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炎症对射血分数保留的心脏代谢性心力衰竭的影响

Contributions of Inflammation to Cardiometabolic Heart Failure with Preserved Ejection Fraction.

作者信息

Thorp Edward B, Filipp Mallory

机构信息

Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA; email:

出版信息

Annu Rev Pathol. 2025 Jan;20(1):143-167. doi: 10.1146/annurev-pathmechdis-111523-023405. Epub 2025 Jan 2.

Abstract

The most common form of heart failure is heart failure with preserved ejection fraction (HFpEF). While heterogeneous in origin, the most common form of HFpEF is the cardiometabolic manifestation. Obesity and aging promote systemic inflammation that appears integral to cardiometabolic HFpEF pathophysiology. Accumulation of immune cells within the heart, fueled by an altered metabolome, contribute to cardiac inflammation and fibrosis. In spite of this, broad anti-inflammatory therapy has not shown significant benefit in patient outcomes. Thus, understanding of the nuances to metabolic and age-related inflammation during HFpEF is paramount for more targeted interventions. Here, we review clinical evidence of inflammation in the context of HFpEF and summarize our mechanistic understanding of immunometabolic inflammation, highlighting pathways of therapeutic potential along the way.

摘要

最常见的心力衰竭形式是射血分数保留的心力衰竭(HFpEF)。虽然其病因具有异质性,但HFpEF最常见的形式是心脏代谢表现。肥胖和衰老会促进全身炎症,而这种炎症似乎是心脏代谢性HFpEF病理生理学不可或缺的一部分。在代谢组改变的推动下,心脏内免疫细胞的积聚导致心脏炎症和纤维化。尽管如此,广泛的抗炎治疗在患者预后方面并未显示出显著益处。因此,了解HFpEF期间代谢和年龄相关炎症的细微差别对于更有针对性的干预至关重要。在此,我们回顾了HFpEF背景下炎症的临床证据,并总结了我们对免疫代谢炎症的机制理解,在此过程中突出了具有治疗潜力的途径。

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