Metabolomics : Official journal of the Metabolomic Society · 2025
Plasma non-targeted metabolomics unravels the metabolic features of normal trans-right heart.
СтатьяНазвание и аннотация: Перевод в очереди
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Qian Xifeng, Deng Yuanrui, Guo Tingting, Huang Xin, Yan Chaowu, Gao Xin, Wu Yan, Yan Xinxin, Liu Zhiqiang, Hu Song, Tan Jiangshan, Chong Lingtao, Zhu Shengsong, Ma Mingjie, Ye Mengting, Hua Lu, Cao Jian, Wang Xiaojian
Аннотация
INTRODUCTION: Right heart (RH), as a junction between the venous system and pulmonary circulation, gains great emphasis on exploring the relevant pathological mechanism of many cardiopulmonary diseases. Although these pathogensis researches centering on RH-related diseases advance, the physiological mechanism research of the RH is scarce.
OBJECTIVES: This study aimed to accurately unravel the metabolic features of normal trans-RH through non-targeted metabolomics.
METHODS: Patent foramen ovale (PFO) participants with normal function of RH were recruited and their blood samples from superior vena cava (SVC) and pulmonary artery (PA) were collected through right cardiac catheterization. Non-targeted metabolomics analysis based on UHPLC-MS/MS was utilized to generate the metabolic feature of trans-RH by comparing the metabolites change from SVC to PA, revealing its physiological gradient metabolic mechanism.
RESULTS: 1060 metabolites were tentatively identified in blood samples from 28 PFO participants. 51 differential metabolites were defined based on screening criteria after flowing through RH, including 39 down-regulated metabolites and 12 up-regulated metabolites. Among them, phosphatidylcholines, sphingomyelins, amino acids, triacylglycerol, neopterin, and tetradecanedioic acid were the most relevant.
CONCLUSION: Our study provides a more profound and extensive understanding of the psychological metabolism of trans-RH, expanding the current knowledge of normal RH function and providing clues for the pathogenesis research of RH-related diseases.
OBJECTIVES: This study aimed to accurately unravel the metabolic features of normal trans-RH through non-targeted metabolomics.
METHODS: Patent foramen ovale (PFO) participants with normal function of RH were recruited and their blood samples from superior vena cava (SVC) and pulmonary artery (PA) were collected through right cardiac catheterization. Non-targeted metabolomics analysis based on UHPLC-MS/MS was utilized to generate the metabolic feature of trans-RH by comparing the metabolites change from SVC to PA, revealing its physiological gradient metabolic mechanism.
RESULTS: 1060 metabolites were tentatively identified in blood samples from 28 PFO participants. 51 differential metabolites were defined based on screening criteria after flowing through RH, including 39 down-regulated metabolites and 12 up-regulated metabolites. Among them, phosphatidylcholines, sphingomyelins, amino acids, triacylglycerol, neopterin, and tetradecanedioic acid were the most relevant.
CONCLUSION: Our study provides a more profound and extensive understanding of the psychological metabolism of trans-RH, expanding the current knowledge of normal RH function and providing clues for the pathogenesis research of RH-related diseases.