Effects of acute fructose loading on levels of serum uric acid-a pilot study.


Journal

European journal of clinical investigation
ISSN: 1365-2362
Titre abrégé: Eur J Clin Invest
Pays: England
ID NLM: 0245331

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 01 06 2018
revised: 28 09 2018
accepted: 22 10 2018
pubmed: 29 10 2018
medline: 23 7 2019
entrez: 29 10 2018
Statut: ppublish

Résumé

Fructose intake may lead to hyperuricaemia, which is associated with increased risk and progression of kidney disease. We aimed to explore the acute effects of fructose loading from different sources, with and without a pizza, on levels of serum uric acid in patients with chronic kidney disease (CKD), type 2 diabetes (T2D) without CKD, and in healthy subjects (HS). The study included six HS, and three CKD stage 4-5 and seven T2D patients. Drinks consumed were blueberry drink (17.5 g fructose), Coca-Cola (18 g fructose) and fructose drink (35 g fructose). The drinks were also combined with pizza, in total six interventions. Serum samples were collected fasting and 30, 60, 90 and 120 minutes after intake and also 240 minutes after drink + pizza, and analysed for fructose, uric acid and triglycerides. Postprandial responses were explored using repeated-measure ANOVA. Baseline serum uric acid levels were increased in CKD (P = 0.037). There were significant differences in serum fructose and serum uric levels over time between drinks and drinks + pizza for all groups (P < 0.001 and P < 0.05, respectively). The highest peak in serum fructose followed the fructose drink interventions and the lowest the blueberry drink. The fructose drink interventions gave the highest responses in serum uric acid and the lowest responses followed the blueberry drink. Triglycerides increased following pizza interventions (P < 0.001). Intake of fructose increases serum uric acid. The fructose intake via a blueberry drink induced lowest increase and thus may be protective.

Sections du résumé

BACKGROUND BACKGROUND
Fructose intake may lead to hyperuricaemia, which is associated with increased risk and progression of kidney disease. We aimed to explore the acute effects of fructose loading from different sources, with and without a pizza, on levels of serum uric acid in patients with chronic kidney disease (CKD), type 2 diabetes (T2D) without CKD, and in healthy subjects (HS).
METHODS METHODS
The study included six HS, and three CKD stage 4-5 and seven T2D patients. Drinks consumed were blueberry drink (17.5 g fructose), Coca-Cola (18 g fructose) and fructose drink (35 g fructose). The drinks were also combined with pizza, in total six interventions. Serum samples were collected fasting and 30, 60, 90 and 120 minutes after intake and also 240 minutes after drink + pizza, and analysed for fructose, uric acid and triglycerides. Postprandial responses were explored using repeated-measure ANOVA.
RESULTS RESULTS
Baseline serum uric acid levels were increased in CKD (P = 0.037). There were significant differences in serum fructose and serum uric levels over time between drinks and drinks + pizza for all groups (P < 0.001 and P < 0.05, respectively). The highest peak in serum fructose followed the fructose drink interventions and the lowest the blueberry drink. The fructose drink interventions gave the highest responses in serum uric acid and the lowest responses followed the blueberry drink. Triglycerides increased following pizza interventions (P < 0.001).
CONCLUSIONS CONCLUSIONS
Intake of fructose increases serum uric acid. The fructose intake via a blueberry drink induced lowest increase and thus may be protective.

Identifiants

pubmed: 30368775
doi: 10.1111/eci.13040
doi:

Substances chimiques

Sweetening Agents 0
Triglycerides 0
Uric Acid 268B43MJ25
Fructose 30237-26-4

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13040

Subventions

Organisme : The Family Erling Persson Foundation
Organisme : The Diabetic Theme Centre
Organisme : Swedish Research Council

Informations de copyright

© 2018 Stichting European Society for Clinical Investigation Journal Foundation.

Auteurs

Camilla Olofsson (C)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Björn Anderstam (B)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Ann-Christin Bragfors-Helin (AC)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Monica Eriksson (M)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Abdul R Qureshi (AR)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Bengt Lindholm (B)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Agneta Hilding (A)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

Wieslaw Wiczkowski (W)

Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland.

Nicola Orsini (N)

Department of Public Health Sciences, Karolinska Institutet, Stockholm, Sweden.

Peter Stenvinkel (P)

Division of Renal Medicine M99, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Neda Rajamand Ekberg (N)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

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Classifications MeSH