Jehi Tony, Dos Santos Hildemar, Kwok-Hinsley Gigi
School of Public Health and Health Sciences, California State University, Dominguez Hills (CSUDH), Carson, USA.
Preventive Care, School of Public Health, Loma Linda University, Loma Linda, USA.
Cureus. 2024 Nov 26;16(11):e74509. doi: 10.7759/cureus.74509. eCollection 2024 Nov.
Variation in common taste receptor type 2 member 38 (TAS2R38) haplotypes is associated with bitter taste sensitivity, but there is not much or inconsistent evidence on association with food cravings and with chronic disease risk factors. We have conducted a cross-sectional study to assess whether genetically defined taster groups would differ in their sensitivity to bitter-tasting compounds, cravings for various food groups, and risk of chronic disease risk factors. Methodology: A total of 116 non-diabetic individuals were recruited from the Loma Linda University (LLU) campus. Various measures were carried out to examine genetic variations, bitter sensitivity, anthropometrics, food cravings, and participant demographics. Taster status was determined based on TAS2R38 haplotypes, classifying participants as super-tasters, tasters, or non-tasters. Analysis of Covariance (ANCOVA) models were used to examine differences among the three TAS2R38 genetic groups in bitter taste sensitivity, food cravings, body mass index (BMI), non-fasting blood glucose, and family history of type 2 diabetes (T2D).
A significant difference in sensitivity to the bitter taste compounds thiourea and phenylthiocarbamide (PTC) was observed among the three TAS2R38 genetic groups ( < 0.01). The sensitivity scores of the bitter taste compounds thiourea and PTC were lowest for super-tasters and highest for non-tasters (-41.283 and -0.233 for thiourea; -32.983 and 3.380 for PTC, respectively). Moreover, super-tasters had a significantly higher cravings score than non-tasters for starchy foods (2.641 vs. 2.183, respectively). Tasters had a significantly higher cravings score than non-tasters for bitter foods (2.306 vs. 1.740, respectively). No significant differences were observed across the TAS2R38 genetic-based taste groups for the chronic disease risk factors, BMI non-fasting blood glucose, and family history of T2D.
Super-tasters had the lowest taste sensitivity for bitter compounds and the highest cravings for bitter foods, which suggests that they might be more likely to consume bitter foods. Examining the genetic differences in taste preferences and sensitivities may pave the way for effective and individualized dietary plans and intervention strategies targeting chronic disease prevention, treatment, and management.
常见味觉受体2型成员38(TAS2R38)单倍型的变异与苦味敏感度相关,但关于其与食物渴望及慢性病风险因素的关联,证据不多或并不一致。我们开展了一项横断面研究,以评估基因定义的味觉者群体在对苦味化合物的敏感度、对各类食物的渴望程度以及慢性病风险因素方面是否存在差异。
从洛马林达大学(LLU)校园招募了116名非糖尿病个体。进行了多项测量,以检测基因变异、苦味敏感度、人体测量指标、食物渴望程度及参与者的人口统计学信息。根据TAS2R38单倍型确定味觉者状态,将参与者分为超级味觉者、味觉者或非味觉者。采用协方差分析(ANCOVA)模型,研究三个TAS2R38基因群体在苦味敏感度、食物渴望程度、体重指数(BMI)、非空腹血糖以及2型糖尿病(T2D)家族史方面的差异。
在三个TAS2R38基因群体中,观察到对苦味化合物硫脲和苯硫脲(PTC)的敏感度存在显著差异( < 0.01)。超级味觉者对硫脲和PTC这两种苦味化合物的敏感度得分最低,非味觉者最高(硫脲分别为-41.283和-0.233;PTC分别为-32.983和3.380)。此外,超级味觉者对淀粉类食物的渴望得分显著高于非味觉者(分别为2.641和2.183)。味觉者对苦味食物的渴望得分显著高于非味觉者(分别为2.306和1.740)。在基于TAS2R38基因的味觉群体中,未观察到慢性病风险因素、BMI、非空腹血糖及T2D家族史方面的显著差异。
超级味觉者对苦味化合物的味觉敏感度最低,对苦味食物的渴望程度最高,这表明他们可能更倾向于食用苦味食物。研究味觉偏好和敏感度的基因差异,可能为针对慢性病预防、治疗和管理的有效且个性化的饮食计划及干预策略铺平道路。