茶摄入量和糖尿病之间没有遗传因果关系:一项双样本孟德尔随机研究

Hui Cheng, Da-Yuan Zhong, Yu-Mei Liu
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摘要

背景:以前的研究表明,茶摄入(TI)对糖尿病有潜在的降低风险的作用。然而,TI对不同类型糖尿病的具体影响及其潜在机制尚不清楚。为了进一步探讨这一主题,我们进行了全面的调查,评估TI与各种类型糖尿病的因果关系,以及其对血糖(Glu)和糖化血红蛋白(HbA1)的影响。方法:我们从IEU数据库中收集TI、糖尿病、1型糖尿病(T1D)、2型糖尿病(T2D)、Glu、HbA1、绿茶摄入量、草药茶摄入量和路易波士茶摄入量的全基因组关联研究数据。随后,我们使用TwoSampleMR软件包进行了双样本孟德尔随机化分析。结果:我们的分析显示TI与糖尿病、T1D、血糖、HbA1c或T2D发病率之间没有因果关系的证据。同样,绿茶摄入与糖尿病、T1D、T2D、Glu或HbA1c之间没有遗传因果关系。这同样适用于草药茶和路易波士茶的摄入,因为与糖尿病、T1D、T2D、Glu或HbA1c没有遗传因果关系。结论:根据我们的研究结果,没有迹象表明TI与所有类型糖尿病的发病率之间存在因果关系,无论特定的茶类型如何。然而,为了全面了解TI对糖尿病发病率的潜在影响,包括摄入的数量和时间,需要通过额外的孟德尔随机化研究进行进一步评估
本文章由计算机程序翻译,如有差异,请以英文原文为准。
No genetic causal relationship between tea intake and diabetes: a two-sample Mendelian randomization study
Background: Previous studies have suggested a potential risk-reducing effect of tea intake (TI) on diabetes. However, the specific impacts of TI on different types of diabetes and its underlying mechanisms remain unclear. To further explore this topic, we conducted a comprehensive investigation to assess the causal relationship between TI and various types of diabetes, as well as its effects on blood glucose (Glu) and glycated hemoglobin (HbA1). Methods: We collected genome-wide association study data for TI, diabetes, type 1 diabetes (T1D), type 2 diabetes (T2D), Glu, HbA1, green tea intake, herbal tea intake, and Rooibos tea intake from the IEU database. Subsequently, we performed two-sample Mendelian randomization analysis using the TwoSampleMR package. Results: Our analysis revealed no evidence of a causal relationship between TI and the incidence of diabetes, T1D, blood Glu, HbA1c, or T2D. Similarly, no genetic causal relationship was found between green tea intake and diabetes, T1D, T2D, Glu, or HbA1c. The same applied to herbal tea intake and Rooibos tea intake, as there was no genetic causal link with diabetes, T1D, T2D, Glu, or HbA1c. Conclusion: Based on our findings, there is no indication of a causal relationship between TI and the incidence of all types of diabetes, regardless of the specific tea type. However, to comprehensively understand the potential effects of TI on diabetes incidence, including the quantity and timing of intake, further evaluation through additional Mendelian randomization studies is warranted
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