[Etiological dissection in common anti-islet autoantibody-negative patients with type 1 diabetes]

Zhonghua Yi Xue Za Zhi. 2004 Aug 2;84(15):1247-51.
[Article in Chinese]

Abstract

Objective: To explore the immunological and genetic factors of common anti-islet autoantibody-negative patients with type 1 diabetes.

Methods: Specimens of peripheral blood were collected from 33 common autoantibody (GAD-Ab, IA2-Ab, IAA, TGA and TPO-Ab) negative diabetic patients with new-onset of unprovoked ketosis (or ketoacidosis), and genome DNA was extracted. The antibodies to carboxypeptide-H (CPH) and SOX13 (ICA12) were detected by radioligand assay. The gene mutations of MODY3 (HNF-1alpha) and MODY6 (NeuroD1/Beta2) were detected by PCR-SSCP sequencing. Mitochondrial gene mutations were analyzed with PCR-RFLP.

Results: Two (6%) of the patients were SOX13-Ab positive, while none of them was positive for CPH-Ab. Gene mutation detection found one case of a new mutation, R321H (CGC-->CAC) in the exon 5 of HNF-1alpha gene and one case with ND1 mt3316 G-->A mutation in mitochondrial DNA. In addition to the diabetes-associated mutations described above, seven polymorphisms of HNF-1alpha gene, including L17L, I27L, L459L, S487N, IVS5 + 9 C > G, IVS6-42 G > T, and IVS7 + 7 G > A, and one NeuroD1/Beta2 gene polymorphic variant Ala45Thr, were found.

Conclusion: Autoimmunity and gene mutations (such as MODY3 and mitochondrial genes mutations) may be etiological in a few cases initially diagnosed as autoantibody-negative type 1 diabetes. Autoimmunity and MODY and mitochondrial diabetes should be excluded if idiopathic type 1 (type 1B) diabetes is diagnosed.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Autoantibodies / blood*
  • Autoantibodies / immunology
  • Autoantigens / immunology*
  • Carboxypeptidase H / immunology
  • DNA-Binding Proteins / immunology
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetes Mellitus, Type 1 / immunology*
  • Female
  • Hepatocyte Nuclear Factor 1
  • Hepatocyte Nuclear Factor 1-alpha
  • High Mobility Group Proteins / immunology*
  • Humans
  • Islets of Langerhans / immunology
  • Male
  • Middle Aged
  • Nuclear Proteins / immunology
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • SOXD Transcription Factors
  • Transcription Factors / immunology

Substances

  • Autoantibodies
  • Autoantigens
  • DNA-Binding Proteins
  • HNF1A protein, human
  • Hepatocyte Nuclear Factor 1-alpha
  • High Mobility Group Proteins
  • Nuclear Proteins
  • SOX13 protein, human
  • SOXD Transcription Factors
  • Transcription Factors
  • Hepatocyte Nuclear Factor 1
  • Carboxypeptidase H