心力衰竭的表观遗传信号:早期诊断和有效治疗的新机会

K. A. Aitbaev, I. T. Murkamilov, V. V. Fomin, I. O. Kudaibergenova, F. A. Yusupov, Z. A. Aidarov
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引用次数: 0

摘要

心力衰竭(HF)是一种严重的临床综合征,具有很高的发病率和死亡率。根据HF的发生机制,临床主要分为两种形式:心力衰竭伴射血分数降低(HFrEF)和心力衰竭伴射血分数保留(HFpEF)。虽然已经开发出有效和特异性的治疗方法,导致近年来这种HF的患病率有所下降,但HFpEF患者的预后仍然不利,目前还没有有效的治疗方法。因此,寻找新的分子靶点和治疗途径被认为是现代医学的重要任务。该领域获得的数据揭示了表观遗传信号在HFpEF发展的转录程序调控中的关键作用,这有助于开发能够逆转转录变化的选择性表观遗传药物,从而延缓或阻止HFpEF的进展。进一步深入研究个体表观遗传景观可能为HFpEF的个性化表观遗传生物标志物和治疗方法的开发提供机会。这篇综述的目的是考虑表观遗传加工的作用,以及它在HFpEF的诊断和治疗的可能性。
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Epigenetic signals in heart failure: new opportunities for early diagnosis and eff ective therapy
Heart failure (HF) is a severe clinical syndrome associated with signifi cant morbidity and mortality. According to the mechanisms of HF development, it is divided into two main clinical forms: heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF). While eff ective and specifi c treatment methods have been developed for HFrEF, leading to a decrease in the prevalence of this form of HF in recent years, the prognosis for patients with HFpEF remains unfavourable, and eff ective treatment methods do not yet exist. Therefore, the identifi cation of new molecular targets and therapeutic approaches is considered an important task of modern medicine. Data obtained in this fi eld have revealed the key involvement of epigenetic signals in the regulation of transcriptional programs underlying the development of HFpEF, which has contributed to the development of selective epigenetic drugs capable of reversing transcriptional changes and thus delaying or preventing the progression of HFpEF. Further thorough investigation of individual epigenetic landscapes may provide opportunities in the future for the development of personalized epigenetic biomarkers and treatment methods for HFpEF. The aim of this review is to consider the role of epigenetic processing, as well as its diagnostic and therapeutic possibilities in HFpEF.
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