Highlights
- •Omega-3 fatty acids and heart rate recovery are important for cardiovascular health.
- •We observed a significant association between the two in 13,912 healthy adults.
- •This association was independent of fitness level and was steeper in women.
- •These findings suggest a potential cardioprotective mechanism for n-3 PUFA.
Abstract
Background
Previous studies have suggested that omega-3 polyunsaturated fatty acids (n-3 PUFA)
can favorably influence cardiac autonomic tone. However, data regarding n-3 PUFA status
and heart rate recovery (HRR) in healthy adults are sparse.
Purpose
To examine the association between n-3 PUFA status and HRR.
Methods
Participants included 13,912 patients who underwent a comprehensive examination at
the Cooper Clinic, Dallas TX. Fitness was determined from a maximal exercise test.
HRR was calculated by subtracting the heart rate at 1, 3, and 5 min of an active recovery
period from the maximal heart rate. Participants were categorized as having a low
(<4%), normal (4–8%) or optimal (>8%) Omega-3 Index (O3I) (i.e., erythrocyte levels
of eicosapentaenoic and docosahexaenoic acids). Multiple linear regression was used
to model the association between O3I and HRR adjusting for age, maximal METs, body
mass index, and smoking by sex.
Results
Higher categories of O3I were associated with greater HRR at 1 min (men: 23.7, 23.9,
24.6 beats/min; women: 23.9, 24.6, 25.9 and 3 min (men: 52.4, 52.9, 53.6 beats/min;
women: 51.9, 53.4, 54.6), p trend <0.01 for all. Corresponding HRR at 5 min were (men:
60.0, 60.2, 60.7 beats/min, p trend=0.09; women: 59.4, 60.8, 61.6, p trend <0.001).
The HRR gradients across O3I categories were steeper in women than men at 1, 3, and
5 min (p<0.03 for all sex x O3I category interactions with HRR).
Conclusions
A direct relationship between HRR and O3I values was observed in both men and women,
with a steeper gradient in women. These findings suggest a potential cardioprotective
mechanism for n-3 PUFA.
Keywords
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Article info
Publication history
Published online: November 13, 2020
Accepted:
November 7,
2020
Received in revised form:
October 7,
2020
Received:
July 30,
2020
Identification
Copyright
© 2020 Elsevier Ltd. All rights reserved.