Department of Cardiology, Hekinan City Hospital.
Department of Laboratory Medicine, Fujita Health University Hospital.
Int Heart J. 2024 Sep 30;65(5):841-848. doi: 10.1536/ihj.24-080. Epub 2024 Sep 12.
Acute heart failure is an important cause of unplanned hospitalizations and poses a significant burden through increased mortality and frequent hospitalizations. Heart failure with preserved ejection fraction (HFpEF) presents as a diverse condition characterized by complex cardiovascular and non-cardiovascular pathology. This study aimed to identify distinct clinical phenotypes in acute decompensated HFpEF (ADHF) using cluster analysis and assess their prognostic significance. We applied a latent class analysis to 1,281 ADHF patients admitted to a single cardiac intensive care unit between 2008 and 2022 with a left ventricular ejection fraction ≥ 50%. We used 83 factors obtained at hospitalization. We evaluated the association between phenogroups and clinical outcomes using either Cox regression model or Fine-Gray competing risk model. We identified 4 phenogroups: Phenogroup 1 (n = 133, 10%) included younger patients with metabolic disorders and a low level of B-type natriuretic peptide (BNP); Phenogroup 2 (n = 346, 27%) had systemic congestion and high BNP levels; Phenogroup 3 (n = 514, 40%) had multiple comorbidities and vascular disorders; Phenogroup 4 (n = 288, 22%) included older patients with bradyarrhythmia and atrial fibrillation. After adjusting for age, sex, and Get with the Guidelines-Heart Failure risk score, Phenogroup 2 had the highest risk of all-cause death and cardiac death. In conclusion, we identified 4 clinically relevant phenogroups of ADHF patients, each associated with different adverse outcomes. Phenotyping may provide a better understanding of the underlying mechanisms involved in the heterogeneity of ADHF and decompensation. Furthermore, it may facilitate the search for phenotype-specific therapeutic strategies.
急性心力衰竭是计划性住院的重要原因,其导致的死亡率增加和频繁住院给患者带来了巨大的负担。射血分数保留的心力衰竭(HFpEF)表现为一种多样化的病症,其特征是复杂的心血管和非心血管病理。本研究旨在通过聚类分析确定急性失代偿性 HFpEF(ADHF)的不同临床表型,并评估其预后意义。我们对 2008 年至 2022 年期间在单一心脏重症监护病房住院的左心室射血分数≥50%的 1281 例 ADHF 患者进行了潜在类别分析。我们使用了住院时获得的 83 个因素。我们使用 Cox 回归模型或 Fine-Gray 竞争风险模型评估了表型组与临床结局之间的关联。我们确定了 4 个表型组:表型组 1(n=133,10%)包括年轻、患有代谢紊乱且 B 型利钠肽(BNP)水平较低的患者;表型组 2(n=346,27%)存在全身性充血和高 BNP 水平;表型组 3(n=514,40%)有多种合并症和血管疾病;表型组 4(n=288,22%)包括患有心动过缓和心房颤动的老年患者。在校正年龄、性别和 Get with the Guidelines-Heart Failure 风险评分后,表型组 2 的全因死亡和心脏死亡风险最高。总之,我们确定了 4 种具有临床意义的 ADHF 患者表型组,每个表型组与不同的不良结局相关。表型分析可能有助于更好地了解 ADHF 异质性和失代偿的潜在机制。此外,它可能有助于寻找表型特异性的治疗策略。