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Title:Effects of proprotein convertase subtilisin-kexin type 9 inhibitors on inflammatory and hemostatic parameters in post myocardial infarction patients
Authors:ID Rehberger Likozar, Andreja (Author)
ID Ugovšek, Sabina (Author)
ID Šebeštjen, Miran (Author)
Files:.pdf PDF - Presentation file, download (1,92 MB)
MD5: 9804FC28ED4DCA5D32373D31BA05FBB9
 
URL URL - Source URL, visit https://www.sciencedirect.com/science/article/pii/S001429992300746X?via%3Dihub
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Despite progress in treatment, elevated levels of low-density lipoprotein cholesterol (LDL-C) and lipoprotein (a) (Lp(a)), represent a significant part of the residual risk. Both are associated with inflammation and the coagulation fibrinolytic system. The purpose of our research was to evaluate the effect of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) on lipid parameters and indicators of inflammation, coagulation and fibrinolysis. We included 100 post myocardial infarction (MI) patients with insufficiently controlled LDL-C values despite the maximum dose of statin, and highly elevated Lp(a). Patients received alirocumab or evolocumab (150 mg sc or 140 mg sc every two weeks, respectively), or placebo for 6 months. In patients receiving PCSK9i, a significant decrease in total cholesterol (TC), LDL-C, triglycerides (TG) and Lp(a), and an increase in high density lipoprotein cholesterol (p < 0.001 for all) was found. Before treatment, the concentrations of TC, LDL-C and TG correlated with the concentrations of thrombin activatable fibrinolysis inhibitor (r = 0.41, p < 0.001; r = 0.353, p < 0.001; r = 0.311, p = 0.003, respectively), and plasminogen activator inhibitor-1 (r = 0.302, p = 0.007; r = 0.218, p = 0.049; r = 0.278; p = 0.013, respectively). The concentrations of TC and LDL-C correlated with overall fibrinolytic potential (r = −0.220, p = 0.034; r = −0.207, p = 0.047, respectively). The concentration of TG was related to the concentration of interleukin 6 (r = 0.290, p = 0.004) and interleukin 8 (r = 0.332, p = 0.001). No correlations between Lp(a) and inflammatory or hemostatic variables were found. No associations were found after treatment. Our results show that inflammatory cytokines and fibrinolytic parameters are related to LDL-C and not Lp(a) in post-MI patients before and with neither of them following PCSK9i treatment.
Keywords:inflammation, hemostasis, PCSK9 inhibitors, LDL cholesterol, lipoprotein (a)
Publication status:Published
Publication version:Version of Record
Year of publishing:2024
Number of pages:str. 1-8
Numbering:Vol. 963, iss. [article no.] 176232
PID:20.500.12556/DiRROS-29837 New window
UDC:616-002
ISSN on article:0014-2999
DOI:10.1016/j.ejphar.2023.176232 New window
COBISS.SI-ID:179035139 New window
Publication date in DiRROS:08.06.2026
Views:170
Downloads:162
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Record is a part of a journal

Title:European Journal of Pharmacology
Shortened title:Eur. J. Pharmacol.
Publisher:North-Holland
ISSN:0014-2999
COBISS.SI-ID:224279 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0308-2019
Name:Ateroskleroza in tromboza

Funder:Other - Other funder or multiple funders
Funding programme:Univerzitetni klinični center Ljubljana
Project number:20220011
Name:Vpliv zaviralcev PCSK9 na celične subpopulacije v periferni krvi bolnikov z ishemično boleznijo srca

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.

Secondary language

Language:Slovenian
Keywords:vnetje, hemostaza, inhibitorji PCSK9, LDL holesterol, lipoprotein (a)


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