To identify reasons for the high incidence rates of stomach cancer in Poland, we conducted a population-based case-control study in Warsaw. Cases were residents aged 21 to 79 years who were newly diagnosed with stomach cancer between March 1, 1994, and April 30, 1997. Controls were randomly selected
Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland
β Scribed by Fang Fang Zhang; Lifang Hou; Mary Beth Terry; Jolanta Lissowska; Alfredo Morabia; Jinbo Chen; Meredith Yeager; Witold Zatonski; Stephen Chanock; Wong-Ho Chow
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- French
- Weight
- 82 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
Genetic variations increasing blood levels of acetaldehyde, the first metabolite of alcohol, refrain their carriers from drinking alcohol but may also put them at increased risk of cancer because of the mutagenic and carcinogenic effect of acetaldehyde. In a populationβbased study of 305 cases and 428 controls in Warsaw, Poland, we evaluated the effect of polymorphisms in alcohol metabolizing genes, including ADH1B (Ex9+5C>T, Ex3+23A>G, Ex3+58A>T and Ex9+77A>G), ADH1C (Ex8β56A>G and Ex6β14G>A) and ALDH2 (Ex1+82A>G), on levels of alcohol drinking and susceptibility of stomach cancer. We found that among control subjects frequency of alcohol drinking varied by alcohol metabolizing genotype. In particular, the weekly consumption of individuals carrying the AA, GA and GG genotypes of ALDH2 Ex1+82A >G polymorphism were 3.75, 2.26 and 1.53 drinks, respectively (p= 0.04). However, none of the assessed polymorphisms in these 3 genes had a measurable effect on stomach cancer risk. When stratified by ALDH2 Ex1+82A>G polymorphism, alcoholβrelated increases in stomach cancer risk were restricted to individuals with the AG/GG genotypes, with a more than 2βfold risk among daily drinkers (OR = 2.63, 95% CI = 1.00β6.88) and 3βfold risk (OR = 3.66, 95% CI = 1.19β11.24) among those with 40 or more drinkβyears. In summary, our results suggested that the ALDH2 Ex1+82 G allele may be functionally deficient in eliminating acetaldehyde and discourage alcohol drinking. Furthermore, heavy drinkers of alcohol who were genetically prone to accumulate acetaldehyde may face an increased risk of stomach cancer. Β© 2007 WileyβLiss, Inc.
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