Inflammatory cell content of coronary thrombi is dependent on thrombus age in patients with ST-elevation myocardial infarction. Issue 1 (January 2017)
- Record Type:
- Journal Article
- Title:
- Inflammatory cell content of coronary thrombi is dependent on thrombus age in patients with ST-elevation myocardial infarction. Issue 1 (January 2017)
- Main Title:
- Inflammatory cell content of coronary thrombi is dependent on thrombus age in patients with ST-elevation myocardial infarction
- Authors:
- Fuijkschot, Wessel W.
Groothuizen, Wouter E.
Appelman, Yolande
Radonic, Teodora
van Royen, Niels
van Leeuwen, Maarten A.H.
Krijnen, Paul A.J.
van der Wal, Allard C.
Smulders, Yvo M.
Niessen, Hans W.M. - Abstract:
- Abstract: Background: ST-elevation myocardial infarction (STEMI) is typically caused by an occlusive coronary thrombus. The process of intracoronary thrombus formation is poorly understood. It is known that inflammatory cells play a role in the formation and resolution of venous thrombi, however their role in coronary thrombosis is not clear. We therefore analyzed inflammatory cells in thrombi derived from patients with STEMI in relation to histologically classified thrombus age. Methods: Thrombus aspirates of 113 patients treated with primary percutaneous coronary intervention were prospectively collected and classified (fresh, lytic, or organized) based on hematoxylin and eosin staining. The density of inflammatory cells neutrophils (MPO), monocytes/macrophages (CD68), lymphocytes (CD45), and the platelet area (CD31), were visualized using immunohistochemistry. Patients' history, medication, and laboratory data were registered. Results: Fresh thrombi (76.1%) were the most abundant as compared to lytic (16.8%) and organized (7.1%) thrombi. Neutrophils were significantly less present in organized (169 cells/mm 2 ) compared to fresh (327 cells/mm 2 ) and lytic thrombi (311 cells/mm 2 ). Monocytes/macrophages were significantly more present in lytic (471 cells/mm 2 ) than in fresh (312 cells/mm 2 ) thrombi. We additionally found that thrombi from patients aged <50 years as compared to >50 years old contained significantly more neutrophils and monocytes/macrophages irrespectiveAbstract: Background: ST-elevation myocardial infarction (STEMI) is typically caused by an occlusive coronary thrombus. The process of intracoronary thrombus formation is poorly understood. It is known that inflammatory cells play a role in the formation and resolution of venous thrombi, however their role in coronary thrombosis is not clear. We therefore analyzed inflammatory cells in thrombi derived from patients with STEMI in relation to histologically classified thrombus age. Methods: Thrombus aspirates of 113 patients treated with primary percutaneous coronary intervention were prospectively collected and classified (fresh, lytic, or organized) based on hematoxylin and eosin staining. The density of inflammatory cells neutrophils (MPO), monocytes/macrophages (CD68), lymphocytes (CD45), and the platelet area (CD31), were visualized using immunohistochemistry. Patients' history, medication, and laboratory data were registered. Results: Fresh thrombi (76.1%) were the most abundant as compared to lytic (16.8%) and organized (7.1%) thrombi. Neutrophils were significantly less present in organized (169 cells/mm 2 ) compared to fresh (327 cells/mm 2 ) and lytic thrombi (311 cells/mm 2 ). Monocytes/macrophages were significantly more present in lytic (471 cells/mm 2 ) than in fresh (312 cells/mm 2 ) thrombi. We additionally found that thrombi from patients aged <50 years as compared to >50 years old contained significantly more neutrophils and monocytes/macrophages irrespective of thrombus age. Furthermore platelet area was smaller in patients on aspirin again irrespective of thrombus age. No gender differences were found. Conclusions: The composition of inflammatory cells differs with thrombus age in thrombosuction material of STEMI patients that in part depends on patient age and medication. … (more)
- Is Part Of:
- Journal of cardiology. Volume 69:Issue 1(2017:Jan.)
- Journal:
- Journal of cardiology
- Issue:
- Volume 69:Issue 1(2017:Jan.)
- Issue Display:
- Volume 69, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 69
- Issue:
- 1
- Issue Sort Value:
- 2017-0069-0001-0000
- Page Start:
- 394
- Page End:
- 400
- Publication Date:
- 2017-01
- Subjects:
- Thrombosis -- Immunohistochemistry -- Myocardial ischemia -- Cardiovascular -- Inflammation
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.clinicalkey.com/dura/browse/journalIssue/09145087 ↗
http://www.sciencedirect.com/science/journal/09145087 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jjcc.2016.10.003 ↗
- Languages:
- English
- ISSNs:
- 0914-5087
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4954.864200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1999.xml