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Endogenous cortisol excess confers a unique lipid signature and metabolic network. | LitMetric

AI Article Synopsis

  • Chronic cortisol excess, such as that seen in Cushing syndrome (CS), leads to significant metabolic changes, resembling those seen in metabolic syndrome, but more pronounced in CS patients, which aren’t fully captured by traditional biomarkers.
  • A study analyzed the serum metabolome of 25 active CS patients and 25 matched controls, using advanced technology to identify 93 significantly altered metabolites linked to CS, including increased sulfur amino acids and lipids, while essential amino acids and certain fatty acids were decreased.
  • The findings revealed a distinct metabolic signature for CS, with high classification accuracy for identifying patients, and highlighted the unique lipidomic changes and amino acid alterations tied to chronic hypercortisolemia, offering new insights into the condition’s cardiomet

Article 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.

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Source
http://dx.doi.org/10.1007/s00109-021-02076-0DOI Listing

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