Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, 20520, Finland.
Steno Diabetes Center Copenhagen, 2820, Gentofte, Denmark.
Sci Rep. 2018 Jul 13;8(1):10635. doi: 10.1038/s41598-018-28907-8.
Type 1 diabetes (T1D) is one of the most prevalent autoimmune diseases among children in Western countries. Earlier metabolomics studies suggest that T1D is preceded by dysregulation of lipid metabolism. Here we used a lipidomics approach to analyze molecular lipids in a prospective series of 428 plasma samples from 40 children who progressed to T1D (PT1D), 40 children who developed at least a single islet autoantibody but did not progress to T1D during the follow-up (P1Ab) and 40 matched controls (CTR). Sphingomyelins were found to be persistently downregulated in PT1D when compared to the P1Ab and CTR groups. Triacylglycerols and phosphatidylcholines were mainly downregulated in PT1D as compared to P1Ab at the age of 3 months. Our study suggests that distinct lipidomic signatures characterize children who progressed to islet autoimmunity or overt T1D, which may be helpful in the identification of at-risk children before the initiation of autoimmunity.
1 型糖尿病(T1D)是西方国家儿童中最常见的自身免疫性疾病之一。早期的代谢组学研究表明,T1D 是脂质代谢失调的前兆。在这里,我们使用脂质组学方法分析了 40 名进展为 T1D(PT1D)的儿童、40 名在随访期间至少产生一种胰岛自身抗体但未进展为 T1D 的儿童(P1Ab)和 40 名匹配对照(CTR)的 428 份前瞻性血浆样本中的分子脂质。与 P1Ab 和 CTR 组相比,PT1D 中鞘磷脂持续下调。与 P1Ab 相比,PT1D 在 3 个月时三酰基甘油和磷脂酰胆碱主要下调。我们的研究表明,不同的脂质组学特征可用于区分进展为胰岛自身免疫或显性 T1D 的儿童,这可能有助于在自身免疫开始前识别处于危险中的儿童。