Integration of methylation quantitative trait loci (mQTL) on dietary intake on DNA methylation levels: an example of n-3 PUFA and ABCA1 gene

被引:0
作者
Fujii, Ryosuke [1 ,2 ]
Ando, Yoshitaka [3 ]
Yamada, Hiroya [4 ]
Tsuboi, Yoshiki [1 ]
Munetsuna, Eiji [5 ]
Yamazaki, Mirai [6 ]
Mizuno, Genki [7 ]
Maeda, Keisuke [8 ]
Ohashi, Koji [3 ]
Ishikawa, Hiroaki [3 ]
Watanabe, Mami [1 ]
Imaeda, Nahomi [9 ]
Goto, Chiho [10 ]
Wakai, Kenji [11 ]
Hashimoto, Shuji [4 ]
Suzuki, Koji [1 ]
机构
[1] Fujita Hlth Univ, Sch Med Sci, Dept Prevent Med Sci, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Japan
[2] Univ Lubeck, Inst Biomed, Eurac Res, Via Alessandro Volta 21, Bolzano, Italy
[3] Fujita Hlth Univ, Sch Med Sci, Dept Informat Clin Med, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Japan
[4] Fujita Hlth Univ, Sch Med, Dept Hyg, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Japan
[5] Fujita Hlth Univ, Sch Med, Dept Biochem, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Japan
[6] Kagawa Prefectural Univ Hlth Sci, Dept Med Technol, 281-1 Hara,Mure Cho, Takamatsu, Japan
[7] Tokyo Univ Technol, Sch Hlth Sci, Dept Med Technol, 5-23-22 Nishi-Kamata,Ota Ku, Tokyo, Japan
[8] Fujita Hlth Univ, Sch Med Sci, Dept Clin Physiol, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Japan
[9] Shigakkan Univ, Fac Wellness, Dept Nutr, 55 Nakoyama, Yokonemachi, Obu, Japan
[10] Nagoya Bunri Univ, Dept Hlth & Nutr, 365 Maeda, Inazawa City, Inazawa, Japan
[11] Nagoya Univ, Grad Sch Med, Dept Prevent Med, 65 Tsurumai Cho,Showa Ku, Nagoya, Japan
基金
日本学术振兴会;
关键词
CORONARY-ARTERY-DISEASE; ADIPOSE-TISSUE; VARIANTS; PATTERNS; IMPACT; LIPIDS;
D O I
10.1038/s41430-023-01315-6
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
BackgroundEpigenetic studies have reported relationships between dietary nutrient intake and methylation levels. However, genetic variants that may affect DNA methylation (DNAm) pattern, called methylation quantitative loci (mQTL), are usually overlooked in these analyses. We investigated whether mQTL change the relationship between dietary nutrient intake and leukocyte DNAm levels with an example of estimated fatty acid intake and ATP-binding cassette transporter A1 (ABCA1).MethodsA cross-sectional study on 231 participants (108 men, mean age: 62.7 y) without clinical history of cancer and no prescriptions for dyslipidemia. We measured leukocyte DNAm levels of 8 CpG sites within ABCA1 gene by pyrosequencing method and used mean methylation levels for statistical analysis. TaqMan assay was used for genotyping a genetic variant of ABCA1 (rs1800976). Dietary fatty acid intake was estimated with a validated food frequency questionnaire and adjusted for total energy intake by using residual methods.ResultsMean ABCA1 DNAm levels were 5% lower with the number of minor alleles in rs1800976 (CC, 40.6%; CG, 35.9%; GG, 30.6%). Higher dietary n-3 PUFA intake was associated with lower ABCA1 DNAm levels (1st (ref) vs. 4th, & beta; [95% CI]: -2.52 [-4.77, -0.28]). After controlling for rs180076, the association between dietary n-3 PUFA intake and ABCA1 DNAm levels was attenuated, but still showed an independent association (1st (ref) vs. 4th, & beta; [95% CI]: -2.00 [-3.84, -0.18]). The interaction of mQTL and dietary n-3 PUFA intake on DNAm levels was not significant.ConclusionsThis result suggested that dietary n-3 PUFA intake would be an independent predictor of DNAm levels in ABCA1 gene after adjusting for individual genetic background. Considering mQTL need to broaden into other genes and nutrients for deeper understanding of DNA methylation, which can contribute to personalized nutritional intervention.
引用
收藏
页码:881 / 887
页数:7
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