Mamic Petra, Snyder Michael, Tang W H Wilson
Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford University, Stanford, California, USA; Department of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, USA.
Department of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, USA.
J Am Coll Cardiol. 2023 May 2;81(17):1729-1739. doi: 10.1016/j.jacc.2023.02.045.
Despite therapeutic advances, chronic heart failure (HF) is still associated with significant risk of morbidity and mortality. The course of disease and responses to therapies vary widely among individuals with HF, highlighting the need for precision medicine approaches. Gut microbiome stands to be an important aspect of precision medicine in HF. Exploratory clinical studies have revealed shared patterns of gut microbiome dysregulation in this disease, with mechanistic animal studies providing evidence for active involvement of the gut microbiome in development and pathophysiology of HF. Deeper insights into gut microbiome-host interactions in patients with HF promise to deliver novel disease biomarkers, preventative and therapeutic targets, and improve disease risk stratification. This knowledge may enable a paradigm shift in how we care for patients with HF, and pave the path toward improved clinical outcomes through personalized HF care.
尽管治疗取得了进展,但慢性心力衰竭(HF)仍然与较高的发病率和死亡率风险相关。HF患者的病程和对治疗的反应差异很大,这凸显了精准医学方法的必要性。肠道微生物群可能是HF精准医学的一个重要方面。探索性临床研究揭示了该疾病中肠道微生物群失调的共同模式,机制性动物研究为肠道微生物群积极参与HF的发展和病理生理学提供了证据。对HF患者肠道微生物群与宿主相互作用的更深入了解有望提供新的疾病生物标志物、预防和治疗靶点,并改善疾病风险分层。这些知识可能会使我们对HF患者的护理方式发生范式转变,并通过个性化的HF护理为改善临床结果铺平道路。