Plasma ceramides are elevated in female children and adolescents with type 2 diabetes

Ximena Lopez, Allison B. Goldfine, William L. Holland, Ruth Gordillo, Philipp E. Scherer

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

Accumulation of ceramides within tissues induces insulin resistance. Moreover, adiponectin exerts its beneficial metabolic effects at least partially through ceramide catabolism. We hypothesized that specific plasma ceramide subspecies are elevated in obese children and adolescents with type 2 diabetes (T2D), and that they inversely correlate with adiponectin and measures of insulin sensitivity. This was a cross-sectional study. Participants included 14 obese female subjects with T2D, ages 10-17, and 14 lean healthy controls of the same age and gender. Fasting plasma ceramide subspecies were measured by quantitative tandem mass spectrometry. Subjects with T2D had higher concentrations of C22:0 and C20:0 ceramides, with a 2-fold increase in C18:0 ceramide and C24:1 dihydroceramide (p<0.05). C22:0, C20:0 and C18:0 ceramide correlated with decreased adiponectin concentrations, increased HOMA-IR, BMI Z-score, triglyceride and fasting blood glucose concentrations (p<0.05). Plasma levels of C18:0, C20:0 and C22:0 ceramide, as well as C24:1 dihydroceramide, were elevated in obese female children and adolescents with T2D. This may be a reflection of tissue insulin resistance and could be a result of low adiponectin levels.

Original languageEnglish (US)
Pages (from-to)995-998
Number of pages4
JournalJournal of Pediatric Endocrinology and Metabolism
Volume26
Issue number9-10
DOIs
StatePublished - Oct 2013

Keywords

  • Adolescents
  • Ceramides
  • Children
  • Insulin resistance
  • Obesity
  • Type 2 diabetes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Fingerprint

Dive into the research topics of 'Plasma ceramides are elevated in female children and adolescents with type 2 diabetes'. Together they form a unique fingerprint.

Cite this