Literature DB >> 21180247

Plasma myeloperoxidase levels in patients with acute ischemic stroke.

Inimoara Mihaela Cojocaru1, M Cojocaru, Iuliana Iliescu, Ludmila Botnaru, Camelia Vidiţa Gurban, Felicia Sfrijan, R Tănăsescu.   

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.

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Year:  2010        PMID: 21180247

Source DB:  PubMed          Journal:  Rom J Intern Med        ISSN: 1220-4749


  5 in total

1.  DNA Hypomethylation of the MPO Gene in Peripheral Blood Leukocytes Is Associated with Cerebral Stroke in the Acute Phase.

Authors:  Olga Bushueva; Ekaterina Barysheva; Anton Markov; Andrey Belykh; Iuliia Koroleva; Egor Churkin; Alexey Polonikov; Vladimir Ivanov; Maria Nazarenko
Journal:  J Mol Neurosci       Date:  2021-04-17       Impact factor: 3.444

2.  Ischaemic stroke and the recanalization drug tissue plasminogen activator interfere with antibacterial phagocyte function.

Authors:  Antje Vogelgesang; Claudia Lange; Lara Blümke; Georg Laage; Sarah Rümpel; Sönke Langner; Barbara M Bröker; Alexander Dressel; Johanna Ruhnau
Journal:  J Neuroinflammation       Date:  2017-07-21       Impact factor: 8.322

3.  Inhibition of myeloperoxidase oxidant production by N-acetyl lysyltyrosylcysteine amide reduces brain damage in a murine model of stroke.

Authors:  Guoliang Yu; Ye Liang; Ziming Huang; Deron W Jones; Kirkwood A Pritchard; Hao Zhang
Journal:  J Neuroinflammation       Date:  2016-05-24       Impact factor: 8.322

4.  Pilot study to assess visualization and therapy of inflammatory mechanisms after vessel reopening in a mouse stroke model.

Authors:  Ebba Beller; Laura Reuter; Anne Kluge; Christine Preibisch; Ute Lindauer; Alexei Bogdanov; Friederike Lämmer; Claire Delbridge; Kaspar Matiasek; Benedikt J Schwaiger; Tobias Boeckh-Behrens; Claus Zimmer; Alexandra S Gersing
Journal:  Sci Rep       Date:  2018-01-15       Impact factor: 4.379

5.  Taurine Protects against Postischemic Brain Injury via the Antioxidant Activity of Taurine Chloramine.

Authors:  Song-I Seol; Hyun Jae Kim; Eun Bi Choi; In Soon Kang; Hye-Kyung Lee; Ja-Kyeong Lee; Chaekyun Kim
Journal:  Antioxidants (Basel)       Date:  2021-03-02
  5 in total

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