Fayyaz Ahmed U, Eltony Muhammad, Prokop Larry J, Koepp Katlyn E, Borlaug Barry A, Dasari Surendra, Bois Melanie C, Margulies Kenneth B, Maleszewski Joesph J, Wang Ying, Redfield Margaret M
Department of Cardiovascular Disease, Division of Circulatory Failure, Mayo Clinic, Rochester, MN, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Nat Rev Cardiol. 2025 Feb;22(2):90-104. doi: 10.1038/s41569-024-01067-1. Epub 2024 Aug 28.
Heart failure with preserved ejection fraction (HFpEF) is a major, worldwide health-care problem. Few therapies for HFpEF exist because the pathophysiology of this condition is poorly defined and, increasingly, postulated to be diverse. Although perturbations in other organs contribute to the clinical profile in HFpEF, altered cardiac structure, function or both are the primary causes of this heart failure syndrome. Therefore, studying myocardial tissue is fundamental to improve pathophysiological insights and therapeutic discovery in HFpEF. Most studies of myocardial changes in HFpEF have relied on cardiac tissue from animal models without (or with limited) confirmatory studies in human cardiac tissue. Animal models of HFpEF have evolved based on theoretical HFpEF aetiologies, but these models might not reflect the complex pathophysiology of human HFpEF. The focus of this Review is the pathophysiological insights gained from studies of human HFpEF myocardium. We outline the rationale for these studies, the challenges and opportunities in obtaining myocardial tissue from patients with HFpEF and relevant comparator groups, the analytical approaches, the pathophysiological insights gained to date and the remaining knowledge gaps. Our objective is to provide a roadmap for future studies of cardiac tissue from diverse cohorts of patients with HFpEF, coupling discovery biology with measures to account for pathophysiological diversity.
射血分数保留的心力衰竭(HFpEF)是一个全球性的重大医疗保健问题。针对HFpEF的治疗方法很少,因为这种疾病的病理生理学定义尚不明确,而且越来越多地被认为具有多样性。虽然其他器官的功能紊乱会导致HFpEF的临床症状,但心脏结构或功能的改变,或两者兼而有之,是这种心力衰竭综合征的主要原因。因此,研究心肌组织对于增进对HFpEF病理生理学的理解以及发现新的治疗方法至关重要。大多数关于HFpEF心肌变化的研究都依赖于动物模型的心脏组织,而缺乏(或仅有有限的)在人体心脏组织中的验证性研究。HFpEF的动物模型是基于理论上的HFpEF病因发展而来的,但这些模型可能无法反映人类HFpEF复杂的病理生理学。本综述的重点是从对人类HFpEF心肌的研究中获得的病理生理学见解。我们概述了这些研究的基本原理、从HFpEF患者及相关对照人群获取心肌组织的挑战与机遇、分析方法、迄今获得的病理生理学见解以及尚存的知识空白。我们的目标是为未来针对不同HFpEF患者群体的心脏组织研究提供路线图,将发现生物学与考虑病理生理多样性的措施相结合。