Hidalgo Vira Nicole, Oyarce Karina, Valladares Vega Macarena, Goldfield Gary S, Guzmán-Gutiérrez Enrique, Obregón Ana M
Escuela de Tecnología Médica, Facultad de Medicina y Ciencia, Universidad San Sebastián, Concepción, Chile.
Escuela de Nutrición y Dietética, Facultad de Ciencias para el Cuidado de la Salud, Universidad San Sebastián, Concepción, Chile.
Front Behav Neurosci. 2023 Mar 31;17:1067384. doi: 10.3389/fnbeh.2023.1067384. eCollection 2023.
Different systems regulate food intake. In the reward system, dopamine (DA) is the main neurotransmitter, and a variety of genetic variants (rs1799732 and rs1800497) are associated with addiction. Addiction is a highly polygenic disease, where each allelic variant adds a small amount of vulnerability. Polymorphisms rs1799732 and rs1800497 are associated with eating behavior and hedonic hunger, but links to food addiction remain unclear. To evaluate the association between the bilocus profile (rs1799732-rs1800497) of the dopaminergic pathway with food reinforcement and food addiction in Chilean adults. A cross-sectional study recruited a convenience sample of 97 obese, 25 overweight, and 99 normal-weight adults (18-35 years). Anthropometric measurements were performed by standard procedures and eating behavior was assessed using the: Food Reinforcement Value Questionnaire (FRVQ) and Yale Food Addiction scale (YFAS). The DRD2 genotypes were determined by TaqMan assays (rs1800497 and rs1799732). A bilocus composite score was calculated. In the normal weight group, individuals who were heterozygous for the rs1977932 variant (G/del) showed higher body weight (-value 0.01) and abdominal circumference (-value 0.01) compared to those who were homozygous (G/G). When analyzing rs1800497, a significant difference in BMI was observed for the normal weight group (-value 0.02) where heterozygous showed higher BMI. In the obese group, homozygous A1/A1 showed higher BMI in comparison to A1/A2 and A2/A2 (-value 0.03). Also, a significant difference in food reinforcement was observed in the rs1800497, where homozygous for the variant (A1A1) show less reinforcement (-value 0.01).In relation to the bilocus score in the total sample, 11% showed "very low dopaminergic signaling", 24.4% were "under", 49.7% showed "intermediate signaling", 12.7% showed "high" and 1.4% showed "very high". No significant genotypic differences were observed in food reinforcement and food addiction by bilocus score. The results indicate that the genetic variants rs1799732 and rs1800497 (Taq1A) were associated with anthropometric measurements but not with food addiction or food reinforcement in Chilean university students. These results suggest that other genotypes, such as rs4680 and rs6277, which affect DA signaling capacity through a multilocus composite score, should be studied. Level V: Evidence obtained from a cross-sectional descriptive study.
不同的系统调节食物摄入。在奖赏系统中,多巴胺(DA)是主要的神经递质,多种基因变异(rs1799732和rs1800497)与成瘾有关。成瘾是一种高度多基因的疾病,每个等位基因变异都会增加少量的易感性。多态性rs1799732和rs1800497与饮食行为和享乐性饥饿有关,但与食物成瘾的联系仍不清楚。为了评估智利成年人中多巴胺能通路的双基因座图谱(rs1799732 - rs1800497)与食物强化及食物成瘾之间的关联。一项横断面研究招募了一个便利样本,包括97名肥胖、25名超重和99名正常体重的成年人(18 - 35岁)。通过标准程序进行人体测量,并使用食物强化价值问卷(FRVQ)和耶鲁食物成瘾量表(YFAS)评估饮食行为。通过TaqMan分析确定DRD2基因型(rs1800497和rs1799732)。计算双基因座综合评分。在正常体重组中,rs1977932变异(G/del)的杂合子个体与纯合子(G/G)个体相比,体重更高(p值0.01),腹围更大(p值0.01)。在分析rs1800497时,正常体重组的BMI存在显著差异(p值0.02),杂合子的BMI更高。在肥胖组中,纯合子A1/A1与A1/A2和A2/A2相比,BMI更高(p值0.03)。此外,在rs1800497中观察到食物强化存在显著差异,该变异的纯合子(A1A1)显示出较少的强化(p值0.01)。关于总样本中的双基因座评分,11%显示“多巴胺能信号极低”,24.4%为“低于正常”,49.7%显示“中等信号”,12.7%显示“高”,1.4%显示“非常高”。按双基因座评分在食物强化和食物成瘾方面未观察到显著的基因型差异。结果表明,基因变异rs1799732和rs1800497(Taq1A)与智利大学生的人体测量指标有关,但与食物成瘾或食物强化无关。这些结果表明,应该研究其他通过多基因座综合评分影响DA信号传导能力的基因型,如rs4680和rs6277。证据等级:V级:从横断面描述性研究中获得的证据。