TY - JOUR
T1 - A genome-wide association study on fish consumption in a Japanese population—the Japan Multi-Institutional Collaborative Cohort study
AU - for the J-MICC Research Group
AU - Suzuki, Taro
AU - Nakamura, Yasuyuki
AU - Matsuo, Keitaro
AU - Oze, Isao
AU - Doi, Yukio
AU - Narita, Akira
AU - Shimizu, Atsushi
AU - Imaeda, Nahomi
AU - Goto, Chiho
AU - Matsui, Kenji
AU - Nakatochi, Masahiro
AU - Miura, Katsuyuki
AU - Takashima, Naoyuki
AU - Kuriki, Kiyonori
AU - Shimanoe, Chisato
AU - Tanaka, Keitaro
AU - Ikezaki, Hiroaki
AU - Murata, Masayuki
AU - Ibusuki, Rie
AU - Takezaki, Toshiro
AU - Koyanagi, Yuriko
AU - Ito, Hidemi
AU - Matsui, Daisuke
AU - Koyama, Teruhide
AU - Mikami, Haruo
AU - Nakamura, Yohko
AU - Suzuki, Sadao
AU - Nishiyama, Takeshi
AU - Katsuura-Kamano, Sakurako
AU - Arisawa, Kokichi
AU - Takeuchi, Kenji
AU - Tamura, Takashi
AU - Okada, Rieko
AU - Kubo, Yoko
AU - Momozawa, Yukihide
AU - Kubo, Michiaki
AU - Kita, Yoshikuni
AU - Wakai, Kenji
AU - Wakai, Kenji
AU - Mikami, Haruo
AU - Nagase, Hiroki
AU - Narimatsu, Hiroto
AU - Kuriki, Kiyonori
AU - Suzuki, Sadao
AU - Matsuo, Keitaro
AU - Hishida, Asahi
AU - Kita, Yoshikuni
AU - Miura, Katsuyuki
AU - Uehara, Ritei
AU - Arisawa, Kokichi
N1 - Funding Information:
Acknowledgements We would like to thank all the staff at the Laboratory for Genotyping Development, Center for the Integrative Medical Sciences, RIKEN, and the staff of the BioBank Japan project. This study was supported by a Grants-in-Aid for Scientific Research for Priority Areas of Cancer (No. 17015018) and Innovative Areas (No. 221S0001), and by JSPS KAKENHI Grants (No. 16H06277) from the Japanese Ministry of Education, Culture, Sports, Science and Technology. This work was also supported in part by a Grant-in-Aid from the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant B Numbers 24390165, 20390184, 17390186. This study was supported in part by funding for the BioBank Japan Project from the Japan Agency for Medical Research and development from April 2015, and the Ministry of Education, Culture, Sports, Science and Technology from April 2003 to March 2015.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/3
Y1 - 2021/3
N2 - Background/objective: Although benefits of fish consumption for health are well known, a significant percentage of individuals dislike eating fish. Fish consumption may be influenced by genetic factors in addition to environmental factors. We conducted a genome-wide association study (GWAS) to find genetic variations that affect fish consumption in a Japanese population. Methods: We performed a two-stage GWAS on fish consumption using 13,739 discovery samples from the Japan Multi-Institutional Collaborative Cohort study, and 2845 replication samples from the other population. We used a semi-quantitative food frequency questionnaire to estimate food intake. Association of the imputed variants with fish consumption was analyzed by separate linear regression models per variant, with adjustments for age, sex, energy intake, principal component analysis components 1–10, and alcohol intake (g/day). We also performed conditional analysis. Results: We found 27 single nucleotide polymorphisms (SNPs) located in 12q24 and 14q32.12 that were associated with fish consumption. The 19 SNPs were located at 11 genes including six lead SNPs at the BRAP, ACAD10, ALDH2, NAA25, and HECTD4 regions on 12q24.12-13, and CCDC197 region on 14q32.12. In replication samples, all five SNPs located on chromosome 12 were replicated successfully, but the one on chromosome 14 was not. Conditional analyses revealed that the five lead variants in chromosome 12 were in fact the same signal. Conclusion: We found that new SNPs in the 12q24 locus were related to fish intake in two Japanese populations. The associations between SNPs on chromosome 12 and fish intake were strongly confounded by drinking status.
AB - Background/objective: Although benefits of fish consumption for health are well known, a significant percentage of individuals dislike eating fish. Fish consumption may be influenced by genetic factors in addition to environmental factors. We conducted a genome-wide association study (GWAS) to find genetic variations that affect fish consumption in a Japanese population. Methods: We performed a two-stage GWAS on fish consumption using 13,739 discovery samples from the Japan Multi-Institutional Collaborative Cohort study, and 2845 replication samples from the other population. We used a semi-quantitative food frequency questionnaire to estimate food intake. Association of the imputed variants with fish consumption was analyzed by separate linear regression models per variant, with adjustments for age, sex, energy intake, principal component analysis components 1–10, and alcohol intake (g/day). We also performed conditional analysis. Results: We found 27 single nucleotide polymorphisms (SNPs) located in 12q24 and 14q32.12 that were associated with fish consumption. The 19 SNPs were located at 11 genes including six lead SNPs at the BRAP, ACAD10, ALDH2, NAA25, and HECTD4 regions on 12q24.12-13, and CCDC197 region on 14q32.12. In replication samples, all five SNPs located on chromosome 12 were replicated successfully, but the one on chromosome 14 was not. Conditional analyses revealed that the five lead variants in chromosome 12 were in fact the same signal. Conclusion: We found that new SNPs in the 12q24 locus were related to fish intake in two Japanese populations. The associations between SNPs on chromosome 12 and fish intake were strongly confounded by drinking status.
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U2 - 10.1038/s41430-020-00702-7
DO - 10.1038/s41430-020-00702-7
M3 - Article
C2 - 32895509
AN - SCOPUS:85090302355
SN - 0954-3007
VL - 75
SP - 480
EP - 488
JO - European Journal of Clinical Nutrition
JF - European Journal of Clinical Nutrition
IS - 3
ER -