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Gluten Problems and Solutions
by Stephen Gislason MD

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Stephen Gislason's Preface

What is Gluten?

What is Celiac Disease?

Gluten & Food

Digestive Tract Permeability

Diseases Related to Celiac Disease

Allergy

Digestive Tract Permeability

Diseases Related to Celiac Disease

Gluten-Free Diet Revision

Celiac Diagnosis

Gluten Psychiatry
Dermatitis Herpetiformis
Celiac Disease & Cancer

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The Alpha Nutrition Program is Gluten free

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Celiac Disease Study Guide  

Increased Intestinal Permeability

Patients with celiac disease have circulating antibodies to food proteins; they also have circulating immune complexes, revealing increased permeability of the digestive tract to macromolecules, especially gluten and other food proteins.  The reduction or absence of an intestinal IgA barrier that increases absorption of antigenic material from the gut. Antibodies to some of the food antigens can cross react with the host's self components and can produce autoimmune disease. Measurements of GIT permeability are important tools of research and clinical assessment.

Elemental Formulas Solve Permeability Problems

Elemental nutrient formulas are designed to solve the problem of increased GIT permeability. By excluding potential antigens from Alpha Nutrition formulas, nutrients are provided in a safe context. All proteins and peptides are excluded. Hydrolyzed proteins are not used so that there is no risk of peptide effects.  Instead of proteins or hydrolyzed proteins, free l-form amino acids are provided.   The individual amino acids fall into two groups: the essential AA's, which must be ingested, and the non-essential AA's, which can be synthesized in the body and need not appear in the food. Nine amino acids are considered essential nutrients, while another eleven or so can be synthesized from the essential amino acids. All 19 nutrient amino acids are included in the Alpha Nutrition Formulas as individual amino acids rated at 100% purity, with the highest solubility attainable. 

Abstracts

GIT Permeability Abstracts

Lymphocytic gastritis and gastric permeability in patients with celiac disease.

Author Vogelsang H; Oberhuber G; Wyatt J
Address Department of Gastroenterology and Hepatology, University Clinic of Internal Medicine IV, Vienna, Austria.
Source Gastroenterology, 1996 Jul, 111:1, 73-7

 

Abstract Lymphocytic gastritis is associated with celiac disease. Gastric permeability can now be assessed by a sucrose test, and intestinal permeability measured by a lactulose/mannitol test is increased in untreated celiac patients. The aim of this study was to prospectively compare gastric and intestinal permeability with histological changes of the stomach and small bowel in patients with celiac disease. METHODS: Gastric and intestinal permeability were measured by oral or duodenal (during endoscopy) administration of a triple sugar solution containing 20 g sucrose, 10 g lactulose, and 5 g mannitol in 100 mL water in 43 adult patients with celiac disease (28 without diet) and in 30 healthy controls. Endoscopical biopsy specimens were taken from the antrum and distal duodenum and investigated for intraepithelial lymphocyte counts. RESULTS: Urinary sucrose excretion decreased after duodenal administration (n = 8) as opposed to oral administration and thus measured gastric permeability in celiac disease. Gastric permeability was elevated in 60% of the celiac patients and correlated with antral intraepithelial lymphocyte counts. Intestinal permeability (measured by a lactulose/mannitol test) was also elevated in 69% of the celiac patients and correlated with duodenal intraepithelial counts. CONCLUSIONS: There is a high prevalence of lymphocytic gastritis in untreated celiac disease associated with elevated gastric permeability. Celiac disease seems to be a general disorder of the gastrointestinal tract associated with disturbed permeability.
 

Gut permeability to human alpha-lactalbumin, beta-lactoglobulin, mannitol, and lactulose in celiac disease.

Author Kuitunen M; Savilahti E
Address Children's Hospital, University of Helsinki, Finland.
Source J Pediatr Gastroenterol Nutr, 1996 Feb, 22:2, 197-204

 

Abstract Our objective was to examine the permeability of the gut to protein macromolecules and sugar probes and their possible association in celiac disease patients. We studied the permeability to human alpha-lactalbumin, beta-lactoglobulin, mannitol, and lactulose on 46 occasions in 33 celiac disease patients in various phases of the disease; in addition, mannitol and lactulose permeability was studied in 18 healthy controls. Lactalbumin absorption was detected in 19 of 42 patients tested, more often in celiac disease patients with villous atrophy than in those with normal jejunal biopsy (p = 0.01). Higher absorption of lactalbumin was found in patients with subtotal villous atrophy than in those with normal biopsy (p = 0.02). beta-lactoglobulin was found in four of 42 patients tested. Less mannitol was absorbed by patients with either subtotal or partial villous atrophy than by those with normal histology (p = 0.001 and 0.006, respectively). Lactulose recovery was higher in newly diagnosed patients and patients with subtotal villous atrophy than in controls (p = 0.007 and 0.03, respectively). The lactulose/mannitol ratio was higher in newly diagnosed patients and patients with villous atrophy than in controls (p = 0.002 and 0.002, respectively). The correlation between permeability to lactalbumin and mannitol and lactulose was poor. We conclude that permeability to proteins and sugar molecules is abnormal in celiac disease patients with mucosal damage and that they probably reflect different mechanisms of penetration.

Follow-up of celiac disease with D-xylose breath test.

Author Casellas F; De Torres I; Malagelada JR
Address Digestive System Research Unit, Hospital General Vall d'Hebron, Barcelona, Spain.
Source Dig Dis Sci, 1996 Oct, 41:10, 2106-11

 

Abstract Hydrogen breath tests (H2-BT) are commonly used to diagnose carbohydrate malabsorption. Specifically, the H2-BT with D-xylose has been shown to be as valid as the traditional urinary test for the recognition of intestinal malabsorption. We have now investigated the H2-BT with D-xylose in the follow-up of patients with celiac disease. Seventeen patients with celiac disease established clinically and confirmed by jejunal biopsy were studied. H2-BT was performed before and after treatment with a gluten-free diet for at least five months. Alveolar breath samples were obtained before administering orally 25 g of D-xylose and thereafter at 30 min intervals for 5 hr. Samples were analyzed for H2 by chromatography. Simultaneously, the 5-hr urinary excretion of D-xylose was determined by colorimetry. Gluten removal significantly decreased the H2 delta change (from 56.5 +/- 5.9 ppm to 32.2 +/- 8.8, P < 0.05). A similar decrease was observed in the area under the curve (P < 0.05). Conversely, urinary D-xylose excretion increased significantly (P < 0.05). Eleven of the 17 celiacs clinically improved after treatment. The H2-BT normalized in every patient who entered remission on the gluten-free diet, whereas the urinary D-xylose excretion remained abnormal in six of them. In the six nonresponder patients the H2-BT remained high in five, whereas urinary D-xylose excretion paradoxically normalized in 2. We conclude that H2-BT with D-xylose is a useful and practical test for the follow-up of celiac disease and is simpler and more reliable than the urinary D-xylose test.

Screening for celiac disease in first-degree relatives of patients with celiac disease by lactulose/mannitol test.

Author Vogelsang H; Wyatt J; Penner E; Lochs H
Address Department of Gastroenterology, University of Vienna, Austria.
Source Am J Gastroenterol, 1995 Oct, 90:10, 1838-42

 

Abstract OBJECTIVES: In first-degree relatives of celiac patients, the risk of oligosymptomatic celiac disease is elevated. These individuals therefore also have a higher potential for malignancy or nutritional deficiencies. Lactulose/mannitol permeability is increased in untreated celiac patients and has been recommended to screen for celiac disease. We investigated the usefulness of a lactulose/mannitol home test kit for screening first-degree relatives home test kit for screening first-degree relatives of celiac patients. METHODS: The lactulose/mannitol test was performed at home by 111 first-degree relatives. These subjects received the test kit from celiac index patients, were instructed by an information sheet how to carry out the test, and were asked about their symptoms by questionnaire. When lactulose/mannitol permeability was abnormal, endomysial antibodies were tested by immunofluorescence. Any relatives with positive endomysial antibodies were then biopsied. To investigate the specificity of the lactulose/mannitol test for celiac disease, 40 patients with nonspecific gastrointestinal symptoms were tested. RESULTS: Lactulose/mannitol permeability was elevated in 34 (31%) relatives, but only nine (8%) of those relatives showed positive endomysial antibodies. Flat mucosa was found in all nine relatives after biopsy. The prevalence of celiac disease was much higher (42%) among 12 relatives who contacted the outpatient clinic themselves because of symptoms. Seventy-one percent of the remaining 21 relatives with elevated permeability demonstrated normal intestinal permeability at a control test within 1 yr. CONCLUSION: By combining the lactulose/mannitol test with endomysial antibody testing, we have developed a good strategy for use in screening for celiac disease among first-degree relatives.

Assessing the site of increased intestinal permeability in coeliac and inflammatory bowel disease.

Author Teahon K; Somasundaram S; Smith T; Menzies I; Bjarnason I
Address Department of Clinical Pharmacology, University of Newcastle upon Tyne.
Source Gut, 1996 Jun, 38:6, 864-9

 

Abstract The precise site of intestinal permeability changes in patients with coeliac and inflammatory bowel disease is unknown. AIMS: To design a non-invasive technique for the localisation of altered gastrointestinal permeability to 51chromium labelled EDTA (51CrEDTA). The method depends on comparing and defining concentration/time profiles in serum of a series of simultaneously ingested indicators with a well defined absorption site (3-0-methyl-D-glucose (jejunal indicator), 57cobalt labelled vitamin B12 (ileal indicator), and sulphasalazine (caecal-colonic indicator)) in relation to simultaneously ingested 51CrEDTA. SUBJECTS: Five normal controls, six patients with untreated coeliac disease, five with Crohn's ileitis, and five with pan-ulcerative colitis underwent study, which entailed the simultaneous ingestion of the above four test substances followed, during the next 24 hours, by timed serial collection of urine and serum for marker analysis. RESULTS: Urinary excretion of 51CrEDTA was significantly increased in all patient groups. Analysis of serum appearances and profiles of the markers suggested that the increased intestinal permeation of 51CrEDTA took place in the diseased jejunum in patients with coeliac disease, predominantly in the ileum in Crohn's disease and in the colon in the patients with pan-ulcerative colitis. CONCLUSION: A new non-invasive technique has been assessed that permits the localisation of the site of permeability changes with the gastrointestinal tract.

Measurement of sugar probes in serum: an alternative to urine measurement in intestinal permeability testing.

Author Fleming SC; Duncan A; Russell RI; Laker MF
Address Department of Clinical Biochemistry, University of Newcastle upon Tyne, UK.
Source Clin Chem, 1996 Mar, 42:3, 445-8

 

Abstract The percentage dose of lactulose and mannitol excreted in urine after oral ingestion is used as a noninvasive method of assessing small intestinal permeability. The collection of incomplete or inaccurately timed urine samples can lead to errors in estimation of sugar probe molecules. We describe an HPLC method for the simultaneous determination of lactulose and mannitol in serum after oral ingestion of test sugars. We applied the test to healthy volunteers and to subjects undergoing jejunal biopsy for suspected gluten-sensitive enteropathy. The ratio of concentrations of lactulose and mannitol in serum discriminated well between subjects with a normal biopsy and those with villous atrophy, discrimination being best at 90 min postdose. The results agree well with lactulose:mannitol ratios determined in urine (r= 0.88), and the two methods can be used interchangeably. The determination of mannitol and lactulose in serum provides an acceptable alternative to urine collection and may be particularly useful in young children. It also reduces the time spent on the investigation from 5 h to 90 min.

Recommendations Alpha Nutrition is gluten-free and is recommended as the diet revision strategy for anyone with diagnosed celiac disease, or any person with symptoms suggestive of gluten allergy.

 

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