Key result
Higher miR-16-5p levels linked to impaired LV global longitudinal strain in pediatric hypertension.
Why the study?
The role of circulating microRNAs in the pathophysiology of cardiac remodeling in primary hypertension remains incompletely understood.
Are circulating microRNA levels (specifically miR-16-5p) associated with subclinical myocardial strain impairment in children with untreated primary hypertension?
Cross-Sectional (n=107)
No
Are circulating microRNA levels (specifically miR-16-5p) associated with subclinical myocardial strain impairment in children with untreated primary hypertension?
Effect estimate: beta = 0.331 (95% CI 0.084-0.578)
p-value: p=0.010
Circulating miR-16-5p is independently associated with impaired left ventricular global longitudinal strain in children with primary hypertension, suggesting its potential as an early biomarker of subclinical myocardial remodeling.
miR-16-5p association with impaired LV GLS supports biomarker exploration in pediatric hypertension; leaves open prospective validation before clinical adoption.
The role of circulating microRNAs in the pathophysiology of cardiac remodeling in primary hypertension (PH) remains incompletely understood. Left ventricular global longitudinal strain (LV GLS) is a sensitive marker of subclinical systolic dysfunction and can be used to monitor early cardiac involvement in cardiovascular and renal diseases. To the best of our knowledge, this is the first study to demonstrate an association between circulating miR-16 and LV GLS in children. The study aimed to evaluate the expression levels of miR-16-5p, -21-5p, -27a-3p, -27b-3p, -133a-3p, and -145-5p in untreated children with PH and examine their associations with LV GLS. 50 children with PH and 57 normotensive controls were evaluated for circulating microRNA expression levels and echocardiographic parameters, including LV GLS. Comprehensive anthropometric, biochemical, blood pressure, and arterial indices were also assessed. Among the analyzed microRNAs, miR-16-5p exhibited a positive association with LV GLS (R = 0.305, p = 0.031), whereas miR-27b-3p demonstrated a negative association (R = −0.330, p < 0.001). Compared with controls, hypertensive children exhibited significantly higher (i.e., less negative) LV GLS (r = 0.29, p = 0.002), indicating early systolic dysfunction occurring already at an early stage of the disease. In conclusion, these findings support the idea that specific microRNAs might play a differential role in early myocardial functional alterations in pediatric PH. Higher miR-16 expression levels may be associated with impaired myocardial deformation, potentially reflecting its involvement in early maladaptive myocardial remodeling. Furthermore, LV GLS may represent a sensitive and clinically informative marker of early myocardial dysfunction beyond traditional echocardiographic parameters in this population.
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Szyszka et al. (2026) conducted a cross-sectional in Pediatric Primary Hypertension (n=107). Circulating miR-16-5p and miR-27b-3p vs. Normotensive healthy peers was evaluated on Association between miR-16-5p expression levels and Left Ventricular Global Longitudinal Strain (LV GLS) (beta = 0.331, 95% CI 0.084-0.578, p=0.010). In children with primary hypertension, higher circulating miR-16-5p levels were independently associated with impaired (less negative) left ventricular global longitudinal strain (beta 0.331, p=0.010).
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