Genetic architecture of alcohol consumption identified by a genotype-stratified GWAS and impact on esophageal cancer risk in Japanese people

An East Asian-specific variant on ( rs671, G>A) is the major genetic determinant of alcohol consumption. We performed an rs671 genotype-stratified genome-wide association study meta-analysis of alcohol consumption in 175,672 Japanese individuals to explore gene-gene interactions with rs671 behind...

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Veröffentlicht in:Science advances 2024-01, Vol.10 (4), p.eade2780
Hauptverfasser: Koyanagi, Yuriko N, Nakatochi, Masahiro, Namba, Shinichi, Oze, Isao, Charvat, Hadrien, Narita, Akira, Kawaguchi, Takahisa, Ikezaki, Hiroaki, Hishida, Asahi, Hara, Megumi, Takezaki, Toshiro, Koyama, Teruhide, Nakamura, Yohko, Suzuki, Sadao, Katsuura-Kamano, Sakurako, Kuriki, Kiyonori, Nakamura, Yasuyuki, Takeuchi, Kenji, Hozawa, Atsushi, Kinoshita, Kengo, Sutoh, Yoichi, Tanno, Kozo, Shimizu, Atsushi, Ito, Hidemi, Kasugai, Yumiko, Kawakatsu, Yukino, Taniyama, Yukari, Tajika, Masahiro, Shimizu, Yasuhiro, Suzuki, Etsuji, Hosono, Yasuyuki, Imoto, Issei, Tabara, Yasuharu, Takahashi, Meiko, Setoh, Kazuya, Matsuda, Koichi, Nakano, Shiori, Goto, Atsushi, Katagiri, Ryoko, Yamaji, Taiki, Sawada, Norie, Tsugane, Shoichiro, Wakai, Kenji, Yamamoto, Masayuki, Sasaki, Makoto, Matsuda, Fumihiko, Okada, Yukinori, Iwasaki, Motoki, Brennan, Paul, Matsuo, Keitaro
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Sprache:eng
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Zusammenfassung:An East Asian-specific variant on ( rs671, G>A) is the major genetic determinant of alcohol consumption. We performed an rs671 genotype-stratified genome-wide association study meta-analysis of alcohol consumption in 175,672 Japanese individuals to explore gene-gene interactions with rs671 behind drinking behavior. The analysis identified three genome-wide significant loci ( , , and ) in wild-type homozygotes and six ( , , , , , and ) in heterozygotes, with five showing genome-wide significant interaction with rs671. Genetic correlation analyses revealed ancestry-specific genetic architecture in heterozygotes. Of the discovered loci, four ( , , , and ) were suggested to interact with rs671 in the risk of esophageal cancer, a representative alcohol-related disease. Our results identify the genotype-specific genetic architecture of alcohol consumption and reveal its potential impact on alcohol-related disease risk.
ISSN:2375-2548
2375-2548
DOI:10.1126/sciadv.ade2780