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Randomized Controlled Trial
. 2016 Apr;29(4):476-83.
doi: 10.1093/ajh/hpv126. Epub 2015 Aug 1.

Differential Effect of Initiating Moderate Red Wine Consumption on 24-h Blood Pressure by Alcohol Dehydrogenase Genotypes: Randomized Trial in Type 2 Diabetes

Affiliations
Randomized Controlled Trial

Differential Effect of Initiating Moderate Red Wine Consumption on 24-h Blood Pressure by Alcohol Dehydrogenase Genotypes: Randomized Trial in Type 2 Diabetes

Yftach Gepner et al. Am J Hypertens. 2016 Apr.

Abstract

Aims: Observational studies report inconsistent associations between moderate alcohol intake and blood pressure (BP). In a sub-study of a larger randomized controlled trial, we assessed the effect of initiating moderate red wine consumption on 24-h BP recordings and the effect of a common genetic variant of alcohol dehydrogenases (ADH) among patients with type 2 diabetes.

Methods: Fifty-four type 2 diabetes, alcohol abstainers were randomized to consume 150 ml/dinner dry red wine or mineral water. Both groups were guided to adhere to a Mediterranean diet, without caloric restriction. We measured 24-h ambulatory BP monitoring (ABPM) at baseline and after 6 months.

Results: Participants (age = 57 years; 85% men; mean 24-h BP = 129/77 mm Hg) had 92% 6-month retention. After 6 months of intervention, the average 24-h BP did not differ between the wine and water groups. A transient decrease in BP was observed in the red wine group at midnight (3-4 hours after wine intake: systolic BP: red wine = -10.6mm Hg vs. mineral water = +2.3 mm Hg; P = 0.031) and the following morning at 7-9 am (red wine: -6.2mm Hg vs. mineral water: +5.6mm Hg; P = 0.014). In a second post hoc sub-analysis among the red wine consumers, individuals who were homozygous for the gene encoding ADH1B*2 variant (Arg48His; rs1229984, TT, fast ethanol metabolizers), exhibited a reduction in mean 24-h systolic BP (-8.0mm Hg vs. +3.7 mm Hg; P = 0.002) and pulse pressure (-3.8 mm Hg vs. +1.2 mm Hg; P = 0.032) compared to heterozygotes and those homozygous for the ADH1B*1 variant (CC, slow metabolizers).

Conclusions: Initiating moderate red wine consumption at dinner among type 2 diabetes patients does not have a discernable effect on mean 24-h BP. Yet, a modest temporal BP reduction could be documented, and a more pronounced BP-lowering effect is suggested among fast ethanol metabolizers.

Clinical trials registration: ClinicalTrials.gov Identifier: NCT00784433.

Keywords: ambulatory measurement; blood pressure; hypertension; moderate alcohol; pulse pressure; randomized controlled trial; type 2 diabetes..

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Figures

Figure 1.
Figure 1.
Baseline average systolic and diastolic ambulatory blood pressure monitoring over 24 hours of the red wine and mineral water groups. Red wine (n = 27), mineral water (n = 27). Black (wine group) and white (water group) points present means of ABPM in each hour.
Figure 2.
Figure 2.
The effect of 6-month wine intervention on changes of systolic BP (a), diastolic BP (b) and pulse pressure (c) from baseline; results from 24-h ambulatory blood pressure monitoring. Black (wine group, n = 24) and white (water group, n = 26) points present delta of ABPM in each hour after 6 months.
Figure 3.
Figure 3.
The effect of ethanol metabolism genotypes on mean 24-h systolic blood pressure and pulse pressure; changes over 6 months of intervention among the wine group. Slow (black bar; n = 12) and fast (white bar; n = 9) ethanol metabolizers.

References

    1. Guidelines Subcommittee. World Health Organization–International Society of Hypertension Guidelines for the Management of Hypertension. J Hypertens 1999; 17:151–183 - PubMed
    1. Ronksley PE, Brien SE, Turner BJ, Mukamal KJ, Ghali WA. Association of alcohol consumption with selected cardiovascular disease outcomes: a systematic review and meta-analysis. BMJ 2011; 342:d671. - PMC - PubMed
    1. Tolstrup J, Jensen MK, Tjønneland A, Overvad K, Mukamal KJ, Grønbaek M. Prospective study of alcohol drinking patterns and coronary heart disease in women and men. BMJ 2006; 332:1244–1248. - PMC - PubMed
    1. Tanasescu M, Hu FB, Willett WC, Stampfer MJ, Rimm EB. Alcohol consumption and risk of coronary heart disease among men with type 2 diabetes mellitus. J Am Coll Cardiol 2001; 38:1836–1842. - PubMed
    1. Solomon CG, Hu FB, Stampfer MJ, Colditz GA, Speizer FE, Rimm EB, Willett WC, Manson JE. Moderate alcohol consumption and risk of coronary heart disease among women with type 2 diabetes mellitus. Circulation 2000; 102:494–499. - PubMed

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