Birth weight in newborn infants with different diabetes‐associated HLA genotypes in three neighbouring countries: Finland, Estonia and Russian Karelia

Abstract Background Human leukocyte antigen (HLA) genotypes associated with increased risk for type 1 diabetes mellitus (T1D) have been reported to be associated with increased birth weight. We set out to investigate the association between HLA haplotypes conferring risk for T1D and birth weight and...

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Bibliographic Details
Published in:Diabetes/Metabolism Research and Reviews
Main Authors: Peet, Aleksandr, Kool, Pille, Ilonen, Jorma, Knip, Mikael, Tillmann, Vallo
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2012
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Online Access:http://dx.doi.org/10.1002/dmrr.2303
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fdmrr.2303
https://onlinelibrary.wiley.com/doi/pdf/10.1002/dmrr.2303
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Summary:Abstract Background Human leukocyte antigen (HLA) genotypes associated with increased risk for type 1 diabetes mellitus (T1D) have been reported to be associated with increased birth weight. We set out to investigate the association between HLA haplotypes conferring risk for T1D and birth weight and search for possible differences in the strength of these associations among populations with contrasting incidence of T1D. Methods As a part of the EU‐funded DIABIMMUNE study, genotyping for the HLA haplotypes associated with T1D was performed in 8369 newborn infants from Estonia, Finland and Russian Karelia. Infants born before 35 gestational weeks, from mothers with diabetes, and multiple pregnancies were excluded. Relative birth weight, expressed in standard deviation scores, was estimated for each gestational week, sex and country. The standard deviation scores were calculated internally using the actual population studied. According to their HLA haplotypes, participants were divided into risk groups, and the distribution of birth weight between quartiles was analysed. Results We did not find any direct association between various HLA risk‐associated genotypes (HLA DR3‐DQ2/DR4‐DQ8, DR3‐DQ2/X or DR4‐DQ8/X) and birth weight. We observed a significant relationship between increased relative birth weight and the protective HLA‐DR2‐DQ6 and DR13‐DQ6 haplotypes. This association was significant only when these haplotypes were found together with the DR4‐DQ8 haplotype. Conclusions The previously reported association between HLA‐risk haplotypes for T1D and an increased birth weight was not confirmed. This suggests that the mechanisms behind the association between high birth weight and risk for T1D may be not directly HLA related. Copyright © 2012 John Wiley & Sons, Ltd.