An open-label randomised pilot trial on safety of wheat variety C273 in patients with adult celiac disease

Author:

Grover Jasmine1,Chhuneja Parveen2,Midha Vandana3,Singh Arshdeep1ORCID,Mahajan Ramit4,Mehta Varun4,Verma Ramneek5,Bansal Ekta6,Deka Dipak5,Bansal Namita7,Sood Neena8,Narang Vikram8,Sood Ajit9ORCID

Affiliation:

1. Department of Gastroenterology, Dayanand Medical College and Hospital, Ludhiana, Punjab, India

2. School of Agricultural Biotechnology, Punjab Agricultural University, Ludhiana, Punjab, India

3. Department of Internal Medicine, Dayanand Medical College and Hospital, Ludhiana, Punjab, India

4. Department of Gastroenterology, Dayanand Medical College and Hospital, Ludhiana, India

5. School of Animal Biotechnology, Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana, Punjab, India

6. Department of Biochemistry, Dayanand Medical College and Hospital, Ludhiana, Punjab, India

7. Statistician, Research and Development Centre, Dayanand Medical College, Ludhiana, Punjab, India

8. Department of Pathology, Dayanand Medical College and Hospital, Ludhiana, Punjab, India

9. Department of Gastroenterology, Dayanand Medical College and Hospital, 6-E, Tagore Nagar, Civil Lines, Ludhiana, Punjab 141001, India

Abstract

Background: The only effective treatment for celiac disease (CeD) is gluten free diet (GFD). However, GFD is restrictive and efforts are being made to explore alternative therapies including safer wheat varieties. Wheat variety C273 has been previously identified to have reduced load of intact T-cell stimulatory epitopes via in silico and in vitro analysis. Methods: Adult patients diagnosed with CeD and recovered on GFD were included in the study. Patients were randomised into two groups in a 2:1 ratio. Patients in group I had graded introduction of C273 wheat in diet, maintained for 24 weeks; in Group II, wheat was restricted with continuation of GFD. Clinical symptoms, serology [anti-tissue transglutaminase (anti-tTG), anti-endomysial antibody (anti-EMA)], circulating inflammatory biomarkers [intestinal fatty-acid binding protein (I-FABP), plasma citrulline, interferon-γ (IFN-γ)] and histology were evaluated periodically. Final evaluation was performed at week 28. Results: A total of 15 patients were enrolled (Group I: n = 10, Group II: n = 5). All patients except two in Group I remained compliant. None of the remaining eight patients in group I developed symptoms. No significant changes in serology (anti-tTG, anti-EMA) and histology were observed between the two groups at 28 weeks ( p > 0.05). Significant changes in plasma citrulline(29.87 ± 8.98 versus 36.58 ± 3.09, p = 0.049) and IFN-γ (44.56 ± 9.74 versus 33.50 ± 3.68; p = 0.031) were observed in Group I. Conclusion: Consumption of C273 wheat did not result in development of symptoms or evident changes in serology and histology at 28 weeks. However, variations in circulating inflammatory markers were noted. Larger randomised trials are needed to corroborate these findings. Clinical Trials Registry-India: CTRI/2018/06/014521.

Publisher

SAGE Publications

Subject

Gastroenterology

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1. Treatment of gluten-related disorders;Gluten-Related Disorders;2022

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