Application of Metabolomics and the Discovery of Potential Serum Biomarkers for Diuretic Resistance in Heart Failure.

IF 1.9 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Reviews in cardiovascular medicine Pub Date : 2025-04-22 eCollection Date: 2025-04-01 DOI:10.31083/RCM27001
Yipin Yu, Qiong Yi, Chenglong Yang, Xudong Song, Duoting Tan, Qinghua Peng, Xiang Sun, Hao Liang
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引用次数: 0

Abstract

Background: Diuretic resistance (DR) is characterized by insufficient fluid and sodium excretion enhancement despite maximum loop diuretic doses, indicating a phenotype of refractory heart failure (HF). Recently, metabolomics has emerged as a crucial tool for diagnosing and understanding the pathogenesis of various diseases. This study aimed to differentiate diuretic-resistant patients from non-resistant HF to identify biomarkers linked to the emergence of DR.

Methods: Serum samples from HF patients, both with and without DR, were subjected to non-targeted metabolomic analysis using liquid chromatography-tandem mass spectrometry. Metabolite variations between groups were identified using principal component analysis and orthogonal partial least-square discriminant analysis. Metabolic pathways were assessed through the Kyoto Encyclopedia of Genes and Genomes database enrichment analysis, and potential biomarkers were determined using receiver operating characteristic curves (ROCs).

Results: In total, 192 metabolites exhibited significant differences across the two sample groups. Among these, up-regulation was observed in 164 metabolites, while 28 metabolites were down-regulated. A total of 28 pathways involving neuroactive ligand-receptor interaction and amino acid biosynthesis were affected. The top five metabolites identified by ROC analysis as potential DR biomarkers were hydroxykynurenine, perillic acid, adrenic acid, 5-acetamidovalerate, and adipic acid.

Conclusions: Significant differences in metabolite profiles were observed between the diuretic-resistant and non-diuretic-resistant groups among patients with HF. The top five differentially expressed endogenous metabolites were hydroxykynurenine, perillic acid, adrenic acid, 5-acetamidovalerate, and adipic acid. The metabolic primary pathways implicated in DR were noted as amino acid, energy, and nucleotide metabolism.

Clinical trial registration: This study was registered with the China Clinical Trials Registry (https://www.chictr.org.cn/hvshowproject.html?id=197183&v=1.7, ChiCTR2100053587).

代谢组学的应用和发现利尿抵抗在心力衰竭中的潜在血清生物标志物。
背景:利尿剂抵抗(DR)的特征是尽管利尿剂剂量最大,但液体和钠排泄不足,表明一种难治性心力衰竭(HF)的表型。近年来,代谢组学已成为诊断和了解各种疾病发病机制的重要工具。本研究旨在区分利尿剂耐药患者和非耐药HF患者,以确定与DR发生相关的生物标志物。方法:采用液相色谱-串联质谱法对伴有和不伴有DR的HF患者的血清样本进行非靶向代谢组学分析。利用主成分分析和正交偏最小二乘判别分析鉴定各组间代谢物差异。通过京都基因和基因组百科全书数据库富集分析评估代谢途径,并使用受试者工作特征曲线(roc)确定潜在的生物标志物。结果:共有192种代谢物在两个样本组中表现出显著差异。其中,164种代谢物上调,28种代谢物下调。涉及神经活性配体-受体相互作用和氨基酸生物合成的28条通路受到影响。ROC分析确定的潜在DR生物标志物前五名代谢物分别是羟基尿氨酸、紫苏酸、肾上腺酸、5-乙酰氨基戊酸和己二酸。结论:在心衰患者中,利尿剂抵抗组和非利尿剂抵抗组之间的代谢物谱存在显著差异。内源代谢物中差异表达最多的5种分别是羟基尿氨酸、紫苏酸、肾上腺酸、5-乙酰氨基戊酸和己二酸。与DR相关的代谢主要途径是氨基酸、能量和核苷酸代谢。临床试验注册:本研究已在中国临床试验注册中心注册(https://www.chictr.org.cn/hvshowproject.html?id=197183&v=1.7, ChiCTR2100053587)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reviews in cardiovascular medicine
Reviews in cardiovascular medicine 医学-心血管系统
CiteScore
2.70
自引率
3.70%
发文量
377
审稿时长
1 months
期刊介绍: RCM is an international, peer-reviewed, open access journal. RCM publishes research articles, review papers and short communications on cardiovascular medicine as well as research on cardiovascular disease. We aim to provide a forum for publishing papers which explore the pathogenesis and promote the progression of cardiac and vascular diseases. We also seek to establish an interdisciplinary platform, focusing on translational issues, to facilitate the advancement of research, clinical treatment and diagnostic procedures. Heart surgery, cardiovascular imaging, risk factors and various clinical cardiac & vascular research will be considered.
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