Circulating YKL-40 in myelofibrosis a potential novel biomarker of disease activity and the inflammatory state

Mads Emil Bjørn1, Christen Lykkegaard Andersen, Morten Krogh Jensen

  • 1Institute for Inflammation Research, Department of Infectious Diseases and Rheumatology, Copenhagen University Hospital, Rigshospitalet, Denmark.

Insights

YKL-40 is elevated in myelofibrosis, a myeloproliferative neoplasm. This biomarker may reflect chronic inflammation and disease burden in MPNs, potentially aiding in disease monitoring.

Area of Science:

  • Biochemistry
  • Hematology
  • Oncology

Background:

  • Chronic myeloproliferative neoplasms (MPNs), including essential thrombocythaemia (ET), polycythaemia vera (PV), and myelofibrosis (PMF), are characterized by chronic inflammation.
  • YKL-40 is a biomarker associated with disease burden and chronic inflammation in various conditions, including cardiovascular diseases and cancers.
  • MPNs carry a significant cardiovascular disease burden, suggesting a potential role for inflammation-related biomarkers.

Purpose of the Study:

  • To investigate whether circulating YKL-40 levels can serve as a novel disease marker reflecting the inflammatory process in MPNs.
  • To assess YKL-40 levels in patients with ET, PV, and PMF compared to healthy controls.

Main Methods:

  • Enzyme-linked immunosorbent assay (ELISA) was used to measure serum YKL-40 levels.
  • The study included 15 patients with ET, 16 with PV, 17 with PMF, and 30 healthy controls.

Main Results:

  • YKL-40 levels were significantly elevated in patients with PMF (median 43 ng/mL) compared to healthy controls (median 28 ng/mL, P = 0.033).
  • A trend of increasing YKL-40 levels from ET to PV to PMF was observed, potentially indicating the cumulative impact of disease processes.

Conclusions:

  • Circulating YKL-40 is significantly elevated in myelofibrosis, suggesting its potential as a biomarker for disease burden and inflammation in MPNs.
  • Further research may explore YKL-40's utility in monitoring disease progression and therapeutic response in MPNs.

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