4.7 Article

Alcohol intake and cardiovascular risk factors: A Mendelian randomisation study

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SCIENTIFIC REPORTS
卷 5, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep18422

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资金

  1. Korean Genome Analysis Project [4845-301]
  2. Korean Genome and Epidemiology Study [4851-302]
  3. Korea Biobank Project [4851-307, KBP-2014-062]
  4. Korea Center for Disease Control and Prevention, Republic of Korea
  5. BAsic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and future Planning [2015R1A2A1A15054758]
  6. Medical Research Council Integrative Epidemiology Unit
  7. Oak Foundation
  8. National Research Foundation of Korea [2015R1A2A1A15054758] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  9. MRC [MC_UU_12013/1, MC_UU_12013/2] Funding Source: UKRI
  10. Medical Research Council [MC_UU_12013/1, MC_UU_12013/2] Funding Source: researchfish

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Mendelian randomisation studies from Asia suggest detrimental influences of alcohol on cardiovascular risk factors, but such associations are observed mainly in men. The absence of associations of genetic variants (e.g. rs671 in ALDH2) with such risk factors in women - who drank little in these populations -provides evidence that the observations are not due to genetic pleiotropy. Here, we present a Mendelian randomisation study in a South Korean population (3,365 men and 3,787 women) that 1) provides robust evidence that alcohol consumption adversely affects several cardiovascular disease risk factors, including blood pressure, waist to hip ratio, fasting blood glucose and triglyceride levels. Alcohol also increases HDL cholesterol and lowers LDL cholesterol. Our study also 2) replicates sex differences in associations which suggests pleiotropy does not underlie the associations, 3) provides further evidence that association is not due to pleiotropy by showing null effects in male non-drinkers, and 4) illustrates a way to measure population-level association where alcohol intake is stratified by sex. In conclusion, population-level instrumental variable estimation (utilizing interaction of rs671 in ALDH2 and sex as an instrument) strengthens causal inference regarding the largely adverse influence of alcohol intake on cardiovascular health in an Asian population.

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