Nadziakiewicz Paulina, Szczurek-Wasilewicz Wioletta, Jurkiewicz Michał, Skrzypek Michał, Gorzkowska Agnieszka, Gąsior Mariusz, Szyguła-Jurkiewicz Bożena
Student's Scientific Society, 3rd Department of Cardiology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.
2nd Department of Cardiology and Angiology, Silesian Center for Heart Diseases, 41-800 Zabrze, Poland.
Biomedicines. 2025 Aug 22;13(9):2048. doi: 10.3390/biomedicines13092048.
: Diagnosing and predicting outcomes in elderly patients with heart failure (HF) is challenging due to atypical symptoms and the limited value of natriuretic peptides, highlighting the need to search for new risk stratification biomarkers in this population. : We aimed to analyze factors associated with the composite endpoint (all-cause mortality or decompensated HF-related hospitalization) within six months of follow-up in elderly patients with left ventricular systolic dysfunction and decompensated HF, with particular emphasis on copeptin concentration. : This is a retrospective observational study based on prospectively collected data of 279 consecutive elderly patients hospitalized between 2018 and 2023 due to decompensated HF. Inclusion criteria were age > 65 years, history of HF diagnosed at least two years before the index hospitalization, and left ventricular ejection fraction < 40% on admission echocardiography. Serum copeptin levels were measured using an Enzyme-Linked Immunosorbent Assay (ELISA) (Human Copeptin ELISA kit, Sunred Biological Technology Co, Shanghai, China). The primary endpoint was all-cause mortality or decompensated HF-related hospitalization during the six-month follow-up. : The median age of the study population was 77 years (IQR: 69-79), and 221 (79.2%) were male. The composite endpoint occurred in 110 patients (38.1%). Multivariable analysis showed that serum concentrations of copeptin [hazard ratio (HR) 1.053 (1.042-1.064), < 0.0001], bilirubin [HR 1.085 (1.057-1.114), < 0.0001], uric acid [HR 1.005 (1.003-1.006), < 0.0001], high-sensitivity C-reactive protein (hs-CRP) [HR 1.208 (1.088-1.342), < 0.0001], and sodium [HR 1.111 (1.025-1.203), = 0.01], as well as ischemic etiology of HF [HR 3.969 (2.396-6.575), < 0.0001], were independently associated with worse outcomes. : Our study demonstrated that higher concentrations of copeptin, bilirubin, hs-CRP, and uric acid, as well as lower sodium levels and ischemic etiology of HF, were independently associated with all-cause mortality or HF-related hospitalization during a six-month follow-up in elderly patients with decompensated HF.
由于非典型症状以及利钠肽价值有限,老年心力衰竭(HF)患者的诊断和预后预测具有挑战性,这凸显了在此人群中寻找新的风险分层生物标志物的必要性。我们旨在分析左心室收缩功能障碍和失代偿性HF老年患者随访6个月内与复合终点(全因死亡率或失代偿性HF相关住院)相关的因素,尤其关注 copeptin 浓度。这是一项基于2018年至2023年间因失代偿性HF连续住院的279例老年患者前瞻性收集数据的回顾性观察研究。纳入标准为年龄>65岁、在本次住院前至少两年诊断为HF的病史以及入院超声心动图显示左心室射血分数<40%。使用酶联免疫吸附测定(ELISA)(人 copeptin ELISA试剂盒,上海顺源生物技术有限公司)测量血清 copeptin 水平。主要终点是6个月随访期间的全因死亡率或失代偿性HF相关住院。研究人群的中位年龄为77岁(IQR:69 - 79),221例(79.2%)为男性。110例患者(38.1%)出现复合终点。多变量分析显示,copeptin血清浓度[风险比(HR)1.053(1.042 - 1.064),P < 0.0001]、胆红素[HR 1.085(1.057 - 1.114),P < 0.0001]、尿酸[HR 1.005(1.003 - 1.006),P < 0.0001]、高敏C反应蛋白(hs - CRP)[HR 1.208(1.088 - 1.342),P < 0.0001]和钠[HR 1.111(1.025 - 1.203),P = 0.01],以及HF的缺血病因[HR 3.969(2.396 - 6.575),P < 0.0001],均与更差的预后独立相关。我们的研究表明,较高浓度的copeptin、胆红素、hs - CRP和尿酸,以及较低的钠水平和HF的缺血病因,在失代偿性HF老年患者6个月随访期间与全因死亡率或HF相关住院独立相关。