Li Ke, Cardoso Cristiano, Moctezuma-Ramirez Angel, Elgalad Abdelmotagaly, Perin Emerson
Center for Preclinical Cardiovascular Research, The Texas Heart Institute, Houston, TX, United States.
Center for Clinical Research, The Texas Heart Institute, Houston, TX, United States.
Front Cardiovasc Med. 2023 Mar 23;10:1099453. doi: 10.3389/fcvm.2023.1099453. eCollection 2023.
Heart failure with preserved ejection fraction (HFpEF) is characterized by a complex, heterogeneous spectrum of pathologic features combined with average left ventricular volume and diastolic dysfunction. HFpEF is a significant public health problem associated with high morbidity and mortality rates. Currently, effective treatments for HFpEF represent the greatest unmet need in cardiovascular medicine. A lack of an efficient preclinical model has hampered the development of new devices and medications for HFpEF. Because large animal models have similar physiologic traits as humans and appropriate organ sizes, they are the best option for limiting practical constraints. HFpEF is a highly integrated, multiorgan, systemic disorder requiring a multipronged investigative approach. Here, we review the large animal models of HFpEF reported to date and describe the methods that have been used to create HFpEF, including surgery-induced pressure overloading, medicine-induced pressure overloading, and diet-induced metabolic syndrome. In addition, for the first time to our knowledge, we use two established clinical HFpEF algorithms (HFA-PEFF and H2FPEF scores) to evaluate the currently available large animal models. We also discuss new technologies, such as continuous remote pressure monitors and inflatable aortic cuffs, as well as how the models could be improved. Based on current progress and our own experience, we believe an efficient large animal model of HFpEF should simultaneously encompass multiple pathophysiologic factors, along with multiorgan dysfunction. This could be fully evaluated through available methods (imaging, blood work). Although many models have been studied, only a few studies completely meet clinical score standards. Therefore, it is critical to address the deficiencies of each model and incorporate novel techniques to establish a more reliable model, which will help facilitate the understanding of HFpEF mechanisms and the development of a treatment.
射血分数保留的心力衰竭(HFpEF)的特征是一系列复杂、异质性的病理特征,同时伴有平均左心室容积和舒张功能障碍。HFpEF是一个重大的公共卫生问题,与高发病率和死亡率相关。目前,针对HFpEF的有效治疗是心血管医学中尚未满足的最大需求。缺乏有效的临床前模型阻碍了用于HFpEF的新设备和药物的开发。由于大型动物模型具有与人类相似的生理特征和合适的器官大小,它们是限制实际限制的最佳选择。HFpEF是一种高度整合的多器官系统性疾病,需要多方面的研究方法。在这里,我们回顾了迄今为止报道的HFpEF大型动物模型,并描述了用于创建HFpEF的方法,包括手术诱导的压力过载、药物诱导的压力过载和饮食诱导的代谢综合征。此外,据我们所知,我们首次使用两种已建立的临床HFpEF算法(HFA-PEFF和H2FPEF评分)来评估目前可用的大型动物模型。我们还讨论了新技术,如连续远程压力监测器和可充气主动脉袖带,以及如何改进这些模型。基于目前的进展和我们自己的经验,我们认为一个有效的HFpEF大型动物模型应该同时包含多个病理生理因素以及多器官功能障碍。这可以通过可用方法(成像、血液检查)进行全面评估。尽管已经研究了许多模型,但只有少数研究完全符合临床评分标准。因此,解决每个模型的不足之处并纳入新技术以建立更可靠的模型至关重要,这将有助于促进对HFpEF机制的理解和治疗方法的开发。