Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section?

Pediatr Diabetes. 2011 Mar;12(2):91-4. doi: 10.1111/j.1399-5448.2010.00669.x. Epub 2010 Sep 6.

Abstract

Background and objective: Maternal age at birth, birth weight, and cesarean section has been associated with a weak but significant increase in risk of type 1 diabetes. The objective was to assess whether the relative risk for type 1 diabetes conferred by established susceptibility loci human leukocyte antigen (HLA)-DQ, INS, and PTPN22 differed depending on these perinatal factors.

Methods: We employed a case-control study with 456 cases of type 1 diabetes diagnosed before 15 yr of age and 1377 population-based control children. HLA genotypes were divided into high to moderate risk (DQ8/DQ2, DQ8/DQ8, DQ8/X, DQ2/DQ2) vs. all other genotypes. Case-only analysis using logistic regression was used to test for significant interaction.

Results: There was no significant difference in the relative risks conferred by HLA-DQ, INS, or PTPN22 by maternal age, birth weight, or mode of delivery, except the relative risk conferred by PTPN22 which was 2.11 [95% confidence interval (CI): 1.64-2.72] for those born vaginally and 0.99 (95% CI: 0.50-1.99) for those born by cesarean section [p(interaction) = 0.028].

Conclusion: The relative risks conferred by the three established susceptibility genes investigated here were independent of the perinatal factors, apart from a possible interaction between PTPN22 and mode of delivery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Birth Weight / genetics
  • Birth Weight / physiology*
  • Case-Control Studies
  • Cesarean Section*
  • Child
  • Diabetes Mellitus, Type 1 / etiology*
  • Diabetes Mellitus, Type 1 / genetics
  • Female
  • Genetic Predisposition to Disease / etiology
  • HLA-DQ Antigens / genetics*
  • Humans
  • Infant, Newborn
  • Insulin / genetics*
  • Male
  • Maternal Age*
  • Polymorphism, Genetic* / physiology
  • Pregnancy
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22 / genetics*
  • Risk

Substances

  • HLA-DQ Antigens
  • Insulin
  • PTPN22 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22