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PCSK9 inhibitors increase CD34+ but not other endothelial progenitor cells in patients with chronic coronary disease and increased Lp(a) values
ID
Ugovšek, Sabina
(
Author
),
ID
Rehberger Likozar, Andreja
(
Author
),
ID
Levstek, Tina
(
Author
),
ID
Trebušak Podkrajšek, Katarina
(
Author
),
ID
Zupan, Janja
(
Author
),
ID
Marka, Frieda
(
Author
),
ID
Trimmel, Tamara
(
Author
),
ID
Brekalo, Mira
(
Author
),
ID
Speidl, Walter
(
Author
),
ID
Hohensinner, Philipp
(
Author
),
ID
Haider, Patrick
(
Author
),
ID
Šebeštjen, Miran
(
Author
)
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https://www.thieme-connect.de/products/ejournals/abstract/10.1055/a-2901-2564
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Abstract
Background: Endothelial dysfunction is an independent predictor of cardiovascular events in patients with established atherosclerosis, while the circulating levels of endothelial progenitor cells (EPCs) reflect active endothelial function in heart failure patients. Although protein convertase subtilisin/kexin type 9 (PCSK9) inhibitors (PCSK9i) lower lipid concentration and reduce cardiovascular events, their impact on endothelial function remains poorly understood. Purpose: We aimed to examine the effect of PCSK9i on the levels of EPCs in the peripheral blood of patients with chronic coronary disease and significantly elevated lipoprotein(a) (Lp(a)) concentrations. Methods: In this randomized, double-blind, placebo-controlled trial, we included 100 statin-treated patients at least 6 months post-myocardial infarction with elevated Lp(a) values. The patients received PCSK9i or a placebo every 2 weeks for 6 months. Biochemical and flow cytometric analyses of peripheral blood mononuclear cells were performed at baseline and after 6 months. Results: Treatment with PCSK9i increased the levels of mature EPCs (CD34+ ) compared with placebo (p = 0.003). In contrast, no significant effects were observed on early EPC subtypes (CD34+ CD309+, CD34+ CD133+, CD133+ CD309+, and CD133+; p = 0.611, p = 0.451, p = 0.739, and p = 0.161, respectively). The increase in mature EPCs (CD34+ ) levels did not correlate with changes in PCSK9 concentration. No associations were detected between changes in PCSK9 concentration and changes in levels of EPC subtypes predominantly expressing CD309, nor between changes in levels of any EPCs and lipoprotein concentration variations at baseline or at the end of the study. Conclusion: In patients with chronic coronary disease, treatment with PCSK9i increases circulating levels of mature CD34+ EPCs, without affecting other EPC subtypes.
Language:
English
Keywords:
endothelial function
,
endothelial progenitor cells
,
CD34+
,
lipoprotein(a)
,
proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors (PCSK9i)
,
myocardial infarction
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2026
Number of pages:
12 str.
Numbering:
Vol. 10, art. a29012564
PID:
20.500.12556/RUL-185247
UDC:
616.1
ISSN on article:
2512-9465
DOI:
10.1055/a-2901-2564
COBISS.SI-ID:
284577027
Publication date in RUL:
04.08.2026
Views:
271
Downloads:
102
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Title:
TH open
Publisher:
Thieme
ISSN:
2512-9465
COBISS.SI-ID:
131788291
Licences
License:
CC BY-NC-ND 4.0, Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
Link:
http://creativecommons.org/licenses/by-nc-nd/4.0/
Description:
The most restrictive Creative Commons license. This only allows people to download and share the work for no commercial gain and for no other purposes.
Secondary language
Language:
Slovenian
Keywords:
endotelijska funkcija
,
CD34+
,
lipoprotein (a)
,
miokardni infarkt
Projects
Funder:
University Medical Centre Ljubljana
Project number:
20240051
Funder:
University Medical Centre Ljubljana
Project number:
20250023
Funder:
Amgen
Funder:
Sanofi
Funder:
Medizinische Universität Wien
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P3-0308
Name:
Ateroskleroza in tromboza
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0170
Name:
Molekulski mehanizmi uravnavanja celičnih procesov v povezavi z nekaterimi boleznimi pri človeku
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0420
Name:
Napredna imunološka zdravila in celični pristopi v farmaciji
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