Heart rate variability in myotonic dystrophy type 1 patients

Arq Bras Cardiol. 2012 Apr;98(4):353-60. doi: 10.1590/s0066-782x2012005000021. Epub 2012 Mar 8.
[Article in English, Portuguese]

Abstract

Background: Cardiac involvement is common in myotonic dystrophy (MD) patients. Heart rate variability (HRV) is a simple and reliable technique that can be useful for studying the influence of the autonomic nervous system on the heart.

Objective: Study heart rate variability in patients with type 1 MD.

Methods: We studied HRV during 5-minute recordings in MD patients and in a healthy control group. We analyzed frequency domains (LF and HF) in normalized units (nu) and sympathovagal balance, in the sitting and supine position.

Results: Seventeen patients (10 men and 7 women) and seventeen matched healthy individuals (10 men and 7 women) were studied. Sympathetic and parasympathetic modulations of the heart increased in male MD patients from supine to sitting position in 19% of LFnu and the LF/HF ratio rose by 42.3%. In the sitting position, male MD patients exhibited significantly higher sympathovagal balances in 50.9% compared to healthy control individuals. HRV was influenced by both gender and disease. Gender influenced LFnu in the supine position while the LF/HF ratio and HFnu were affected in both positions. Post hoc analyses showed that gender significantly impacts MD patients and healthy individuals in different ways (p < 0.01). The low frequency domain in the sitting position (LFnu) was significantly influenced by the disease.

Conclusion: The results of this study suggest that the sympathetic drive in middle-aged male MD patients who are not severely impaired and present moderate disease duration seems to be greater than in healthy matched individuals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analysis of Variance
  • Autonomic Nervous System / physiology
  • Body Mass Index
  • Case-Control Studies
  • Female
  • Heart Rate / physiology*
  • Humans
  • Male
  • Middle Aged
  • Myotonic Dystrophy / physiopathology*
  • Sex Factors
  • Time Factors