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Carnitine is a friend in HFpEF and foe in HFrEF

  • Huiqing Wang
  • , Haoran Wei
  • , Mingming Zhao
  • , Junfang Wu
  • , Min Fei
  • , Nan Lin
  • , Rui Zhan
  • , Qingyuan Liu
  • , Qi Zhang
  • , Xiaodong Yao
  • , Yufei Wu
  • , Wenxin Shan
  • , Hongtu Cui
  • , Liang Ji
  • , Bing Pan
  • , Lu Fang
  • , Yujie Zhu
  • , Xin Li
  • , Yansong Guo
  • , Dao Wen Wang
  • Lemin Zheng
  • Peking University Health Science Center
  • Tongji Medical College of Huazhong University of Science and Technology
  • Peking University
  • Fujian Medical University
  • Beijing Tiantan Hospital, Capital Medical University
  • North Sichuan Medical College

科研成果: 期刊稿件文章同行评审

3 引用 (Scopus)

摘要

Heart failure (HF) is a global concern, particularly HF with preserved ejection fraction (HFpEF), lacking effective treatments. Understanding the differences of metabolic profiles between HFpEF and HFrEF (heart failure with reduced ejection fraction) patients is crucial for therapeutic advancements. In this study, pseudotargeted metabolomics was employed to analyze for disparities of plasma metabolic profiles between HFpEF and HFrEF in two cohorts: discovery (n = 514) and validation (n = 3368). Plasma-free carnitine levels were significant changed in HF patients. A non-linear and U-shaped (for HFpEF) or J-shaped (for HFrEF) association between circulating free carnitine levels and the composite risk of cardiac events were observed. Interestingly, HFpEF patients with low free carnitine (≤40.18 μmol/L) displayed a poorer survival, contrasting with HFrEF where higher levels (≥35.67 μmol/L) were linked to poorer outcomes, indicating distinct metabolism pathways. In conclusion, these findings offer insights into HFpEF metabolic profiles, suggesting potential therapeutic targets.

源语言英语
文章编号111018
期刊iScience
27
10
DOI
出版状态已出版 - 18 10月 2024

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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