Association of the TPO gene in Colombian families with type 1 diabetes

Authors

  • Javier Gutiérrez Achury Universidad de Antioquia
  • Vital Balthazar González Universidad de Antioquia
  • Gabriel Bedoya Berrío Universidad de Antioquia
  • Andres Ruíz Linares Universidad de Antioquia
  • Federico Uribe Londoño Universidad de Antioquia
  • Juan Manuel Alfaro Universidad de Antioquia
  • Nicolas Pineda Trujillo Universidad de Antioquia

DOI:

https://doi.org/10.17533/udea.iatreia.11107

Abstract

We have found linkage and association of type 1 diabetes (T1D) to 2p25. The TPO gene lies within this region. Our aim was to test the association of this gene with the susceptibility to T1D in a group of Colombian families, all of them originated in Antioquia, a special population in northwestern Colombia. One hundred familial trios with type 1 diabetes (T1D) were analyzed. They had already been studied for anti-glutamic acid descarboxilase (GAD) antibodies and the marker locus D2S319. For further characterization, the probands were tested for autoantibodies against insulin, TPO and thyrosine phosphatase 2 (IA-2). Two single nucleotide polymorphisms (SNPs) (rs4927611 and rs732609) were tested in TPO. These two markers were chosen considering that the polymorphism changes the encoded amino-acid and a minor allele frequency, MAF, ≥ 0.3. SNP typing was carried out by means of the polymerase chain reaction/restriction fragment length polymorphisms (PCR-RFLP) and the tetraprimer amplification refractory mutation system (ARMS-PCR) methods. Hardy-Weinberg equilibrium (HWE) and linkage disequilibrium (LD) analyses were separately tested on both parents and probands. Genetic association was tested by the transmission disequilibrium test (TDT).

It was found that 86% of the patients presented at least one of the three auto-antibodies tested. Both parents and probands were found in HWE for both SNPs. In addition, the two markers were found in tight LD (p < 0.0001). A haplotype associated with susceptibility to the disease was identified

(p = 0.0116).

Autoimmunity was found in a proportion similar to that previously reported. It was found that a haplotype at TPO gene is associated with the disease. Such haplotype is characterized by alleles G and A at rs4927611 and rs732609 SNPs, respectively. Our results suggest a possible causative participation of the TPO gene in T1D. In order to verify them, a sample of equivalent size is currently being collected, from the same population in Colombia.

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Author Biographies

Javier Gutiérrez Achury, Universidad de Antioquia

Mapeo Genético, Departamento de Pediatría, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

Vital Balthazar González, Universidad de Antioquia

Mapeo Genético, Departamento de Pediatría, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

Gabriel Bedoya Berrío, Universidad de Antioquia

Laboratorio de Genética Molecular (GENMOL), Universidad de Antioquia, Medellín, Colombia.

Andres Ruíz Linares, Universidad de Antioquia

Laboratorio de Genética Molecular (GENMOL), Universidad de Antioquia, Medellín, Colombia.

Department of Biology, University College London, London UK.

Federico Uribe Londoño, Universidad de Antioquia

Departamento de Endocrinología y Metabolismo, Universidad de Antioquia, Medellín, Colombia.

Juan Manuel Alfaro, Universidad de Antioquia

Mapeo Genético, Departamento de Pediatría, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

Nicolas Pineda Trujillo, Universidad de Antioquia

Mapeo Genético, Departamento de Pediatría, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.

Published

2012-02-10

How to Cite

1.
Gutiérrez Achury J, Balthazar González V, Bedoya Berrío G, Ruíz Linares A, Uribe Londoño F, Alfaro JM, Pineda Trujillo N. Association of the TPO gene in Colombian families with type 1 diabetes. Iatreia [Internet]. 2012 Feb. 10 [cited 2025 Dec. 13];22(4):Pág. 323-329. Available from: https://revistas.udea.edu.co/index.php/iatreia/article/view/11107

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Original research

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