建立24小时尿蔗糖加果糖作为总糖摄入量的预测性生物标志物。

Laurence S Freedman, Victor Kipnis, Douglas Midthune, John Commins, Brian Barrett, Virag Sagi-Kiss, Susana A Palma-Duran, Carol S Johnston, Diane M O'Brien, Natasha Tasevska
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引用次数: 6

摘要

背景:在英国(UK)和亚利桑那州(AZ)进行的两项喂养研究中,研究了24小时尿蔗糖和果糖(24uSF)作为总糖摄入量的生物标志物。我们比较了这些人群中生物标志物的表现,测试它是否符合预测性生物标志物的标准。方法:UK和AZ喂养研究分别纳入13名和98名参与者,年龄在18至70岁之间,在控制条件下食用正常饮食。在每个研究中建立了24uSF与总糖和个人特征相关的线性混合模型并进行了比较。阿斯利康校准的生物标志物方程被应用于生成生物标志物估计的英国参与者的总糖摄入量。还检验了模型在AZ研究亚群中的稳定性。结果:两项研究的模型系数相似[例如,log(总糖):UK 0.99, AZ 1.03, P = 0.67],校准的生物标志物个人特异性偏差与人与人之间方差的比值(UK 0.32, AZ 0.25, P = 0.68)。AZ方程估计的UK log(总糖摄入量)的均方预测误差为0.27,与AZ研究估计的0.28相似。在AZ研究中,log(总糖)的回归系数在年龄、性别和体重指数亚群中是相似的。结论:两项研究中相似的模型系数以及AZ方程对英国糖摄入量的良好预测表明,24uSF符合预测生物标志物的标准。在其他人群中测试生物标志物性能是可取的。影响:24uSF生物标志物的应用将能够更好地评估糖摄入在慢性疾病(包括癌症)风险中的作用。见普伦蒂斯的相关评论,第1151页。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Establishing 24-Hour Urinary Sucrose Plus Fructose as a Predictive Biomarker for Total Sugars Intake.

Establishing 24-Hour Urinary Sucrose Plus Fructose as a Predictive Biomarker for Total Sugars Intake.

Background: Twenty-four-hour urinary sucrose and fructose (24uSF) has been studied as a biomarker of total sugars intake in two feeding studies conducted in the United Kingdom (UK) and Arizona (AZ). We compare the biomarker performance in these populations, testing whether it meets the criteria for a predictive biomarker.

Methods: The UK and AZ feeding studies included 13 and 98 participants, respectively, aged 18 to 70 years, consuming their usual diet under controlled conditions. Linear mixed models relating 24uSF to total sugars and personal characteristics were developed in each study and compared. The AZ calibrated biomarker equation was applied to generate biomarker-estimated total sugars intake in UK participants. Stability of the model across AZ study subpopulations was also examined.

Results: Model coefficients were similar between the two studies [e.g., log(total sugars): UK 0.99, AZ 1.03, P = 0.67], as was the ratio of calibrated biomarker person-specific bias to between-person variance (UK 0.32, AZ 0.25, P = 0.68). The AZ equation estimated UK log(total sugar intakes) with mean squared prediction error of 0.27, similar to the AZ study estimate (0.28). Within the AZ study, the regression coefficients of log(total sugars) were similar across age, gender, and body mass index subpopulations.

Conclusions: Similar model coefficients in the two studies and good prediction of UK sugar intakes by the AZ equation suggest that 24uSF meets the criteria for a predictive biomarker. Testing the biomarker performance in other populations is advisable.

Impact: Applications of the 24uSF biomarker will enable improved assessment of the role of sugars intake in risk of chronic disease, including cancer. See related commentary by Prentice, p. 1151.

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