Serum YKL-40/chitinase 3-like protein 1 level is an independent predictor of atherosclerosis development in patients with obstructive sleep apnea syndrome

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Objective: The inflammatory process plays an important role in the development of cardiovascular complications in patients with obstructive sleep apnea syndrome (OSAS). YKL-40/chitinase 3-like protein 1 is a novel biomarker of systemic inflammation. This study aimed to investigate whether carotid intima-media thickness (CIMT), a useful marker for early atherosclerosis, is associated with serum YKL-40/chitinase 3-like protein 1 levels in patients with normotensive and nondiabetic OSAS. Methods: The study included 40 OSAS patients and 40 age-sex- and body mass index-matched healthy controls. Serum YKL-40 levels were detected by enzyme-linked immunosorbent assay. CIMT was measured by B-mode ultrasound. Results: The patients with OSAS had significantly increased CIMT and higher YKL-40 and high sensitivity C-reactive protein (hsCRP) levels than those of the controls. CIMT was strongly correlated with serum YKL-40 levels (r=0.694, p<0.001), hsCRP (r=0.622, p<0.001), age (r=0.525, p=0.001), and weakly correlated with apnea-hypopnea index (AHI) (r=0.365, p=0.021) and the percentage of recording time spent (PRTS) of oxygen saturation <90% (r=0.488, p=0.001). Moreover, it was detected that serum YKL-40 levels were strongly correlated with AHI (r=0.617, p<0.001), and weakly correlated with SaO2 <90% of PRTS (r=0.394, p=0.012) and hsCRP (r=0.486, p=0.001). In multiple regression analyses, age and serum levels of YKL-40 and hsCRP were found to be independent predictors of CIMT. Conclusion: In patients with OSAS, CIMT was increased. This increase was associated with serum YKL-40 level. Increased serum level of YKL-40 may be an early predictor of atherosclerosis development in patients with OSAS. © 2015 Türk Kardiyoloji Derneʇí.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15475Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.5543/tkda.2015.56805Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBakirci, Eftal Murat
dc.contributor.authorÜnver, Edhem
dc.contributor.authorDeʇirmenci, Hüsnü
dc.contributor.authorKivanç, Tülay
dc.contributor.authorGünay, Murat
dc.contributor.authorHamur, Hikmet
dc.contributor.authorBüyüklü, Mutlu
dc.contributor.authorCeyhun, Gökhan
dc.contributor.authorTopal, Ergun
dc.contributor.authorÇoban, Taha Abdulkadir
dc.date.accessioned2026-10-18T20:30:19.143657829Z
dc.date.available2026-10-18T20:30:19.143657829Z
dc.date.issued2015
dc.description.abstractObjective: The inflammatory process plays an important role in the development of cardiovascular complications in patients with obstructive sleep apnea syndrome (OSAS). YKL-40/chitinase 3-like protein 1 is a novel biomarker of systemic inflammation. This study aimed to investigate whether carotid intima-media thickness (CIMT), a useful marker for early atherosclerosis, is associated with serum YKL-40/chitinase 3-like protein 1 levels in patients with normotensive and nondiabetic OSAS. Methods: The study included 40 OSAS patients and 40 age-sex- and body mass index-matched healthy controls. Serum YKL-40 levels were detected by enzyme-linked immunosorbent assay. CIMT was measured by B-mode ultrasound. Results: The patients with OSAS had significantly increased CIMT and higher YKL-40 and high sensitivity C-reactive protein (hsCRP) levels than those of the controls. CIMT was strongly correlated with serum YKL-40 levels (r=0.694, p<0.001), hsCRP (r=0.622, p<0.001), age (r=0.525, p=0.001), and weakly correlated with apnea-hypopnea index (AHI) (r=0.365, p=0.021) and the percentage of recording time spent (PRTS) of oxygen saturation <90% (r=0.488, p=0.001). Moreover, it was detected that serum YKL-40 levels were strongly correlated with AHI (r=0.617, p<0.001), and weakly correlated with SaO2 <90% of PRTS (r=0.394, p=0.012) and hsCRP (r=0.486, p=0.001). In multiple regression analyses, age and serum levels of YKL-40 and hsCRP were found to be independent predictors of CIMT. Conclusion: In patients with OSAS, CIMT was increased. This increase was associated with serum YKL-40 level. Increased serum level of YKL-40 may be an early predictor of atherosclerosis development in patients with OSAS. © 2015 Türk Kardiyoloji Derneʇí.
dc.description.sponsorshipThis study is supported by Erzincan University Committee for Scientific Research Projects (EUBAP No: SAG-A-070114-0050).
dc.identifier.doi10.5543/tkda.2015.56805
dc.identifier.endpage339
dc.identifier.issn1016-5169
dc.identifier.issue4
dc.identifier.pmid26142786
dc.identifier.scopus2-s2.0-84941567716
dc.identifier.startpage333
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15475
dc.identifier.volume43
dc.identifier.wosWOS:000421966900003
dc.language.isoen
dc.publisherTurkish Society of Cardiology
dc.relation.ispartofTurk Kardiyoloji Dernegi Arsivi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarotid intima-media thickness
dc.subjectCoronary artery disease
dc.subjectInflammation
dc.subjectObstructive
dc.subjectSleep apnea
dc.subjectYKL-40
dc.subjectAdipokines
dc.subjectAdult
dc.subjectAtherosclerosis
dc.subjectFemale
dc.subjectHumans
dc.subjectLectins
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPolysomnography
dc.subjectProspective Studies
dc.subjectSleep Apnea, Obstructive
dc.subjectbiological marker
dc.subjectC reactive protein
dc.subjectchitinase 3 like protein 1
dc.subjectunclassified drug
dc.subjectadipocytokine
dc.subjectCHI3L1 protein, human
dc.subjectlectin
dc.subjectapnea hypopnea index
dc.subjectarterial wall thickness
dc.subjectArticle
dc.subjectB scan
dc.subjectblood level
dc.subjectbody mass
dc.titleSerum YKL-40/chitinase 3-like protein 1 level is an independent predictor of atherosclerosis development in patients with obstructive sleep apnea syndrome
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus17
rdl.citation.wos15
rdl.departmentDepartment of Cardiology, Erzincan University Faculty of Medicine, Erzincan, Turkey. eftalka@yahoo.com. | Department of Pulmonary Diseases, Erzincan University Faculty of Medicine, Erzincan, Turkey. | Department of Cardiology, Erzincan University Faculty of Medicine, Erzincan, Turkey. | Department of Biochemistry, Erzincan University Faculty of Medicine, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexEmerging Sources Citation Index (ESCI)