Exp Clin Endocrinol Diabetes 2011; 119(10): 618-620
DOI: 10.1055/s-0031-1280799
Short Communication
© J. A. Barth Verlag in George Thieme Verlag KG Stuttgart · New York

Pancreatic Autoantibodies, HLA DR and PTPN22 Polymorphisms in First Degree Relatives of Patients with Type 1 Diabetes and Multiethnic Background

B. Barone
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
J. R. Dantas
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
M. H. Almeida
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
B. S. Anna-Gomes
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
M.D. R. Bencke-Gongalves
2   Nuclear Medicine Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
M. S. Albernaz
2   Nuclear Medicine Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
M. R. Rodrigues
2   Nuclear Medicine Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
L. Zajdenverg
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
R. Kupfer
3   Diabetes Section, Instituto Estadual de Diabetes e Endocrinologia Luiz Capriglione (IEDE), Rio de Janeiro/RJ, Brazil
,
A. Milech
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
M. Rodacki
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
,
J.E. P. Oliveira
1   Nutrology Section, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro/RJ, Brazil
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 21. Januar 2011
first decision 09. April 2011

accepted 31. Mai 2011

Publikationsdatum:
08. November 2011 (online)

Abstract

Aim:

To evaluate the prevalence of pancreatic auto-antibodies (PAb) as well as its relationship with HLA DR B1 and PTPN22 polymorphisms in first degree relatives (FDR) of Brazilian patients with Type 1 diabetes (T1D) and multiethnic background.

Methods:

FDR of patients with T1D were interviewed and blood was sampled for PAb measurement, HLA DRB1 and PTPN22 genotyping. Genotyping was also performed in index cases.

Results:

In FDR (n=78), 16.7% presented at least one PAb. These individuals had a higher prevalence of HLA DRB1* 03 than others (p=0.03), without differences in PTPN22 genotyping. While the genetic profile was similar in FDR with PAb and their index cases, those without PAb had a lower frequency of HLA DR B1 * 03 than their correspondent patients (p=0.009).

Conclusion:

In this multiethnic population, a significant proportion of FDR of T1D patients had PAb, which was associated with HLA DR B1 * 03 but not with the PTPN22 polymorphism.

Type 1 diabetes and relatives: Antibodies, genetics

 
  • References

  • 1 Rewers M, Norris JM, Eisenbarth GS et al. Beta-cell autoantibodies in infants and toddlers without IDDM relatives: diabetes autoimmunity study in the young (DAISY). J Autoimmun 1996; 9: 405-410
  • 2 Ziegler AG, Hillebrand B, Rabl W et al. On the appearance of islet associated autoimmunity in offspring of diabetic mothers: a prospective study from birth. Diabetologia 1993; 36: 402-408
  • 3 Butty V, Campbell C, Mathis D et al. Impact of diabetes susceptibility loci on progression from pre-diabetes to diabetes in at-risk individuals of the diabetes prevention trial-type 1 (DPT-1). Diabetes 2008; 57: 2348-2359
  • 4 Fernandes AP, Louzada-Junior P, Foss MC et al. HLA-DRB1, DQB1, and DQA1 allele profile in Brazilian patients with type 1 diabetes mellitus. Ann NY Acad Sci 2002; 958: 305-308
  • 5 Diagnosis and Classification/Pathogenesis. In Medical Management of Type I Diabetes. 4 ed. Bode BW. Ed. Alexandria (Virginia), American Diabetes Association. 2004: 4-18
  • 6 Rodacki M, Zajdenverg L, Tortora RP et al. Characteristics of childhood and adult-onset type 1 diabetes in a multi-ethnic population. Diabetes Res Clin Pract 2005; 69 (Suppl. 01) 22-8
  • 7 Saccucci P, Del DE, Rapini N et al. Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy. Tissue Antigens 2008; 71: 234-237
  • 8 Kawasaki E, Awata T, Ikegami H et al. Systematic search for single nucleotide polymorphisms in a lymphoid tyrosine phosphatase gene (PTPN22): association between a promoter polymorphism and type 1 diabetes in Asian populations. Am J Med Genet A 2006; 140: 586-593
  • 9 Mori M, Yamada R, Kobayashi K et al. Ethnic differences in allele frequency of autoimmune-disease-associated SNPs. J Hum Genet 2005; 50: 264-266
  • 10 Chagastelles PC, Romitti M, Trein MR et al. Association between the 1858 T allele of the protein tyrosine phosphatase nonreceptor type 22 and type 1 diabetes in a Brazilian population. Tissue Antigens 2010; (in press)
  • 11 Barker JM, Barriga KJ, Yu L et al. Prediction of autoantibody positivity and progression to type 1 diabetes: Diabetes Autoimmunity Study in the Young (DAISY). J Clin Endocrinol Metab 2004; 89: 3896-3902
  • 12 Decochez K, Truyen I, van der AB et al. Combined positivity for HLA DQ2/DQ8 and IA-2 antibodies defines population at high risk of developing type 1 diabetes. Diabetologia 2005; 48: 687-694
  • 13 Lammi N, Blomstedt PA, Moltchanova E et al. Marked temporal increase in the incidence of type 1 and type 2 diabetes among young adults in Finland. Diabetologia 2008; 51: 897-899
  • 14 Redondo MJ, Eisenbarth GS. Genetic control of autoimmunity in Type I diabetes and associated disorders. Diabetologia 2002; 45: 605-622
  • 15 Gomez LM, Anaya JM, Gonzalez CI et al. PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases. Genes Immun 2005; 6: 628-631