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Folate, alcohol, ADH1B and ALDH2 and colorectal cancer risk

Bibliographic Data

ID15097018
AuthorsJu Eun Seol (Sookmyung Women's University), Jeongseon Kim (0000-0002-0889-2686, National Cancer Center), Bong-Hwa Lee (Hallym University Sacred Heart Hospital), Dae-Yong Hwang, Dae–Yong Hwang (0000-0001-9082-8431, Konkuk University Medical Center), Jinyoung Jeong (0000-0003-0381-3958, Hallym University), Hun-Jae Lee, Hun Jae Lee (0000-0002-0163-6815, Inha University), Yoon-Ok Ahn, Yoon‐Ok Ahn (Seoul National University), Jung Eun Lee (0000-0003-0917-2872, Seoul National University), Dong-Hyun Kim (0000-0001-6815-3319, Hallym University, corresponding author)
Year2021
Volume24
Issue4
Pages677-684
Publication date2021-03-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenuePublic Health Nutrition (JOURNAL)
Journal identifiersISSN: 1368-9800 • E-ISSN: 1475-2727
PublisherCambridge University Press (CUP) (PUBLISHER)
DOI10.1017/s136898001900452x
PMID32223781
OpenAlexW3013364759
LanguageEN
References cited24

Objective: There is limited evidence on the interaction by alcohol dehydrogenase 2 ( ADH1B ) (rs1229984) and aldehyde dehydrogenase 2 ( ALDH2 ) (rs671) regarding the associations of alcohol and a methyl diet (low folate and high alcohol intake) with cancer risk, partly because of rare polymorphisms in Western populations. Design: In a case–control study, we estimated the ORs and 95 % CIs to evaluate the associations of ADH1B and ALDH2 genotypes with colorectal cancer (CRC) and the joint association between methyl diets and ADH1B and ALDH2 polymorphisms with CRC risk using logistic regression models. Setting: A hospital-based case–control study. Participants: In total, 1001 CRC cases and 899 cancer-free controls admitted to two university hospitals. Results: We found that alcohol intake increased the risk of CRC; OR (95 % CI) was 2·02 (1·41, 2·87) for ≥60 g/d drinkers compared with non-drinkers ( P trend ALDH2 with methyl diets and CRC. We observed a 9·08-fold (95 % CI 1·93, 42·60) higher risk of CRC for low-methyl diets compared with high-methyl diets among individuals with an A allele of ALDH2 , but the association was not apparent among those with ALDH2 GG ( P interaction = 0·02). Conclusions: Our data support the evidence that gene–methyl diet interactions may be involved in CRC risk in East Asian populations, showing that a low-methyl diet increased the risk of CRC among individuals with an A allele of ALDH2

ADH1B · ALDH2 · Allele · Biology · Cancer · Case-control study · Colorectal cancer · Dehydrogenase · Environmental health · Enzyme · Gene · Logistic regression · Odds ratio · Alcohol Consumption and Health Effects · Epigenetics and DNA Methylation · Folate and B Vitamins Research · Medicine · Biochemistry · Genetics · Internal Medicine · Oncology

  • Total Energy Intake

    Walter C Willett, Walter Willett et al.•American Journal of Epidemiology•1986

Citation velocityhistorical
Highly citedNo

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