Fructose metabolism and noncommunicable diseases: recent findings and new research perspectives
Abstract
Purpose of review There is increasing concern that dietary fructose may contribute to the development of noncommunicable diseases. This review identifies major new findings related to fructose's physiological or adverse effects. Recent findings Fructose is mainly processed in splanchnic organs (gut, liver, kidneys) to glucose, lactate, and fatty acids, which can then be oxidized in extrasplanchnic organs and tissues. There is growing evidence that splanchnic lactate production, linked to extrasplanchnic lactate metabolism, represents a major fructose disposal pathway during and after exercise. Chronic excess fructose intake can be directly responsible for an increase in intrahepatic fat concentration and for the development of hepatic, but not muscle insulin resistance. Although it has long been thought that fructose was exclusively metabolized in splanchnic organs, several recent reports provide indirect that some fructose may also be metabolized in extrasplanchnic cells, such as adipocytes, muscle, or brain cells; the quantity of fructose directly metabolized in extrasplanchnic cells, and its physiological consequences, remain however unknown. There is also growing evidence that endogenous fructose production from glucose occurs in humans and may have important physiological functions, but may also be associated with adverse health effects. Summary Fructose is a physiological nutrient which, when consumed in excess, may have adverse metabolic effects, mainly in the liver (h…
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High dietary fructose intake has been proposed to induce adverse health effects and has been associated with the development of metabolic disease.
“It should be noted that high dietary fructose intake has been proposed to induce adverse health effects and has been associated with the development of metabolic disease (Hannou et al. 2018; Tappy, 2018).”
From Fructose co‐ingestion to increase carbohydrate availability in athletes (2019) · cites this paper as Tappy, 2018
Cites
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Altered brain response to drinking glucose and fructose in obese adolescents
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Fructose co‐ingestion to increase carbohydrate availability in athletes
Fuchs, C. J., Gonzalez, J. T., & van Loon, L. J. C. (2019) · The Journal of Physiology · doi:10.1113/jp277116 · Cited by 63 · see citing works
“…fructose appears to be actively metabolized in the splanchnic area (i.e. intestine, liver and kidneys), whereas glucose appears to be largely transmitted passively from the splanchnic area into the systemic circulation (Gonzalez et al. 2017; Tappy & Rosset, 2017; Jang et al. 2018; Tappy, 2018; Fig.”
Background
- Authors
- Tappy, L.
- Affiliations
- Hôpital intercantonal de la Broye (CH)
- Corresponding author
- Tappy, Luc
- ORCID
- Tappy, Luc
- Venue
- Current Opinion in Clinical Nutrition & Metabolic Care
- Published
- 2018-05
- Volume
- 21
- Issue
- 3
- Pages
- 214-222
- ISSN
- 1363-1950 (ISSN-L)
- OpenAlex
- W2790391108
- Cited by
- 37
- References
- 3
- Citations by year
- 2026: 1 · 2025: 2 · 2023: 3 · 2022: 4 · 2021: 7 · 2020: 8 · 2019: 8 · 2018: 4
- FWCI
- 1.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Opinion in Clinical Nutrition & Metabolic Care (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- fructose metabolism, non-communicable diseases, splanchnic metabolism, lactate metabolism, hepatic insulin resistance, intrahepatic fat
- MeSH terms
- Noncommunicable Diseases, Dietary Sugars, Adipose Tissue, Diet, Dietary Carbohydrates, Fatty Acids, Feeding Behavior, Fructose, Glucose, Humans, Insulin, Insulin Resistance, Liver, Muscles, Exercise, Lactic Acid
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