The effects of repeated binge drinking on arterial stiffness and urinary norepinephrine levels in young adults.

OBJECTIVES: The aim of this study was to investigate the effect of repeated binge drinking and moderate alcohol consumption in young adults on arterial stiffness and sympathetic activity. METHODS: We enrolled 49 healthy young adults, free of cardiovascular diseases (25 men; age: 23.5 ±â€Š0.4 years; BMI: 23.4 ±â€Š0.4 kg/m; mean ±â€ŠS.E). Individuals included were those with a history of repeated binge drinking (>2 years duration; n = 20), drank at moderate levels (MODs, >5 years duration; n = 16) and abstained from alcohol (last 2-3 years; n = 13). Arterial stiffness was assessed using carotid to femoral pulse wave velocity (cfPWV) and sympathetic activity was assessed using 24-h urinary norepinephrine levels. Also measured was aortic SBP and augmentation index (AIx), a measure of wave reflection. RESULTS: Binge drinkers and MODs had higher cfPWV than alcohol abstainers (0.6 and 0.5 m/s, respectively; P ≤ 0.04). In addition, binge drinkers had higher urinary norepinephrine levels than MODs and alcohol abstainers (P < 0.05). Higher cfPWV were correlated with higher norepinephrine levels (r = 0.35. P = 0.02). Aortic SBP (P = 0.2) and AIx (P = 0.96) were similar among binge drinkers, MODs and alcohol abstainers. CONCLUSION: Our findings suggest that repeated exposure to alcohol, regardless of drinking pattern, may increase aortic arterial stiffness in healthy young adults. In addition, sympathetic activation, reflected by increased 24-h urinary norepinephrine levels, may contribute to alcohol-induced arterial stiffening in young adults.

Urinary isoxanthohumol is a specific and accurate biomarker of beer consumption.

Biomarkers of food consumption are a powerful tool to obtain more objective measurements of dietary exposure and to monitor compliance in clinical trials. In this study, we evaluated the effectiveness of urinary isoxanthohumol (IX) excretion as an accurate biomarker of beer consumption. A dose-response clinical trial, a randomized, crossover clinical trial, and a cohort study were performed. In the dose-response trial, 41 young volunteers (males and females, aged 28 ± 3 y) consumed different doses of beer at night and a spot urine sample was collected the following morning. In the clinical trial, 33 males with high cardiovascular risk (aged 61 ± 7 y) randomly were administered 30 g of ethanol/d as gin or beer, or an equivalent amount of polyphenols as nonalcoholic beer for 4 wk. Additionally, a subsample of 46 volunteers from the PREDIMED (Prevenciόn con Dieta Mediterránea) study (males and females, aged 63 ± 5 y) was also evaluated. Prenylflavonoids were quantified in urine samples by liquid chromatography coupled to mass spectrometry. IX urinary recovery increased linearly with the size of the beer dose in male volunteers. A significant increase in IX excretion (4.0 ± 1.6 µg/g creatinine) was found after consumption of beer and nonalcoholic beer for 4 wk (P < 0.001). Receiver operating characteristic curves showed that IX is able to discriminate between beer consumers and abstainers with a sensitivity of 67% and specificity of 100% (positive predictive value = 70%, negative predictive value = 100% in real-life conditions). IX in urine samples was found to be a specific and accurate biomarker of beer consumption and may be a powerful tool in epidemiologic studies.

The effects of binge drinking behaviour on recovery and performance after a rugby match.

OBJECTIVES: This study compared the effects of "normal" post-game behaviour with recommended behaviour on physical performance in the days after a rugby union game. Additionally, the habitual drinking habits of rugby players were identified. DESIGN: Prospective cohort study. METHODS: After a rugby game, 26 players were split by team into a customary behaviour group (CB), who carried out their usual post-game behaviour, or recommended behaviour group (RB), whose diet and activity was controlled in the hours after the game. Counter movement jump, lower-body strength, repeated sprint ability, CK and hydration status were measured prior to and in the days after the game. Twenty-four hour behaviour recall questionnaires where completed throughout the trial period. The Alcohol Use Disorders Identification Test (AUDIT) was also administered to participants. RESULTS: Compared to baseline values, large volumes of alcohol (p<0.01) and a loss in sleep (p<0.001) was reported by the CB group in the hours after the game. Measures of performance and hydration status were unchanged over time and no difference was evident between groups (all p<0.05). Total AUDIT scores for all participants were 17.7 ± 5. CK was elevated in the days following the game (p<0.001). CONCLUSIONS: Physical performance was not affected by participation in a game of senior club rugby, irrespective of post-game behaviour and possible muscle damage. AUDIT scores indicate that club rugby players may be at risk of serious alcohol related harm, with post-game binge drinking likely to be a major contributor.