Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure

被引:3
作者
Jiang, Xiyun [1 ]
Anasanti, Mila D. [2 ]
Drenos, Fotios [1 ]
Blakemore, Alexandra, I [1 ,3 ]
Pazoki, Raha [1 ,4 ]
机构
[1] Brunel Univ London, Coll Hlth Med & Life Sci, Dept Life Sci, Div Biosci, London UB8 3PH, England
[2] Nusa Mandiri Univ, Fac Informat Technol, Jakarta 10450, Indonesia
[3] Imperial Coll London, Fac Med, Dept Metab Digest & Reprod, London W12 7TA, England
[4] Imperial Coll London, Sch Publ Hlth, Dept Epidemiol & Biostat, London W12 7TA, England
基金
英国医学研究理事会;
关键词
genetics of alcohol; urinary sodium; cardiovascular traits; MENDELIAN RANDOMIZATION; SALT INTAKE; INSTRUMENTS; BIAS; CONSUMPTION; ASSOCIATION; REGRESSION; REDUCTION;
D O I
10.3390/healthcare10071296
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Alcohol consumption is linked to urinary sodium excretion and both of these traits are linked to hypertension and cardiovascular diseases (CVDs). The interplay between alcohol consumption and sodium on hypertension, and cardiovascular diseases (CVDs) is not well-described. Here, we used genetically predicted alcohol consumption and explored the relationships between alcohol consumption, urinary sodium, hypertension, and CVDs. Methods: We performed a comparative analysis among 295,189 participants from the prospective cohort of the UK Biobank (baseline data collected between 2006 and 2010). We created a genetic risk score (GRS) using 105 published genetic variants in Europeans that were associated with alcohol consumption. We explored the relationships between GRS, alcohol consumption, urinary sodium, blood pressure traits, and incident CVD. We used linear and logistic regression and Cox proportional hazards (PH) models and Mendelian randomization in our analysis. Results: The median follow-up time for composite CVD and stroke were 6.1 years and 7.1 years respectively. Our analyses showed that high alcohol consumption is linked to low urinary sodium excretion. Our results showed that high alcohol GRS was associated with high blood pressure and higher risk of stroke and supported an interaction effect between alcohol GRS and urinary sodium on stage 2 hypertension (P-interaction = 0.03) and CVD (P-interaction = 0.03), i.e., in the presence of high urinary sodium excretion, the effect of alcohol GRS on blood pressure may be enhanced. Conclusions: Our results show that urinary sodium excretion may offset the risk posed by genetic risk of alcohol consumption.
引用
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页数:13
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