Subfatin, asprosin, alamandine and maresin-1 in cerebral ischemia, intracranial and subarachnoid hemorrhages

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OBJECTIVE: Cerebrovascular diseases (CVDs) remain an important public health issue due to the increasing number of deaths worldwide. Changes in the synthesis and release of peptides in CVDs may play an important role in elucidating the physiopathology of the disease. Therefore, this study was to investigate the fate of maresin-1 (MaR-1), subfatin (SUB), asprosin (ASP), and alamandine (ALA) levels in patients with cerebral infarction (CI), intracranial hemorrhage (ICH), subarachnoid hemorrhage (SAH) evaluated within the scope of CVDs, and voluntary healthy controls. PATIENTS AND METHODS: The study participants were divided into 4 groups: CI patients, ICH patients, SAH patients, and healthy volunteers. The diagnosis of CVDs was made based on the National Institutes of Health Stroke Scale (NIHSS), Intracerebral Hemorrhage Score (ICHS), Botterel-Hunt-Hess Scale (BHHS), and cranial computed tomography (CT). The levels of MaR- 1 (ng/mL), SUB (ng/mL), ASP (ng/mL), and ALA (pg/mL) in the blood samples collected from the participants were studied using the ELISA method. Other parameters included in the study were obtained from the patient records of our hospital. RESULTS: The comparison of MaR-1 [(control 1.38 ± 0.14), SAH (0.98 ± 0.087), CI (0.67 ± 0.04), ICH (0.51 ± 0.03)], SUB [(control (13.2 ± 1.4), SAH (10.1 ± 1.2), CI (7.9 ± 0.8), ICH (5.8 ± 0.5)], and ALA [(control (67.2 ± 7.9), SAH (58.2 ± 4.3), CI (42.1 ± 3.7), and ICH (34.2 ±3.9)] values revealed a significant decrease compared to the control values. The comparison of the ASP values of SAH, CI, and ICH patients and control values (11.6 ± 1.2) showed significantly higher asprosin values in SAH (13.8 ± 1.1), CI (15.4 ± 1.2) and ICH (28.9 ± 2.8) patients. Similarly, systolic blood pressure (SBP), diastolic blood pressure (DBP), and glucose levels of CKD patients were also high. CONCLUSIONS: Decreased MaR-1, SUB, ALA and increased ASP compared to the control values may play a role in the physiopathology of these diseases. MaR-1, SUB, ALA, and ASP differences between SAH, CI and ICH patients may also guide clinicians along with SBP, DBP and glucose values. © 2023 Verduci Editore s.r.l. All rights reserved.

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AlanDeğerDil
dc.contributor.authorAlbayrak, S.
dc.contributor.authorAydin, M.A.
dc.contributor.authorUgur, K.
dc.contributor.authorHanbeyoglu, O.
dc.contributor.authorAydin, S.
dc.contributor.authorErol, E.
dc.contributor.authorKilinc, A.
dc.contributor.authorAcar, V.
dc.contributor.authorSahin, İ.
dc.date.accessioned2026-10-18T20:27:08.318239823Z
dc.date.available2026-10-18T20:27:08.318239823Z
dc.date.issued2023
dc.description.abstractOBJECTIVE: Cerebrovascular diseases (CVDs) remain an important public health issue due to the increasing number of deaths worldwide. Changes in the synthesis and release of peptides in CVDs may play an important role in elucidating the physiopathology of the disease. Therefore, this study was to investigate the fate of maresin-1 (MaR-1), subfatin (SUB), asprosin (ASP), and alamandine (ALA) levels in patients with cerebral infarction (CI), intracranial hemorrhage (ICH), subarachnoid hemorrhage (SAH) evaluated within the scope of CVDs, and voluntary healthy controls. PATIENTS AND METHODS: The study participants were divided into 4 groups: CI patients, ICH patients, SAH patients, and healthy volunteers. The diagnosis of CVDs was made based on the National Institutes of Health Stroke Scale (NIHSS), Intracerebral Hemorrhage Score (ICHS), Botterel-Hunt-Hess Scale (BHHS), and cranial computed tomography (CT). The levels of MaR- 1 (ng/mL), SUB (ng/mL), ASP (ng/mL), and ALA (pg/mL) in the blood samples collected from the participants were studied using the ELISA method. Other parameters included in the study were obtained from the patient records of our hospital. RESULTS: The comparison of MaR-1 [(control 1.38 ± 0.14), SAH (0.98 ± 0.087), CI (0.67 ± 0.04), ICH (0.51 ± 0.03)], SUB [(control (13.2 ± 1.4), SAH (10.1 ± 1.2), CI (7.9 ± 0.8), ICH (5.8 ± 0.5)], and ALA [(control (67.2 ± 7.9), SAH (58.2 ± 4.3), CI (42.1 ± 3.7), and ICH (34.2 ±3.9)] values revealed a significant decrease compared to the control values. The comparison of the ASP values of SAH, CI, and ICH patients and control values (11.6 ± 1.2) showed significantly higher asprosin values in SAH (13.8 ± 1.1), CI (15.4 ± 1.2) and ICH (28.9 ± 2.8) patients. Similarly, systolic blood pressure (SBP), diastolic blood pressure (DBP), and glucose levels of CKD patients were also high. CONCLUSIONS: Decreased MaR-1, SUB, ALA and increased ASP compared to the control values may play a role in the physiopathology of these diseases. MaR-1, SUB, ALA, and ASP differences between SAH, CI and ICH patients may also guide clinicians along with SBP, DBP and glucose values. © 2023 Verduci Editore s.r.l. All rights reserved.
dc.identifier.doi10.26355/eurrev_202305_32453
dc.identifier.endpage4480
dc.identifier.issn1128-3602
dc.identifier.issue10
dc.identifier.pmid37259728
dc.identifier.scopus2-s2.0-85160789219
dc.identifier.startpage4471
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12209
dc.identifier.volume27
dc.identifier.wosWOS:001021187100018
dc.language.isoen
dc.publisherVerduci Editore s.r.l
dc.relation.ispartofEuropean Review for Medical and Pharmacological Sciences
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAlamandine
dc.subjectAsprosin
dc.subjectCerebral ischemia
dc.subjectHemorrhagy
dc.subjectMaresin-1
dc.subjectSubfatin
dc.subjectBrain Ischemia
dc.subjectCerebral Hemorrhage
dc.subjectCerebral Infarction
dc.subjectGlucose
dc.subjectHumans
dc.subjectIntracranial Hemorrhages
dc.subjectSubarachnoid Hemorrhage
dc.subjectUnited States
dc.subjectadipocytokine
dc.subjectangiotensin
dc.subjectdocosahexaenoic acid
dc.subjectmaresin 1
dc.subjectpeptide hormone
dc.subjectrenin
dc.subjectunclassified drug
dc.subjectaged
dc.subjectArticle
dc.subjectblood sampling
dc.subjectBotterel Hunt Hess Scale
dc.subjectbrain hemorrhage
dc.subjectbrain infarction
dc.subjectcerebrovascular disease
dc.subjectchronic kidney failure
dc.subjectcomputer assisted tomography
dc.titleSubfatin, asprosin, alamandine and maresin-1 in cerebral ischemia, intracranial and subarachnoid hemorrhages
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus7
rdl.citation.wos5
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)