。本综述总结了关于代谢性心肌病的文献,重点关注长链脂肪酸氧化障碍和巴斯综合征。我们强调了各种模型的心脏检测结果,并讨论了hiPSC技术作为临床相关疾病模型的潜力。

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