Mediation analysis unveils a carcinogenic effect of ADH1B rs1229984 through mechanisms other than change in drinking intensity: oesophageal cancer case-control study

Author:

Sugimoto Yukihiro123,Koyanagi Yuriko N43,Kawakatsu Yukino23,Oze Isao23,Taniyama Yukari43,Kasugai Yumiko235,Tanaka Tsutomu6,Abe Tetsuya7,Tajika Masahiro6,Shimizu Yasuhiro7,Ito Hidemi438,Wakai Kenji1,Matsuo Keitaro235

Affiliation:

1. Department of Preventive Medicine, Nagoya University Graduate School of Medicine , Nagoya , Japan

2. Division of Cancer Epidemiology and Prevention , Department of Preventive Medicine, , Nagoya , Japan

3. Aichi Cancer Center Research Institute , Department of Preventive Medicine, , Nagoya , Japan

4. Division of Cancer Information and Control , Department of Preventive Medicine, , Nagoya , Japan

5. Department of Cancer Epidemiology, Nagoya University Graduate School of Medicine , Nagoya , Japan

6. Department of Endoscopy, Aichi Cancer Center Hospital , Nagoya , Japan

7. Department of Gastroenterological Surgery, Aichi Cancer Center Hospital , Nagoya , Japan

8. Department of Descriptive Cancer Epidemiology, Nagoya University Graduate School of Medicine , Nagoya , Japan

Abstract

Abstract Background Ingested alcohol is predominantly oxidized to acetaldehyde by alcohol dehydrogenase 1B (ADH1B), and acetaldehyde is further oxidized to acetate mainly by aldehyde dehydrogenase 2 (ALDH2). Although alcohol consumption is a convincing risk factor for oesophageal cancer, the role of ADH1B rs1229984 (His48Arg), the single-nucleotide polymorphism associated with slow alcohol metabolism, in oesophageal cancer development is unclear. Because this single-nucleotide polymorphism is associated with both increased risk of oesophageal cancer and drinking intensity, its association with oesophageal cancer might operate either through a direct pathway independently of drinking intensity, via an indirect pathway mediated by drinking intensity, or both. Methods To disentangle these different pathways, we applied a mediation analysis to an oesophageal cancer case-control study (600 cases and 865 controls) by defining the ADH1B Arg allele and alcohol consumption as exposure and mediator, respectively, and decomposed the total-effect odds ratio of the ADH1B Arg allele into direct- and indirect-effect odds ratio. Results The ADH1B Arg allele was associated with oesophageal cancer risk through pathways other than change in drinking intensity (direct-effect odds ratio, 2.03; 95% confidence interval, 1.41–2.92), in addition to the indirect pathway mediated by drinking intensity (indirect-effect odds ratio, 1.27; 95% confidence interval, 1.05–1.53). Further analyses by stratifying genotypes of ALDH2 rs671 (Glu504Lys), the functional single-nucleotide polymorphism that strongly attenuates the enzymatic activity, showed significant direct-effect odds ratio within each stratum. Conclusions These results indicate that ADH1B Arg allele contributes to oesophageal cancer risk by slowing alcohol breakdown, in addition to its effect on the amount of alcohol consumed.

Funder

Ministry of Education, Science, Sports, Culture and Technology of Japan Priority Areas of Cancer

Innovative Areas

Japan Society for the Promotion of Science

Ministry of Health, Labour and Welfare of Japan

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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