Impact of BMI and waist circumference on epigenome-wide DNA methylation and identification of epigenetic biomarkers in blood: an EWAS in multi-ethnic Asian individuals

被引:23
作者
Chen, Yuqing [1 ,2 ]
Kassam, Irfahan [1 ,2 ,3 ]
Lau, Suk Hiang [4 ]
Kooner, Jaspal S. [5 ,6 ,7 ,8 ]
Wilson, Rory [9 ]
Peters, Annette [10 ,11 ]
Winkelmann, Juliane [12 ,13 ,14 ,15 ]
Chambers, John C. [5 ,6 ,7 ,16 ,17 ]
Chow, Vincent T. [18 ]
Khor, Chiea Chuen [19 ,20 ]
van Dam, Rob M. [1 ,2 ,21 ,22 ]
Teo, Yik-Ying [1 ,2 ,3 ]
Loh, Marie [16 ,17 ,23 ]
Sim, Xueling [1 ,2 ]
机构
[1] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, 12 Sci Dr 2,10-01,Tahir Fdn Bldg, Singapore 117549, Singapore
[2] Natl Univ Hlth Syst, 12 Sci Dr 2,10-01,Tahir Fdn Bldg, Singapore 117549, Singapore
[3] Natl Univ Singapore, Life Sci Inst, Singapore, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol & Immunol, Singapore, Singapore
[5] London North West Healthcare NHS Trust, Ealing Hosp, Dept Cardiol, Harrow, Middx, England
[6] Imperial Coll London, Imperial Coll Healthcare NHS Trust, London, England
[7] Imperial Coll London, MRC PHE Ctr Environm & Hlth, London, England
[8] Imperial Coll London, Natl Heart & Lung Inst, London, England
[9] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Res Unit Mol Epidemiol, Inst Epidemiol, D-85764 Neuherberg, Bavaria, Germany
[10] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Inst Epidemiol, Neuherberg, Germany
[11] Partner Site Munich Heart Alliance, German Ctr Cardiovasc Res, Munich, Germany
[12] Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany
[13] Tech Univ Munich, Inst Human Genet, Klinikum Rechts Isar, Munich, Germany
[14] Tech Univ Munich, Lehrstuhl Neurogenet, Munich, Germany
[15] Munich Cluster Syst Neurol, Munich, Germany
[16] Nanyang Technol Univ, Lee Kong Chian Sch Med, 11 Mandalay Rd,Lee Kong Chian Clin Sci Bldg, Singapore 308232, Singapore
[17] Imperial Coll London, Dept Epidemiol & Biostat, London, England
[18] Natl Univ Singapore, Natl Univ Hlth Syst, Infect Dis Translat Res Program, Dept Microbiol & Immunol,Yong Loo Lin Sch Med, Singapore, Singapore
[19] Agcy Sci Technol & Res, Genome Inst Singapore, Singapore, Singapore
[20] Singapore Natl Eye Ctr, Singapore Eye Res Inst, Singapore, Singapore
[21] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA USA
[22] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[23] Natl Skin Ctr, Singapore, Singapore
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
DNA methylation; Epigenome-wide association study; Obesity; Body mass index; Waist circumference; Inflammation; Metabolites; BODY-MASS INDEX; INSULIN-RESISTANCE; OBESITY; ASSOCIATION; LOCI; DISEASE; PROFILE; GENE; INFLAMMATION; ADIPOSITY;
D O I
10.1186/s13148-021-01162-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The prevalence of obesity and its related chronic diseases have been increasing especially in Asian countries. Obesity-related genetic variants have been identified, but these explain little of the variation in BMI. Recent studies reported associations between DNA methylation and obesity, mostly in non-Asian populations. Methods We performed an epigenome-wide association study (EWAS) on general adiposity (body mass index, BMI) and abdominal adiposity (waist circumference, WC) in 409 multi-ethnic Asian individuals and replicated BMI and waist-associated DNA methylation CpGs identified in other populations. The cross-lagged panel model and Mendelian randomization were used to assess the temporal relationship between methylation and BMI. The temporal relationship between the identified CpGs and inflammation and metabolic markers was also examined. Results EWAS identified 116 DNA methylation CpGs independently associated with BMI and eight independently associated with WC at false discovery rate P-FDR < 0.05 in 409 Asian samples. We replicated 110 BMI-associated CpGs previously reported in Europeans and identified six novel BMI-associated CpGs and two novel WC-associated CpGs. We observed high consistency in association direction of effect compared to studies in other populations. Causal relationship analyses indicated that BMI was more likely to be the cause of DNA methylation alteration, rather than the consequence. The causal analyses using BMI-associated methylation risk score also suggested that higher levels of the inflammation marker IL-6 were likely the consequence of methylation change. Conclusion Our study provides evidence of an association between obesity and DNA methylation in multi-ethnic Asians and suggests that obesity can drive methylation change. The results also suggested possible causal influence that obesity-related methylation changes might have on inflammation and lipoprotein levels.
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页数:13
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