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Gain of function variants in PCSK9 gene in high risk patients after myocardial infarction with increased lipoprotein (a) values and treated with statins
ID
Ugovšek, Sabina
(
Avtor
),
ID
Rehberger Likozar, Andreja
(
Avtor
),
ID
Levstek, Tina
(
Avtor
),
ID
Trebušak Podkrajšek, Katarina
(
Avtor
),
ID
Zupan, Janja
(
Avtor
),
ID
Antonić, Slobodan
(
Avtor
),
ID
Šebeštjen, Miran
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(1,71 MB)
MD5: 080B2CFAAC0EB205AD92F17B2CC90D37
URL - Izvorni URL, za dostop obiščite
https://www.nature.com/articles/s41598-025-12432-6
Galerija slik
Izvleček
The proprotein convertase subtilisin/kexin type 9 (PCSK9) regulates lipid metabolism, inflammation and haemostasis. Pathogenic gain-of-function variants in the PCSK9 gene are causative of autosomal-dominant form of familial hypercholesterolemia, while several PCSK9 alleles have been associated with elevated levels of low-density lipoprotein cholesterol (LDL-C) and an increased risk of cardiovascular disease. Elevated lipoprotein(a) (Lp(a)) levels, regardless of LDL-C levels, as well as functional and morphological changes in the arterial vessel wall predict future cardiovascular events. In our study, we aimed to identify whether treatment with statins nullifies the effect of four gain-of-function gene variants in PCSK9 on lipoproteins and arterial wall properties in high-risk post-myocardial infarction patients with severely elevated Lp(a) levels. We included 68 patients after myocardial infarction with elevated Lp(a) levels on maximal statin therapy. Biochemical analysis of lipid parameters and total PCSK9 levels were performed. Arterial wall properties were measured by ultrasound. Genotyping was performed for four gain-of-function, i.e. rs11206510, rs2479409, rs2479408 and rs1711503, and one intergenic, rs11591147 PCSK9 single nucleotide polymorphisms. The results showed no association between studied PCSK9 gene variants and lipid parameters, PCSK9 levels and arterial wall properties in our patient cohort. Clinical, biochemical and arterial wall parameters did not differ between the group with lower compared to group with higher number of PCSK9 alleles. Our results suggest that in high-risk patients after myocardial infarction with increased Lp(a) levels treated with statins the studied PCSK9 gain-of-function gene variants are associated neither with lipoproteins nor with arterial wall properties.
Jezik:
Angleški jezik
Ključne besede:
PCSK9 polymorphisms
,
lipoprotein(a)
,
endothelial dysfunction
,
total PCSK9 levels
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2025
Št. strani:
11 str.
Številčenje:
Vol. 15, art. 26753
PID:
20.500.12556/RUL-171412
UDK:
616.127-005.8
ISSN pri članku:
2045-2322
DOI:
10.1038/s41598-025-12432-6
COBISS.SI-ID:
244049155
Datum objave v RUL:
26.08.2025
Število ogledov:
206
Število prenosov:
65
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Scientific reports
Skrajšan naslov:
Sci. rep.
Založnik:
Nature Publishing Group
ISSN:
2045-2322
COBISS.SI-ID:
18727432
Licence
Licenca:
CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:
Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
polimorfizmi PCSK9
,
lipoprotein(a)
,
endotelijska disfunkcija
,
skupne ravni PCSK9
,
miokardni infarkt
Projekti
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P3-0308
Naslov:
Ateroskleroza in tromboza
Financer:
ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:
P1-0170
Naslov:
Molekulski mehanizmi uravnavanja celičnih procesov v povezavi z nekaterimi boleznimi pri človeku
Financer:
University Medical Centre Ljubljana
Program financ.:
University Medical Centre Ljubljana
Naslov:
20240051
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