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Soluble CD163 correlates with lipid metabolic adaptations in type 1 diabetes patients during ketoacidosis.

AbstractINTRODUCTION:
Diabetic ketoacidosis (DKA) is associated with inflammation and increased lipolysis. The macrophage activation marker, soluble CD163 (sCD163), is associated with obesity, non-alcoholic fatty liver disease and type 2 diabetes. We aimed to investigate whether sCD163 correlates with key elements of lipolysis in type 1 diabetes patients during mild DKA.
MATERIALS AND METHODS:
We investigated nine patients with type 1 diabetes twice during: (i) euglycemic control conditions and a bolus of saline; and (ii) hyperglycemic ketotic conditions induced by lipopolysaccharide administration combined with insulin deprivation. Blood samples, indirect calorimetry, palmitate tracer and adipose tissue biopsies were used to investigate lipid metabolism.
RESULTS:
We observed a significant increase in plasma sCD163 levels after lipopolysaccharide exposure (P < 0.001). Concentrations of sCD163 were positively correlated with plasma concentrations of free fatty acids, palmitate rate of appearance and lipid oxidation rates, and negatively correlated to the expression of G0/G1 switch 2 gene messenger ribonucleic acid content in adipose tissue (P < 0.01 for all). Furthermore, sCD163 levels correlated positively with plasma peak concentrations of cortisol, glucagon, tumor necrosis factor-α, interleukin-6 and interleukin-10 (P < 0.01 for all). Data on lipolysis and inflammation have previously been published.
CONCLUSIONS:
Macrophage activation assessed by sCD163 might play an important role in DKA, as it correlates strongly with important components of lipid metabolism including free fatty acids, palmitate, lipid oxidation, G0/G1 switch 2 gene and pro-inflammatory cytokines during initial steps of DKA. These results are novel and add important knowledge to the field of DKA.
AuthorsMads Svart, Nikolaj Rittig, Niels Møller, Holger J Møller, Henning Gronbaek
JournalJournal of diabetes investigation (J Diabetes Investig) Vol. 10 Issue 1 Pg. 67-72 (Jan 2019) ISSN: 2040-1124 [Electronic] Japan
PMID29802679 (Publication Type: Clinical Trial, Journal Article)
Copyright© 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.
Chemical References
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD163 antigen
  • Inflammation Mediators
  • Lipopolysaccharides
  • Receptors, Cell Surface
Topics
  • Adult
  • Antigens, CD (metabolism)
  • Antigens, Differentiation, Myelomonocytic (metabolism)
  • Diabetes Mellitus, Type 1 (metabolism)
  • Diabetic Ketoacidosis (chemically induced, metabolism)
  • Humans
  • Inflammation (chemically induced, metabolism)
  • Inflammation Mediators (metabolism)
  • Lipid Metabolism
  • Lipopolysaccharides (administration & dosage)
  • Male
  • Receptors, Cell Surface (metabolism)
  • Young Adult

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