A longitudinal plasma lipidomics dataset from children who developed islet autoimmunity and type 1 diabetes

Santosh Lamichhane1, Linda Ahonen2, Thomas Sparholt Dyrlund2

  • 1Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku 20520, Finland.

Scientific Data
|November 14, 2018
PubMed

Insights

Researchers analyzed infant lipid profiles to identify early markers for type 1 diabetes (T1D). This longitudinal dataset aids in understanding T1D development and age-dependent metabolic changes.

Area of Science:

  • Metabolomics
  • Pediatric Endocrinology
  • Immunology

Background:

  • Early prediction and prevention of type 1 diabetes (T1D) remain significant unmet medical needs.
  • Prior metabolomics research indicates that children developing T1D exhibit unique metabolic profiles in infancy, preceding islet autoimmunity.
  • The specificity of these persistent metabolic disturbances concerning T1D progression requires further investigation.

Purpose of the Study:

  • To present a longitudinal plasma lipidomics dataset for analyzing early metabolic changes associated with type 1 diabetes development.
  • To facilitate research into the age-dependent progression of islet autoimmunity and T1D.
  • To support the development of analytical methods for longitudinal multivariate data.

Main Methods:

  • Collected longitudinal plasma lipidomics data from three groups of children: those progressing to T1D, those developing single islet autoantibodies without T1D, and matched controls.
  • Data were collected at six time points: 3, 6, 12, 18, 24, and 36 months of age.
  • The dataset includes 40 children in each group, totaling 120 participants.

Main Results:

  • The study provides a comprehensive dataset detailing plasma lipidomic profiles over the first three years of life.
  • This data captures metabolic variations in children who develop T1D, islet autoimmunity, or remain healthy.
  • The dataset allows for the examination of age-specific lipidomic alterations.

Conclusions:

  • The presented dataset is valuable for investigating the early metabolic signatures of type 1 diabetes.
  • It enables further research into the relationship between lipid metabolism, islet autoimmunity, and T1D onset during early childhood.
  • The data can also serve as a resource for advancing statistical and computational methods for analyzing complex longitudinal biological data.

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