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水合作用与代谢健康早期关联证据的探索之旅。

A Journey through the Early Evidence Linking Hydration to Metabolic Health.

机构信息

Health, Hydration and Nutrition Science Department, Danone Research, Palaiseau, France.

Department of Clinical Science, Skåne University Hospital, Lund University, Malmö, Sweden.

出版信息

Ann Nutr Metab. 2020;76 Suppl 1:4-9. doi: 10.1159/000515021. Epub 2021 Mar 26.

Abstract

The idea that water intake or hydration may play an intrinsic, independent role in modulating metabolic disease risk is relatively recent. Here, we outline the journey from early experimental works to more recent evidence linking water and hydration to metabolic health. It has been known for decades that individuals with existing metabolic dysfunction experience challenges to body water balance and have elevated arginine vasopressin (AVP), a key hormone regulating body fluid homeostasis. Later, intervention studies demonstrated that altering fluid balance in these individuals could worsen their condition, suggesting that hydration played a role in modulating glycemic control. More recently, observational and interventional studies in healthy individuals have implicated the hydration-vasopressin axis in the pathophysiology of metabolic diseases. Individuals with higher AVP (or its surrogate, copeptin) are at higher risk for developing type 2 diabetes and components of the metabolic syndrome, an association that remains even when controlling for known risk factors. Supporting preclinical work also suggests a causal role for AVP in metabolic dysfunction. It is known that individuals who habitually drink less fluids tend to have higher circulating AVP, which may be lowered by increasing water intake. In the short term, water supplementation in habitual low drinkers with high copeptin may reduce fasting glucose or glucagon, generating a proof of concept for the role of water supplementation in reducing incident metabolic disease. A large randomized trial is ongoing to determine whether water supplementation for 1 year in subjects with low water intake can meaningfully reduce fasting glucose, risk of new-onset diabetes, and other cardiometabolic risk factors.

摘要

水的摄入或水合作用可能对调节代谢性疾病风险起到内在的、独立的作用,这一观点相对较新。在这里,我们概述了从早期的实验工作到最近的证据,将水和水合作用与代谢健康联系起来的过程。几十年来,人们已经知道,患有现有代谢功能障碍的个体在维持身体水分平衡方面存在挑战,并且其精氨酸加压素(AVP)水平升高,这是一种调节体液平衡的关键激素。后来的干预研究表明,改变这些个体的液体平衡可能会使他们的病情恶化,这表明水合作用在调节血糖控制方面发挥了作用。最近,对健康个体的观察性和干预性研究表明,水合-加压素轴与代谢性疾病的病理生理学有关。具有较高 AVP(或其替代物, copeptin)的个体患 2 型糖尿病和代谢综合征成分的风险更高,即使在控制已知危险因素的情况下,这种关联仍然存在。支持临床前工作的证据还表明,AVP 在代谢功能障碍中具有因果关系。众所周知,习惯性少饮水的个体往往具有较高的循环 AVP,而增加水的摄入可以降低 AVP。在短期内,高 copeptin 的习惯性低饮水者补充水分可能会降低空腹血糖或胰高血糖素,为水补充在降低代谢性疾病发病风险中的作用提供了概念验证。一项大型随机试验正在进行中,以确定在低水摄入的受试者中补充水 1 年是否可以显著降低空腹血糖、新发糖尿病风险和其他心血管代谢危险因素。

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