The Growth/Differentiation Factor-15 in Chronic Heart Failure: New Challenge in Biomarker-Guided Therapy?

A. Berezin
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引用次数: 1

Abstract

Heart failure (HF) biomarker-guided therapy is promising method, which directs to improving of clinical status, attenuation of admission/readmission to the hospital and reduces of mortality rate. Many biological markers, i.e. inflammatory cytokines, are under consideration as a surrogate target for HF treatment, while there is known biomarkers with established predictive value, such as natriuretic peptides. However, discovery of new biomarkers reflecting various underlying mechanisms of HF and appearing to be surrogate targets for biomarkerguided therapy is promising. Nowadays, growth differentiation factor 15 (GDF-15) is suggested a target biomarker for HF treatment. Although elevated level of GDF-15 associated with HF development, progression, and prognosis, there is not represented evidence regarding direct comparison of this biomarker with other clinical risk predictors and biomarkers. Moreover, GDF-15 might serve as a contributor to endothelial progenitor cells (EPC) dysfunction by inducing EPC death/autophagy and limiting their response to angiopoetic and reparative effects. The short communication is discussed whether GDF-15 is good molecular target for HF guided therapy.
生长/分化因子-15在慢性心力衰竭中的作用:生物标志物引导治疗的新挑战?
心衰(HF)生物标志物引导治疗是一种很有前途的治疗方法,有助于改善心衰的临床状况,减少住院/再入院率,降低病死率。许多生物标志物,如炎症细胞因子,正在考虑作为心衰治疗的替代靶标,而已知的生物标志物具有确定的预测价值,如利钠肽。然而,新的生物标志物的发现反映了HF的各种潜在机制,似乎是生物标志物引导治疗的替代靶点,这是有希望的。目前,生长分化因子15 (growth differentiation factor 15, GDF-15)被认为是治疗心衰的靶标生物标志物。虽然GDF-15水平升高与HF的发生、进展和预后相关,但没有证据表明该生物标志物与其他临床风险预测因子和生物标志物直接比较。此外,GDF-15可能通过诱导内皮祖细胞死亡/自噬并限制其对血管生成和修复作用的反应而导致内皮祖细胞(EPC)功能障碍。讨论了GDF-15是否是心衰引导治疗的良好分子靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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