肝纤维化评分与心力衰竭患者全因死亡率和心血管死亡率的关系。

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Ziyu Guo, Zixiang Ye, Qinfeng Xu, Yike Li, Jingang Zheng
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引用次数: 0

摘要

本研究旨在探讨肝纤维化(通过纤维化评分确定)与高血压患者全因死亡率和心血管死亡率的关系。该研究从 NHANES 数据库(1999 年至 2018 年)中收集了人口统计学和临床数据。共有 1356 名高血压患者参与了我们的分析。在中位 70 个月的随访期间,455 名患者死亡。与幸存者相比,死亡组的 LFSs 水平明显升高。RCS 分析显示,各种 LFSs 与全因死亡率和心血管死亡率之间存在线性关系。KM 曲线和 Cox 回归模型表明,较高的 FIB-4(≥ 1.637)、NFS(≥ -0.064)和 AST/ALT 比值(≥ 1.172)与较高的全因死亡风险相关[Cox 模型 2:FIB-4 调整后危险比(aHR),1.24;95% CI,1.04-1.48;NFS aHR,1.19;95% CI,1.01-1.38;AST/ALT 比值 aHR,1.25;95% CI,1.07-1.47]和心衰患者的心血管死亡风险(FIB-4 aHR,1.28;95% CI,1.07-1.67;AST/ALT 比值 aHR,1.39;95% CI,1.08-1.79)。ROC曲线显示,FIB-4、NFS和AST/ALT比值是心衰患者全因死亡率(AUC分别为0.715、0.707和0.715)和心血管死亡率(AUC分别为0.658、0.657和0.659)的重要预测指标。随机生存森林显示,FIB-4、AST/ALT 比值和 NFS 是潜在影响心力衰竭死亡率的重要因素。在亚组分析中也观察到了一致的关联。肝纤维化评分(FIB-4、NFS和AST/ALT比值)与心衰患者的全因死亡率和心血管死亡率密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of liver fibrosis scores with all-cause and cardiovascular mortality in patients with heart failure

Association of liver fibrosis scores with all-cause and cardiovascular mortality in patients with heart failure

The aim of this study was to examine the relationship of liver fibrosis (determined via fibrosis scores) with all-cause mortality and cardiovascular mortality in HF patients. The study examined demographic and clinical data were collected from NHANES database (1999 to 2018). A total of 1356 HF patients were enrolled in our analysis. During a median follow-up time of 70 months, 455 patients died. Compared to the survivors, the death group showed significantly elevated LFSs levels. RCS analysis revealed a linear relationship between various LFSs and all-cause and cardiovascular mortality. KM curves and Cox regression models indicated that higher FIB-4 (≥ 1.637), NFS (≥ −0.064), and AST/ALT ratio (≥ 1.172) were linked to higher risk of all-cause mortality [Cox model 2: FIB-4 adjusted hazard ratio (aHR), 1.24; 95% CI, 1.04–1.48; NFS aHR, 1.19; 95% CI, 1.01–1.38; AST/ALT ratio aHR, 1.25; 95% CI, 1.07–1.47] and cardiovascular mortality in heart failure patients (FIB-4 aHR, 1.28; 95% CI, 1.07–1.67; AST/ALT ratio aHR, 1.39; 95% CI, 1.08–1.79). ROC curves indicated that FIB-4, NFS, and the AST/ALT ratio were important predicators of all-cause mortality (AUC: 0.715, 0.707, and 0.715, respectively) and cardiovascular mortality (AUC: 0.658, 0.657, and 0.659, respectively) in heart failure patients. Random survival forests showed that FIB-4, AST/ALT ratio, and NFS emerged as important factors potentially influencing mortality of HF. Consistent associations were observed in subgroup analysis. Liver fibrosis scores (FIB-4, NFS, and AST/ALT ratio) were strongly linked to all-cause and cardiovascular mortality in heart failure patients.

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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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