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Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa

BACKGROUND: Antibody serology is an important tool in the investigation of celiac disease (CD), but does not always correlate with mucosal appearance in the small intestine. Patients with positive CD serology but normal mucosa (Marsh 0) are at increased risk of future CD. In this study we describe a...

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Autores principales: Ludvigsson, Jonas F, Brandt, Lena, Montgomery, Scott M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724402/
https://www.ncbi.nlm.nih.gov/pubmed/19624815
http://dx.doi.org/10.1186/1471-230X-9-57
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author Ludvigsson, Jonas F
Brandt, Lena
Montgomery, Scott M
author_facet Ludvigsson, Jonas F
Brandt, Lena
Montgomery, Scott M
author_sort Ludvigsson, Jonas F
collection PubMed
description BACKGROUND: Antibody serology is an important tool in the investigation of celiac disease (CD), but does not always correlate with mucosal appearance in the small intestine. Patients with positive CD serology but normal mucosa (Marsh 0) are at increased risk of future CD. In this study we describe a model for identifying and characterizing individuals with normal mucosa but positive CD serology. Such individuals are sometimes referred to as having latent CD. METHODS: The records of ten Swedish pathology departments were used to identify individuals with biopsies indicating normal duodenal/jejunal mucosa. Using the national personal identification number, these data were linked with CD serology data (antigliadin, antiendomysial and tissue transglutaminase antibodies); and we thereby identified 3,736 individuals with normal mucosa but positive CD serology. Two independent reviewers then manually reviewed their biopsy reports to estimate comorbidity. We also randomly selected 112 individuals for validation through patient chart review. RESULTS: The majority of the 3,736 individuals were females (62%). Children (0–15 years) made up 21.4%. The median number of biopsy specimen was 3. Our review of biopsy reports found that other gastrointestinal comorbidity was rare (inflammatory bowel disease: 0.4%; helicobacter pylori infection: 0.2%). Some 22% individuals selected for patient chart review had a relative with CD. The most common symptoms among these individuals were diarrhea (46%) and abdominal pain (45%), while 26% had anemia. Although 27% of the individuals selected for validation had been informed about gluten-free diet, only 13% were adhering to a gluten-free diet at the end of follow-up. CONCLUSION: Individuals with positive CD serology but normal mucosa often have CD-like symptoms and a family history of CD.
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spelling pubmed-27244022009-08-11 Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa Ludvigsson, Jonas F Brandt, Lena Montgomery, Scott M BMC Gastroenterol Research Article BACKGROUND: Antibody serology is an important tool in the investigation of celiac disease (CD), but does not always correlate with mucosal appearance in the small intestine. Patients with positive CD serology but normal mucosa (Marsh 0) are at increased risk of future CD. In this study we describe a model for identifying and characterizing individuals with normal mucosa but positive CD serology. Such individuals are sometimes referred to as having latent CD. METHODS: The records of ten Swedish pathology departments were used to identify individuals with biopsies indicating normal duodenal/jejunal mucosa. Using the national personal identification number, these data were linked with CD serology data (antigliadin, antiendomysial and tissue transglutaminase antibodies); and we thereby identified 3,736 individuals with normal mucosa but positive CD serology. Two independent reviewers then manually reviewed their biopsy reports to estimate comorbidity. We also randomly selected 112 individuals for validation through patient chart review. RESULTS: The majority of the 3,736 individuals were females (62%). Children (0–15 years) made up 21.4%. The median number of biopsy specimen was 3. Our review of biopsy reports found that other gastrointestinal comorbidity was rare (inflammatory bowel disease: 0.4%; helicobacter pylori infection: 0.2%). Some 22% individuals selected for patient chart review had a relative with CD. The most common symptoms among these individuals were diarrhea (46%) and abdominal pain (45%), while 26% had anemia. Although 27% of the individuals selected for validation had been informed about gluten-free diet, only 13% were adhering to a gluten-free diet at the end of follow-up. CONCLUSION: Individuals with positive CD serology but normal mucosa often have CD-like symptoms and a family history of CD. BioMed Central 2009-07-22 /pmc/articles/PMC2724402/ /pubmed/19624815 http://dx.doi.org/10.1186/1471-230X-9-57 Text en Copyright ©2009 Ludvigsson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ludvigsson, Jonas F
Brandt, Lena
Montgomery, Scott M
Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title_full Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title_fullStr Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title_full_unstemmed Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title_short Symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
title_sort symptoms and signs in individuals with serology positive for celiac disease but normal mucosa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724402/
https://www.ncbi.nlm.nih.gov/pubmed/19624815
http://dx.doi.org/10.1186/1471-230X-9-57
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