Krischer Jeffrey P, Lynch Kristian F, Lernmark Åke, Hagopian William A, Rewers Marian J, She Jin-Xiong, Toppari Jorma, Ziegler Anette-G, Akolkar Beena
Health Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, FL
Health Informatics Institute, Morsani College of Medicine, University of South Florida, Tampa, FL.
Diabetes Care. 2017 Sep;40(9):1194-1202. doi: 10.2337/dc17-0238. Epub 2017 Jun 23.
We tested the associations between genetic background and selected environmental exposures with respect to islet autoantibodies and type 1 diabetes.
Infants with HLA-DR high-risk genotypes were prospectively followed for diabetes-related autoantibodies. Single nucleotide polymorphisms (SNPs) came from the Illumina ImmunoChip and environmental exposure data were by parental report. Children were followed to age 6 years.
Insulin autoantibodies occurred earlier than GAD antibody (GADA) and then declined, while GADA incidence rose and remained constant (significant in HLA-DR4 but not in the DR3/3 children). The presence of SNPs rs2476601 () and rs2292239 () demonstrated increased risk of both autoantibodies to insulin (IAA) only and GADA only. SNP rs689 () was protective of IAA only, but not of GADA only. The rs3757247 () SNP demonstrated increased risk of GADA only. Male sex, father or sibling as the diabetic proband, introduction of probiotics under 28 days of age, and weight at age 12 months were associated with IAA only, but only father as the diabetic proband and weight at age 12 months were associated with GADA only. Mother as the diabetic proband was not a significant risk factor.
These results show clear differences in the initiation of autoimmunity according to genetic factors and environmental exposures that give rise to IAA or GADA as the first appearing indication of autoimmunity.
我们测试了遗传背景和特定环境暴露与胰岛自身抗体及1型糖尿病之间的关联。
对具有HLA - DR高危基因型的婴儿进行前瞻性随访,观察与糖尿病相关的自身抗体。单核苷酸多态性(SNP)数据来自Illumina免疫芯片,环境暴露数据通过父母报告获取。对儿童随访至6岁。
胰岛素自身抗体比谷氨酸脱羧酶抗体(GADA)出现得早,随后下降,而GADA的发病率上升并保持稳定(在HLA - DR4儿童中显著,但在DR3/3儿童中不显著)。SNP rs2476601()和rs2292239()的存在表明仅胰岛素自身抗体(IAA)和仅GADA的风险增加。SNP rs689()仅对IAA有保护作用,对仅GADA无保护作用。SNP rs3757247()仅表明GADA的风险增加。男性、父亲或兄弟姐妹为糖尿病先证者、28天龄前引入益生菌以及12个月龄时的体重仅与IAA相关,但仅父亲为糖尿病先证者和12个月龄时的体重仅与GADA相关。母亲为糖尿病先证者不是显著的风险因素。
这些结果表明,根据遗传因素和环境暴露,自身免疫的起始存在明显差异,这些因素导致IAA或GADA作为自身免疫的首次出现迹象。