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Published on: May 29, 2020
Cord-Blood Lipidome in Progression to Islet Autoimmunity and Type 1 Diabetes
Santosh Lamichhane1, Linda Ahonen2, Thomas Sparholt Dyrlund3
1Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland. santosh.lamichhane@utu.fi.
Insights
Newborns who later develop type 1 diabetes (T1D) have distinct cord blood lipid profiles. Specific sphingomyelin and cholesterol ester levels at birth can predict T1D progression risk.
Area of Science:
- Metabolomics
- Pediatric Endocrinology
- Immunology
Background:
- Altered serum lipid profiles at birth are associated with later progression to type 1 diabetes (T1D).
- Understanding early lipidomic differences may identify infants at high risk for T1D.
Purpose of the Study:
- To compare cord blood lipidomic profiles in infants who progress to T1D, those who develop autoantibodies without T1D, and healthy controls.
- To identify specific lipids and lipid signatures predictive of T1D progression.
Main Methods:
- Cord blood samples were analyzed for lipidome composition.
- Three groups were studied: progressors to T1D (PT1D), autoantibody-positive non-progressors (P1Ab), and controls (CTR).
- Statistical analysis and receiver operating characteristic (ROC) curve analysis were used to identify predictive lipid signatures.
Main Results:
- Phospholipids, particularly sphingomyelins, were significantly lower in PT1D infants compared to P1Ab and CTR groups.
- Cholesterol esters were elevated in the PT1D group relative to the other groups.
- A five-lipid signature achieved an area under the ROC curve (AUROC) of 0.83 for predicting T1D progression.
Conclusions:
- Cord blood lipidomic profiles at birth differ between infants who progress to T1D and those who do not.
- Specific lipid alterations, including sphingomyelins and cholesterol esters, are associated with future T1D development.
- Early lipidomic profiling shows promise for predicting type 1 diabetes risk in newborns.
Abstract:
Previous studies suggest that children who progress to type 1 diabetes (T1D) later in life already have an altered serum lipid molecular profile at birth. Here, we compared cord blood lipidome across the three study groups: children who progressed to T1D (PT1D; n = 30), children who developed at least one islet autoantibody but did not progress to T1D during the follow-up (P1Ab; n = 33), and their age-matched controls (CTR; n = 38). We found that phospholipids, specifically sphingomyelins, were lower in T1D progressors when compared to P1Ab and the CTR. Cholesterol esters remained higher in PT1D when compared to other groups. A signature comprising five lipids was predictive of the risk of progression to T1D, with an area under the receiver operating characteristic curve (AUROC) of 0.83. Our findings provide further evidence that the lipidomic profiles of newborn infants who progress to T1D later in life are different from lipidomic profiles in P1Ab and CTR.
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