Pedram Pardis, Zhai Guangju, Gulliver Wayne, Zhang Hongwei, Sun Guang
Memorial University, Faculty of Medicine, 300 Prince Philip Drive; St.John's, NL, A1B3V6, Canada.
Appetite. 2017 Aug 1;115:71-79. doi: 10.1016/j.appet.2017.01.004. Epub 2017 Jan 20.
Food addiction (FA) is a distinguished clinical feature affecting about 5% adults of the general population in Canada. FA contributes to obesity, however, the underlying genes in FA are largely unknown. The aim of the current study was to search for FA candidate genes using an exome sequencing followed by a verification study using the most significantly associated identified genes. From a total of 752 adults, 24 subjects were selected including 8 obese with high and 8 obese with low/zero FA clinical symptom score (FAO, NFO), and 8 healthy controls with normal BMI and low/zero FA symptom score (Ctrl). Exome sequencing was completed in all three groups. The top 100 SNPs identified were categorized into 5 subgroups based on gene functions: addiction (Ad), psychological disorders, energy metabolism and obesity, and cancer, unknown function or with other diseases. In the verification study, the top 19 SNPs in the Addiction subgroup were genotyped in the entire 752 subjects using Sequenom iPLEX Gold genotyping technology. Comparison of NFO with Ctrl, and FAO with NFO, Ctrl and the combined group of NFO + Ctrl revealed 19 SNPs associated with Ad genes including, TIRAP, MMADHC, ERAP1, NTM, MYPN, GRID1, ITPR2, GPSM1, ZCCHC14, TNN, PPARD, CACNA1C, SIM1, and DRD2. Genetic association analysis was performed. The major allele A of rs2511521 located in DRD2 (OR = 3.1(95% CI 1.1-8.2)) and the minor allele T of rs625413 located in TIRAP (OR = 2.5(95% CI 1.1-5.8)) in NFO subjects significantly associated with increased risk of food addiction. Using a combination of exome sequencing method and a candidate gene association approach two new FA candidate genes are identified. Further study on the rest of the genes in the other four categories will be warranted.
食物成瘾(FA)是一种显著的临床特征,影响着加拿大约5%的成年普通人群。食物成瘾会导致肥胖,然而,食物成瘾背后的基因在很大程度上尚不明确。本研究的目的是通过外显子组测序寻找食物成瘾候选基因,随后使用最显著相关的已鉴定基因进行验证研究。从总共752名成年人中,选取了24名受试者,包括8名具有高食物成瘾临床症状评分的肥胖者(FAO)、8名具有低/零食物成瘾临床症状评分的肥胖者(NFO),以及8名体重指数正常且食物成瘾症状评分为低/零的健康对照者(Ctrl)。对所有三组进行了外显子组测序。根据基因功能,将鉴定出的前100个单核苷酸多态性(SNP)分为5个亚组:成瘾(Ad)、心理障碍、能量代谢与肥胖、癌症、功能未知或与其他疾病相关。在验证研究中,使用Sequenom iPLEX Gold基因分型技术对整个752名受试者进行了成瘾亚组中前19个SNP的基因分型。将NFO与Ctrl进行比较,以及将FAO与NFO、Ctrl和NFO + Ctrl的合并组进行比较,发现了19个与Ad基因相关的SNP,包括TIRAP、MMADHC、ERAP1、NTM、MYPN、GRID1、ITPR2、GPSM1、ZCCHC14、TNN、PPARD、CACNA1C、SIM1和DRD2。进行了基因关联分析。在NFO受试者中,位于DRD2的rs2511521的主要等位基因A(OR = 3.1(95% CI 1.1 - 8.2))和位于TIRAP的rs625413的次要等位基因T(OR = 2.5(95% CI 1.1 - 5.8))与食物成瘾风险增加显著相关。使用外显子组测序方法和候选基因关联方法相结合,鉴定出了两个新的食物成瘾候选基因。对其他四个类别中其余基因的进一步研究将是必要的。