Plasma YKL-40 - a BMI-independent marker of type 2 diabetes

  1. Anders R Nielsen (rinnov{at}rh.dk)1,
  2. Christian Erikstrup1,
  3. Julia S. Johansen2,
  4. Christian P. Fischer1,
  5. Peter Plomgaard1,
  6. Rikke Krogh-Madsen1,
  7. Sarah Taudorf1,
  8. Birgitte Lindegaard1 and
  9. Bente K Pedersen1
  1. 1The Centre of Inflammation and Metabolism, Department of Infectious Diseases and CMRC, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Denmark
  2. 2Department of Rheumatology, Herlev Hospital, University of Copenhagen, Denmark

    Abstract

    Objective. YKL-40 is produced by macrophages and plasma YKL-40 is elevated in patients with diseases characterized by inflammation. In the present study, YKL-40 was examined in relation to obesity, inflammation, and type 2 diabetes mellitus (T2DM).

    Research Design and Methods. Plasma YKL-40 and adipose tissue YKL-40 mRNA levels were investigated in 199 subjects divided into four groups depending on the presence or absence of T2DM and obesity. In addition, plasma YKL-40 was examined in healthy subjects during a hyperglycaemic clamp, where the plasma glucose level was kept at 15 mM for 3 hours and during a hyperinsulinaemic euglycaemic clamp.

    Results. Patients with T2DM had higher plasma YKL-40 (76.7 vs. 45.1 ng/ml, p = 0.0001), but not higher expression in adipose tissue YKL-40 mRNA (1.20 vs. 0.98, p = 0.2), compared to subjects with a normal glucose tolerance. Within the groups with normal glucose tolerance and T2DM, obesity subgroups showed no difference with respect to either plasma YKL-40 or adipose tissue YKL-40 mRNA levels. Multivariate regression analysis showed that plasma YKL-40 was associated with fasting plasma glucose (β = 0.5, p = 0.0014) and plasma IL-6 (β = 0.2, p = 0.0303). Plasma YKL-40 was not related to parameters of obesity. There were no changes in plasma YKL-40 in healthy subjects during either hyperglycaemic or hyperinsulinaemic euglycaemic clamps.

    Conclusions. Plasma YKL-40 was identified as an obesity-independent marker of T2DM, related to fasting plasma glucose and plasma IL-6 levels.

    Footnotes

      • Received February 10, 2008.
      • Accepted July 17, 2008.