Lactose Malabsorption and Lactose Intolerance in Children with Inflammatory Bowel Diseases [PDF]
Gastroenterology Research and Practice, 2019 Background. Insufficient vitamin D and calcium intake associated with the restricted intake of milk and dairy products can lead to poor health outcomes like malnutrition and abnormal bone mineralization.
Martyna Jasielska +1 more
doaj +3 more sources
13910C>T and 22018G>A LCT gene polymorphisms in diagnosing hypolactasia in children. [PDF]
United European Gastroenterol J, 2019 Background Primary lactose intolerance (PLI) is a gradual decrease of lactase activity that usually manifests at the age of 1–5 years. It has been proved that PLI is related to a single‐nucleotide polymorphism of the lactase (LCT) gene. Objective An evaluation was performed on the usefulness of genetic tests in detecting LCT 13910C>T and 22018G>A ...
Tomczonek-Moruś J +4 more
europepmc +4 more sources
Effects of exogenous lactase administration on hydrogen breath excretion and intestinal symptoms in patients presenting lactose malabsorption and intolerance [PDF]
BioMed Research International, Volume 2014, Issue 1, 2014., 2014 To establish whether supplementation with a standard oral dose of Beta-Galactosidase affects hydrogen breath excretion in patients presenting with lactose malabsorption.
Boi, MF, Gilli, A, Ibba, I, Usai, P
core +3 more sources
Perceived food intolerances can guide personalization of the FODMAP diet but not the choice of dietary intervention. [PDF]
JGH Open, 2023 JGH Open, Volume 7, Issue 11, Page 737-739, November 2023.
Rhys-Jones D, Yao CK, Gibson PR.
europepmc +2 more sources
Regulation of intestinal lactase in adult hypolactasia. [PDF]
Journal of Clinical Investigation, 1992 Relative deficiency of intestinal lactase activity during adulthood, adult hypolactasia, is a common condition worldwide. We studied the regulation of lactase-phlorizin hydrolase in normal and adult hypolactasic subjects by correlating transcript abundance in intestinal biopsies with relative synthetic rates for the protein in cultured intestinal ...
M Lloyd +8 more
openalex +4 more sources
Congruency of Genetic Predisposition to Lactase Persistence and Lactose Breath Test. [PDF]
Nutrients, 2019 The physiological decline of lactase production in adulthood, in some individuals, is responsible for the so-called “Lactose Intolerance.” This clinical syndrome presents with gastrointestinal and non-gastrointestinal symptoms following the consumption ...
Coluccia E +10 more
europepmc +3 more sources
A felnőttkori hypolactasia születésikohorsz-vizsgálata [PDF]
Orvosi Hetilap, 2019 Abstract: Introduction and aim: To assess the prevalence of lactase gene promoter C/T13910 phenotypes in patients with lactose intolerance symptoms and to analyze the birth-cohort phenomenon in lactose-intolerant patients. Method: 1266 patients consulted between 2010 and 2017 were enrolled.
György Miklós Buzás
openalex +4 more sources
Phase IV noninferiority controlled randomized trial to evaluate the impact on diagnostic thinking and patient management and the test-retest reproducibility of the Gaxilose test for hypolactasia diagnosis. [PDF]
Medicine (Baltimore), 2018 Monsalve-Hernando C +13 more
europepmc +2 more sources
The lactase persistence genotype is a protective factor for the metabolic syndrome [PDF]
Genetics and Molecular Biology, 2014 The Metabolic Syndrome (MetS) is defined as a pattern of metabolic disturbances, which include central obesity, insulin resistance and hyperglycemia, dyslipidemia, and hypertension.
Deise C. Friedrich +6 more
doaj +3 more sources