Plasma ceramides are elevated in obese subjects with type 2 diabetes and correlate with the severity of insulin resistance
- PMID: 19008343
- PMCID: PMC2628606
- DOI: 10.2337/db08-1228
Plasma ceramides are elevated in obese subjects with type 2 diabetes and correlate with the severity of insulin resistance
Abstract
Objective: To quantitate plasma ceramide subspecies concentrations in obese subjects with type 2 diabetes and relate these plasma levels to the severity of insulin resistance. Ceramides are a putative mediator of insulin resistance and lipotoxicity, and accumulation of ceramides within tissues in obese and diabetic subjects has been well described.
Research design and methods: We analyzed fasting plasma ceramide subspecies by quantitative tandem mass spectrometry in 13 obese type 2 diabetic patients and 14 lean healthy control subjects. Results were related to insulin sensitivity measured with the hyperinsulinemic-euglycemic clamp technique and with plasma tumor necrosis factor-alpha (TNF-alpha) levels, a marker of inflammation. Ceramide species (C18:1, 18:0, 20:0, 24:1, and 24:0) were quantified using electrospray ionization tandem mass spectrometry after separation with high-performance liquid chromatography.
Results: Insulin sensitivity (mg x kg(-1) x min(-1)) was lower in type 2 diabetic patients (4.90 +/- 0.3) versus control subjects (9.6 +/- 0.4) (P < 0.0001). Type 2 diabetic subjects had higher (P < 0.05) concentrations of C18:0, C20:0, C24:1, and total ceramide. Insulin sensitivity was inversely correlated with C18:0, C20:0, C24:1, C24:0, and total ceramide (all P < 0.01). Plasma TNF-alpha concentration was increased (P < 0.05) in type 2 diabetic subjects and correlated with increased C18:1 and C18:0 ceramide subspecies.
Conclusions: Plasma ceramide levels are elevated in type 2 diabetic subjects and may contribute to insulin resistance through activation of inflammatory mediators, such as TNF-alpha.
Figures
Comment in
-
Inflammation, insulin resistance, and type 2 diabetes: back to the future?Diabetes. 2009 Feb;58(2):307-8. doi: 10.2337/db08-1656. Diabetes. 2009. PMID: 19171748 Free PMC article. No abstract available.
References
-
- DeFronzo RA: Pathogenesis of type 2 diabetes mellitus. Med Clin N Am 88: 787–835, 2004 - PubMed
-
- Unger R: Minireview. Weapons of lean body mass destruction: the role of ectopic lipids in the metabolic syndrome. Endocrinology 144: 5159–5165, 2003 - PubMed
-
- DeFronzo RA: Dysfunctional fat cells, lipotoxicity and type 2 diabetes. Int J Clin Pract Suppl 9–21, 2004 - PubMed
-
- Summers SA: Ceramides in insulin resistance and lipotoxicity. Prog Lipid Res 45: 42–72, 2006 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- M01-RR-01346/RR/NCRR NIH HHS/United States
- R01 DK024092/DK/NIDDK NIH HHS/United States
- 5K12RR023264/RR/NCRR NIH HHS/United States
- AG-12834/AG/NIA NIH HHS/United States
- DK-24092/DK/NIDDK NIH HHS/United States
- R56 DK024092/DK/NIDDK NIH HHS/United States
- T32 HL007887/HL/NHLBI NIH HHS/United States
- R01 AG012834/AG/NIA NIH HHS/United States
- T32 DK007319/DK/NIDDK NIH HHS/United States
- M01 RR001346/RR/NCRR NIH HHS/United States
- K12 RR023264/RR/NCRR NIH HHS/United States
- R29 AG012834/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous
