5 results on '"Peroxidase -- blood"'
Search Results
2. A new easy method for specific measurement of active myeloperoxidase in human biological fluids and tissue extracts.
- Author
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Franck, Thierry, Kohnen, Stephan S., Zouaoui Boudjeltia, Karim, Van Antwerpen, Pierre, Bosseloir, Alain, Niesten, A, Gach, O, Nys, Marie, Deby-Dupont, Ginette, Serteyn, Didier, Franck, Thierry, Kohnen, Stephan S., Zouaoui Boudjeltia, Karim, Van Antwerpen, Pierre, Bosseloir, Alain, Niesten, A, Gach, O, Nys, Marie, Deby-Dupont, Ginette, and Serteyn, Didier
- Abstract
The SIEFED ("Specific Immunological Extraction Followed by Enzymatic Detection") method already developed for the specific detection of the activity of equine myeloperoxidase (MPO) was adapted for the specific measurement of active human MPO in biological fluids or tissue extracts. The method consists of the extraction of MPO from aqueous solutions by immobilized anti-MPO antibodies followed by a washing (to eliminate the extraction medium and the biological fluid with their possible interfering molecules) and the measurement of the activity of MPO with a detection system containing a fluorogenic substrate, H(2)O(2) and nitrite ions as reaction enhancer. The SIEFED was applied to study active MPO in human biological fluids (plasma, bronchoalveolar lavage fluid and supernatant from carotids extracts). The SIEFED for human MPO has a sensitivity limit of 0.080 mU/mL and showed good precision with intra- and inter-assay coefficients of variation below 10 and 20% respectively within a broad range of MPO activities establish from 0.156 to 473 mU/mL. The SIEFED for human MPO will be useful for the specific detection of active MPO in complex fluids and can be complementary to an ELISA to determine an active/total MPO ratio in healthy volunteers and patients especially in case of chronic or acute inflammatory diseases., Journal Article, SCOPUS: ar.j, info:eu-repo/semantics/published
- Published
- 2009
3. Coronary stenting is associated with an acute increase in plasma myeloperoxidase in stable angina patients but not in patients with acute myocardial infarction.
- Author
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Aminian, Adel, Zouaoui Boudjeltia, Karim, Babar, Sajida, Van Antwerpen, Pierre, Lefebvre, Pascal, Crasset, Vincent, Leone, Attilio, Ducobu, Jean, Friart, Alain, Vanhaeverbeek, Michel, Aminian, Adel, Zouaoui Boudjeltia, Karim, Babar, Sajida, Van Antwerpen, Pierre, Lefebvre, Pascal, Crasset, Vincent, Leone, Attilio, Ducobu, Jean, Friart, Alain, and Vanhaeverbeek, Michel
- Abstract
BACKGROUND: Myeloperoxidase (MPO) has emerged as a critical mediator in the physiopathology of atherosclerosis from plaque formation and growth until destabilization and rupture leading to acute coronary syndrome (ACS). Using coronary stenting as a model of plaque injury, we aimed to determine the evolution of systemic MPO levels following coronary stenting in stable angina patients and in patients with acute myocardial infarction (AMI). METHODS: Plasma levels of MPO, lactoferrin, interleukin (IL)-6, C-reactive protein and PMN counts were assessed in 13 patients with Non-ST-elevation myocardial infarction (NSTEMI) (Group A) and in 29 patients with stable angina pectoris (Group B), undergoing coronary stenting. Serial blood samples were taken before angioplasty (baseline) and at 1, 6 and 24 h following initial balloon inflation. RESULTS: Following angioplasty, the overall plasma MPO levels significantly increased at 1 h in group B (120.5+/-79.0 to 166+/-79.5, p=0.003) but not in group A (121+/-63.4 to 124.7+/-76.9, p=0.753). In Group B, the increase in MPO levels at 1 h were significantly higher in the presence of complex lesions compared to patients with simple lesions (p=0.023). Lactoferrin levels showed no change over time except for a significant decrease at 6 h in group B. CONCLUSIONS: In stable angina patients, coronary stenting is associated with an acute and transient increase in plasma MPO levels, but not in lactoferrin levels, with an enhanced response in the presence of complex lesions. In contrast, we observed no changes in plasma MPO and lactoferrin levels following stenting in patients with AMI. Given its pro-inflammatory properties, the potential implication of MPO release on clinical outcome in stable patients undergoing stenting needs further investigation., Comparative Study, Journal Article, info:eu-repo/semantics/published
- Published
- 2009
4. Pancreatic cellular injury after cardiac surgery with cardiopulmonary bypass: frequency, time course and risk factors.
- Author
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Nys, Monique, Venneman, Ingrid, Deby-Dupont, Ginette, Preiser, Jean-Charles, Vanbelle, Sophie, Albert, Adelin, Camus, Gérard, Damas, Pierre, Larbuisson, Robert, Lamy, Maurice, Nys, Monique, Venneman, Ingrid, Deby-Dupont, Ginette, Preiser, Jean-Charles, Vanbelle, Sophie, Albert, Adelin, Camus, Gérard, Damas, Pierre, Larbuisson, Robert, and Lamy, Maurice
- Abstract
Although often clinically silent, pancreatic cellular injury (PCI) is relatively frequent after cardiac surgery with cardiopulmonary bypass; and its etiology and time course are largely unknown. We defined PCI as the simultaneous presence of abnormal values of pancreatic isoamylase and immunoreactive trypsin (IRT). The frequency and time evolution of PCI were assessed in this condition using assays for specific exocrine pancreatic enzymes. Correlations with inflammatory markers were searched for preoperative risk factors. One hundred ninety-three patients submitted to cardiac surgery were enrolled prospectively. Blood IRT, amylase, pancreatic isoamylase, lipase, and markers of inflammation (alpha1-protease inhibitor, alpha2-macroglobulin, myeloperoxidase) were measured preoperatively and postoperatively until day 8. The postoperative increase in plasma levels of pancreatic enzymes and urinary IRT was biphasic in all patients: early after surgery and later (from day 4 to 8 after surgery). One hundred thirty-three patients (69%) experienced PCI, with mean IRT, isoamylase, and alpha1-protease inhibitor values higher for each sample than that in patients without PCI. By multiple regression analysis, we found preoperative values of plasma IRT >or=40 ng/mL, amylase >or=42 IU/mL, and pancreatic isoamylase >or=20 IU/L associated with a higher incidence of postsurgery PCI (P < 0.005). In the PCI patients, a significant correlation was found between the 4 pancreatic enzymes and urinary IRT, total calcium, myeloperoxidase, alpha1-protease inhibitor, and alpha2-macroglobulin. These data support a high prevalence of postoperative PCI after cardiac surgery with cardiopulmonary bypass, typically biphasic and clinically silent, especially when pancreatic enzymes were elevated preoperatively., Clinical Trial, Journal Article, info:eu-repo/semantics/published
- Published
- 2007
5. Temporal Dissociation between Myeloperoxidase (MPO)-Modified LDL and MPO Elevations during Chronic Sleep Restriction and Recovery in Healthy Young Men
- Author
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Dany Brohée, Karim Zouaoui Boudjeltia, Maria José Esposito, Myriam Kerkhofs, Nicole Moguilevsky, Luc Vanhamme, Michal Dyzma, Patricia Stenuit, Pierre Van Antwerpen, Brice Faraut, Michel Vanhaeverbeek, Boudjeltia K.Z., Faraut B., Esposito M.J., Stenuit P., Dyzma M., Van Antwerpen P., Brohée D., Vanhamme l., Moguilevsky N., Vanhaeverbeek M., and Kerkhofs M.
- Subjects
Male ,Time Factors ,Anatomy and Physiology ,genetic structures ,lcsh:Medicine ,Leukocytes -- metabolism ,Sciences biomédicales en général ,Cardiovascular ,Fibrinogen ,Inflammation Mediators -- blood ,Sleep -- physiology ,CARDIOVASCULAR RISK FACTORS ,Leukocytes ,Pathology ,Sleep Deprivation -- blood -- physiopathology ,OXIDATIVE STRESS ,Insulin-Like Growth Factor I ,Young adult ,lcsh:Science ,Sleep restriction ,INFLAMMATORY PROCESSESS ,Multidisciplinary ,biology ,Lipoproteins, LDL ,Médecine interne ,C-Reactive Protein ,SLEEP RESTRICTION ,Neurology ,Health ,Myeloperoxidase ,Medicine ,Analysis of variance ,Peroxidase -- blood ,Inflammation Mediators ,medicine.symptom ,Insulin-Like Growth Factor I -- metabolism ,Research Article ,medicine.drug ,Adult ,medicine.medical_specialty ,Immunology ,Inflammation ,Microbiology ,Young Adult ,Diagnostic Medicine ,Internal medicine ,medicine ,Humans ,Biology ,Peroxidase ,Interleukin-8 -- blood ,business.industry ,Acute Cardiovascular Problems ,Physiologie pathologique ,Interleukin-8 ,lcsh:R ,C-reactive protein ,Immunity ,C-Reactive Protein -- metabolism ,Fibrinogen -- metabolism ,SLEEP LOSS ,Sleep deprivation ,Endocrinology ,biology.protein ,Lipoproteins, LDL -- metabolism ,Sleep Deprivation ,Clinical Immunology ,lcsh:Q ,Sleep ,Physiological Processes ,Sleep Disorders ,business ,Biomarkers ,General Pathology - Abstract
Many studies have evaluated the ways in which sleep disturbances may influence inflammation and the possible links of this effect to cardiovascular risk. Our objective was to investigate the effects of chronic sleep restriction and recovery on several blood cardiovascular biomarkers., Journal Article, Research Support, Non-U.S. Gov't, SCOPUS: ar.j, info:eu-repo/semantics/published
- Published
- 2011
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