Abstract

Nonclassic apparent mineralocorticoid excess (NC-AME) is proposed as a novel clinical condition with a mild phenotypic spectrum that ranges from normotension to severe hypertension. This condition is mainly characterized by a high serum cortisol to cortisone ratio (F/E) and concomitant low cortisone (E), however further metabolic changes in NC-AME have not been studied. A cross-sectional study was performed in a primary-care cohort of 396 Chilean subjects, which were classified in two groups: NC-AME (n = 28) and healthy controls (n = 27). A discovery study based in untargeted metabolomics assay in serum samples from both groups was performed by UPLC-Q-TOF/MS. Global metabolomic variations were assayed by principal component analysis and further compared by orthogonal partial least-squares discriminant analysis (OPLS-DA). NC-AME subjects exhibited higher values of blood pressure, fractional excretion of potassium, and lower plasma renin activity and urinary sodium to potassium ratio. Metabolomic analyses showed 36 differentially regulated metabolites between NC-AME and control subjects. A ROC curve analyses identified eight metabolites with high discriminatory capacity between NC-AME and control subjects. Moreover, gamma-l-glutamyl-l-methionine sulfoxide and 5-sulfoxymethylfurfural, exhibited significant association with cortisone, which are potential biomarkers of NC-AME, however further assays should elucidate its biological role in setup and progression of this phenotype.

Highlights

  • Nonclassic apparent mineralocorticoid excess (NC-Apparent mineralocorticoid excess (AME)) is proposed as a novel clinical condition with a mild phenotypic spectrum that ranges from normotension to severe hypertension

  • The discovery study was based on an untargeted metabolomic analysis of serum samples from Nonclassic apparent mineralocorticoid excess (NC-AME) patients and identified 36 differentially regulated metabolites, 3 upregulated metabolites and 33 downregulated metabolites

  • We observed that l-dopachrome and S-phenylmercapturic acid (SPMA) had the highest sensitivity and specificity to discriminate the NC-AME condition, followed by bilirubin, l-iditol, deoxyribose 1-phosphate, citric acid, gamma-l-glutamyl-l-methionine sulfoxide and 5-sulfoxymethylfurfural (SMF)

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Summary

Introduction

Nonclassic apparent mineralocorticoid excess (NC-AME) is proposed as a novel clinical condition with a mild phenotypic spectrum that ranges from normotension to severe hypertension. This condition is mainly characterized by a high serum cortisol to cortisone ratio (F/E) and concomitant low cortisone (E), further metabolic changes in NC-AME have not been studied. Recent studies by our group identified mild forms of AME syndrome that we named nonclassic apparent mineralocorticoid excess (NC-AME), which is proposed to be a condition with a wider and milder phenotypical spectrum than was identified for A­ ME5,7,9–12 and is primarily characterized by a high F/E ratio and low c­ ortisone[9].

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