Key result
Higher alcohol intake is linked to lower peripheral arterial stiffness in young men but not women.
Why the study?
The relationship between alcohol consumption and vascular function remains controversial, prompting investigation into how alcohol intake and beverage type relate to arterial stiffness in young adults by sex.
Does alcohol consumption affect peripheral arterial stiffness in young adults?
Cross-Sectional (n=501)
Does alcohol consumption affect peripheral arterial stiffness in young adults?
Effect estimate: β = -0.002 (95% CI -0.004 to -0.001)
Alcohol consumption in young adults is associated with sex-specific differences in peripheral arterial stiffness, though the cross-sectional design precludes causal inferences.
Alcohol intake modestly linked to lower peripheral stiffness in young men only; cross-sectional data leave open causality and preclude practice changes.
Background: The relationship between alcohol consumption and vascular function remains controversial. This study aimed to examine the association between total alcohol intake, type of alcoholic beverage, and arterial stiffness across different vascular territories in young Spanish adults, with special attention to sex-specific patterns. Methods: A descriptive cross-sectional study was conducted. Using consecutive non-probability sampling, 501 participants (222 men and 279 women) aged 18–34 years, were recruited from the urban population of Salamanca. Alcohol consumption was assessed using a standardized questionnaire and quantified in grams per week overall and by different types of drinks (wine, beer or spirits drinks). Arterial stiffness was evaluated using pulse pressure (PP), carotid–femoral pulse wave velocity (cf-PWV), brachial–ankle pulse wave velocity (ba-PWV), cardio–ankle vascular index (CAVI), and central augmentation index corrected to a heart rate of 75 beats per minute (CAIx75). Results: The mean age of the sample was 26.58 ± 4.40 years, and was significantly higher in men than in women (27.04 ± 4.41 vs. 26.22 ± 4.37 years; p = 0.040). The mean values for vascular function parameters were as follows: PP 42.86 ± 8.45 mmHg, cf-PWV 5.60 ± 1.29 m/s, ba-PWV 38 10.80 ± 1.01 m/s, CAVI 6.13 ± 0.75, and CAIx75 7.71 ± 19.74. Participants reporting alcohol consumption showed lower ba-PWV values compared with abstainers, while no consistent associations were observed for central arterial stiffness parameters. In sex-stratified analyses, higher total alcohol intake (β = −0.002, 95% CI: −0.004–−0.001), as well as beer (β = −0.004, 95% CI: −0.007–−0.001), and spirit consumption (β = −0.004, 95% CI: −0.006–−0.001), were inversely associated with ba-PWV exclusively in men. In women, spirit consumption was positively associated with CAIx75 (β = 0.044, 95% CI: 0.006–0.081). The magnitude of the observed differences in ba-PWV was modest and occurred in a predominantly low-risk population. Conclusions: In young adults, alcohol consumption was associated with differences in peripheral arterial stiffness, primarily reflected by ba-PWV, with clear sex-specific patterns. These findings do not support a causal or protective effect of alcohol consumption and should be interpreted cautiously due to the cross-sectional design of the study. The results highlight the importance of considering sex and vascular territory when evaluating early markers of vascular aging in young populations. Clinical trial registration: [ClinicalTrials.gov], identifier [NCT05819840].
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Vicente-Prieto et al. (2026) conducted a cross-sectional in Healthy young adults (n=501). Alcohol consumption vs. Abstainers was evaluated on Brachial-ankle pulse wave velocity (ba-PWV) associated with total alcohol intake in men (β = -0.002, 95% CI -0.004 to -0.001). In young men, higher total alcohol intake was inversely associated with peripheral arterial stiffness measured by ba-PWV (β = -0.002; 95% CI -0.004 to -0.001), but this was not observed in women.
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