Pediatric endocrinology

Circulating miR-1-3p precedes adrenarche and modulates adrenocortical steroidogenesis via protein kinase C signaling

J Clin Endocrinol MetabPublished Prospective cohort study

Main finding · Serum miR-1-3p levelsResult — go to the resultFold change 2

Authors' conclusion

Elevated circulating miR-1-3p precedes clinical adrenarche and enhances steroidogenesis in vitro.

Study context

Population
Children in the population-based PANIC study, followed at ages 7, 9 and 15 years; cases 20 girls, controls 11 girls
Participants
34 vs 24
Exposure
Children with signs of adrenarche at age 9 vs age-matched controls
  • Casesn = 34
  • Controlsn = 24reference
Outcome
Longitudinal serum miRNA expression and in vitro effects of candidate microRNAs (miRNAs) on adrenal steroidogenesis and gene expression
Follow-up
Ages 7, 9, and 15 years
Methodological detailsnested within the population-based PANIC study, longitudinal follow-up, age-matched controls, combined with in vitro experimental analyses (NCI-H295R cells)
  • Nested within the population-based PANIC study
  • Longitudinal follow-up
  • Age-matched controls
  • Combined with in vitro experimental analyses (NCI-H295R cells)

Main finding

Serum miR-1-3p levels · age 7 years

Fold change

2

P < 0.001

As reported in the abstract

Observational data: associations, not effects.

Further findings

Serum miR-1-3p over time

In both groups, miR-1-3p levels declined during adrenarchal and pubertal development

In vitro miR-1-3p overexpression (NCI-H295R)

Increased steroidogenic activity (approximately, on average)
1.5-fold
Upregulated genes
208
Downregulated genes
140
No change in expression of canonical steroidogenic enzyme genes
Genes identified include PRKCA (encoding protein kinase C (PKC)), enriched in the zona reticularis (ZR) and involved in steroidogenic signaling

Original publication

Circulating miR-1-3p precedes adrenarche and modulates adrenocortical steroidogenesis via protein kinase C signaling. J Clin Endocrinol Metab. Published 19 August 2026. doi:10.1210/clinem/dgag341

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