Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis.
Background: Limited data on a short series of patients suggest that lymphocytic enteritis (classically considered as latent coeliac disease) may produce symptoms of malabsorption, although the true prevalence of this situation is unknown. Serological markers of coeliac disease are of little diagnost...
| Autores: | , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2006 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/18670 |
| Acceso en línea: | https://hdl.handle.net/2445/18670 |
| Access Level: | acceso abierto |
| Palabra clave: | Enteritis Malaltia celíaca Celiac disease |
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Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis.Esteve i Comas, MariaRosinach, MercèFernández Bañares, FernandoFarré i Masip, CarmeSalas Martínez, AzucenaAlsina, M.Vilar, P.Abad, ÁguedaForné Bardera, MontserratMariné i Guillem, MeritxellSantaolalla Sala, RebecaEspinós, J. C.Viver i Pi-Suñer, Josep M.EnteritisMalaltia celíacaCeliac diseaseEnteritisBackground: Limited data on a short series of patients suggest that lymphocytic enteritis (classically considered as latent coeliac disease) may produce symptoms of malabsorption, although the true prevalence of this situation is unknown. Serological markers of coeliac disease are of little diagnostic value in identifying these patients. Aims: To evaluate the usefulness of human leucocyte antigen-DQ2 genotyping followed by duodenal biopsy for the detection of gluten-sensitive enteropathy in first-degree relatives of patients with coeliac disease and to assess the clinical relevance of lymphocytic enteritis diagnosed with this screening strategy. Patients and methods: 221 first-degree relatives of 82 DQ2+ patients with coeliac disease were consecutively included. Duodenal biopsy (for histological examination and tissue transglutaminase antibody assay in culture supernatant) was carried out on all DQ2+ relatives. Clinical features, biochemical parameters and bone mineral density were recorded. Results: 130 relatives (58.8%) were DQ2+, showing the following histological stages: 64 (49.2%) Marsh 0; 32 (24.6%) Marsh I; 1 (0.8%) Marsh II; 13 (10.0%) Marsh III; 15.4% refused the biopsy. 49 relatives showed gluten sensitive enteropathy, 46 with histological abnormalities and 3 with Marsh 0 but positive tissue transglutaminase antibody in culture supernatant. Only 17 of 221 relatives had positive serological markers. Differences in the diagnostic yield between the proposed strategy and serology were significant (22.2% v 7.2%, p<0.001). Relatives with Marsh I and Marsh II¿III were more often symptomatic (56.3% and 53.8%, respectively) than relatives with normal mucosa (21.1%; p=0.002). Marsh I relatives had more severe abdominal pain (p=0.006), severe distension (p=0.047) and anaemia (p=0.038) than those with Marsh 0. The prevalence of abnormal bone mineral density was similar in relatives with Marsh I (37%) and Marsh III (44.4%). Conclusions: The high number of symptomatic patients with lymphocytic enteritis (Marsh I) supports the need for a strategy based on human leucocyte antigen-DQ2 genotyping followed by duodenal biopsy in relatives of patients with coeliac disease and modifies the current concept that villous atrophy is required to prescribe a gluten-free diet.BMJ Group2006info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/18670Articles publicats en revistes (Medicina)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció digital del document publicat a: http://dx.doi.org/10.1136/gut.2006.095299Gut, 2006, vol. 55, núm. 12, p. 1739-1745http://dx.doi.org/10.1136/gut.2006.095299(c) BMJ Publishing Group Ltd and British Society of Gastroenterology, 2006info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/186702026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| title |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| spellingShingle |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. Esteve i Comas, Maria Enteritis Malaltia celíaca Celiac disease Enteritis |
| title_short |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| title_full |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| title_fullStr |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| title_full_unstemmed |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| title_sort |
Spectrum of gluten sensitive enteropathy in first degree relatives of patients with coeliac disease: clinical relevance of lymphocytic enteritis. |
| dc.creator.none.fl_str_mv |
Esteve i Comas, Maria Rosinach, Mercè Fernández Bañares, Fernando Farré i Masip, Carme Salas Martínez, Azucena Alsina, M. Vilar, P. Abad, Águeda Forné Bardera, Montserrat Mariné i Guillem, Meritxell Santaolalla Sala, Rebeca Espinós, J. C. Viver i Pi-Suñer, Josep M. |
| author |
Esteve i Comas, Maria |
| author_facet |
Esteve i Comas, Maria Rosinach, Mercè Fernández Bañares, Fernando Farré i Masip, Carme Salas Martínez, Azucena Alsina, M. Vilar, P. Abad, Águeda Forné Bardera, Montserrat Mariné i Guillem, Meritxell Santaolalla Sala, Rebeca Espinós, J. C. Viver i Pi-Suñer, Josep M. |
| author_role |
author |
| author2 |
Rosinach, Mercè Fernández Bañares, Fernando Farré i Masip, Carme Salas Martínez, Azucena Alsina, M. Vilar, P. Abad, Águeda Forné Bardera, Montserrat Mariné i Guillem, Meritxell Santaolalla Sala, Rebeca Espinós, J. C. Viver i Pi-Suñer, Josep M. |
| author2_role |
author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Enteritis Malaltia celíaca Celiac disease Enteritis |
| topic |
Enteritis Malaltia celíaca Celiac disease Enteritis |
| description |
Background: Limited data on a short series of patients suggest that lymphocytic enteritis (classically considered as latent coeliac disease) may produce symptoms of malabsorption, although the true prevalence of this situation is unknown. Serological markers of coeliac disease are of little diagnostic value in identifying these patients. Aims: To evaluate the usefulness of human leucocyte antigen-DQ2 genotyping followed by duodenal biopsy for the detection of gluten-sensitive enteropathy in first-degree relatives of patients with coeliac disease and to assess the clinical relevance of lymphocytic enteritis diagnosed with this screening strategy. Patients and methods: 221 first-degree relatives of 82 DQ2+ patients with coeliac disease were consecutively included. Duodenal biopsy (for histological examination and tissue transglutaminase antibody assay in culture supernatant) was carried out on all DQ2+ relatives. Clinical features, biochemical parameters and bone mineral density were recorded. Results: 130 relatives (58.8%) were DQ2+, showing the following histological stages: 64 (49.2%) Marsh 0; 32 (24.6%) Marsh I; 1 (0.8%) Marsh II; 13 (10.0%) Marsh III; 15.4% refused the biopsy. 49 relatives showed gluten sensitive enteropathy, 46 with histological abnormalities and 3 with Marsh 0 but positive tissue transglutaminase antibody in culture supernatant. Only 17 of 221 relatives had positive serological markers. Differences in the diagnostic yield between the proposed strategy and serology were significant (22.2% v 7.2%, p<0.001). Relatives with Marsh I and Marsh II¿III were more often symptomatic (56.3% and 53.8%, respectively) than relatives with normal mucosa (21.1%; p=0.002). Marsh I relatives had more severe abdominal pain (p=0.006), severe distension (p=0.047) and anaemia (p=0.038) than those with Marsh 0. The prevalence of abnormal bone mineral density was similar in relatives with Marsh I (37%) and Marsh III (44.4%). Conclusions: The high number of symptomatic patients with lymphocytic enteritis (Marsh I) supports the need for a strategy based on human leucocyte antigen-DQ2 genotyping followed by duodenal biopsy in relatives of patients with coeliac disease and modifies the current concept that villous atrophy is required to prescribe a gluten-free diet. |
| publishDate |
2006 |
| dc.date.none.fl_str_mv |
2006 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/18670 |
| url |
https://hdl.handle.net/2445/18670 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció digital del document publicat a: http://dx.doi.org/10.1136/gut.2006.095299 Gut, 2006, vol. 55, núm. 12, p. 1739-1745 http://dx.doi.org/10.1136/gut.2006.095299 |
| dc.rights.none.fl_str_mv |
(c) BMJ Publishing Group Ltd and British Society of Gastroenterology, 2006 info:eu-repo/semantics/openAccess |
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(c) BMJ Publishing Group Ltd and British Society of Gastroenterology, 2006 |
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openAccess |
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application/pdf |
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BMJ Group |
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BMJ Group |
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Articles publicats en revistes (Medicina) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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