van den Dolder Floor W, Dinani Rafeeh, Warnaar Vincent A J, Vučković Sofija, Passadouro Adriana S, Nassar Ali A, Ramsaroep Azhaar X, Burchell George B, Schoonmade Linda J, van der Velden Jolanda, Goversen Birgit
Department of Physiology, Amsterdam University Medical Center (UMC), Location VUmc, Amsterdam, the Netherlands; Amsterdam Cardiovascular Sciences, Heart Failure and Arrhythmias, Amsterdam, the Netherlands.
Department of Physiology, Amsterdam University Medical Center (UMC), Location VUmc, Amsterdam, the Netherlands; Vascular Surgery, Department of Molecular Medicine and Surgery, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
JACC Basic Transl Sci. 2025 Apr;10(4):511-546. doi: 10.1016/j.jacbts.2024.10.017. Epub 2025 Jan 15.
To advance research in hypertrophic cardiomyopathy (HCM), and guide researchers in choosing the optimal model to answer their research questions, we performed a systematic review of all models investigating HCM induced by gene variants ranging from animal models to human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). Our research question entailed: which experimental models of HCM have been created thus far, and which major hallmarks of HCM do they present? Out of the 603 included papers, the majority included animal models, though a clear transition to hiPSC-CM is visible since 2010. Our review showed that only 36 mouse models showed minimal 4 out of 6 HCM disease markers (cell/cardiac hypertrophy, disarray, fibrosis, diastolic dysfunction, and arrhythmias), while only 17 hiPSC-CM models showed 3 out of 4 HCM cell characteristics. Our review emphasizes the need to better report data on sample size, sex, age, and relevant disease-specific characteristics.
为了推动肥厚型心肌病(HCM)的研究,并指导研究人员选择最佳模型来回答他们的研究问题,我们对所有研究基因变异诱导的HCM模型进行了系统综述,范围从动物模型到人类诱导多能干细胞衍生的心肌细胞(hiPSC-CM)。我们的研究问题包括:迄今为止创建了哪些HCM实验模型,它们呈现出哪些HCM的主要特征?在纳入的603篇论文中,大多数涉及动物模型,不过自2010年以来向hiPSC-CM的明显转变是可见的。我们的综述表明,只有36个小鼠模型显示出6个HCM疾病标志物中的至少4个(细胞/心脏肥大、排列紊乱、纤维化、舒张功能障碍和心律失常),而只有17个hiPSC-CM模型显示出4个HCM细胞特征中的3个。我们的综述强调需要更好地报告关于样本量、性别、年龄和相关疾病特异性特征的数据。