4.3 Article

Clinical, biochemical, and miRNA profile of subjects with positive screening of primary aldosteronism and nonclassic apparent mineralocorticoid excess

Journal

ENDOCRINE
Volume 77, Issue 2, Pages 380-391

Publisher

SPRINGER
DOI: 10.1007/s12020-022-03103-x

Keywords

Hypertension; Mineralocorticoid; MicroRNAs

Funding

  1. ANIDCONICYT FONDECYT [1212006]
  2. FONDECYT [3200646]
  3. CONICYT-FONDEQUIP [EQM150023]
  4. ANID-Millennium Science Initiative Program-IMII [P09/016-F, ICN09_016]
  5. CORFO [BMRC-13CTI-21526-P1]
  6. SOCHED [2019-09]
  7. CETRENUC

Ask authors/readers for more resources

This study identified adult subjects with a combined condition of nonclassic apparent mineralocorticoid excess (NCAME) and primary aldosteronism (PA), who had higher blood pressure and increased markers of renal and endothelial damage. Additionally, certain miRNA expressions were associated with this novel combined phenotype.
Primary aldosteronism (PA) and nonclassic apparent mineralocorticoid excess (NCAME) have been recognized as endocrine-related conditions having a broad clinical-biochemical spectrum, spanning from normotension to severe arterial hypertension (AHT). However, the coexistence of both phenotypes have not been reported to date. Aim To identify and characterize clinical and biochemical parameters of subjects with both PA and NCAME conditions (NCAME&PA) and study the miRNA cargo in their urinary extracellular vesicles as potential biomarkers for this novel condition. Methods We performed a cross-sectional study of 206 Chilean adult subjects from a primary care cohort. We measured blood pressure (BP), cortisol (F), cortisone (E), aldosterone, plasma renin activity (PRA), microalbuminuria (MAC), plasma NGAL, MMP9, fractional-potassium-excretion (FEK). Subjects were classified as NCAME&PA, PA, NCAME, essential hypertensives (EH), or healthy controls (CTL). EV-miRNAs were quantified by Taqman-qPCR. Results We found that 30.6% subjects had an abnormal endocrine phenotype: NCAME&PA (6.8%), PA (11.2%) or NCAME (12.6%), and the prevalence of AHT was 92.9%, 82.6%, and 65%, respectively. NCAME&PA subjects had both lower cortisone (p < 0.05) and lower PRA (p < 0.0001), higher FEK (p = 0.02) and higher MAC (p = 0.01) than EH or CTL. NCAME&PA subjects had also higher NGAL levels than CTL and PA (p < 0.05). Exosome miR-192, miR-133a and miR-21 expression decreased with phenotype severity and correlated with BP and PRA (p < 0.05). Conclusion We identified adult subjects with a combined condition of NCAME and PA associated with higher BP, increased renal and endothelial damage markers than control and EH. Additionally, we observed a differential expression of a specific miRNAs, suggesting a potential role of these miRNAs associated to this novel combined phenotype.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available