Methylation levels of the SCD1 gene promoter and LINE-1 repeat region are associated with weight change: An intervention study

被引:46
作者
Maria Martin-Nunez, Gracia [1 ,2 ]
Cabrera-Mulero, Rebeca [1 ]
Rubio-Martin, Elehazara [1 ,2 ]
Rojo-Martinez, Gemma [1 ,2 ]
Olveira, Gabriel [1 ,2 ]
Valdes, Sergio [1 ,2 ]
Soriguer, Federico [1 ,2 ]
Castano, Luis [2 ,3 ,4 ]
Morcillo, Sonsoles [2 ,3 ,4 ]
机构
[1] Hosp Reg Univ, Inst Invest Biomed Malaga IBIMA, UGCI Endocrinol & Nutr, Malaga, Spain
[2] CIBER Diabet & Enfermedades Metab Asociadas CIBER, Barcelona, Spain
[3] Hosp Cruces, Endocrinol & Diabet Res Grp, Baracaldo 48903, Bizkaia, Spain
[4] Univ Basque Country UPV EHU, Baracaldo, Spain
关键词
Body weight; Diet; DNA methylation; Intervention study; STEAROYL-COA DESATURASE-1; CARDIOVASCULAR-DISEASE RISK; CANCER-FREE POPULATION; DNA METHYLATION; MEDITERRANEAN DIET; GLOBAL METHYLATION; PERIPHERAL-BLOOD; EPIGENETICS; OBESITY; EXPRESSION;
D O I
10.1002/mnfr.201400079
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: Epigenetic processes may be affected by environmental factors. DNA methylation measured in LINE-1 elements (LINE-1, long interspersed nucleotide element-1) correlates with LINE-1 DNA methylation. Variations in stearoyl CoA desaturase (SCD) activity (a key enzyme in the fatty acid metabolism) may be involved in various processes that can lead to diseases such as obesity. We evaluated whether changes in diet after a nutritional intervention would be associated with changes in LINE-1 DNA methylation and/or specific methylation of SCD1 gene promoter. Methods and results: Design: Prospective cohort intervention study with a control group. We recorded phenotypic, anthropometric, biochemical, and nutritional information at baseline and 1 year later. DNA methylation was quantified by pyrosequencing. LINE-1 DNA methylation and SCD1 gene promoter methylation levels were similar at the beginning of the study in both populations, whereas after a year these levels were higher in the control group (p < 0.001). In the intervention group, those subjects who lost weight showed higher levels of SCD1 gene promoter methylation after the intervention. Subjects with lower adherence to a Mediterranean diet experienced larger changes in LINE-1 methylation. Conclusion: DNA methylation levels were associated with weight change and with adherence to a Mediterranean diet.
引用
收藏
页码:1528 / 1536
页数:9
相关论文
共 48 条
[1]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[2]  
2-S
[3]  
[Anonymous], 2012, R LANG ENV STAT COMP
[4]   Ischemic Heart Disease and Stroke in Relation to Blood DNA Methylation [J].
Baccarelli, Andrea ;
Wright, Robert ;
Bollati, Valentina ;
Litonjua, Augusto ;
Zanobetti, Antonella ;
Tarantini, Letizia ;
Sparrow, David ;
Vokonas, Pantel ;
Schwartz, Joel .
EPIDEMIOLOGY, 2010, 21 (06) :819-828
[5]   Perceptions of epigenetics [J].
Bird, Adrian .
NATURE, 2007, 447 (7143) :396-398
[6]   Differential epigenomic and transcriptomic responses in subcutaneous adipose tissue between low and high responders to caloric restriction [J].
Bouchard, Luigi ;
Rabasa-Lhoret, Remi ;
Faraj, May ;
Lavoie, Marie-Eve ;
Mill, Jonathan ;
Perusse, Louis ;
Vohl, Marie-Claude .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2010, 91 (02) :309-320
[7]   Individuality and epigenetics in obesity [J].
Campion, J. ;
Milagro, F. I. ;
Martinez, J. A. .
OBESITY REVIEWS, 2009, 10 (04) :383-392
[8]   Epigenetics and Obesity [J].
Campion, Javier ;
Milagro, Fermin ;
Alfredo Martinez, J. .
GENES AND OBESITY, 2010, 94 :291-347
[9]   TNF-α Promoter Methylation as a Predictive Biomarker for Weight-loss Response [J].
Campion, Javier ;
Milagro, Fermin I. ;
Goyenechea, Estibaliz ;
Alfredo Martinez, J. .
OBESITY, 2009, 17 (06) :1293-1297
[10]   Cardiovascular disease risk factors and DNA methylation at the LINE-1 repeat region in peripheral blood from Samoan islanders [J].
Cash, Haley L. ;
McGarvey, Stephen T. ;
Houseman, E. Andres ;
Marsit, Carmen J. ;
Hawley, Nicola L. ;
Lambert-Messerlian, Geralyn M. ;
Viali, Satupaitea ;
Tuitele, John ;
Kelsey, Karl T. .
EPIGENETICS, 2011, 6 (10) :1257-1264