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Published on: February 12, 2016
Plasma myeloperoxidase levels in patients with acute ischemic stroke
Inimoara Mihaela Cojocaru1, M Cojocaru, Iuliana Iliescu
1"Carol Davila" University of Medicine and Pharmacy, Department of Neurology, "Colentina" Clinical Hospital, Bucharest, Romania. inimioaramihaela_cojocaru@yahoo.com
Abstract:
Myeloperoxidase (MPO) is a glycoprotein released by activated polymorphonuclear neutrophils, which takes part in the defence of the organism through production of hypochlorous acid (HOCl), a potent oxidant. MPO has a role in pathogenesis of atherosclerosis. The aim of the study was to evaluate the time course of MPO plasma levels in the early stage of ischemic stroke. The study included 78 patients with acute ischemic stroke, 46 females and 32 males, mean age 74.3 +/- 6.8 years. Blood samples for MPO measurement were taken within 24 hours after the onset of ischemic stroke. Seventy-two patients served as matched controls 43 females and 29 males, mean age 71.3 +/- 6.4 years. MPO was measured in plasma using the Abbott Architect platform (Abbott Diagnostics Inc., Abbott Parck IL). Comparisons between patients and controls and patients group were expressed as relative risk with its 95% confidence interval (RR [95% CI]), where a lower limit > 1.0 was considered significant. All p values were determined by Fischer's exact test. A value of p < 0.05 was considered statistically significant. Mean plasma MPO level was in patients with acute ischemic stroke 583 +/- 48 pmol/L. Seventy-one patients out of seventy-eight patients with ischemic stroke presented mean plasma MPO levels greater than the upper of normal (425 +/- 36 pmol/L, p < 0.0001, (RR 8.188, [95% CI 4.038 to 16.600]). Twelve controls presented mean plasma MPO level greater than the upper of normal. In conclusion, plasma MPO levels were statistically significantly higher in patients after ischemic stroke as compared to controls. MPO has been associated with acute ischemic stroke but its direct role in its pathogenesis has not been established. MPO could be proposed as a potential prognostic marker of such lesions rather than a marker of diagnosis. MPO is a new biomarker and a possible future therapeutic target.
Insights
Elevated myeloperoxidase (MPO) plasma levels were observed in acute ischemic stroke patients compared to controls. MPO may serve as a prognostic marker for stroke, not a diagnostic one.
Area of Science:
- Biochemistry
- Immunology
- Neurology
Background:
- Myeloperoxidase (MPO) is a glycoprotein from neutrophils involved in host defense via hypochlorous acid production.
- MPO plays a role in the pathogenesis of atherosclerosis.
- The role of MPO in acute ischemic stroke requires further investigation.
Purpose of the Study:
- To evaluate the time course of MPO plasma levels in the early stage of ischemic stroke.
- To compare MPO levels in acute ischemic stroke patients with matched controls.
Main Methods:
- The study included 78 patients with acute ischemic stroke and 72 matched controls.
- Plasma MPO levels were measured using the Abbott Architect platform within 24 hours of stroke onset.
- Statistical significance was determined using Fischer's exact test, with p < 0.05 considered significant.
Main Results:
- Mean plasma MPO levels were significantly higher in ischemic stroke patients (583 +/- 48 pmol/L) compared to controls.
- 71 out of 78 stroke patients had MPO levels above the normal upper limit (p < 0.0001, RR 8.188).
- Only 12 control patients exceeded the normal upper limit for MPO levels.
Conclusions:
- Plasma MPO levels are statistically significantly elevated in patients following ischemic stroke.
- MPO is associated with acute ischemic stroke, but its direct role in pathogenesis is not established.
- MPO shows potential as a prognostic marker for ischemic stroke and a future therapeutic target.

