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Alcohol Intake and Blood Pressure: A Systematic Review Implementing a Mendelian Randomization Approach

Author

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  • Lina Chen
  • George Davey Smith
  • Roger M Harbord
  • Sarah J Lewis

Abstract

Background: Alcohol has been reported to be a common and modifiable risk factor for hypertension. However, observational studies are subject to confounding by other behavioural and sociodemographic factors, while clinical trials are difficult to implement and have limited follow-up time. Mendelian randomization can provide robust evidence on the nature of this association by use of a common polymorphism in aldehyde dehydrogenase 2 (ALDH2) as a surrogate for measuring alcohol consumption. ALDH2 encodes a major enzyme involved in alcohol metabolism. Individuals homozygous for the null variant (*2*2) experience adverse symptoms when drinking alcohol and consequently drink considerably less alcohol than wild-type homozygotes (*1*1) or heterozygotes. We hypothesise that this polymorphism may influence the risk of hypertension by affecting alcohol drinking behaviour. Methods and Findings: We carried out fixed effect meta-analyses of the ALDH2 genotype with blood pressure (five studies, n = 7,658) and hypertension (three studies, n = 4,219) using studies identified via systematic review. In males, we obtained an overall odds ratio of 2.42 (95% confidence interval [CI] 1.66–3.55, p = 4.8 × 10−6) for hypertension comparing *1*1 with *2*2 homozygotes and an odds ratio of 1.72 (95% CI 1.17–2.52, p = 0.006) comparing heterozygotes (surrogate for moderate drinkers) with *2*2 homozygotes. Systolic blood pressure was 7.44 mmHg (95% CI 5.39–9.49, p = 1.1 × 10−12) greater among *1*1 than among *2*2 homozygotes, and 4.24 mmHg (95% CI 2.18–6.31, p = 0.00005) greater among heterozygotes than among *2*2 homozygotes. Conclusions: These findings support the hypothesis that alcohol intake has a marked effect on blood pressure and the risk of hypertension. Using a mendelian randomization approach Sarah Lewis and colleagues find strong support for the hypothesis that alcohol intake has a marked effect on blood pressure and the risk of hypertension. Background.: High blood pressure (hypertension) is a common medical condition that affects nearly a third of US and UK adults. Hypertension has no symptoms but can lead to heart attacks or strokes. It is diagnosed by measuring blood pressure—the force that blood moving around the body exerts on the inside of large blood vessels. Blood pressure is highest when the heart is pumping out blood (systolic pressure) and lowest when it is filling up with blood (diastolic pressure). Normal blood pressure is defined as a systolic pressure of less than 130 millimeters of mercury (mmHg) and a diastolic pressure of less than 85 mmHg (a blood pressure of 130/85). A reading of more than 140/90 indicates hypertension. Many factors affect blood pressure, but overweight people and individuals who eat too much salty or fatty foods are at high risk of developing hypertension. Mild hypertension can often be corrected by lifestyle changes, but many people also take antihypertensive drugs to reduce their blood pressure. Why Was This Study Done?: Another modifiable lifestyle factor thought to affect blood pressure is alcohol intake. Observational studies that ask people about their drinking habits and measure their blood pressure suggest that alcohol intake correlates with blood pressure, but they cannot prove a causal link because of “confounding”—other risk factors associated with alcohol drinking, such as diet, might also affect the study participant's blood pressures. A trial that randomly assigns people to different alcohol intakes could provide this proof of causality, but such a trial is impractical. In this study, therefore, the researchers have used “Mendelian randomization” to investigate whether alcohol intake affects blood pressure. An inactive variant of aldehyde dehydrogenase 2 (ALDH2; the enzyme that removes alcohol from the body) has been identified. People who inherit the variant form of this gene from both parents have an ALDH2 *2*2 genotype (genetic makeup) and become flushed and nauseated after drinking. Consequently, they drink less than people with a *1*2 genotype and much less than those with a *1*1 genotype. Because inheritance of these genetic variants does not affect lifestyle factors other than alcohol intake, an association between ALDH2 genotypes and blood pressure would indicate that alcohol intake has an effect on blood pressure without any confounding. What Did the Researchers Do and Find?: The researchers identified ten published studies (mainly done in Japan where the ALDH2 gene variant is common) on associations between ALDH2 genotype and blood pressure or hypertension using a detailed search protocol (a “systematic review”). A meta-analysis (a statistical method for combining the results of independent studies) of the studies that had investigated the association between ALDH2 genotype and hypertension showed that men with the *1*1 genotype (highest alcohol intake) and those with the *1*2 genotype (intermediate alcohol intake) were 2.42 and 1.72 times more likely, respectively, to have hypertension than those with the *2*2 genotype (lowest alcohol intake). There was no association between ALDH2 genotype and hypertension among the women in these studies because they drank very little. Systolic and diastolic blood pressures showed a similar relationship to ALDH2 genotype in a second meta-analysis of relevant studies. Finally, the researchers estimated that for men the lifetime effect of drinking 1 g of alcohol a day (one unit of alcohol contains 8 g of alcohol in the UK and 14 g in the US; recommended daily limits in these countries are 3–4 and 1–2 units, respectively) would be an increase in systolic blood pressure of 0.24 mmHg. What Do These Findings Mean?: These findings support the suggestion that alcohol has a marked effect on blood pressure and hypertension. Consequently, some cases of hypertension could be prevented by encouraging people to reduce their daily alcohol intake. Although the Mendelian randomization approach avoids most of the confounding intrinsic to observational studies, it is possible that a gene near ALDH2 that has no effect on alcohol intake affects blood pressure, since genes are often inherited in blocks. Alternatively, ALDH2 could affect blood pressure independent of alcohol intake. The possibility that ALDH2 could effect blood pressure independently of alcohol is intake made unlikely by the fact that no effect of genotype on blood pressure is seen among women who drink very little. Additional large-scale studies are needed to address these possibilities, to confirm the current finding in more people, and to improve the estimates of the effect that alcohol intake has on blood pressure. Additional Information.: Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.0050052.

Suggested Citation

  • Lina Chen & George Davey Smith & Roger M Harbord & Sarah J Lewis, 2008. "Alcohol Intake and Blood Pressure: A Systematic Review Implementing a Mendelian Randomization Approach," PLOS Medicine, Public Library of Science, vol. 5(3), pages 1-11, March.
  • Handle: RePEc:plo:pmed00:0050052
    DOI: 10.1371/journal.pmed.0050052
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    Citations

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    Cited by:

    1. Oksoo Kim & Bo Hye Kim & Hae Ok Jeon, 2012. "Risk factors related to hazardous alcohol consumption among Korean men with hypertension," Nursing & Health Sciences, John Wiley & Sons, vol. 14(2), pages 204-212, June.
    2. Stephanie Hinke Kessler Scholder & George L. Wehby & Sarah Lewis & Luisa Zuccolo, 2014. "Alcohol Exposure In Utero and Child Academic Achievement," Economic Journal, Royal Economic Society, vol. 0(576), pages 634-667, May.
    3. von Hinke Kessler Scholder S, 2009. "Genetic Markers as Instrumental Variables: An Application to Child Fat Mass and Academic Achievement," Health, Econometrics and Data Group (HEDG) Working Papers 09/25, HEDG, c/o Department of Economics, University of York.
    4. Mengying Wang & Wenyong Li & Ren Zhou & Siyue Wang & Hongchen Zheng & Jin Jiang & Shengfeng Wang & Canqing Yu & Wenjing Gao & Jun Lv & Tao Wu & Weihua Cao & Yonghua Hu & Liming Li & John S. Ji, 2020. "The Paradox Association between Smoking and Blood Pressure among Half Million Chinese People," IJERPH, MDPI, vol. 17(8), pages 1-11, April.
    5. Stephanie von Hinke Kessler Scholder & George Davey Smith & Debbie A. Lawlor & Carol Propper & Frank Windmeijer, 2011. "Mendelian randomization: the use of genes in instrumental variable analyses," Health Economics, John Wiley & Sons, Ltd., vol. 20(8), pages 893-896, August.
    6. Dagmar Drogan & Abigail J Sheldrick & Madlen Schütze & Sven Knüppel & Frank Andersohn & Romina di Giuseppe & Bianca Herrmann & Stefan N Willich & Edeltraut Garbe & Manuela M Bergmann & Heiner Boeing &, 2012. "Alcohol Consumption, Genetic Variants in Alcohol Deydrogenases, and Risk of Cardiovascular Diseases: A Prospective Study and Meta-Analysis," PLOS ONE, Public Library of Science, vol. 7(2), pages 1-11, February.
    7. Chenhao Yu & Huigang Liang & Zhiruo Zhang, 2022. "Does Health Insurance Reduce the Alcohol Consumption? Evidence from China Health and Nutrition Survey," Sustainability, MDPI, vol. 14(9), pages 1-10, May.
    8. Golder, Su & McCambridge, Jim, 2021. "Alcohol, cardiovascular disease and industry funding: A co-authorship network analysis of systematic reviews," Social Science & Medicine, Elsevier, vol. 289(C).
    9. Shiu Lun Au Yeung & Chaoqiang Jiang & Kar Keung Cheng & Benjamin J Cowling & Bin Liu & Weisen Zhang & Tai Hing Lam & Gabriel M Leung & C Mary Schooling, 2013. "Moderate Alcohol Use and Cardiovascular Disease from Mendelian Randomization," PLOS ONE, Public Library of Science, vol. 8(7), pages 1-9, July.
    10. Dixon, Padraig & Hollingworth, William & Harrison, Sean & Davies, Neil M. & Davey Smith, George, 2020. "Mendelian Randomization analysis of the causal effect of adiposity on hospital costs," Journal of Health Economics, Elsevier, vol. 70(C).
    11. Yongho Jee & Susan Park & Eunu Yuk & Sung-il Cho, 2021. "Alcohol Consumption and Cigarette Smoking among Young Adults: An Instrumental Variable Analysis Using Alcohol Flushing," IJERPH, MDPI, vol. 18(21), pages 1-9, October.
    12. Yawen Wang & Yuntong Yao & Yun Chen & Jie Zhou & Yanli Wu & Chaowei Fu & Na Wang & Tao Liu & Kelin Xu, 2022. "Association between Drinking Patterns and Incident Hypertension in Southwest China," IJERPH, MDPI, vol. 19(7), pages 1-20, March.
    13. Yinyin Wu & Juntao Ni & Xiao Cai & Fuzhi Lian & Haiyan Ma & Liangwen Xu & Lei Yang, 2017. "Positive association between ALDH2 rs671 polymorphism and essential hypertension: A case-control study and meta-analysis," PLOS ONE, Public Library of Science, vol. 12(5), pages 1-16, May.

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