Expression of the fructose transporter GLUT5 in patients with fructose malabsorption

Author:

Staubach Pia1,Koch Anna Katharina2,Langhorst Jost2,Schreiber Stefan3,Röcken Christoph1,Helwig Ulf43

Affiliation:

1. Department of Pathology, Christian-Albrechts-University Kiel, Germany

2. Department of Internal and Integrative Medicine, Kliniken Essen-Mitte, University of Duisburg-Essen, Germany

3. Department of Internal Medicine, Christian-Albrechts-University Kiel, Germany

4. Specialist Practice for Internal Medicine, Oldenburg, Oldenburg Germany

Abstract

Abstract Background Patients with abdominal symptoms are frequently diagnosed with fructose malabsorption (FM). Fructose is absorbed by monosaccharide transporters located in the brush border of the human small intestine. The aim of this study was to investigate the histoanatomical distribution of the main fructose transporter GLUT5. Materials and methods We studied 223 patients diagnosed with FM by a hydrogen breath test and grouped according to their response to a fructose-free diet. The control group were 42 healthy individuals and 29 patients with celiac disease (CD). The fructose breath test was done with 50 g fructose. The expression of Glut5 in duodenal biopsy specimens was studied by immunohistochemistry. The Kruskal-Wallis-test and Mann-Whitney U-test were used to carry out the statistical analysis. Results The histoanatomical expression pattern of GLUT5 did not differ significantly between those patients with FM who responded completely to a fructose-free diet (n = 183) and healthy individuals (n = 42); nor did it correlate to H2 production measured in fructose breath testing. In patients with FM, the GLUT5 expression pattern did not differ between those individuals responding to a fructose-free diet and those who did not. However, GLUT5 expression pattern was significantly different in patients with CD (n = 29) compared to patients with FM and to healthy individuals (p = 0.009). Conclusion GLUT5 expression patterns are not be related to adult patients with FM. However, in secondary malabsorption, a decreased GLUT5 expression was found. Further investigation is needed to understand the essential factors in FM and the influence on functional gastrointestinal disorders.

Funder

Registered Society for Science and Education in the Internal Medicine and the University of Kiel Department of Pathology

Publisher

Georg Thieme Verlag KG

Subject

Gastroenterology

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1. GLUT5: structure, functions, diseases and potential applications;Acta Biochimica et Biophysica Sinica;2023-09-07

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