IF 3.9 2区 医学 Q2 NUTRITION & DIETETICS
Yongsheng Zhao, Renyan Zheng, Kexin Luo, Haiyang Zhao, Wanping Xiang
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引用次数: 0

摘要

背景:甜味剂因其低热量和甜味特性被广泛添加到食品和饮料中。然而,过去几十年来,甜味剂在癌症风险中的作用一直是一个广泛争论的话题:我们旨在利用孟德尔随机法(Mendelian randomization,MR)阐明常用天然甜味剂赤藓糖醇与肺癌(LC)风险之间的因果关系:赤藓糖醇及其代谢物的数据来自公开的全基因组关联研究数据。LC 及其亚型的汇总数据来自国际肺癌联盟肺癌跨学科研究和肺癌队列联盟进行的大规模遗传研究。我们进行了独立的双样本 MR 分析,以评估赤藓糖醇与 LC 及其亚型之间的因果关系:逆方差加权法磁共振分析显示,没有证据支持赤藓糖醇与肺癌及其组织学亚型之间存在因果关系。敏感性分析进一步支持了上述结果:我们的研究结果不支持赤藓糖醇与 LC 或其亚型之间存在遗传关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between erythritol and lung cancer: a two-sample Mendelian randomization study.

Background: Sweeteners have been widely added to food and beverages due to their low-calorie and sweetening properties. However, the role of sweeteners in cancer risk has been a subject of extensive debate over the past few decades.

Objective: We aimed to elucidate the causation between the commonly used natural sweetener erythritol and the risk of lung cancer (LC) using Mendelian randomization (MR).

Methods: Data on erythritol and its metabolites were obtained from publicly available genome-wide association studies data. Summary data on LC and its subtypes were obtained from a large-scale genetic study conducted by the Transdisciplinary Research of Cancer in Lung of the International Lung Cancer Consortium and the Lung Cancer Cohort Consortium. We conducted independent two-sample MR analyses to assess the causation between erythritol and LC and its subtypes.

Results: The inverse variance weighted method of MR analysis showed no evidence supporting causation between erythritol and LC or its histological subtypes. Sensitivity analysis further supported the results.

Conclusion: Our study findings do not support genetic association between erythritol and LC or its subtypes.

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来源期刊
Nutrition & Metabolism
Nutrition & Metabolism 医学-营养学
CiteScore
8.40
自引率
0.00%
发文量
78
审稿时长
4-8 weeks
期刊介绍: Nutrition & Metabolism publishes studies with a clear focus on nutrition and metabolism with applications ranging from nutrition needs, exercise physiology, clinical and population studies, as well as the underlying mechanisms in these aspects. The areas of interest for Nutrition & Metabolism encompass studies in molecular nutrition in the context of obesity, diabetes, lipedemias, metabolic syndrome and exercise physiology. Manuscripts related to molecular, cellular and human metabolism, nutrient sensing and nutrient–gene interactions are also in interest, as are submissions that have employed new and innovative strategies like metabolomics/lipidomics or other omic-based biomarkers to predict nutritional status and metabolic diseases. Key areas we wish to encourage submissions from include: -how diet and specific nutrients interact with genes, proteins or metabolites to influence metabolic phenotypes and disease outcomes; -the role of epigenetic factors and the microbiome in the pathogenesis of metabolic diseases and their influence on metabolic responses to diet and food components; -how diet and other environmental factors affect epigenetics and microbiota; the extent to which genetic and nongenetic factors modify personal metabolic responses to diet and food compositions and the mechanisms involved; -how specific biologic networks and nutrient sensing mechanisms attribute to metabolic variability.
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