TY - JOUR
T1 - Alcohol consumption and microvascular dysfunction
T2 - a J-shaped association: The Maastricht Study
AU - van der Heide, Frank C. T.
AU - Eussen, Simone J. P. M.
AU - Houben, Alfons J. H. M.
AU - Henry, Ronald M. A.
AU - Kroon, Abraham A.
AU - van der Kallen, Carla J. H.
AU - Dagnelie, Pieter C.
AU - van Dongen, Martien C. J. M.
AU - Berendschot, Tos T. J. M.
AU - Schouten, Jan S. A. G.
AU - Webers, Carroll A. B.
AU - van Greevenbroek, Marleen M. J.
AU - Wesselius, Anke
AU - Schalkwijk, Casper G.
AU - Koster, Annemarie
AU - Jansen, Jacobus F. A.
AU - Backes, Walter H.
AU - Beulens, Joline W. J.
AU - Stehouwer, Coen D. A.
N1 - Funding Information:
The authors would like to acknowledge ZIO foundation (Vereniging Regionale HuisartsenZorg Heuvelland) for their contribution to The Maastricht Study. The researchers are indebted to the participants for their willingness to participate in the study.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12/1
Y1 - 2023/12/1
N2 - Background: Microvascular dysfunction (MVD) is an important contributor to major clinical disease such as stroke, dementia, depression, retinopathy, and chronic kidney disease. Alcohol consumption may be a determinant of MVD. Objective: Main objectives were (1) to study whether alcohol consumption was associated with MVD as assessed in the brain, retina, skin, kidney and in the blood; and (2) to investigate whether associations differed by history of cardiovascular disease or sex. Design: We used cross-sectional data from The Maastricht Study (N = 3,120 participants, 50.9% men, mean age 60 years, and 27.5% with type 2 diabetes [the latter oversampled by design]). We used regression analyses to study the association between total alcohol (per unit and in the categories, i.e. none, light, moderate, high) and MVD, where all measures of MVD were combined into a total MVD composite score (expressed in SD). We adjusted all associations for potential confounders; and tested for interaction by sex, and history of cardiovascular disease. Additionally we tested for interaction with glucose metabolism status. Results: The association between total alcohol consumption and MVD was non-linear, i.e. J-shaped. Moderate versus light total alcohol consumption was significantly associated with less MVD, after full adjustment (beta [95% confidence interval], -0.10 [-0.19; -0.01]). The shape of the curve differed with sex (P
interaction = 0.03), history of cardiovascular disease (P
interaction < 0.001), and glucose metabolism status (P
interaction = 0.02). Conclusions: The present cross-sectional, population-based study found evidence that alcohol consumption may have an effect on MVD. Hence, although increasing alcohol consumption cannot be recommended as a policy, this study suggests that prevention of MVD may be possible through dietary interventions.
AB - Background: Microvascular dysfunction (MVD) is an important contributor to major clinical disease such as stroke, dementia, depression, retinopathy, and chronic kidney disease. Alcohol consumption may be a determinant of MVD. Objective: Main objectives were (1) to study whether alcohol consumption was associated with MVD as assessed in the brain, retina, skin, kidney and in the blood; and (2) to investigate whether associations differed by history of cardiovascular disease or sex. Design: We used cross-sectional data from The Maastricht Study (N = 3,120 participants, 50.9% men, mean age 60 years, and 27.5% with type 2 diabetes [the latter oversampled by design]). We used regression analyses to study the association between total alcohol (per unit and in the categories, i.e. none, light, moderate, high) and MVD, where all measures of MVD were combined into a total MVD composite score (expressed in SD). We adjusted all associations for potential confounders; and tested for interaction by sex, and history of cardiovascular disease. Additionally we tested for interaction with glucose metabolism status. Results: The association between total alcohol consumption and MVD was non-linear, i.e. J-shaped. Moderate versus light total alcohol consumption was significantly associated with less MVD, after full adjustment (beta [95% confidence interval], -0.10 [-0.19; -0.01]). The shape of the curve differed with sex (P
interaction = 0.03), history of cardiovascular disease (P
interaction < 0.001), and glucose metabolism status (P
interaction = 0.02). Conclusions: The present cross-sectional, population-based study found evidence that alcohol consumption may have an effect on MVD. Hence, although increasing alcohol consumption cannot be recommended as a policy, this study suggests that prevention of MVD may be possible through dietary interventions.
KW - Albuminuria
KW - Alcohol
KW - Beer
KW - Cardiovascular risk factor
KW - Cerebral small vessel disease
KW - Dyslipidemia
KW - Endothelial cell dysfunction
KW - Ethanol
KW - Flicker light-induced increase in retinal microvascular diameter
KW - Heat-induced skin hyperemia
KW - History of cardiovascular disease
KW - Hypertension
KW - Microvascular dysfunction
KW - Microvasculature
KW - Plasma biomarkers
KW - Retinal microvascular diameters
KW - Smoking
KW - Spirits
KW - Type 2 diabetes
KW - Wine
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85151044018&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36964536
U2 - 10.1186/s12933-023-01783-x
DO - 10.1186/s12933-023-01783-x
M3 - Article
C2 - 36964536
SN - 1475-2840
VL - 22
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 67
ER -