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Predicting hypertension subtypes with machine learning using targeted metabolites and their ratios

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-286161
  • Hypertension is a major global health problem with high prevalence and complex associated health risks. Primary hypertension (PHT) is most common and the reasons behind primary hypertension are largely unknown. Endocrine hypertension (EHT) is another complex form of hypertension with an estimated prevalence varying from 3 to 20% depending on the population studied. It occurs due to underlying conditions associated with hormonal excess mainly related to adrenal tumours and sub-categorised: primary aldosteronism (PA), Cushing’s syndrome (CS),Hypertension is a major global health problem with high prevalence and complex associated health risks. Primary hypertension (PHT) is most common and the reasons behind primary hypertension are largely unknown. Endocrine hypertension (EHT) is another complex form of hypertension with an estimated prevalence varying from 3 to 20% depending on the population studied. It occurs due to underlying conditions associated with hormonal excess mainly related to adrenal tumours and sub-categorised: primary aldosteronism (PA), Cushing’s syndrome (CS), pheochromocytoma or functional paraganglioma (PPGL). Endocrine hypertension is often misdiagnosed as primary hypertension, causing delays in treatment for the underlying condition, reduced quality of life, and costly antihypertensive treatment that is often ineffective. This study systematically used targeted metabolomics and high-throughput machine learning methods to predict the key biomarkers in classifying and distinguishing the various subtypes of endocrine and primary hypertension. The trained models successfully classified CS from PHT and EHT from PHT with 92% specificity on the test set. The most prominent targeted metabolites and metabolite ratios for hypertension identification for different disease comparisons were C18:1, C18:2, and Orn/Arg. Sex was identified as an important feature in CS vs. PHT classification.zeige mehrzeige weniger

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Autor(en): Smarti Reel, Parminder S. Reel, Zoran Erlic, Laurence Amar, Alessio Pecori, Casper K. Larsen, Martina Tetti, Christina Pamporaki, Cornelia Prehn, Jerzy Adamski, Aleksander Prejbisz, Filippo Ceccato, Carla Scaroni, Matthias Kroiss, Michael C. Dennedy, Jaap Deinum, Graeme Eisenhofer, Katharina Langton, Paolo Mulatero, Martin Reincke, Gian Paolo Rossi, Livia Lenzini, Eleanor Davies, Anne-Paule Gimenez-Roqueplo, Guillaume Assié, Anne Blanchard, Maria-Christina Zennaro, Felix Beuschlein, Emily R. Jefferson
URN:urn:nbn:de:bvb:20-opus-286161
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Medizinische Klinik und Poliklinik I
Medizinische Fakultät / Comprehensive Cancer Center Mainfranken
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Metabolites
ISSN:2218-1989
Erscheinungsjahr:2022
Band / Jahrgang:12
Heft / Ausgabe:8
Aufsatznummer:755
Originalveröffentlichung / Quelle:Metabolites (2022) 12:8, 755. https://doi.org/10.3390/metabo12080755
DOI:https://doi.org/10.3390/metabo12080755
Sonstige beteiligte Institutionen:Zentraleinheit Klinische Massenspektrometrie
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):Cushing syndrome; biomarkers; hypertension; machine learning; metabolomics; pheochromocytoma/paraganglioma; primary aldosteronism
Datum der Freischaltung:18.08.2023
Datum der Erstveröffentlichung:16.08.2022
EU-Projektnummer / Contract (GA) number:633983
OpenAIRE:OpenAIRE
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International