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Non-diarrheal celiac disease: a report of 31 cases from northern India
Naresh Agarwal1, A S Puri, Rajiv Grover
1Department of Gastroenterology, G B Pant Hospital, New Delhi, India. naresh_al@rediffmail.com
Insights
Non-diarrheal celiac disease (NDCD) accounts for a third of celiac disease cases in India. Common symptoms include failure to thrive in children and refractory anemia in adults, both improving with a gluten-free diet.
Area of Science:
- Gastroenterology
- Pediatrics
- Internal Medicine
Background:
- Non-diarrheal celiac disease (NDCD) presentation is increasingly recognized globally.
- Limited data exists on NDCD in the Indian population.
- This study focuses on characterizing NDCD in a tertiary referral center in Northern India.
Purpose of the Study:
- To investigate the clinical characteristics and outcomes of non-diarrheal celiac disease (NDCD) in Indian patients.
- To emphasize the diagnostic challenges and treatment responses in NDCD.
- To contribute data on NDCD prevalence in India.
Main Methods:
- A 3-year prospective study of consecutive celiac disease (CD) patients at a tertiary referral center.
- Diagnosis confirmed by CD-specific autoantibodies, duodenal biopsy, and gluten-free diet (GFD) response.
- Clinical, hematological, and histological parameters assessed one year post-GFD initiation.
Main Results:
- 31 out of 86 CD patients (36%) had NDCD, with equal distribution in children and adults.
- Failure to thrive in children and refractory anemia in adults were the most common presentations.
- Significant improvements in weight and hemoglobin were observed after one year of GFD, though metabolic bone disease persisted in some.
Conclusions:
- Non-diarrheal celiac disease constitutes a significant proportion of CD cases in India.
- 'Failure to thrive' and 'refractory anemia' are key indicators for NDCD in pediatric and adult populations, respectively.
- Gluten-free diet is effective in improving clinical and hematological parameters in NDCD patients.
Background And Aims:
Non-diarrheal presentation of celiac disease (CD) is being increasingly recognized. Data on this form of CD from India are limited.
Methods:
Consecutive patients with CD presenting to a tertiary referral center in northern India over a 3-year period were studied, with special emphasis on non-diarrheal celiac disease (NDCD). Diagnosis was based on the presence of autoantibodies typical of CD (IgA anti-tissue transglutaminase antibodies and/ or IgA endomysial antibodies), abnormal duodenal biopsy and response to gluten-free diet (GFD). Clinical, hematological and histological responses were assessed over a one-year period after instituting GFD.
Results:
Of 86 patients with CD, 31 (16 children, 15 adult) had NDCD. Mean (SD) age of these children (12 boys) and adults (4 male) was 10.2 (4.2) y and 35.3 (12.0) y, respectively. Failure to thrive was the most common (11/16) presentation in children, as was refractory anemia in adults (10/15). Malabsorption was found in 8 adults (54%) and 10 children (64%) with NCCD. The duration from onset of symptoms to diagnosis was 2.9 (1.5) y in children and 3.3 (0.3) y in adults. There was significant improvement in body weight (children--baseline 18.9 [5.8] Kg, follow up 27.4 [12.4] Kg; adults--baseline 47.6 [18.2] Kg, follow up 54.9 [5.1] Kg) and hemoglobin (children--8.1 [2.0] g/dL to 11.2 [1.4] g/dL; adults--7.3 [2.3] g/dL to 9.7 [1.7] g/dL) in both groups after one year of GFD; duodenal biopsy also improved, with a majority of patients attaining normal to IIIa Marsh grading. Five adults and all children had evidence of metabolic bone disease at presentation, which did not revert completely with GFD. Eight adults and nine children showed dietary transgression 6 weeks after starting GFD.
Conclusion:
NDCD ac-counted for nearly one-third of all cases with CD at our center, with 'failure to thrive' and refractory anemia being the most common presentations in children and adults, respectively.
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