Key result
Adolescents demonstrated a greater mean RR time-interval compared to children (896 vs 813 ms, p=0.007), while adolescent males exhibited lower approximate entropy (p<0.001).
Why the study?
Although linear HRV in childhood and adolescence has been explored, little is known about nonlinear HRV in typically developing children and adolescents.
Does short-term linear and nonlinear heart rate variability differ between childhood and adolescence in typically developing youth?
Cross-Sectional (n=64)
No
Does short-term linear and nonlinear heart rate variability differ between childhood and adolescence in typically developing youth?
Absolute Event Rate: 896% vs 813%
p-value: p=0.007
Typically developing children and adolescents exhibit distinct age- and sex-related differences in nonlinear and linear heart rate variability, highlighting important physiological developmental changes in cardiac autonomic function.
May inform age- and sex-adjusted HRV interpretation in youth; extends linear observations but leaves open clinical utility of nonlinear metrics.
Linear heart rate variability (HRV) quantifies heart rate (HR) changes due to stochastic processes while nonlinear HRV captures the complexity of the HR structure. Although linear HRV in childhood and adolescence has been explored, little is known about nonlinear HRV. The present study characterized short‐term linear and nonlinear HRV in typically‐developing children (7–12 years, n = 35) and adolescents (13–17 years, n = 29). HRV during quiet rest was assessed using a three‐lead electrocardiogram for 5‐min and analyzed using linear (time and frequency domain) and nonlinear (Poincáre analysis, approximate [ApEn] and sample entropy [Sampen], and detrended fluctuation analysis [DFA]) metrics. A greater mean RR time‐interval was observed in adolescents ( p = 0.007). Time‐domain HRV was not different between children and adolescents, although sex differences were observed, such that females had lower linear HRV ( p < 0.05, > 62); namely, standard deviation of the normal sinus interbeat intervals (SDNN) and root mean square of the successive differences between the normal interbeat intervals (RMSSD). ApEn was lower in adolescent males ( p < 0.001, = 86). Short‐term scaling DFA was also lower in adolescents ( p = 0.023, = 64). Poincaré analysis revealed higher nonlinear short‐term ( p < 0.003, = 68) and long‐term variability ( p < 0.001, = 83) in males. Nonlinear metrics correlated with linear indices of parasympathetic tone. Collectively, age and sex differences were observed in nonlinear HRV in children and adolescents. Future research is needed to elucidate the mechanisms underlying nonlinear HRV during development and how these processes are altered in childhood disorders.
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Matias et al. (2026) conducted a cross-sectional in Typically developing children and adolescents (n=64). Adolescence (13-17 years old) vs. Childhood (7-12 years old) was evaluated on Mean RR time-interval (p=0.007). Adolescents demonstrated a greater mean RR time-interval compared to children (896 vs 813 ms, p=0.007), while adolescent males exhibited lower approximate entropy (p<0.001).
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