Total power and high frequency components of heart rate variability and risk factors for atherosclerosis

Nanna Hurwitz Eller1

  • 1Clinic of Occupational Medicine, Hilleroed Hospital, Helsevej 2-4, DK-3400 Hilleroed, Denmark. nael@fa.dk

Insights

Low heart rate variability (HRV) is linked to diabetes and heart disease. This study found waist-hip ratio and HbA1c negatively impact HRV in both sexes, with stress hormones affecting men more significantly. Gender differences in HRV pathophysiology are suggested.

Area of Science:

  • Cardiology
  • Endocrinology
  • Metabolic Syndrome

Background:

  • Low heart rate variability (HRV) is a marker for diabetic neuropathy and ischemic heart disease (IHD).
  • Diabetes precedes HRV changes, which in turn precede atherosclerosis and IHD development.
  • Understanding the association between IHD risk factors and HRV is crucial for early intervention.

Purpose of the Study:

  • To analyze the association between physiological risk factors for IHD and HRV.
  • To investigate potential gender-specific differences in these associations.

Main Methods:

  • Prospective study analyzing data from 1998 and 2002.
  • Included 74 participants (50 women, 24 men) in an HRV sub-study.
  • HRV measured during a clinical stress test and sleep; analyzed using GLM repeated measures.
  • Risk factors included BMI, waist-hip ratio, blood pressure, fibrinogen, cholesterol, HbA1c, and stress hormones (catecholamines, cortisol).

Main Results:

  • In women, waist-hip ratio and HbA1c were negatively associated with total power (TP) and high-frequency variability (HF).
  • Stress hormones showed no significant association with HRV in women.
  • In men, waist-hip ratio, HbA1c, fibrinogen, cortisol, and noradrenaline were negatively associated with TP and HF.

Conclusions:

  • Significant gender differences exist in the associations between IHD risk factors and HRV.
  • Waist-hip ratio and HbA1c negatively impact HRV in both genders.
  • Stress hormones are associated with reduced HRV in men, but not in women, suggesting distinct pathophysiological pathways for IHD between sexes.
Abstract

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