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Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus

BACKGROUND & OBJECTIVES: Celiac disease (CD) and type 1 diabetes mellitus (T1DM) share a common genetic locus and clinical manifestations. The present study was planned to compare clinical, biochemical and hormonal profiles of patients with CD and CD with T1DM. METHODS: Records of CD patients wi...

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Autores principales: Bhadada, Sanjay Kumar, Rastogi, Ashu, Agarwal, Aakash, Kochhar, Rashi, Kochhar, Rakesh, Bhansali, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555061/
https://www.ncbi.nlm.nih.gov/pubmed/28749395
http://dx.doi.org/10.4103/ijmr.IJMR_666_14
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author Bhadada, Sanjay Kumar
Rastogi, Ashu
Agarwal, Aakash
Kochhar, Rashi
Kochhar, Rakesh
Bhansali, Anil
author_facet Bhadada, Sanjay Kumar
Rastogi, Ashu
Agarwal, Aakash
Kochhar, Rashi
Kochhar, Rakesh
Bhansali, Anil
author_sort Bhadada, Sanjay Kumar
collection PubMed
description BACKGROUND & OBJECTIVES: Celiac disease (CD) and type 1 diabetes mellitus (T1DM) share a common genetic locus and clinical manifestations. The present study was planned to compare clinical, biochemical and hormonal profiles of patients with CD and CD with T1DM. METHODS: Records of CD patients with age ≤20 yr, available anthropometric measurements, haematological, biochemical and hormonal workup with tissue transglutaminase IgA antibody and duodenal biopsy (Marsh grade) were screened. The patients were divided into two groups i.e., CD alone (Group A) and concurrent CD with T1DM (Group B). RESULTS: One hundred and nine patients of CD (57 male) with a mean age of 14.9±2.9 yr were evaluated. Of these, 86 (78.9%) patients had CD alone and 23 (13 females) (21.1%) patients had CD with T1DM. The age at diagnosis and the lag duration for the diagnosis of CD were 11.5±4.6 versus 13.8±3.4 yr (P<0.05) and 48.8 ±43.3 versus 20.2±31.8 months (P<0.05) in groups A and B, respectively. The most common histopathological grade was type 3b (59.2%) in group A and type 2 (42.1%) in group B. Short stature (87% vs. 40.9%; P<0.01), anaemia (80.9% vs. 45%, P<0.01) and delayed puberty (61.9% vs. 29.4%; P<0.01) were more common in group A. INTERPRETATION & CONCLUSIONS: Patients with CD alone have a longer lag time to diagnosis and consequent sequel in the form of anaemia, short stature and delayed puberty, as compared to patients with concurrent CD and T1DM.
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spelling pubmed-55550612017-08-30 Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus Bhadada, Sanjay Kumar Rastogi, Ashu Agarwal, Aakash Kochhar, Rashi Kochhar, Rakesh Bhansali, Anil Indian J Med Res Original Articles BACKGROUND & OBJECTIVES: Celiac disease (CD) and type 1 diabetes mellitus (T1DM) share a common genetic locus and clinical manifestations. The present study was planned to compare clinical, biochemical and hormonal profiles of patients with CD and CD with T1DM. METHODS: Records of CD patients with age ≤20 yr, available anthropometric measurements, haematological, biochemical and hormonal workup with tissue transglutaminase IgA antibody and duodenal biopsy (Marsh grade) were screened. The patients were divided into two groups i.e., CD alone (Group A) and concurrent CD with T1DM (Group B). RESULTS: One hundred and nine patients of CD (57 male) with a mean age of 14.9±2.9 yr were evaluated. Of these, 86 (78.9%) patients had CD alone and 23 (13 females) (21.1%) patients had CD with T1DM. The age at diagnosis and the lag duration for the diagnosis of CD were 11.5±4.6 versus 13.8±3.4 yr (P<0.05) and 48.8 ±43.3 versus 20.2±31.8 months (P<0.05) in groups A and B, respectively. The most common histopathological grade was type 3b (59.2%) in group A and type 2 (42.1%) in group B. Short stature (87% vs. 40.9%; P<0.01), anaemia (80.9% vs. 45%, P<0.01) and delayed puberty (61.9% vs. 29.4%; P<0.01) were more common in group A. INTERPRETATION & CONCLUSIONS: Patients with CD alone have a longer lag time to diagnosis and consequent sequel in the form of anaemia, short stature and delayed puberty, as compared to patients with concurrent CD and T1DM. Medknow Publications & Media Pvt Ltd 2017-03 /pmc/articles/PMC5555061/ /pubmed/28749395 http://dx.doi.org/10.4103/ijmr.IJMR_666_14 Text en Copyright: © 2017 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Articles
Bhadada, Sanjay Kumar
Rastogi, Ashu
Agarwal, Aakash
Kochhar, Rashi
Kochhar, Rakesh
Bhansali, Anil
Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title_full Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title_fullStr Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title_full_unstemmed Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title_short Comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
title_sort comparative study of clinical features of patients with celiac disease & those with concurrent celiac disease & type 1 diabetes mellitus
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5555061/
https://www.ncbi.nlm.nih.gov/pubmed/28749395
http://dx.doi.org/10.4103/ijmr.IJMR_666_14
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