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  • 标题:Macronutrient-specific effect of the MTNR1B genotype on lipid levels in response to 2 year weight-loss diets
  • 作者:Leticia Goni ; Dianjianyi Sun ; Yoriko Heianza
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2018
  • 卷号:59
  • 期号:1
  • 页码:155-161
  • DOI:10.1194/jlr.P078634
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Compelling evidence indicates that lipid metabolism is in partial control of the circadian system. In this context, it has been reported that the melatonin receptor 1B ( MTNR1B ) genetic variant influences the dynamics of melatonin secretion, which is involved in the circadian system as a chronobiotic. The objective was to analyze whether the MTNR1B rs10830963 genetic variant was related to changes in lipid levels in response to dietary interventions with different macronutrient distribution in 722 overweight/obese subjects from the POUNDS Lost trial. We did not find a significant association between the MTNR1B genotype and changes in lipid metabolism. However, dietary fat intake significantly modified genetic effects on 2 year changes in total and LDL cholesterol ( P interaction = 0.006 and 0.001, respectively). In the low-fat diet group, carriers of the sleep disruption G allele (minor allele) showed a greater reduction of total cholesterol (β ± SE = −5.78 ± 2.88 mg/dl, P = 0.04) and LDL cholesterol (β ± SE = −7.19 ± 2.37 mg/dl, P = 0.003). Conversely, in the high-fat diet group, subjects carrying the G allele evidenced a smaller decrease in total cholesterol (β ± SE = 5.81 ± 2.65 mg/dl, P = 0.03) and LDL cholesterol (β ± SE = 5.23 ± 2.21 mg/dl, P = 0.002). Subjects carrying the G allele of the circadian rhythm-related MTNR1B variant may present a bigger impact on total and LDL cholesterol when undertaking an energy-restricted low-fat diet.
  • 关键词:clinical trials ; diet and dietary lipids ; cholesterol ; low density lipoprotein ; genetics ; melatonin receptor 1B ; gene-diet interaction ; high-fat diet ; lipid metabolism ; weight-loss intervention
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