Key result
Both low- and high-glycemic index breakfasts decreased low-frequency gain, but only high-GI breakfast decreased very-low frequency phase compared to breakfast omission.
Why the study?
Does low- and high-glycemic index breakfast consumption impact dynamic cerebral autoregulation and plasma BDNF compared to breakfast omission in healthy young men?
RCT (n=10)
Randomized crossover
Does low- and high-glycemic index breakfast consumption impact dynamic cerebral autoregulation and plasma BDNF compared to breakfast omission in healthy young men?
Breakfast consumption improves dynamic cerebral autoregulation in the low-frequency range, but high-glycemic index breakfasts may attenuate regulation against slow changes in arterial pressure.
Answers are grounded in this paper and cite their sources.
Breakfast improves low-frequency cerebral autoregulation versus omission in healthy men; extends evidence on glycemic effects to dynamic cerebrovascular control.
We examined the acute impact of both low- and high-glycemic index (GI) breakfasts on plasma brain-derived neurotrophic factor (BDNF) and dynamic cerebral autoregulation (dCA) compared with breakfast omission. Ten healthy men (age 24 ± 1 yr) performed three trials in a randomized crossover order; omission and Low-GI (GI = 40) and High-GI (GI = 71) breakfast conditions. Middle cerebral artery velocity (transcranial Doppler ultrasonography) and arterial pressure (finger photoplethysmography) were continuously measured for 5 min before and 120 min following breakfast consumption to determine dCA using transfer function analysis. After these measurements of dCA, venous blood samples for the assessment of plasma BDNF were obtained. Moreover, blood glucose was measured before breakfast and every 30 min thereafter. The area under the curve of 2 h postprandial blood glucose in the High-GI trial was higher than the Low-GI trial ( P < 0.01). The GI of the breakfast did not affect BDNF. In addition, both very-low (VLF) and low-frequency (LF) transfer function phase or gains were not changed during the omission trial. In contrast, LF gain (High-GI P < 0.05) and normalized gain (Low-GI P < 0.05) were decreased by both GI trials, while a decrease in VLF phase was observed in only the High-GI trial ( P < 0.05). These findings indicate that breakfast consumption augmented dCA in the LF range but High-GI breakfast attenuated cerebral blood flow regulation against slow change (i.e., the VLF range) in arterial pressure. Thus we propose that breakfast and glycemic control may be an important strategy to optimize cerebrovascular health.
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Tsukamoto et al. (2020) conducted an RCT in Healthy (n=10). Low- and high-glycemic index (GI) breakfasts vs. Breakfast omission was evaluated on Plasma brain-derived neurotrophic factor (BDNF) and dynamic cerebral autoregulation (dCA) (p=<0.05). Both low- and high-glycemic index breakfasts decreased low-frequency gain, but only high-GI breakfast decreased very-low frequency phase compared to breakfast omission.
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