Lee Dong I, Dai Dao-Fu
Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore MD, USA.
Cell Signal (Middlet). 2025;3(1):54-58. doi: 10.46439/signaling.3.057.
Aging contributes significantly to the deterioration of cardiac function and increases the prevalence of heart failure, including those with reduced or preserved ejection fraction. Heart failure with preserved ejection fraction (HFpEF) is highly prevalent in the elderly population and it has become a leading cause of morbidity and mortality in this group. This commentary discusses the important findings and broader implications of the study by Daneshgar . on the role of the anti-aging hormone α-Klotho in alleviating diastolic dysfunction in the aged heart via Sirtuin1 (Sirt1)-mediated pathways. Using aged and Klotho-deficient mouse models, they demonstrated that soluble Klotho (sKL) supplementation improved cardiac diastolic function, reduced left ventricular hypertrophy and fibrosis, and increased capillary density. Mechanistically, the cardioprotective effects of sKL were found to rely on Sirt1-mediated regulation of DNA damage pathways and cardiac protein acetylation. These findings provide new insights into the therapeutic potential of targeting the Klotho-Sirt1 axis for HFpEF and other age-related cardiovascular diseases.
衰老在很大程度上导致心脏功能恶化,并增加心力衰竭的患病率,包括射血分数降低或保留的心力衰竭。射血分数保留的心力衰竭(HFpEF)在老年人群中非常普遍,已成为该群体发病和死亡的主要原因。本评论讨论了Daneshgar等人的研究的重要发现及其更广泛的意义,该研究探讨了抗衰老激素α-klotho通过沉默调节蛋白1(Sirt1)介导的途径减轻老年心脏舒张功能障碍的作用。他们使用老年和Klotho基因缺陷小鼠模型,证明补充可溶性Klotho(sKL)可改善心脏舒张功能,减少左心室肥厚和纤维化,并增加毛细血管密度。从机制上讲,发现sKL的心脏保护作用依赖于Sirt1介导的对DNA损伤途径和心脏蛋白乙酰化的调节。这些发现为针对Klotho-Sirt1轴治疗HFpEF和其他与年龄相关的心血管疾病的治疗潜力提供了新的见解。