膳食支链氨基酸与遗传风险评分对中国人罹患 2 型糖尿病风险的交互作用。

Weiqi Wang, Haiyang Jiang, Ziwei Zhang, Wei Duan, Tianshu Han, Changhao Sun
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引用次数: 0

摘要

背景和目的:以往的研究发现了基因-饮食相互作用对2型糖尿病(T2D)发病的重要影响,但没有关注支链氨基酸(BCAAs),尽管支链氨基酸在糖尿病相关因素中显示出不同的有效性。因此,在本研究中,我们旨在调查膳食中的 BCAAs 是否与遗传易感性相互作用,从而影响中国成年人的 T2D 风险和空腹血糖:在一项嵌套于哈尔滨饮食、营养与慢性非传染性疾病队列研究的病例对照研究中,我们获得了 434 例 T2D 发病病例和 434 例年龄与性别匹配的对照组的数据。通过对 25 个与 T2D 相关的单核苷酸多态性的 T2D 风险等位基因数求和,计算出了非加权遗传风险评分(GRS)。多变量逻辑回归模型和一般线性回归模型用于评估膳食中的 BCAAs 和 GRS 对 T2D 风险和空腹血糖的交互作用:结果:发现GRS和膳食中的BCAAs对T2D风险和空腹血糖有显著的交互作用(交互作用的p分别为0.001和0.004)。与低GRS相比,在BCAA总摄入量最高的三等分人群中,高GRS人群患T2D的几率比为2.98(95% CI 1.54-5.76),但在摄入量最低的人群中则不显著,相当于每三等分人群空腹血糖升高0.39 (0.12) mmol/L和- 0.07 (0.10) mmol/L。换个角度看,比较膳食中 BCAAs 的极端三分位数,低、中、高遗传风险参与者的 T2D 风险几率(95% CIs)分别为 0.46(0.22-0.95)、2.22(1.15-4.31)和 2.90(1.54-5.47)(每三分位数的空腹血糖升高:- 0.23(0.10)、0.18(0.10)和 0.26(0.13)mmol/L):该研究表明,膳食中的 BCAAs 可放大与 T2D 风险和空腹血糖的遗传关联。此外,当遗传易感性也较高时,较高的 BCAA 摄入量与 T2D 呈正相关,但当遗传易感性较低时,则转为负相关。
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Interaction between dietary branched-chain amino acids and genetic risk score on the risk of type 2 diabetes in Chinese.

Background and objectives: Previous studies have found the important gene-diet interactions on type 2 diabetes (T2D) incident but have not followed branched-chain amino acids (BCAAs), even though they have shown heterogeneous effectiveness in diabetes-related factors. So in this study, we aim to investigate whether dietary BCAAs interact with the genetic predisposition in relation to T2D risk and fasting glucose in Chinese adults.

Methods: In a case-control study nested in the Harbin Cohort Study on Diet, Nutrition and Chronic Non-Communicable Diseases, we obtained data for 434 incident T2D cases and 434 controls matched by age and sex. An unweighted genetic risk score (GRS) was calculated for 25 T2D-related single nucleotide polymorphisms by summation of the number of risk alleles for T2D. Multivariate logistic regression models and general linear regression models were used to assess the interaction between dietary BCAAs and GRS on T2D risk and fasting glucose.

Results: Significant interactions were found between GRS and dietary BCAAs on T2D risk and fasting glucose (p for interaction = 0.001 and 0.004, respectively). Comparing with low GRS, the odds ratio of T2D in high GRS were 2.98 (95% CI 1.54-5.76) among those with the highest tertile of total BCAA intake but were non-significant among those with the lowest intake, corresponding to 0.39 (0.12) mmol/L versus - 0.07 (0.10) mmol/L fasting glucose elevation per tertile. Viewed differently, comparing extreme tertiles of dietary BCAAs, the odds ratio (95% CIs) of T2D risk were 0.46 (0.22-0.95), 2.22 (1.15-4.31), and 2.90 (1.54-5.47) (fasting glucose elevation per tertile: - 0.23 (0.10), 0.18 (0.10), and 0.26 (0.13) mmol/L) among participants with low, intermediate, and high genetic risk, respectively.

Conclusions: This study indicated that dietary BCAAs could amplify the genetic association with T2D risk and fasting glucose. Moreover, higher BCAA intake showed positive association with T2D when genetic predisposition was also high but changed to negative when genetic predisposition was low.

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