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Endogenous cortisol excess confers a unique lipid signature and metabolic network

Authors :
Vanesa Flores
Mireia Mora
Gemma Rojo
Felicia A. Hanzu
Ting Hu
Francesc Carmona
Oriol Giró
Guillermo Garcia-Eguren
Gloria Aranda
Marta Iruarrizaga
Ramon Gomis
Arturo Vega-Beyhart
Gregori Casals
Adriana Pané
Laura Boswell
Cristina Alonso
Joaquim Enseñat
Irene Halperin
Oscar Vidal
Source :
Journal of Molecular Medicine. 99:1085-1099
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Chronic cortisol excess induces several alterations on protein, lipid and carbohydrate metabolism resembling those found in the metabolic syndrome. However, patients exposed to prolonged high levels of cortisol in Cushing syndrome (CS) present exceeding cardiometabolic alterations not reflected by conventional biomarkers. Using 3 ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS) platforms, we aimed to characterise the serum metabolome of 25 patients with active endogenous CS and 25 control subjects matched by propensity score (sex, BMI, diabetes mellitus type 2 (T2D), high blood pressure (HBP) and dyslipidaemia) to search for potential disease-specific biomarkers and pathways associated to the clinical comorbidities. A total of 93 metabolites were significantly altered in patients with CS. Increased levels of sulfur amino acids (AA), triacylglycerols, glycerophospholipids, ceramides and cholesteryl esters were observed. Contrarily, concentrations of essential and non-essential AA, polyunsaturated fatty acids, conjugated bile acids and second messenger glycerolipids were decreased. Twenty-four-hour urinary free cortisol (24h-UFC) independently determined the concentration of 21 lipids and 4 AA. A metabolic signature composed by 10 AA and 10 lipid metabolites presented an AUC-ROC of 95% for the classification of CS patients. Through differential network analysis, 152 aberrant associations between metabolites involved in the Lands cycle and Kennedy pathway were identified. Our data indicates that chronic hypercortisolemia confers a unique lipidomic signature and several alterations in numerous AA even when compared to patients with similar metabolic comorbidities providing novel insights of the increased cardiometabolic burden of CS. KEY MESSAGES: • Cortisol excess induces metabolic alterations beyond conventional biomarkers. • The hypercortisolism extent determines the concentration of 21 lipids and 5 aa. • Cortisol excess confers a unique metabolic signature of 20 metabolites. • Kennedy and Lands cycle are profoundly disturbed by cortisol excess.

Details

ISSN :
14321440 and 09462716
Volume :
99
Database :
OpenAIRE
Journal :
Journal of Molecular Medicine
Accession number :
edsair.doi.dedup.....0ca6fc536f5a278fe47c3983adb506e3
Full Text :
https://doi.org/10.1007/s00109-021-02076-0