Food Craving in Obese Subjects: Its Correlation with Atherogenic Index and Feeding Behavior-Related Gene Expression

N. Pérez-Vielma, Á. Miliar-García, M. Gómez-López, María Delfina Marín-Soto, Gerardo Leija-Alva, Víctor Ricardo Aguilera-Sosa
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Abstract

Obesity is influenced by environmental, behavioral, and genetic factors; particularly genes related to the regulation of lipids and addictive behavior. Food craving (FC) is a physiological and behavioral response that triggers the intense desire to ingest food, particularly food with high energy, fat, and/or sweet content. Objective: To evaluate the relationship between the prevalence of FC in obese subjects and blood lipids as well as to determine the transcriptional modulation of CART, DRD2, and FTO. Method: Transverse, comparative, and randomized study including 21 obese participants (BMI, ≥30 kg/m2] and 20 normal weight participants (BMI, ≤25 kg/m2). We determined CART, DRD2, and FTO expressions; evaluated blood lipid levels; and obtained trait scores on the Food Craving Questionnaire-Trait, a multifactorial instrument validated for the Mexican population. Results: The DRD2 expression was significantly increased (p = 0.027) and the CART expression was significantly decreased (p = 0.001) in obese participants compared with normal weight participants. The FTO expression did not show significant differences. Food Craving Questionnaire-Trait showed scores of ≥72 in obese participants. Conclusions: Linear regression model analysis showed that FC is a predictor of atherogenic index (ATH), independently of BMI, and of the gene expression modulation of CART and DRD2.
肥胖受试者的食物渴望:与动脉粥样硬化指数和摄食行为相关基因表达的关系
肥胖受环境、行为和遗传因素的影响;尤其是与脂质调节和成瘾行为有关的基因。食物渴求(FC)是一种生理和行为反应,它触发了摄取食物的强烈欲望,特别是高能量、高脂肪和/或甜的食物。目的:探讨肥胖人群FC患病率与血脂的关系,并确定CART、DRD2和FTO的转录调控。方法:横向、比较、随机研究,包括21名肥胖受试者(BMI≥30 kg/m2)和20名正常体重受试者(BMI≤25 kg/m2)。我们检测了CART、DRD2和FTO的表达;评估血脂水平;并获得了食物渴望问卷的特征分数,这是一种针对墨西哥人口的多因素工具。结果:与正常体重组相比,肥胖组DRD2表达显著升高(p = 0.027), CART表达显著降低(p = 0.001)。FTO的表达差异无统计学意义。肥胖参与者的食物渴望问卷-特质得分≥72。结论:线性回归模型分析显示,FC是动脉粥样硬化指数(ATH)的预测因子,独立于BMI,以及CART和DRD2基因表达调节。
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