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遗传风险评分与饮食脂肪摄入量对巴西年轻成年人脂质相关特征的相互作用。

Interaction between genetic risk score and dietary fat intake on lipid-related traits in Brazilian young adults.

机构信息

Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences and Institute for Cardiovascular and Metabolic Research (ICMR), University of Reading, ReadingRG6 6DZ, UK.

Nutritional Genomics Research Group, Faculty of Nutrition, Federal University of Goiás (UFG), Goiania, Brazil.

出版信息

Br J Nutr. 2024 Sep 14;132(5):575-589. doi: 10.1017/S0007114524001594. Epub 2024 Sep 23.

Abstract

The occurrence of dyslipidaemia, which is an established risk factor for cardiovascular diseases, has been attributed to multiple factors including genetic and environmental factors. We used a genetic risk score (GRS) to assess the interactions between genetic variants and dietary factors on lipid-related traits in a cross-sectional study of 190 Brazilians (mean age: 21 ± 2 years). Dietary intake was assessed by a trained nutritionist using three 24-h dietary recalls. The high GRS was significantly associated with increased concentration of TAG (beta = 0·10 mg/dl, 95 % CI 0·05-0·16; < 0·001), LDL-cholesterol (beta = 0·07 mg/dl, 95 % CI 0·04, 0·11; < 0·0001), total cholesterol (beta = 0·05 mg/dl, 95 % CI: 0·03, 0·07; < 0·0001) and the ratio of TAG to HDL-cholesterol (beta = 0·09 mg/dl, 95 % CI: 0·03, 0·15; = 0·002). Significant interactions were found between the high GRS and total fat intake on TAG:HDL-cholesterol ratio ( = 0·03) and between the high GRS and SFA intake on TAG:HDL-cholesterol ratio ( = 0·03). A high intake of total fat (>31·5 % of energy) and SFA (>8·6 % of energy) was associated with higher TAG:HDL-cholesterol ratio in individuals with the high GRS (beta = 0·14, 95 % CI: 0·06, 0·23; < 0·001 for total fat intake; beta = 0·13, 95 % CI: 0·05, 0·22; = 0·003 for SFA intake). Our study provides evidence that the genetic risk of high TAG:HDL-cholesterol ratio might be modulated by dietary fat intake in Brazilians, and these individuals might benefit from limiting their intake of total fat and SFA.

摘要

血脂异常是心血管疾病的一个既定危险因素,其发生可归因于多种因素,包括遗传和环境因素。我们使用遗传风险评分(GRS)来评估遗传变异与饮食因素之间的相互作用,对 190 名巴西人(平均年龄:21±2 岁)的横断面研究进行了分析。饮食摄入由经过培训的营养师使用三份 24 小时膳食回忆进行评估。高 GRS 与 TAG 浓度升高显著相关(β=0.10mg/dl,95%CI 0.05-0.16;<0.001)、LDL-胆固醇(β=0.07mg/dl,95%CI 0.04,0.11;<0.0001)、总胆固醇(β=0.05mg/dl,95%CI:0.03,0.07;<0.0001)和 TAG/HDL-胆固醇比值(β=0.09mg/dl,95%CI:0.03,0.15;=0.002)。还发现高 GRS 与总脂肪摄入量之间存在显著的相互作用,这种相互作用与 TAG:HDL-胆固醇比值有关(=0.03),而高 GRS 与 SFA 摄入量之间存在显著的相互作用,这种相互作用与 TAG:HDL-胆固醇比值有关(=0.03)。高总脂肪(>31.5%的能量)和 SFA(>8.6%的能量)摄入量与高 GRS 个体的 TAG:HDL-胆固醇比值升高有关(β=0.14,95%CI:0.06,0.23;总脂肪摄入量<0.001;β=0.13,95%CI:0.05,0.22;SFA 摄入量=0.003)。我们的研究提供了证据,表明巴西人高 TAG:HDL-胆固醇比值的遗传风险可能受到饮食脂肪摄入的调节,这些个体可能受益于限制总脂肪和 SFA 的摄入。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1a4/11536265/4a932fca77ef/S0007114524001594_fig1.jpg

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