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基于机制的肌丝调控以治疗射血分数保留的心力衰竭中的舒张功能障碍。

Mechanism-based myofilament manipulation to treat diastolic dysfunction in HFpEF.

作者信息

Dominic Katherine L, Schmidt Alexandra V, Granzier Henk, Campbell Kenneth S, Stelzer Julian E

机构信息

Department of Physiology and Biophysics, School of Medicine, Case Western Reserve University, Cleveland, OH, United States.

Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.

出版信息

Front Physiol. 2024 Dec 12;15:1512550. doi: 10.3389/fphys.2024.1512550. eCollection 2024.

Abstract

Heart failure with preserved ejection fraction (HFpEF) is a major public health challenge, affecting millions worldwide and placing a significant burden on healthcare systems due to high hospitalization rates and limited treatment options. HFpEF is characterized by impaired cardiac relaxation, or diastolic dysfunction. However, there are no therapies that directly treat the primary feature of the disease. This is due in part to the complexity of normal diastolic function, and the challenge of isolating the mechanisms responsible for dysfunction in HFpEF. Without a clear understanding of the mechanisms driving diastolic dysfunction, progress in treatment development has been slow. In this review, we highlight three key areas of molecular dysregulation directly underlying impaired cardiac relaxation in HFpEF: altered calcium sensitivity in the troponin complex, impaired phosphorylation of myosin-binding protein C (cMyBP-C), and reduced titin compliance. We explore how targeting these pathways can restore normal relaxation, improve diastolic function, and potentially provide new therapeutic strategies for HFpEF treatment. Developing effective HFpEF therapies requires precision targeting to balance systolic and diastolic function, avoiding both upstream non-specificity and downstream rigidity. This review highlights three rational molecular targets with a strong mechanistic basis and potential for therapeutic success.

摘要

射血分数保留的心力衰竭(HFpEF)是一项重大的公共卫生挑战,影响着全球数百万人,因其高住院率和有限的治疗选择给医疗系统带来了巨大负担。HFpEF的特征是心脏舒张功能受损,即舒张功能障碍。然而,目前尚无直接治疗该疾病主要特征的疗法。部分原因在于正常舒张功能的复杂性,以及分离HFpEF中功能障碍相关机制的挑战。由于对驱动舒张功能障碍的机制缺乏清晰认识,治疗开发进展缓慢。在本综述中,我们重点介绍了HFpEF中心脏舒张功能受损直接相关的三个关键分子失调领域:肌钙蛋白复合物中钙敏感性改变、肌球蛋白结合蛋白C(cMyBP-C)磷酸化受损以及肌联蛋白顺应性降低。我们探讨了针对这些途径如何恢复正常舒张、改善舒张功能,并有可能为HFpEF治疗提供新的治疗策略。开发有效的HFpEF疗法需要精准靶向,以平衡收缩和舒张功能,避免上游的非特异性和下游的僵化。本综述重点介绍了三个具有强大机制基础和治疗成功潜力的合理分子靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bea/11669688/0cd19286ee86/fphys-15-1512550-g001.jpg

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