Dhilhani Faleel, Ahmed Elzanaty, Vaishnavi Aradhyula, Rohit Vyas, Prabhatchandra R. Dube, Steven T. Haller, Rajesh Gupta, David J. Kennedy, Samer J. Khouri
{"title":"通过机器学习分析确定可预测射血分数保留型心力衰竭患者不良预后的多不饱和脂肪酸代谢物","authors":"Dhilhani Faleel, Ahmed Elzanaty, Vaishnavi Aradhyula, Rohit Vyas, Prabhatchandra R. Dube, Steven T. Haller, Rajesh Gupta, David J. Kennedy, Samer J. Khouri","doi":"10.46570/utjms.vol11-2023-951","DOIUrl":null,"url":null,"abstract":"which molecules were associated with future risk of either all cause death or a combined adverse outcome of death or rehospitalization in the setting of HFpEF. Results: In patients with HFpEF, increased levels of 9(10)-Epome, 15(R)-PGE1, 17-oxoRvD1, TXB3, RvD3, 5(S),15(S)-DiHETE, and 11dh-2,3-dinor TXB2 at baseline were predictive of all cause mortality (all p<0.05). Increased baseline levels of 8-oxoRvD1, MaR1(n-3DPA), PGE3, and 5,6-DiHETrE were predictive of the combined adverse outcome of death or rehospitalization (all p<0.05). Conclusion: These findings support the hypothesis that distinct PUFA metabolites play a significant role in mediating cardiovascular disease in HFpEF. Our study introduces a novel lipidomics framework for the diagnostic and prognostic assessment of cardiovascular risk in HFpEF patients.","PeriodicalId":220681,"journal":{"name":"Translation: The University of Toledo Journal of Medical Sciences","volume":"5 14","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Machine Learning Analysis of Identifies Polyunsaturated Fatty Acid Metabolites Predictive of Adverse Outcomes In Heart Failure with Preserved Ejection Fraction Patients\",\"authors\":\"Dhilhani Faleel, Ahmed Elzanaty, Vaishnavi Aradhyula, Rohit Vyas, Prabhatchandra R. Dube, Steven T. Haller, Rajesh Gupta, David J. Kennedy, Samer J. Khouri\",\"doi\":\"10.46570/utjms.vol11-2023-951\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"which molecules were associated with future risk of either all cause death or a combined adverse outcome of death or rehospitalization in the setting of HFpEF. Results: In patients with HFpEF, increased levels of 9(10)-Epome, 15(R)-PGE1, 17-oxoRvD1, TXB3, RvD3, 5(S),15(S)-DiHETE, and 11dh-2,3-dinor TXB2 at baseline were predictive of all cause mortality (all p<0.05). Increased baseline levels of 8-oxoRvD1, MaR1(n-3DPA), PGE3, and 5,6-DiHETrE were predictive of the combined adverse outcome of death or rehospitalization (all p<0.05). Conclusion: These findings support the hypothesis that distinct PUFA metabolites play a significant role in mediating cardiovascular disease in HFpEF. Our study introduces a novel lipidomics framework for the diagnostic and prognostic assessment of cardiovascular risk in HFpEF patients.\",\"PeriodicalId\":220681,\"journal\":{\"name\":\"Translation: The University of Toledo Journal of Medical Sciences\",\"volume\":\"5 14\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translation: The University of Toledo Journal of Medical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.46570/utjms.vol11-2023-951\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translation: The University of Toledo Journal of Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46570/utjms.vol11-2023-951","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Machine Learning Analysis of Identifies Polyunsaturated Fatty Acid Metabolites Predictive of Adverse Outcomes In Heart Failure with Preserved Ejection Fraction Patients
which molecules were associated with future risk of either all cause death or a combined adverse outcome of death or rehospitalization in the setting of HFpEF. Results: In patients with HFpEF, increased levels of 9(10)-Epome, 15(R)-PGE1, 17-oxoRvD1, TXB3, RvD3, 5(S),15(S)-DiHETE, and 11dh-2,3-dinor TXB2 at baseline were predictive of all cause mortality (all p<0.05). Increased baseline levels of 8-oxoRvD1, MaR1(n-3DPA), PGE3, and 5,6-DiHETrE were predictive of the combined adverse outcome of death or rehospitalization (all p<0.05). Conclusion: These findings support the hypothesis that distinct PUFA metabolites play a significant role in mediating cardiovascular disease in HFpEF. Our study introduces a novel lipidomics framework for the diagnostic and prognostic assessment of cardiovascular risk in HFpEF patients.