Metabolomics Profiling Predicts Ventricular Arrhythmia in Patients with an Implantable Cardioverter Defibrillator

被引:2
作者
Yang, Shengwen [1 ,2 ]
Zhao, Junhan [3 ]
Liu, Xi [4 ]
Wang, Jing [3 ]
Gu, Min [3 ]
Cai, Chi [3 ]
Niu, Hongxia [3 ]
Chen, Liang [5 ]
Hua, Wei [3 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Heart Ctr, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chaoyang Hosp, Beijing Key Lab Hypertens, Beijing, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Arrhythmia Ctr, Arrhythmia Ctr,State Key Lab Cardiovasc Dis,Fuwai, Beijing, Peoples R China
[4] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, China Natl Clin Res Ctr Intervent Med,Dept Cardiol, Shanghai, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Natl Ctr Cardiovasc Dis, Dept Cardiac Surg,State Key Lab Cardiovasc Dis, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Implantable cardioverter defibrillator; Ventricular tachyarrhythmia; Metabolomics; Metabolites; SUDDEN CARDIAC DEATH; RISK STRATIFICATION; N-ACETYLASPARTATE; PHOSPHATIDIC-ACID; EJECTION FRACTION; DISEASE; OVEREXPRESSION; ABNORMALITIES; METABOLISM; COMMITTEE;
D O I
10.1007/s12265-023-10413-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Implantable cardioverter defibrillators (ICDs) reduce sudden cardiac death (SCD) when patients experience life-threatening ventricular arrhythmias ( LTVA). However, current strategies determining ICD patient selection and risk stratification are inefficient. We used metabolomics to assess whether dysregulated metabolites are associated with LTVA and identify potential biomarkers. Baseline plasma samples were collected from 72 patients receiving ICDs. Over a median follow-up of 524.0 days (range 239.0-705.5), LTVA occurred in 23 ( 31.9%) patients (22 effective ICD treatments and 1 SCD). After confounding risk factors adjustment for age, smoking, secondary prevention, and creatine kinase MB, 23 metabolites were significantly associated with LTVA. Pathway analysis revealed LTVA associations with disrupted metabolism of glycine, serine, threonine, and branched chain amino acids. Pathway enrichment analysis identified a panel of 6 metabolites that potentially predicted LTVA, with an area under the receiver operating characteristic curve of 0.8. Future studies are necessary on biological mechanisms and potential clinical use.
引用
收藏
页码:91 / 101
页数:11
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