Results 1 to 10 of about 6,347 (129)

Internalizing psychological symptoms in children and adolescents with fructose malabsorption [PDF]

Frontiers in Psychology
IntroductionDue to an inhibited tryptophan resorption, patients with fructose malabsorption are expected to experience decreased serotonin synthesis. A deficiency of serotonin may cause internalizing mental disorders like depression and anxiety, and a ...
Stephan Bongard
exaly   +7 more sources

Fructose malabsorption and fructan malabsorption are associated in patients with irritable bowel syndrome [PDF]

BMC Gastroenterology
Background Food malabsorption and intolerance is implicated in gastrointestinal symptoms among patients with irritable bowel syndrome (IBS). Key triggers include fructose and fructan.
Twan Sia, Riki O. Tanaka, Albert Mousad, Aditya P. Narayan, Kristen Si, Leeon Bacchus, Hind Ouerghi, Aashka Patel, Arnav Patel, Evan Cunningham, Taylor Epstein, Jerry Fu, Stanley Liu, Raisa Khuda, Paige McDonald, Shibani Mallik, Joanna McNulty, Michelle Pan, John Leung   +18 more
doaj   +4 more sources

Fructose Malabsorption, Gut Microbiota and Clinical Consequences: A Narrative Review of the Current Evidence [PDF]

Life
Fructose malabsorption is characterized as the incomplete absorption of fructose in the small intestine. Fructose is one of the most common monosaccharides in the human diet.
Catarina D Simões, Ana S Sousa, Amelia Sarmento   +2 more
exaly   +4 more sources

Fructose Malabsorption and Intolerance: Effects of Fructose with and without Simultaneous Glucose Ingestion [PDF]

Critical Reviews in Food Science and Nutrition, 2011
Concern exists that increasing fructose consumption, particularly in the form of high-fructose corn syrup, is resulting in increasing rates of fructose intolerance and aggravation of clinical symptoms in individuals with irritable bowel syndrome. Most clinical trials designed to test this hypothesis have used pure fructose, a form not commonly found in
Marie E Latulippe
exaly   +5 more sources

Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption [PDF]

BMC Gastroenterology, 2022
Background While role of ALDOB-related gene variants for hereditary fructose intolerance is well established, contribution of gene variants for acquired fructose malabsorption (e.g. SLC2A5, GLUT5) is not well understood.
Irina Taneva, Dorothee Grumann, Dietmar Schmidt, Elina Taneva, Ulrike von Arnim, Thomas Ansorge, Thomas Wex   +6 more
doaj   +2 more sources

Fructose malabsorption. [PDF]

Mol Cell Pediatr, 2016
Incomplete intestinal absorption of fructose might lead to abdominal complaints such as pain, flatulence and diarrhoea. Whether defect fructose transporters such as GLUT5 or GLUT2 are involved in the pathogenesis of fructose malabsorption is a matter of debate.
Ebert K, Witt H.
europepmc   +4 more sources

Fructose Malabsorption in Systemic Sclerosis. [PDF]

Medicine (Baltimore), 2015
The deleterious effect of fructose, which is increasingly incorporated in many beverages, dairy products, and processed foods, has been described; fructose malabsorption has thus been reported in up to 2.4% of healthy subjects, leading to digestive clinical symptoms (eg, pain, distension, diarrhea). Because digestive involvement is frequent in patients
Marie I, Leroi AM, Gourcerol G, Levesque H, Ménard JF, Ducrotte P.   +5 more
europepmc   +5 more sources

IS THERE A RELATIONSHIP BETWEEN INTESTINAL FRUCTOSE MALABSORPTION, GASTROINTESTINAL SYMPTOMS AFTER FRUCTOSE OVERLOAD, AND BODY ADIPOSITY IN ADOLESCENTS? [PDF]

Arquivos de Gastroenterologia
Background: Over the past several decades, dietary fructose intake has increased significantly, along with the prevalence of obesity. Fructose malabsorption is associated with gastrointestinal symptoms and may lead to fructose intolerance.
Dayane Pêdra Batista de FARIA, Ana Paula Bidutte CORTEZ, Ricardo Palmero OLIVEIRA, Maria Sylvia de Souza VITALLE, Patrícia da Graça Leite SPERIDIÃO, Mauro Batista de MORAIS   +5 more
doaj   +3 more sources

Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review

Diagnostics, 2023
Glucose-galactose malabsorption is a rare inherited autosomal recessive genetic defect. A mutation in the glucose sodium-dependent transporter-1 gene will alter the transportation and absorption of glucose and galactose in the intestine.
Nawaf W Alruwaili
exaly   +3 more sources

Giardia intestinalis and Fructose Malabsorption: A Frequent Association. [PDF]

Nutrients, 2019
Nowadays, scientific studies are emerging on the possible etiological role of intestinal parasites in functional digestive disorders. Our study was carried out with healthy individuals (control group; n = 82) and symptomatic patients with lactose or fructose malabsorption, including positive (malabsorbers; n = 213) and negative (absorbers; n = 56 ...
Trelis M, Taroncher-Ferrer S, Gozalbo M, Ortiz V, Soriano JM, Osuna A, Merino-Torres JF.   +6 more
europepmc   +7 more sources