Felipe Fernandes Pires Barbosa, Marco Antonio Coral Pinto, Álex Ap Rosini Silva, Luisa Oliveira Messias, Vanessa Bertolucci, Pedro Paulo Menezes Scariot, Lucas Miguel de Carvalho, José Geraldo Cardoso Junior, Andréia de Melo Porcari, Leonardo Henrique Dalcheco Messias
{"title":"心肌血运重建手术对血浆代谢组的影响。","authors":"Felipe Fernandes Pires Barbosa, Marco Antonio Coral Pinto, Álex Ap Rosini Silva, Luisa Oliveira Messias, Vanessa Bertolucci, Pedro Paulo Menezes Scariot, Lucas Miguel de Carvalho, José Geraldo Cardoso Junior, Andréia de Melo Porcari, Leonardo Henrique Dalcheco Messias","doi":"10.1007/s11306-025-02316-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Myocardial revascularization (MR) is recommended in acute myocardial infarction. Understanding the physiological disturbances caused by MR may be pertinent for future therapeutic strategies in the postoperative period.</p><p><strong>Objectives: </strong>This study aims to analyze the MR impact on plasma metabolites and investigate potential correlations between them with routinely measured biochemical and clinical parameters in MR, and with the cardiopulmonary bypass time (CPB).</p><p><strong>Methods: </strong>Twenty-five patients had plasma samples collected before and after MR for metabolomic analysis, performed by liquid chromatography coupled with high-resolution mass spectrometry.</p><p><strong>Results: </strong>One hundred eleven ions showed statistically significant differences due to MR and thirteen were identified. Only Pregnenolone Sulfate had its abundance in plasma decreased due to MR. Hydrocortisone succinate, Cortisone, and Corticosterone increased in response to the glucocorticoids administered during surgery. LysoPS 16:1, LysoPC 14:0, Phenylvaleric acid, 13-Hydroxyoctadecadienoic acid, N-Linoleoyl Glutamine, and N-Myristoyl Methionine, along with the significant increase in the white blood cell count are associated with inflammation processes, possibly caused by MR. Furthermore, Pregnenolone sulfate, Pentosidine, Phenylvaleric acid, and N-Myristoyl Methionine were correlated with biochemical/clinical parameters and CPB.</p><p><strong>Conclusion: </strong>These results open new horizons in the interpretation of physiological disturbances caused by MR, as well as provide support for future studies. The scientific community is invited to build upon the outcomes obtained to confirm the associations suggested in this study, advancing the realm of metabolomics and MR.</p>","PeriodicalId":18506,"journal":{"name":"Metabolomics","volume":"21 5","pages":"111"},"PeriodicalIF":3.3000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of myocardial revascularization surgery on the plasma metabolome.\",\"authors\":\"Felipe Fernandes Pires Barbosa, Marco Antonio Coral Pinto, Álex Ap Rosini Silva, Luisa Oliveira Messias, Vanessa Bertolucci, Pedro Paulo Menezes Scariot, Lucas Miguel de Carvalho, José Geraldo Cardoso Junior, Andréia de Melo Porcari, Leonardo Henrique Dalcheco Messias\",\"doi\":\"10.1007/s11306-025-02316-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Myocardial revascularization (MR) is recommended in acute myocardial infarction. Understanding the physiological disturbances caused by MR may be pertinent for future therapeutic strategies in the postoperative period.</p><p><strong>Objectives: </strong>This study aims to analyze the MR impact on plasma metabolites and investigate potential correlations between them with routinely measured biochemical and clinical parameters in MR, and with the cardiopulmonary bypass time (CPB).</p><p><strong>Methods: </strong>Twenty-five patients had plasma samples collected before and after MR for metabolomic analysis, performed by liquid chromatography coupled with high-resolution mass spectrometry.</p><p><strong>Results: </strong>One hundred eleven ions showed statistically significant differences due to MR and thirteen were identified. Only Pregnenolone Sulfate had its abundance in plasma decreased due to MR. Hydrocortisone succinate, Cortisone, and Corticosterone increased in response to the glucocorticoids administered during surgery. LysoPS 16:1, LysoPC 14:0, Phenylvaleric acid, 13-Hydroxyoctadecadienoic acid, N-Linoleoyl Glutamine, and N-Myristoyl Methionine, along with the significant increase in the white blood cell count are associated with inflammation processes, possibly caused by MR. Furthermore, Pregnenolone sulfate, Pentosidine, Phenylvaleric acid, and N-Myristoyl Methionine were correlated with biochemical/clinical parameters and CPB.</p><p><strong>Conclusion: </strong>These results open new horizons in the interpretation of physiological disturbances caused by MR, as well as provide support for future studies. The scientific community is invited to build upon the outcomes obtained to confirm the associations suggested in this study, advancing the realm of metabolomics and MR.</p>\",\"PeriodicalId\":18506,\"journal\":{\"name\":\"Metabolomics\",\"volume\":\"21 5\",\"pages\":\"111\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Metabolomics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11306-025-02316-1\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Metabolomics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11306-025-02316-1","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
Impact of myocardial revascularization surgery on the plasma metabolome.
Introduction: Myocardial revascularization (MR) is recommended in acute myocardial infarction. Understanding the physiological disturbances caused by MR may be pertinent for future therapeutic strategies in the postoperative period.
Objectives: This study aims to analyze the MR impact on plasma metabolites and investigate potential correlations between them with routinely measured biochemical and clinical parameters in MR, and with the cardiopulmonary bypass time (CPB).
Methods: Twenty-five patients had plasma samples collected before and after MR for metabolomic analysis, performed by liquid chromatography coupled with high-resolution mass spectrometry.
Results: One hundred eleven ions showed statistically significant differences due to MR and thirteen were identified. Only Pregnenolone Sulfate had its abundance in plasma decreased due to MR. Hydrocortisone succinate, Cortisone, and Corticosterone increased in response to the glucocorticoids administered during surgery. LysoPS 16:1, LysoPC 14:0, Phenylvaleric acid, 13-Hydroxyoctadecadienoic acid, N-Linoleoyl Glutamine, and N-Myristoyl Methionine, along with the significant increase in the white blood cell count are associated with inflammation processes, possibly caused by MR. Furthermore, Pregnenolone sulfate, Pentosidine, Phenylvaleric acid, and N-Myristoyl Methionine were correlated with biochemical/clinical parameters and CPB.
Conclusion: These results open new horizons in the interpretation of physiological disturbances caused by MR, as well as provide support for future studies. The scientific community is invited to build upon the outcomes obtained to confirm the associations suggested in this study, advancing the realm of metabolomics and MR.
期刊介绍:
Metabolomics publishes current research regarding the development of technology platforms for metabolomics. This includes, but is not limited to:
metabolomic applications within man, including pre-clinical and clinical
pharmacometabolomics for precision medicine
metabolic profiling and fingerprinting
metabolite target analysis
metabolomic applications within animals, plants and microbes
transcriptomics and proteomics in systems biology
Metabolomics is an indispensable platform for researchers using new post-genomics approaches, to discover networks and interactions between metabolites, pharmaceuticals, SNPs, proteins and more. Its articles go beyond the genome and metabolome, by including original clinical study material together with big data from new emerging technologies.