Increased PCSK9 associated with cIMT in AS: A useful marker for subclinical atherosclerosis in patients with ankylosing spondylitis

dc.authorid0000-0001-8288-9744
dc.authorid0000-0002-4367-2355
dc.authorid0000-0003-1711-5157
dc.authorid0000-0002-8519-5382
dc.authorid0000-0002-7173-3530
dc.authorid0000-0002-8044-7616
dc.authorid0000-0001-8028-1671
dc.contributor.authorKarakoyun, Ahmet
dc.contributor.authorAkkubak, Yasemin
dc.contributor.authorGöktepe, Mevlüt Hakan
dc.contributor.authorYılmaz, Pınar Diydem
dc.contributor.authorKadıyoran, Cengiz
dc.contributor.authorOğul, Mustafa
dc.contributor.authorKucuk, Adem
dc.date.accessioned2025-02-07T13:13:23Z
dc.date.available2025-02-07T13:13:23Z
dc.date.issued2024
dc.departmentTıp Fakültesi
dc.description.abstractThis study aims to investigate the relationship between proprotein convertase subtilisin/ kexin type 9 (PCSK9) levels and subclinical atherosclerosis (SA) in patients with ankylosing spondylitis (AS). Patients and methods: Between January 2022 and March 2022, a total of 56 patients (33 males, 23 females; mean age: 37.8±9.3 years; range, 20 to 60 years) who were under regular follow-up in our clinic and fulfilled the criteria of the Modified New York Diagnostic Criteria for AS and American College of Rheumatology (ACR) for AS were included. Age-and sex-matched 56 healthy volunteers (25 males, 31 females; mean age: 38.4±8.2 years; range, 20 to 60 years) were also recruited as the control group. Demographic, clinical, and laboratory data were recorded. The PCSK9 level and carotid intima-media thickness (cIMT) were evaluated using appropriate methods. Results: The mean serum PCSK9 levels in AS patients (609.3±149.9 vs. 136.3±120.8 ng/mL, p<0.001) and the mean cIMT values (0.51±0.19 vs. 0.43±0.08 mm, p=0.003) were higher than healthy controls. In the multivariate stepwise regression analysis, there was an independent relationship between SA and PCSK9 (?=0.324, p=0.001). Additionally, there was an independent relationship between carotid plaque and PCSK9 (?=0.265, p=0.006). Based on the receiver operating characteristic curve analysis, the optimal PCSK9 cut-off value for plaque was 472.0 ng/mL, sensitivity 90.9%, specificity 65.0% (area under the curve [AUC]=0.759; 95% CI: 0.660-0.857, p=0.005). The optimal PCSK9 cut-off value for SA was 459.5 ng/mL, sensitivity 63.2%, specificity 63.0% (AUC=0.625; 95% CI: 0.512-0.739, p=0.031). Conclusion: Our study showed that serum PCSK9 levels in patients with AS were higher than that in healthy individuals and were associated with SA and arterial plaque formation.
dc.identifier.doi10.46497/ArchRheumatol.2024.10625
dc.identifier.endpage661en_US
dc.identifier.issn2618-6500
dc.identifier.issue4en_US
dc.identifier.startpage652en_US
dc.identifier.urihttps://dx.doi.org/10.46497/ArchRheumatol.2024.10625
dc.identifier.urihttps://hdl.handle.net/20.500.12451/12939
dc.identifier.volume39en_US
dc.language.isoen
dc.publisherTurkish League Against Rheumatism (TLAR)
dc.relation.ispartofArchives of Rheumatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAnkylosing Spondylitis
dc.subjectCarotid Intima-media Thickness
dc.subjectProprotein Convertase Subtilisin/kexin type 9
dc.subjectSubclinical Atherosclerosis
dc.titleIncreased PCSK9 associated with cIMT in AS: A useful marker for subclinical atherosclerosis in patients with ankylosing spondylitis
dc.typeArticle

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