Blood pressure variability and left ventricular mass index in children

Bojko Bjelakovic1, Stevo Lukic, Vladislav Vukomanovic

  • 1Clinic of Pediatrics, Clinical Center, Nis, Serbia; Medical Faculty, University of Nis, Nis, Serbia.

Insights

Blood pressure variability indices are not reliable for identifying children at risk for left ventricular hypertrophy. Body mass index is a more significant predictor of left ventricular mass index in pediatric hypertension.

Area of Science:

  • Pediatric Cardiology
  • Hypertension Research
  • Cardiovascular Imaging

Background:

  • Blood pressure variability (BPV) implications on subclinical organ damage in children remain unclear.
  • Standard and novel BPV indices require evaluation for predicting left ventricular hypertrophy (LVH) in pediatric hypertension.

Purpose of the Study:

  • To assess the clinical utility of weighted standard deviation (wBPSD) and real average variability (ARV) for identifying children at risk for LVH.
  • To compare these novel BPV indices with standard ambulatory blood pressure monitoring (ABPM) parameters.

Main Methods:

  • Echocardiography was used to estimate left ventricular mass index (LVMI) in 67 children with suspected hypertension.
  • Analysis included correlation and regression models using 24-hour wBPSD, 24-hour ARV, average 24-hour systolic blood pressure (SBP), and 24-hour SBP load.

Main Results:

  • A significant positive correlation was found between 24-hour wBPSD and LVMI (ρ=0.389; P=.002).
  • No correlation was observed between 24-hour ARV and LVMI (P>.05).
  • After adjusting for body mass index (BMI), the correlation between 24-hour wBPSD and LVMI became weak (ρ=0.3; P=.022), and BMI emerged as the only significant independent predictor of LVMI (P=.028).

Conclusions:

  • Current BPV indices, including 24-hour wBPSD and 24-hour ARV, are not clinically reliable for identifying children at risk for LVH.
  • The association of wBPSD with LVMI is negligible and primarily influenced by BMI.
  • Further research is needed to identify reliable BPV markers for subclinical organ damage in pediatric hypertension.

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