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韩国人的苦味受体基因变异(rs10246939)、膳食营养素摄入量与生物临床参数

Bitter Taste Receptor Genetic Variation (rs10246939), Dietary Nutrient Intake, and Bio-Clinical Parameters in Koreans.

作者信息

Choi Jeong-Hwa

机构信息

Department of Food Science and Nutrition, Keimyung University, Daegu 42601, Korea.

出版信息

Clin Nutr Res. 2023 Jan 26;12(1):40-53. doi: 10.7762/cnr.2023.12.1.40. eCollection 2023 Jan.

DOI:10.7762/cnr.2023.12.1.40
PMID:36793779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9900072/
Abstract

Differential bitterness perception associated with genetic polymorphism in the bitter taste receptor gene taste 2 receptor member 38 () may influence an individual's food preferences, nutrition consumption, and eventually chronic nutrition-related disorders including cardiovascular disease. Therefore, the effect of genetic variations on nutritional intake and clinical markers needs to be elaborated for health and disease prevention. In this study, we conducted sex-stratified analysis to examine the association between genetic variant rs10246939 A > G with daily nutritional intake, blood pressure, and lipid parameters in Korean adults (males = 1,311 and females = 2,191). We used the data from the Multi Rural Communities Cohort, Korean Genome and Epidemiology Study. Findings suggested that the genetic variant rs10246939 was associated with dietary intake of micronutrients including calcium (adjusted p = 0.007), phosphorous (adjusted p = 0.016), potassium (adjusted p = 0.022), vitamin C (adjusted p = 0.009), and vitamin E (adjusted p = 0.005) in females. However, this genetic variant did not influence blood glucose, lipid profile parameters, and other blood pressure markers. These may suggest that this genetic variation is associated with nutritional intake, but its clinical effect was not found. More studies are needed to explore whether genotype may be a potential predictive marker for the risk of metabolic diseases via modulation of dietary intake.

摘要

苦味味觉受体基因味觉2受体成员38()中的基因多态性所导致的不同苦味感知,可能会影响个体的食物偏好、营养摄入,并最终影响包括心血管疾病在内的慢性营养相关疾病。因此,为了健康和疾病预防,需要详细阐述基因变异对营养摄入和临床指标的影响。在本研究中,我们进行了性别分层分析,以检验韩国成年人(男性=1311人,女性=2191人)中基因变异rs10246939 A>G与每日营养摄入、血压和血脂参数之间的关联。我们使用了来自韩国基因组与流行病学研究多农村社区队列的数据。研究结果表明,基因变异rs10246939与女性的钙(校正p=0.007)、磷(校正p=0.016)、钾(校正p=0.022)、维生素C(校正p=0.009)和维生素E(校正p=0.005)等微量营养素的饮食摄入有关。然而,这种基因变异并未影响血糖、血脂参数和其他血压指标。这可能表明这种基因变异与营养摄入有关,但其临床影响尚未发现。需要更多的研究来探索基因型是否可能通过调节饮食摄入成为代谢疾病风险的潜在预测标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e4/9900072/854961f09475/cnr-12-40-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e4/9900072/854961f09475/cnr-12-40-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e4/9900072/854961f09475/cnr-12-40-g001.jpg

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