Associations of plasma MMP-9 and MPO with functional outcome in moderate to severe acute ischemic stroke

Vivian Vogt1, Christoph Vollmuth1, Guido Stoll2

  • 1Department of Neurology, University Hospital Würzburg, Würzburg, Germany.

Scientific Reports
|July 10, 2026
PubMed

Insights

Higher levels of matrix metalloproteinase-9 (MMP-9) and myeloperoxidase (MPO) in acute ischemic stroke (AIS) patients correlate with poorer functional outcomes. These neutrophil-derived biomarkers reflect inflammation and may complement existing predictors.

Area of Science:

  • Neuroscience
  • Immunology
  • Biochemistry

Background:

  • Inflammation is central to acute ischemic stroke (AIS) pathophysiology.
  • Neutrophil granulocytes are key players in the post-stroke immune response.
  • Neutrophil degranulation releases matrix metalloproteinase-9 (MMP-9) and myeloperoxidase (MPO), impacting stroke outcomes.

Purpose of the Study:

  • To investigate the association between systemic MMP-9 and MPO levels and functional outcomes in moderate to severe AIS.
  • To explore the pathophysiological relevance of these biomarkers in relation to neutrophil counts.
  • To assess their role alongside established clinical predictors.

Main Methods:

  • Prospective single-center cohort study of 279 patients with moderate to severe AIS (NIHSS ≥ 6).
  • Blood samples collected up to 48 hours post-symptom onset for plasma MMP-9 (zymography) and MPO (ELISA) measurement.
  • Differential blood count performed simultaneously; functional outcome assessed using modified Rankin Scale (mRS) at 3 months.

Main Results:

  • Significantly higher plasma MMP-9 and MPO levels in patients with poor functional outcome (mRS ≥ 3) compared to those with good outcomes.
  • MMP-9 and MPO concentrations correlated positively with neutrophil counts.
  • Both biomarkers showed significant association with poor outcome in unadjusted analyses.

Conclusions:

  • Systemic MMP-9 and MPO plasma concentrations are associated with functional outcomes in moderate to severe AIS.
  • These biomarkers reflect neutrophil-driven inflammatory processes post-stroke.
  • Their primary value may be in complementing, rather than independently predicting, stroke outcomes.

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