We examined the association between heart rate variability (HRV) and duration of type 2 diabetes among 155 female and 106 male subjects: mean±SD for duration=49.6±65.6 and 57.3±77.1 months, respectively, p=0.38. Among males, duration of diabetes was independently and inversely associated with vagal-heart rate modulation (high frequency (HF) power, 0.15-0.40 Hz, standardised ß = -0.32, p=0.001; root mean square of successive differences between R-R intervals, ß = -0.26, p=0.006) and total R-R variability (standard deviation of normal R-R intervals, ß = -0.36, p=0.001); but not among females (p≥0.80 for each HRV index). In contrast, HF was inversely associated with age of diabetes diagnosis (ß = -0.16, p=0.04) and 10-year absolute risk for coronary heart disease (ß = -0.16, p=0.04) among female subjects. Longitudinal research is needed to establish whether risk factors for early cardiac autonomic impairment differ among men and women with type 2 diabetes. domain measures are obtained by spectral analysis of recurrent cycles of R-R variation within established frequency bandwidths that correspond to sympathetic, vagal and non-neural modulation of the sinus node cycle length. Among individuals with diabetes, decreased HRV is independently associated with impaired lipid and glucose metabolism, as well as incident coronary heart disease (CHD), myocardial infarction and mortality. 2,9,10 With the exception of one investigation, 11 there is consistent evidence that the duration of type 1 and 2 diabetes is inversely associated with HRV measures of total R-R variability and vagal-heart rate modulation. 4,10,[12][13][14][15][16][17][18] Few studies have investigated sex-based differences in factors that potentially influence HRV impairment among patients with
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