This study was designed to examine the association of heart rate variabilit
y (HRV) with blood glucose levels in a large community-based population. Pr
evious reports have shown HRV to be reduced in diabetics, suggesting the pr
esence of abnormalities in neural regulatory mechanisms. There is scant inf
ormation about HRV across the spectrum of blood glucose levels in a populat
ion-based cohort. One thousand nine hundred nineteen men and women from the
Framingham Offspring Study, who underwent ambulatory electrocardiographic
recordings at a routine examination, were eligible. HRV variables included
the SD of normal RR intervals (SDNN), high-frequency (HF, 0.15 to 0.40 Hz)
and low-frequency (LF, 0.04 to 0.15 Hz) power, and LF/HF ratio. Pasting pla
sma glucose levels were used to classify subjects as normal (<110 mg/dl; n
= 1,779), as having impaired fasting glucose levels (110 to 125 mg/dl; n =
56), and as having diabetes mellitus (DM greater than or equal to 126 mg/dl
or receiving therapy; n = 84). SDNN, LF and HF power, and LF/HF ratio were
inversely related to plasma glucose levels (p <0.0001). SDNN and LF and HF
powers were reduced in DM subjects (4.28 +/- 0.03, 6.03 +/- 0.08, and 4.95
+/- 0.09) and in subjects with impaired fasting glucose levels (4.37 +/- 0
.04, 6.26 +/- 0.10, and 5.06 +/- 0.11) compared with those with normal fast
ing glucose (4.51 +/- 0.01, 6.77 +/- 0.02, and 5.55 +/- 0.02, all p <0.005)
, respectively. After adjusting for covariates (age, sex, heart rate, body
mass index, antihypertensive and cardiac medications, systolic and diastoli
c blood pressures, smoking, and alcohol and coffee consumption), LF power a
nd LF/HF ratio were lower in DM subjects than in those with normal fasting
glucose (p <0.005). HRV is inversely associated with plasma glucose levels
and is reduced in diabetics as well as in subjects with impaired fasting gl
ucose levels. Additional research is needed to determine if low HRV contrib
utes to the increased cardiovascular morbidity and mortality described in s
ubjects with hyperglycemia. (C) 2000 by Excerpta Medica, Inc.