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Decreased Serum Salusin-β Levels Are Independently Associated with Gestational Diabetes Mellitus

dc.contributor.authorSonay, Hanise Ozkan
dc.contributor.authorOkuturlar, Yildiz
dc.contributor.authorCokicli, Esra
dc.contributor.authorSahtiyanci, Berrak
dc.contributor.authorUtku, Irem Kirac
dc.contributor.authorSeckin, Kerem Doga
dc.contributor.authorEkinci, Iskender
dc.contributor.authorDuran, Eda Nur
dc.contributor.authorAnataca, Gulden
dc.contributor.authorOnal, Burak
dc.contributor.authorKumbasar, Abdulbaki
dc.contributor.authorAkarsu, Murat
dc.contributor.authorTabak, Omur
dc.date.accessioned2026-11-05T11:00:15Z
dc.date.issued2026
dc.description.abstractBackground: Gestational diabetes mellitus (GDM) is characterized by pregnancy-induced insulin resistance and beta-cell dysfunction and is increasingly recognized as a state of cardiometabolic and endothelial dysregulation. Salusin-beta, a bioactive peptide implicated in vascular inflammation and metabolic disorders, may play a role in GDM pathophysiology. However, data regarding its clinical relevance in GDM remain limited. Objective: This study aimed to compare serum salusin-beta levels between women with GDM and healthy pregnant controls and to evaluate its diagnostic performance. Methods: This prospective study included 144 pregnant women between 24 and 28 weeks of gestation (70 with GDM and 74 healthy controls). GDM was diagnosed using a 75-g oral glucose tolerance test according to American Diabetes Association criteria. Serum salusin-beta levels were measured using ELISA. Between-group comparisons were performed using appropriate parametric or non-parametric tests. Multivariable logistic regression analysis was performed to evaluate the independent association between salusin-beta and GDM. Sensitivity analyses using an expanded adjustment model were also conducted. Diagnostic performance was evaluated using receiver operating characteristic (ROC) curve analysis. Results: Salusin-beta levels were significantly lower in women with GDM compared to controls (68.53 [53.05-84.27] vs. 128.03 [76.74-261.35] pg/mL; p < 0.001). In the expanded multivariable logistic regression analysis, lower serum salusin-beta levels remained independently associated with GDM (OR = 0.990, 95% CI: 0.985-0.996, p = 0.001). ROC analysis demonstrated acceptable discriminatory performance (AUC = 0.754, 95% CI: 0.672-0.833). The optimal cut-off value of 87.1 pg/mL yielded 80.0% sensitivity and 66.2% specificity. Conclusions: Serum salusin-beta levels are significantly reduced in women with GDM and independently associated with disease presence. Although not sufficient as a standalone diagnostic marker, salusin-beta demonstrates moderate discriminatory ability and may serve as a complementary biomarker reflecting vascular and metabolic dysregulation in GDM.
dc.description.issue7
dc.description.pages1602
dc.description.sponsorshipThis research received no external funding.
dc.description.volume14
dc.identifier.doi10.3390/biomedicines14071602
dc.identifier.issn2227-9059
dc.identifier.urihttps://doi.org/10.3390/biomedicines14071602
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10371
dc.identifier.wosWOS:001832469400001
dc.language.isoen
dc.publisherMDPI
dc.relation.hasversion10.3390/biomedicines14071602
dc.relation.ispartofBIOMEDICINES
dc.subjectgestational diabetes mellitus
dc.subjectbiomarkers
dc.subjectinsulin resistance
dc.subjectendothelial dysfunction
dc.subjectinflammation
dc.subjectpregnancy
dc.subjectglucose intolerance
dc.subjectoxidative stress
dc.subjectcardiometabolic risk
dc.subjectsalusin-beta
dc.subjectMATERNAL OBESITY
dc.subjectDYSFUNCTION
dc.subjectWOMEN
dc.subjectMARKERS
dc.subjectBiochemistry & Molecular Biology
dc.subjectMedicine, Research & Experimental
dc.subjectPharmacology & Pharmacy
dc.subjectResearch & Experimental Medicine
dc.titleDecreased Serum Salusin-β Levels Are Independently Associated with Gestational Diabetes Mellitus
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue7
oaire.citation.volume14
person.identifier.ridHTO-1602-2023
person.identifier.ridMIP-3425-2025
person.identifier.ridGPS-9145-2022
person.identifier.ridAGV-9329-2022
person.identifier.ridX-3647-2018
person.identifier.ridGPX-1872-2022

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