Division of Cardiology, Department of Medicine, Feinberg School of Medicine (A.S., C.W.Y., S.J.S., E.M.N., D.M.L.-J., S.S.K.), Northwestern University, Chicago, IL.
Department of Preventive Medicine, Feinberg School of Medicine (A.S., L.J.R.-T., P.G., D.M.L.-J., S.S.K.), Northwestern University, Chicago, IL.
Circ Heart Fail. 2021 Feb;14(2):e007761. doi: 10.1161/CIRCHEARTFAILURE.120.007761. Epub 2021 Feb 4.
Targeted prevention of heart failure (HF) remains a critical need given the high prevalence of HF morbidity and mortality. Similar to risk-based prevention of atherosclerotic cardiovascular disease, optimal HF prevention strategies should include quantification of risk in the individual patient. In this review, we discuss incorporation of a quantitative risk-based approach into the existing HF staging landscape and the clinical opportunity that exists to translate available data on risk estimation to help guide personalized decision making. We first summarize the recent development of key HF risk prediction tools that can be applied broadly at a population level to estimate risk of incident HF. Next, we provide an in-depth description of the clinical utility of biomarkers to personalize risk estimation in select patients at the highest risk of developing HF. We also discuss integration of genomics-enhanced approaches (eg, ) and other risk-enhancing features to reclassify risk with a precision medicine approach to HF prevention. Although sequential testing is very likely to identify low and high-risk individuals with excellent accuracy, whether or not interventions based on these risk models prevent HF in clinical practice requires prompt attention including randomized placebo-controlled trials of candidate therapies in risk-enriched populations. We conclude with a summary of unanswered questions and gaps in evidence that must be addressed to move the field of HF risk assessment forward.
鉴于心力衰竭(HF)发病率和死亡率高,靶向预防 HF 仍然是一个关键需求。与基于风险的动脉粥样硬化性心血管疾病预防类似,最佳 HF 预防策略应包括在个体患者中量化风险。在这篇综述中,我们讨论了将定量风险方法纳入现有的 HF 分期领域,以及将现有的风险估计数据转化为帮助指导个性化决策的临床机会。我们首先总结了最近开发的关键 HF 风险预测工具,这些工具可广泛应用于人群,以估计新发 HF 的风险。接下来,我们深入描述了生物标志物在选择处于 HF 发展最高风险的患者中进行个体化风险估计的临床实用性。我们还讨论了基因组增强方法(例如)和其他风险增强特征的整合,以采用精准医学方法重新分类 HF 预防的风险。尽管连续测试很可能以极高的准确性识别低风险和高风险个体,但这些风险模型是否能在临床实践中预防 HF 需要引起关注,包括在风险丰富人群中进行候选治疗的随机安慰剂对照试验。我们总结了尚未解决的问题和证据差距,必须解决这些问题才能推动 HF 风险评估领域的发展。