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|a Schneeman, Barbara
|e [editor]
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|a Scanning for new evidence on riboflavin to support a dietary reference intake review
|h Elektronische Ressource
|c Barbara O. Schneeman, Ann L. Yaktine, and Alice Vorosmarti, editors ; Committee on Scanning for New Evidence on Riboflavin to Support a Dietary Reference Intake Review, Food and Nutrition Board, Health and Medicine Division
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| 260 |
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|a Washington, DC
|b The National Academies Press
|c 2021, [2021]
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| 300 |
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|a 1 PDF file (ix, 63 pages)
|b illustrations
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|a Includes bibliographical references
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|a Yaktine, Ann L.
|e [editor]
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|a Vorosmarti, Alice
|e [editor]
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|a National Academies of Sciences, Engineering, and Medicine (U.S.)
|b Committee on Scanning for New Evidence on Riboflavin to Support a Dietary Reference Intake Review
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|a eng
|2 ISO 639-2
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| 989 |
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|b NCBI
|a National Center for Biotechnology Information
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|a Consensus study report
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|u https://www.ncbi.nlm.nih.gov/books/NBK572709
|3 Volltext
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|a 641.1
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|a 572/.39
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|a The Dietary Reference Intakes (DRIs) are a set of evidence-based nutrient reference values for intakes that include the full range of age, gender, and life stage groups in the US and Canada. At the request of the U.S. Department of Agriculture, Agricultural Research Service and the U.S. Department of Health and Human Services, Food and Drug Administration, Center for Food Safety and Applied Nutrition, the National Academies of Science, Engineering, and Medicine convened an ad hoc committee to carry out a literature search and evidence scan of the peer-reviewed published literature on indicators of nutritional requirements, toxicity, and chronic disease risk reduction for riboflavin. Scanning for New Evidence on Riboflavin to Support a Dietary Reference Intake Review builds on the methodology for evidence scanning nutrients (which have existing DRIs) to determine whether there is new and relevant knowledge available that may merit a formal reexamination of DRIs for riboflavin. This report offers comments on the methodological approach to the evidence scan and discusses its findings and interpretation of the process to provide the study sponsors with a greater context to support their interpretation and application of the reported results
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