Baroreceptor sensitivity, kidney function and cardiovascular risk in prepubescent boys with normal versus elevated

Aletta S Uys1,2, Wayne Smith3,4, Annemarie Wentzel3,4

  • 1Hypertension in Africa Research Team (HART), North-West University, Potchefstroom, South Africa. lisa.uys@nwu.ac.za.

PubMed

Insights

Reduced baroreceptor sensitivity (BRS) is linked to kidney function in boys with normal blood pressure (BP). In boys with elevated BP, familial risk, obesity, and Black ethnicity are associated with lower BRS, increasing cardiovascular disease risk.

Area of Science:

  • Pediatrics
  • Cardiology
  • Nephrology

Background:

  • Reduced baroreceptor sensitivity (BRS) is linked to obesity in children, but not blood pressure (BP).
  • Offspring of hypertensive parents exhibit reduced BRS, potentially increasing hypertension and kidney dysfunction risk.
  • Familial cardiovascular and lifestyle risks are critical factors in pediatric cardiovascular health.

Purpose of the Study:

  • To investigate the relationships between BRS, kidney function, and familial risk factors in prepubescent boys.
  • To explore these associations across varying blood pressure (BP) levels in young boys.

Main Methods:

  • Study included 81 prepubescent boys (aged 6-8 years), stratified by normal or elevated BP.
  • Assessed anthropometrics (BMI, BMIz), cardiovascular measures (BP, BRS via Finometer), and kidney function (uACR).
  • Collected demographic data on familial cardiovascular and lifestyle risk via questionnaires.

Main Results:

  • No significant differences in BRS or uACR between normal and elevated BP groups.
  • In normal BP boys, inverse association found between BRS and uACR (p=0.009).
  • In elevated BP boys, BRS associated with familial risk (p=0.002), BMIz (p=0.020), and Black ethnicity (p=0.024), but not uACR.

Conclusions:

  • A cardioprotective relationship exists between BRS and kidney function in boys with normal BP.
  • In boys with elevated BP, increased cardiovascular disease risk is linked to lower BRS, influenced by familial risk, adiposity, and Black ethnicity.

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