Prentice Ross L
Division of Public Health Sciences, Fred Hutchinson Cancer Center, Department of Biostatistics, University of Washington, 1100 Fairview Avenue North, P.O. Box 19024, Seattle, WA 98109-1024, USA.
Metabolites. 2024 May 10;14(5):276. doi: 10.3390/metabo14050276.
Metabolomics profiles from blood, urine, or other body fluids have the potential to assess intakes of foods and nutrients objectively, thereby strengthening nutritional epidemiology research. Metabolomics platforms may include targeted components that estimate the relative concentrations for individual metabolites in a predetermined set, or global components, typically involving mass spectrometry, that estimate relative concentrations more broadly. While a specific metabolite concentration usually correlates with the intake of a single food or food group, multiple metabolites may be correlated with the intake of certain foods or with specific nutrient intakes, each of which may be expressed in absolute terms or relative to total energy intake. Here, I briefly review the progress over the past 20 years on the development and application intake biomarkers for foods/food groups, nutrients, and dietary patterns, primarily by drawing from several recent reviews. In doing so, I emphasize the criteria and study designs for candidate biomarker identification, biomarker validation, and intake biomarker application. The use of intake biomarkers for diet and chronic disease association studies is still infrequent in nutritional epidemiology research. My comments here will derive primarily from our research group's recent contributions to the Women's Health Initiative cohorts. I will complete the contribution by describing some opportunities to build on the collective 20 years of effort, including opportunities related to the metabolomics profiling of blood and urine specimens from human feeding studies that approximate habitual diets.
来自血液、尿液或其他体液的代谢组学图谱有潜力客观评估食物和营养素的摄入量,从而加强营养流行病学研究。代谢组学平台可能包括估计预定组中单个代谢物相对浓度的靶向成分,或通常涉及质谱分析、更广泛地估计相对浓度的整体成分。虽然特定代谢物浓度通常与单一食物或食物组的摄入量相关,但多种代谢物可能与某些食物的摄入量或特定营养素摄入量相关,其中每一种都可以用绝对量表示或相对于总能量摄入量表示。在此,我主要借鉴最近的几篇综述,简要回顾过去20年在食物/食物组、营养素和饮食模式的摄入量生物标志物的开发和应用方面取得的进展。在此过程中,我强调了候选生物标志物识别、生物标志物验证和摄入量生物标志物应用的标准和研究设计。在营养流行病学研究中,饮食与慢性病关联研究中摄入量生物标志物的使用仍然很少见。我在此的评论将主要来自我们研究小组最近对妇女健康倡议队列研究的贡献。我将通过描述基于20年集体努力的一些机会来完善这一贡献,包括与来自接近习惯饮食的人体喂养研究的血液和尿液样本的代谢组学分析相关的机会。