Surendran Shelini, Jayashri Ramamoorthy, Drysdale Lauren, Bodhini Dhanasekaran, Lakshmipriya Nagarajan, Shanthi Rani Coimbatore Subramanian, Sudha Vasudevan, Lovegrove Julie A, Anjana Ranjit M, Mohan Viswanathan, Radha Venkatesan, Pradeepa Rajendra, Vimaleswaran Karani S
1Hugh Sinclair Unit of Human Nutrition and Institute for Cardiovascular and Metabolic Research (ICMR), Department of Food and Nutritional Sciences, University of Reading, Whiteknights, PO Box 226, Reading, RG6 6AP UK.
Department of Diabetology, Madras Diabetes Research Foundation and Dr. Mohan's Diabetes Specialities Centre, WHO Collaborating Centre for Non-communicable Diseases Prevention and Control, ICMR Centre for Advanced Research on Diabetes, Gopalapuram, Chennai, 600086 India.
Genes Nutr. 2019 Sep 5;14:26. doi: 10.1186/s12263-019-0649-3. eCollection 2019.
Low vitamin B12 concentrations have been associated with major clinical outcomes, including adiposity, in Indian populations. The Fat mass and obesity-associated gene () is an established obesity-susceptibility locus; however, it remains unknown whether it influences vitamin B12 status. Hence, we investigated the association of two previously studied polymorphisms with vitamin B12 concentrations and metabolic disease-related outcomes and examined whether these associations were modified by dietary factors and physical activity.
A total of 176 individuals with type 2 diabetes, 152 with pre-diabetes, and 220 normal glucose-tolerant individuals were randomly selected from the Chennai Urban Rural Epidemiology Study. Anthropometric, clinical, and biochemical investigations, which included body mass index (BMI), waist circumference, vitamin B12, homocysteine, and folic acid were measured. A validated food frequency questionnaire was used for dietary assessment and self-reported physical activity measures were collected. An unweighted genetic risk score (GRS) was calculated for two single-nucleotide polymorphisms (rs8050136 and rs2388405) by summation of the number of risk alleles for obesity. Interaction analyses were performed by including the interaction terms in the regression model.
The GRS was significantly associated with increased BMI ( = 0.009) and risk of obesity ( = 0.023). Individuals carrying more than one risk allele for the GRS had 13.13% lower vitamin B12 concentrations, compared to individuals carrying zero risk alleles ( = 0.018). No associations between the GRS and folic acid and homocysteine concentrations were observed. Furthermore, no statistically significant GRS-diet or GRS-physical activity interactions with vitamin B12, folic acid, homocysteine or metabolic-disease outcomes were observed.
The study shows for the first time that a genetic risk score using two SNPs is associated with lower vitamin B12 concentrations; however, we did not identify any evidence for the influence of lifestyle factors on this association. Further replication studies in larger cohorts are warranted to investigate the association between the GRS and vitamin B12 concentrations.
在印度人群中,低维生素B12浓度与包括肥胖在内的主要临床结局相关。脂肪量和肥胖相关基因( )是一个已确定的肥胖易感性位点;然而,它是否影响维生素B12水平尚不清楚。因此,我们研究了两个先前研究过的 多态性与维生素B12浓度及代谢疾病相关结局之间的关联,并检验了这些关联是否会受到饮食因素和体育活动的影响。
从金奈城乡流行病学研究中随机选取了176名2型糖尿病患者、152名糖尿病前期患者和220名糖耐量正常的个体。进行了人体测量、临床和生化检查,包括测量体重指数(BMI)、腰围、维生素B12、同型半胱氨酸和叶酸。使用经过验证的食物频率问卷进行饮食评估,并收集自我报告的体育活动量。通过对肥胖风险等位基因数量求和,计算了两个 单核苷酸多态性(rs8050136和rs2388405)的非加权遗传风险评分(GRS)。通过在回归模型中纳入交互项进行交互分析。
GRS与BMI升高( = 0.009)和肥胖风险( = 0.023)显著相关。与携带零个风险等位基因的个体相比,携带一个以上GRS风险等位基因的个体维生素B12浓度低13.13%( = 0.018)。未观察到GRS与叶酸和同型半胱氨酸浓度之间的关联。此外,未观察到GRS与饮食或GRS与体育活动与维生素B12、叶酸、同型半胱氨酸或代谢疾病结局之间存在统计学显著的交互作用。
该研究首次表明,使用两个 单核苷酸多态性的遗传风险评分与较低的维生素B12浓度相关;然而,我们没有发现任何证据表明生活方式因素对这种关联有影响。有必要在更大的队列中进行进一步的重复研究,以调查GRS与维生素B12浓度之间的关联。