The value of [1-14C] phenylacetic oil as a clinical test for malassimilation was evaluated in 20 normal volunteers, 20 patients with various non-gastrointestinal illnesses, 10 patients with malabsorption, and 7 patients with maldigestion. All subjects were given a test meal composed of 0.5 ml of 14C-phenylacetic oil (0.5 muCi) in 30 g of cheese and 40 g of bread. The test was simultaneously run with D-xylose. Urine was collected over a 5 h period and assayed for 14C and D-xylose. Mean urinary recovery of 14C label in volunteers was 65 +/- 15% of th: administered dose. All 10 patients with malabsorption had abnormal D-xylose excretion and excreted less than 35% of the 14C-phenylacetate. 6 of 7 patients with maldigestion excreted less than 15%, while in the 7th patient excretion of 14C label was borderline (35%). 4 of the 7 patients with maldigestion had abnormal D-xylose excretion, probably as a result of bacterial overgrowth. The procedure described is a cost-effective, simple, rapid, and safe test for fat absorption which may be conveniently run with a D-xylose excretion test.
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http://dx.doi.org/10.1016/s0140-6736(80)90717-5 | DOI Listing |
Clin Nutr ESPEN
February 2025
Medical Affairs, Pediatric Medical Nutrition, Nestlé Health Science, Switzerland.
Background & Aims: Enteral formulas containing predigested lipids to support the needs of patients with fat maldigestion are currently unavailable. Monoacylglycerol (MAG)-rich oils offer potential benefits for fat absorption without prior digestion, but their safety and tolerability in enteral formulas need evaluation. We assessed the safety and tolerability of a new formula containing predigested lipids in the form of MAG-rich oil.
View Article and Find Full Text PDFCureus
November 2024
Department of Public Health, The Ministry of Health, Manama, BHR.
Introduction Children with cystic fibrosis (CF) have lipid maldigestion due to pancreatic insufficiency, which causes malabsorption of fat-soluble vitamins. The primary objective of this study was to assess the prevalence of vitamin E deficiency among children with CF. The secondary objective was to examine the correlation between vitamin E levels with demographic data, laboratory findings, and the number of pulmonary exacerbations.
View Article and Find Full Text PDFDig Dis Sci
January 2025
Gastrointestinal Motility Laboratory, Department of Gastroenterology, National Institute of Medical Sciences and Nutrition Salvador Zubirán, Mexico D.F., Mexico.
Background: Irritable bowel syndrome symptoms are associated with diverse pathophysiological mechanisms including small intestinal bacterial overgrowth and food intolerance. Small intestinal bacterial overgrowth leads to the decreased activity of several digestive enzymes, including lactase.
Aims: To assess the efficacy of rifaximin-alpha on the symptoms and lactase activity of patients with irritable bowel syndrome without constipation.
Clin Gastroenterol Hepatol
October 2024
Gastrointestinal Genetics Lab, CIC bioGUNE - BRTA, Derio, Spain; Ikerbasque, Basque Foundation for Science, Bilbao, Spain; Department of Medicine and Surgery, LUM University, Casamassima, Italy. Electronic address:
Background & Aims: Limiting the dietary intake of certain carbohydrates has therapeutic effects in some but not all irritable bowel syndrome (IBS) patients. We investigated genetic variation in human Carbohydrate-Active enZYmes (hCAZymes) genes in relationship to the response to a FODMAP-lowering diet in the DOMINO study.
Methods: hCAZy polymorphism was studied in patients with IBS from the dietary (FODMAP-lowering; n = 196) and medication (otilonium bromide; n = 54) arms of the DOMINO trial via targeted sequencing of 6 genes of interest (AMY2B, LCT, MGAM, MGAM2, SI, and TREH).
J Med Life
June 2024
Faculty of Biology, University of Bucharest, Bucharest, Romania.
Cystic fibrosis (CF) is a recessive inherited disorder caused by genetic mutations in the CF transmembrane conductance regulator () gene. It is a multisystem condition that primarily induces abnormal mucus accumulation in the respiratory system and obstructs the intrapancreatic common bile duct, causing a reduction in the delivery of digestive enzymes to the small intestine. Thus, patients with CF are characterized by maldigestion, malabsorption, and recurrent airway bacterial infections.
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