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Prevalence of autoantibodies in type 1 diabetes mellitus pediatrics in Mazandaran, North of Iran

  • Daniel Zamanfar ORCID logo EMAIL logo , Mohsen Aarabi , Monireh Amini and Mahila Monajati ORCID logo
Published/Copyright: August 17, 2020

Abstract

Objectives

Type 1 diabetes is an autoimmune disease. Its most important immunologic markers are pancreatic beta-cell autoantibodies. This study aimed to determine diabetes mellitus antibodies frequency among children and adolescents with type 1 diabetes.

Methods

This descriptive study evaluated the frequency of four diabetes autoantibodies (glutamic acid decarboxylase 65 autoantibodies [GADA], islet cell autoantibodies [ICA], insulin autoantibodies [IAA], tyrosine phosphatase–like insulinoma antigen-2 antibodies [IA-2A]) and their serum level in children and adolescents diagnosed with type 1 diabetes mellitus at the diabetes department of Bou-Ali-Sina Hospital and Baghban Clinic, Sari, Iran, from March 2012 to March 2018. The relationship between the level of different antibodies and age, gender, and diabetes duration were determined. A two-sided p value less than 0.05 indicated statistical significance.

Results

One hundred forty-two eligible patient records were screened. The average age at diabetes diagnosis was 4.2 ± 4.4 years. The median duration of diabetes was 34.0 (12.7–69.7) months. 53.5% of patients were female, and 81.7% of them had at least one positive autoantibody, and ICA in 66.2%, GADA in 56.3%, IA-2A in 40.1%, and IAA in 21.8% were positive. The type of the autoantibodies and their serum level was similar between females and males but there was a higher rate of positive autoantibodies in females. The level of IA-2A and ICA were in positive and weak correlation with age at diagnosis.

Conclusions

More than 80% of pediatric and adolescent patients with type 1 diabetes were autoantibody-positive. ICA and GADA were the most frequently detected autoantibodies. The presence of antibodies was significantly higher in females.


Corresponding author: Daniel Zamanfar, MD, Associate Professor of Pediatric Endocrinology, Department of Pediatric Endocrinology, Diabetes Research Center of Mazandaran, Mazandaran University of Medical Sciences, Sari, Iran, Phone/Fax: +98 11 33342338,

  1. Research funding: The source of financial grants and other funding was supported by Research Vice Chancellor of Mazandaran University of Medical Sciences.

  2. Author contributions: Zamanfar D. conceptualized and designed the study; Aarabi M. designed and analyzed the data; Amini M. collected the data and Zamanfar D. and Monajati M. drafted the initial manuscript. All authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  3. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The study was approved by the Ethics Committee of the Mazandaran University of Medical Science. Data were collected anonymously. All the principles, outlined in the Helsinki Declaration, were followed during the investigation.

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Received: 2019-08-25
Accepted: 2020-05-13
Published Online: 2020-08-17

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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