High Frequency of Recessive WFS1 Mutations Among Indian Children With Islet Antibody-negative Type 1 Diabetes.

Pratibha Singh, Surya Kumar Singh, Shivendra Verma, Ruchira Vishwakarma, Atul Garg, Kausik Mandal, Uma Kanga, Archana Archana, Jayakrishnan C Menon, Medha Mittal, Vijayalakshmi Bhatia, Siddhnath Sudhanshu, Preeti Dabadghao, Preeti Singh, Aditya Narayan Sarangi, Anju Seth, Eesh Bhatia

Journal: The Journal of clinical endocrinology and metabolism 2024;109(3):e1072-e1082

PMID: 37931151

Abstract

BACKGROUND

While the frequency of islet antibody-negative (idiopathic) type 1 diabetes mellitus (T1DM) is reported to be increased in Indian children, its aetiology has not been studied. We investigated the role of monogenic diabetes in the causation of islet antibody-negative T1DM.

METHODS

We conducted a multicenter, prospective, observational study of 169 Indian children (age 1-18 years) with recent-onset T1DM. All were tested for antibodies against GAD65, islet antigen-2, and zinc transporter 8 using validated ELISA. Thirty-four islet antibody-negative children underwent targeted next-generation sequencing for 31 genes implicated in monogenic diabetes using the Illumina platform. All mutations were confirmed by Sanger sequencing.

RESULTS

Thirty-five (21%) children were negative for all islet antibodies. Twelve patients (7% of entire cohort, 34% of patients with islet antibody-negative T1DM) were detected to have pathogenic or likely pathogenic genetic variants. The most frequently affected locus was WFS1, with 9 patients (5% of entire cohort, 26% of islet antibody-negative). These included 7 children with homozygous and 1 patient each with a compound heterozygous and heterozygous mutation. Children with Wolfram syndrome 1 (WS) presented with severe insulin-requiring diabetes (including 3 patients with ketoacidosis), but other syndromic manifestations were not detected. In 3 patients, heterozygous mutations in HNF4A, ABCC8, and PTF1A loci were detected.

CONCLUSION

Nearly one-quarter of Indian children with islet antibody-negative T1DM had recessive mutations in the WFS1 gene. These patients did not exhibit other features of WS at the time of diagnosis. Testing for monogenic diabetes, especially WS, should be considered in Indian children with antibody-negative T1DM.

© The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: [email protected].

Address: Department of Endocrinology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India.; Department of Paediatrics, Lady Hardinge Medical College, Delhi 110001, India.; Department of Paediatrics, Chacha Nehru Bal Chikitsalay, Delhi 110031, India.; Department of Immunogenetics and Transplant Immunology, All India Institute of Medical Sciences, Delhi 110029, India.; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India.; Department of Microbiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India.; Department of Genome Analytics, BaseSolve Informatics Pvt Ltd, Ahmedabad, Gujrat 380006, India.; Department of General Medicine, GSVM Medical College, Kanpur, Uttar Pradesh 208002, India.; Department of Endocrinology, Banaras Hindu University, Varanasi, Uttar Pradesh 221005, India.
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