Related Experiment Video
Updated: Apr 15, 2026

Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
Recommendations on reporting requirements for flavonoids in research
Douglas A Balentine1, Johanna T Dwyer1, John W Erdman2
1From Unilever, Englewood Cliffs, NJ (DAB); Tufts University, Jean Mayer Human Nutrition Research Center on Aging, Boston, MA (JTD); University of Illinois at Urbana-Champaign, Urbana-Champaign, IL (JWE); Purdue University, West Lafayette, IN (MGF); The Sugar Association, Washington, DC (PCG); USDA Agricultural Research Service, Beltsville, MD (JMH); and Mars, Incorporated, McLean, VA (CLK-U).
Abstract:
Numerous observational and intervention-based human studies support the notion of a beneficial role for dietary flavonoids in human health. Despite these studies, it is not yet possible to make dietary recommendations with regard to the types and amounts of flavonoids to be consumed. The inherent diversity of flavonoid structure, chemistry, and natural distribution in foods lends itself to errors in reporting the types and/or amounts of flavonoids consumed, as well as incomplete recognition of requirements for intervention studies that aim to assess their benefits in a clinical setting. A need exists for guidelines that facilitate the design and reporting of flavonoid research. With a focus on clinical studies, this article 1) outlines limitations commonly encountered in the field of flavonoid research, including the inconsistent use of nomenclature, inappropriate analytic methods, inconsistent use of existing flavonoid databases, and the lack of full consideration in the design of test materials for intervention trials, and 2) provides guidance for future studies with a focus on clinical intervention trials. Adoption of this guidance will facilitate more accurate and interpretable research that will support the development of dietary recommendations regarding the intake of flavonoids.
More Related Videos
Related Concept Videos
Cancer Prevention
Some...
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Reporter Genes
Drug Regulation

