Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism

As an essential vitamin, the role of riboflavin in human diet and health is increasingly being highlighted. Insufficient dietary intake of riboflavin is often reported in nutritional surveys and population studies, even in non-developing countries with abundant sources of riboflavin-rich dietary pro...

Full description

Bibliographic Details
Main Authors: Signe Mosegaard, Graziana Dipace, Peter Bross, Jasper Carlsen, Niels Gregersen, Rikke Katrine Jentoft Olsen
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/11/3847
id doaj-76653ba02a6a47df8efaae84106be4b0
record_format Article
spelling doaj-76653ba02a6a47df8efaae84106be4b02020-11-25T03:10:10ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-05-01213847384710.3390/ijms21113847Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of MetabolismSigne Mosegaard0Graziana Dipace1Peter Bross2Jasper Carlsen3Niels Gregersen4Rikke Katrine Jentoft Olsen5Research Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkResearch Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkResearch Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkResearch Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkResearch Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkResearch Unit for Molecular Medicine, Department for Clinical Medicine, Aarhus University and Aarhus University Hospital, 8200 Aarhus N, DenmarkAs an essential vitamin, the role of riboflavin in human diet and health is increasingly being highlighted. Insufficient dietary intake of riboflavin is often reported in nutritional surveys and population studies, even in non-developing countries with abundant sources of riboflavin-rich dietary products. A latent subclinical riboflavin deficiency can result in a significant clinical phenotype when combined with inborn genetic disturbances or environmental and physiological factors like infections, exercise, diet, aging and pregnancy. Riboflavin, and more importantly its derivatives, flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), play a crucial role in essential cellular processes including mitochondrial energy metabolism, stress responses, vitamin and cofactor biogenesis, where they function as cofactors to ensure the catalytic activity and folding/stability of flavoenzymes. Numerous inborn errors of flavin metabolism and flavoenzyme function have been described, and supplementation with riboflavin has in many cases been shown to be lifesaving or to mitigate symptoms. This review discusses the environmental, physiological and genetic factors that affect cellular riboflavin status. We describe the crucial role of riboflavin for general human health, and the clear benefits of riboflavin treatment in patients with inborn errors of metabolism.https://www.mdpi.com/1422-0067/21/11/3847riboflavinriboflavin deficiencyenergy metabolismmitochondriafatty acid oxidationacyl-CoA dehydrogenases
collection DOAJ
language English
format Article
sources DOAJ
author Signe Mosegaard
Graziana Dipace
Peter Bross
Jasper Carlsen
Niels Gregersen
Rikke Katrine Jentoft Olsen
spellingShingle Signe Mosegaard
Graziana Dipace
Peter Bross
Jasper Carlsen
Niels Gregersen
Rikke Katrine Jentoft Olsen
Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
International Journal of Molecular Sciences
riboflavin
riboflavin deficiency
energy metabolism
mitochondria
fatty acid oxidation
acyl-CoA dehydrogenases
author_facet Signe Mosegaard
Graziana Dipace
Peter Bross
Jasper Carlsen
Niels Gregersen
Rikke Katrine Jentoft Olsen
author_sort Signe Mosegaard
title Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
title_short Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
title_full Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
title_fullStr Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
title_full_unstemmed Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism
title_sort riboflavin deficiency—implications for general human health and inborn errors of metabolism
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-05-01
description As an essential vitamin, the role of riboflavin in human diet and health is increasingly being highlighted. Insufficient dietary intake of riboflavin is often reported in nutritional surveys and population studies, even in non-developing countries with abundant sources of riboflavin-rich dietary products. A latent subclinical riboflavin deficiency can result in a significant clinical phenotype when combined with inborn genetic disturbances or environmental and physiological factors like infections, exercise, diet, aging and pregnancy. Riboflavin, and more importantly its derivatives, flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD), play a crucial role in essential cellular processes including mitochondrial energy metabolism, stress responses, vitamin and cofactor biogenesis, where they function as cofactors to ensure the catalytic activity and folding/stability of flavoenzymes. Numerous inborn errors of flavin metabolism and flavoenzyme function have been described, and supplementation with riboflavin has in many cases been shown to be lifesaving or to mitigate symptoms. This review discusses the environmental, physiological and genetic factors that affect cellular riboflavin status. We describe the crucial role of riboflavin for general human health, and the clear benefits of riboflavin treatment in patients with inborn errors of metabolism.
topic riboflavin
riboflavin deficiency
energy metabolism
mitochondria
fatty acid oxidation
acyl-CoA dehydrogenases
url https://www.mdpi.com/1422-0067/21/11/3847
work_keys_str_mv AT signemosegaard riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
AT grazianadipace riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
AT peterbross riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
AT jaspercarlsen riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
AT nielsgregersen riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
AT rikkekatrinejentoftolsen riboflavindeficiencyimplicationsforgeneralhumanhealthandinbornerrorsofmetabolism
_version_ 1724660127899844608