Distinct features of circulating microparticles and their relationship with disease activity in inflammatory bowel

Evangelos Voudoukis1, Eleni-Kyriaki Vetsika2, Konstantina Giannakopoulou1

  • 1Department of Gastroenterology, Venizelion General Hospital (Evangelos Voudoukis, Konstantina Giannakopoulou, Konstantinos Karmiris, Angeliki Theodoropoulou, Gregorios A. Paspatis), Crete, Greece.

Abstract

Insights

Circulating microparticles (MPs) and platelet-derived MPs (PDMPs) are elevated in inflammatory bowel disease (IBD). The annexin V binding ratio of MPs is a key indicator distinguishing IBD patients from healthy controls.

Area of Science:

  • Immunology
  • Gastroenterology
  • Biochemistry

Background:

  • Circulating microparticles (MPs) and annexin (+) platelet-derived MPs (PDMPs) are implicated in inflammatory bowel disease (IBD).
  • Understanding the characteristics of MPs in IBD is crucial for disease management.

Purpose of the Study:

  • To characterize the abundance, origin, and annexin V binding of MPs in IBD patients.
  • To correlate MP levels with IBD disease characteristics and activity.

Main Methods:

  • A case-control study involving 46 IBD patients (Crohn's disease and ulcerative colitis) and 40 healthy controls (HC).
  • MPs were analyzed for annexin V binding and cell origin using flow cytometry and specific membrane markers.
  • Clinical and laboratory disease activity indices were assessed.

Main Results:

  • IBD patients showed increased annexin (-) PDMPs, total monocyte-derived MPs, and annexin (+) monocyte-derived MPs compared to HC.
  • The annexin (+)/(-) ratio for all MP types was significantly elevated in IBD patients.
  • Active IBD was associated with higher levels of total MPs, PDMPs (both annexin (+) and (-)), and correlated with disease activity indices.

Conclusions:

  • Circulating MPs, particularly annexin (-) PDMPs, are elevated in active IBD.
  • The annexin (+)/(-) ratio of MPs serves as a reliable biomarker for distinguishing IBD patients from healthy individuals.

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