Zhang Ji Cheng, Wang Jin Hua, Lin Jia, Su Guo Ming, Shen Yi Lin, Guo Qi Wei, Cai Jia Jing, Liu Jun Yi, Jia Ke Xin, Fang Ding Zhi
Department of Biochemistry and Molecular Biology, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, People's Republic of China.
Diabetes Metab Syndr Obes. 2023 May 30;16:1555-1565. doi: 10.2147/DMSO.S412983. eCollection 2023.
To explore anthropometric, metabolic and dietary factors associated with and their interplays with the Val66Met polymorphism at brain-derived neurotrophic factor (BDNF) gene () on serum BDNF levels in adolescents.
Serum BDNF levels were quantified using an enzyme-linked immunosorbent assay in 644 high school students (278 males/366 females). A polymerase chain reaction and restriction fragment length polymorphism assay were utilized for Val66Met genotyping followed by verification using DNA sequencing. Serum levels of metabolic characteristics were assayed by routine methods. The intake of macro and micronutrients was collected by a three-day food record.
Serum BDNF levels were found to be significantly different in the subjects with different genotypes of Val66Met (Val/Val homozygotes, 60.05 ± 28.07 ng/mL vs Val/Met heterozygotes, 56.37 ± 29.34 ng/mL vs Met/Met homozygotes, 51.32 ± 24.54 ng/mL, p = 0.022). Among the 36 tested variables, waist-hip ratio (WHR) (β = -0.163, p < 0.001), iodine intake (β = 0.132, p = 0.001), heart rate (β = 0.108, p = 0.005), high-density lipoprotein cholesterol (HDL-C) (β = 0.098, p = 0.011) and dietary fiber intake (β = 0.082, p = 0.084) were the predictor of serum BDNF levels, while SBP (β = 0.097, p = 0.013) and WHR (β = 0.091, p = 0.021) were related with Val66Met. Moreover, WHR was observed to play a partial mediating role in the relationship between Val66Met and serum BDNF levels (95% CI [-1.161, -0.087]) and contribute 13.05% of its total effect on serum BDNF levels.
There are interplays between WHR and Val66Met on serum BDNF levels, which may be among the explanations for the previous heterogeneous reports and provide novel insights into the regulation of serum BDNF levels.
探讨青少年中与脑源性神经营养因子(BDNF)基因Val66Met多态性相关的人体测量学、代谢和饮食因素及其与血清BDNF水平的相互作用。
采用酶联免疫吸附测定法对644名高中生(278名男性/366名女性)的血清BDNF水平进行定量。利用聚合酶链反应和限制性片段长度多态性分析进行Val66Met基因分型,随后使用DNA测序进行验证。通过常规方法检测血清代谢特征水平。通过为期三天的饮食记录收集常量和微量营养素的摄入量。
发现不同Val66Met基因型受试者的血清BDNF水平存在显著差异(Val/Val纯合子,60.05±28.07 ng/mL;Val/Met杂合子,56.37±29.34 ng/mL;Met/Met纯合子,51.32±24.54 ng/mL,p = 0.022)。在36个检测变量中,腰臀比(WHR)(β = -0.163,p < 0.001)、碘摄入量(β = 0.132,p = 0.001)、心率(β = 0.108,p = 0.005)、高密度脂蛋白胆固醇(HDL-C)(β = 0.098,p = 0.011)和膳食纤维摄入量(β = 0.082,p = 0.084)是血清BDNF水平的预测因素,而收缩压(SBP)(β = 0.097,p = 0.013)和WHR(β = 0.091,p = 0.021)与Val66Met相关。此外,观察到WHR在Val66Met与血清BDNF水平之间的关系中起部分中介作用(95%CI[-1.161,-0.087]),并对血清BDNF水平的总效应贡献13.05%。
WHR与Val66Met在血清BDNF水平上存在相互作用,这可能是先前异质性报告的解释之一,并为血清BDNF水平的调节提供了新的见解。