Relationship between increased relative birthweight and infections during pregnancy in children with a high-risk diabetes HLA genotype

Diabetologia. 2007 Jun;50(6):1161-9. doi: 10.1007/s00125-007-0648-6. Epub 2007 Apr 4.

Abstract

Aims/hypothesis: Children with high-risk type 1 diabetes HLA genotype have increased risk of high relative birthweight (HrBW), while cord blood islet autoantibodies decrease the risk. As gestational infections may affect offspring type 1 diabetes risk, the aims were to test whether: (1) children of mothers reporting gestational infections have increased HrBW; (2) gestational infections explain islet autoantibody reduction of HrBW; and (3) gestational infections affect the association between HLA and HrBW.

Subjects and methods: HLA genotypes and autoantibodies to glutamic acid decarboxylase, insulinoma-associated protein 2 and insulin were determined in cord blood of children born to non-diabetic mothers in the Diabetes Prediction in Skåne (DiPiS) study. Mothers reported gestational infections when the child was 2 months old.

Results: Fever or gastroenteritis during pregnancy was reported by 2,848/19,756 mothers (14%); 339 in more than one trimester. Children whose mothers reported infections had increased risk of HrBW (p = 0.0003), particularly in the absence of cord blood islet autoantibodies (interaction between HrBW, islet autoantibodies and infections, p = 0.0005). The effect on HrBW by high-risk HLA-DQ2/8 was aggravated by infections in more than one trimester (odds ratio [OR] = 5.24; p = 0.003) (interaction; p = 0.022). When infections were reported, cord blood islet autoantibodies decreased HrBW (OR = 0.34; p = 0.0002).

Conclusions/interpretation: This study revealed that: (1) gestational fever, gastroenteritis, or both, increased the risk of HrBW; (2) cord blood islet autoantibodies decreased the risk of HrBW only in combination with infections; and (3) infections aggravated the association between HLA-DQ2/8 and HrBW. These data suggest an interaction between HLA, gestational infections, islet autoantibodies and fetal growth.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoantibodies / blood
  • Birth Weight*
  • Child
  • Diabetes Mellitus, Type 1 / epidemiology
  • Diabetes Mellitus, Type 1 / genetics*
  • Female
  • Fetal Development
  • Gastroenteritis / epidemiology
  • Genotype
  • Glutamate Decarboxylase / immunology
  • HLA Antigens / genetics*
  • Humans
  • Infant, Newborn
  • Infections / embryology*
  • Infections / epidemiology*
  • Isoenzymes / immunology
  • Pregnancy
  • Pregnancy Complications

Substances

  • Autoantibodies
  • HLA Antigens
  • Isoenzymes
  • Glutamate Decarboxylase
  • glutamate decarboxylase 2