Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4580
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKaragoz, Ahmet-
dc.contributor.authorKurt, Devrim-
dc.contributor.authorGunaydin, Zeki Yuksel-
dc.contributor.authorVural, Asli-
dc.contributor.authorUsta, Murat-
dc.contributor.authorTosun, Alptekin-
dc.contributor.authorYenercag, Mustafa-
dc.contributor.authorOzdemir, Fatih-
dc.date.accessioned2024-03-15T11:53:58Z-
dc.date.available2024-03-15T11:53:58Z-
dc.date.issued2022-
dc.identifier.citationKaragöz, A., Kurt, D., Günaydin, ZY., Vural, A., Usta, M., Tosun, A., Yenercag, M., Özdemir, F. (2022). A New Insight Into Pathophysiological Mechanism of Abdominal Aortic Aneurysm With Novel Parameters Salusin-β and Arterial Stiffness. Tex. Heart Inst. J., 49(6). https://doi.org/10.4503/THU-21-7561en_US
dc.identifier.issn0730-2347-
dc.identifier.issn1526-6702-
dc.identifier.urihttp://dx.doi.org/10.4503/THU-21-7561-
dc.identifier.urihttps://www.webofscience.com/wos/woscc/full-record/WOS:000899309600001-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4580-
dc.descriptionWoS Categories: Cardiac & Cardiovascular Systemsen_US
dc.descriptionWeb of Science Index: Science Citation Index Expanded (SCI-EXPANDED)en_US
dc.descriptionResearch Areas: Cardiovascular System & Cardiologyen_US
dc.description.abstractBackground: Abdominal aortic aneurysm (AAA) has risk factors similar to those of atherosclerosis. Salusin-beta and arterial stiffness are novel parameters that have been shown to predict atherosclerosis and related cardiovascular disorders. However, their predictive value for detecting AAA remains unclear. Methods: Forty-eight patients with AAA and 47 age- and sex-matched participants without AAA were enrolled in the study. Arterial stiffness parameters were obtained via an oscillometric Mobil-O-Graph PWA Monitor device (IEM GmbH) with integrated ARCSolver software (Australian Institute of Technology). Plasma salusin-beta levels were analyzed using an enzyme-linked immunosorbent assay reagent kit (Abbkine, Inc). The measured salusin-beta levels and arterial stiffness parameters of the AAA and control groups were compared. Results: Salusin-beta levels were significantly lower in patients with AAA (P = .014). There was a significant negative correlation between salusin-p levels and abdominal aorta diameter. No significant difference was detected between AAA and control groups in terms of arterial stiffness parameters (P > .05). In backward multiple regression analysis, the presence of AAA, platelet count, and augmentation index were found to be independent predictors of salusin-beta levels (P = .006 and P = .023, respectively). Conclusion: Arterial stiffness parameters were not found to be associated with AAA. Contrary to previous results regarding atherosclerosis and related cardiovascular disorders, salusin-beta-levels were found to be lower in patients with AAA. Although AAA is thought to have similar risk factors as atherosclerosis, the exact pathophysiologic mechanism remains unclear.en_US
dc.description.sponsorshipCoordinatorship of Scientific Research Projects of Giresun University [SAGBAP-A-150219-47]en_US
dc.language.isoengen_US
dc.publisherTEXAS HEART INST-HOUSTONen_US
dc.relation.isversionof10.4503/THU-21-7561en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAbdominal aortic aneurysm, salusin beta, human, arterial stiffnessen_US
dc.subjectPULSE-WAVE VELOCITY, ALPHA, HYPERTENSION, PREDICTION, INCREASEen_US
dc.titleA New Insight Into Pathophysiological Mechanism of Abdominal Aortic Aneurysm With Novel Parameters Salusin-β and Arterial Stiffnessen_US
dc.typearticleen_US
dc.relation.journalTEXAS HEART INSTITUTE JOURNALen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-0933-7852en_US
dc.contributor.authorID0000-0003-4230-3248en_US
dc.identifier.volume49en_US
dc.identifier.issue6en_US
Appears in Collections:Dahili Tıp Bilimleri

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.