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. 2017 Mar;145(3):334-338.
doi: 10.4103/ijmr.IJMR_666_14.

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

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

Sanjay Kumar Bhadada et al. Indian J Med Res. 2017 Mar.

Abstract

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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Conflict of interest statement

Conflicts of Interest: None.

Figures

Figure
Figure
Endocrinological abnormalities in the two groups of patients.

Comment in

References

    1. Makharia GK, Verma AK, Amarchand R, Bhatnagar S, Das P, Goswami A, et al. Prevalence of celiac disease in the northern part of India: A community based study. J Gastroenterol Hepatol. 2011;26:894–900. - PubMed
    1. Rostom A, Murray JA, Kagnoff MF. American gastroenterological association (AGA) institute technical review on the diagnosis and management of celiac disease. Gastroenterology. 2006;131:1981–2002. - PubMed
    1. Catato F, Montalto G. Celiac disease in the developing countries: A new and challenging public health problem. World J Gastroenetrol. 2007;13:2153–9. - PMC - PubMed
    1. Bhadada SK, Kochhar R, Bhansali A, Dutta U, Kumar PR, Poornachandra KS, et al. Prevalence and clinical profile of celiac disease in type 1 diabetes mellitus in North India. J Gastroenterol Hepatol. 2011;26:378–81. - PubMed
    1. Salardi S, Volta U, Zucchini S, Fiorini E, Maltoni G, Vaira B, et al. Prevalence of celiac disease in children with type 1 diabetes mellitus increased in the mid-1990 s: An 18-year longitudinal study based on anti-endomysial antibodies. J Pediatr Gastroenterol Nutr. 2008;46:612–4. - PubMed

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