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Purpose: Inflammation is a key contributor to coronary heart disease (CHD). Sortilin is a sorting receptor and has been identified as a critical regulator of inflammatory response. Therefore, our study aimed to determine the link between circulating sortilin levels, proinflammatory cytokine levels, and the occurrence of CHD.
Patients And Methods: Our study included 227 CHD patients and 101 matched healthy individuals. Circulating serum levels of sortilin and proinflammatory cytokines, including IL-1β, IL-6 and TNF-α, were assessed by a double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). Linear regression and correlation analyses were used to estimate the associations between sortilin and proinflammatory cytokines. Moreover, six single-nucleotide polymorphisms (SNPs) spanning the sortilin and SORL1 genes were genotyped.
Results: Elevated levels of sortilin (P=0.027) and proinflammatory cytokines IL-1β (P=0.013), IL-6 (P=0.000) and TNF-α (P=0.010) were observed in CHD patients compared to those in healthy controls. Furthermore, sortilin levels were significantly positively correlated with IL-1β (r=0.252, P=0.0001), IL-6 (r=0.250, P=0.0001) and TNF-α (r=0.180, P=0.0064) levels. Notably, sortilin polymorphisms were revealed to be associated with the occurrence of CHD and varying sortilin levels. Subjects with the rs599839 AA risk genotype for CHD had significantly higher sortilin levels than those with the GG and GA genotypes (P=0.000); the same tendency was also observed in the levels of the proinflammatory cytokines IL-1β (P=0.003) and TNF-α (P=0.000). Similarly, GG carriers of rs464218 with increased sortilin levels were found to be at increased risk for CHD (P=0.014). The levels of IL-1β (P=0.025) and IL-6 (P=0.015) were also increased in these patients.
Conclusion: Our findings reveal that high sortilin levels may interact with inflammatory response to contribute to the occurrence of CHD. Considering that our clinical evidence suggests for the first time that sortilin involves in inflammatory response in CHD, the mechanistic role of sortilin in the progression of CHD deserves detailed investigation.
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http://dx.doi.org/10.2147/JIR.S240421 | DOI Listing |
Mol Nutr Food Res
August 2025
Department of Medical Biochemistry, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Sortilin regulates lipid metabolism, adipogenesis, and inflammation in obesity. While the anti-inflammatory and lipid-modulating effects of krill oil (KO) on obesity are well known, its effects on sortilin remain insufficiently investigated. This study investigates the potential effects of KO supplementation on sortilin and pro-inflammatory cytokine levels in rats fed a high-fat diet (HFD).
View Article and Find Full Text PDFClin Chim Acta
August 2025
School of Medicine, Southeast University, Nanjing, China; Department of Nephrology, Nanjing Drum Tower Hospital, Affiliated Hospital of Nanjing University School of Medicine, Nanjing, China. Electronic address:
Background: Cardiovascular disease (CVD) is the principal cause of mortality in chronic kidney disease (CKD) patients. Vascular calcification (VC) and cardiac valve calcification (CVC) significantly contribute to the increased CVD incidence in uremic patients. This study sought to determine the relationship between serum sortilin protein and both VC and CVC in uremic patients.
View Article and Find Full Text PDFBMC Cancer
August 2025
Laboratoire d'Oncologie Moléculaire, Département de Chimie, Université du Québec à Montréal, Montreal, C.P. 8888, Succ. Centre-ville, QC, H3C 3P8, Canada.
Background: The epidermal growth factor receptor (EGFR) plays a significant role in vasculogenic mimicry (VM), a process by which aggressive cancer cells within hypoxic solid tumors form blood vessel-like structures independent of endothelial cells. Mostly attributed to cancer stem cells (CSC), VM is strongly associated with chemoresistance and poor prognosis in glioblastomas (GBMs). The trafficking of EGFR from the plasma membrane is in part regulated by Sortilin (SORT1), a type I membrane glycoprotein with receptor sorting functions.
View Article and Find Full Text PDFSortilin, a type I transmembrane protein encoded by SORT1 and part of the VPS10-domain receptor family, is crucial for intracellular trafficking and APP processing in Alzheimer's disease (AD). It promotes protective α-secretase cleavage to prevent Aβ formation and aids Aβ clearance. However, under certain conditions, sortilin can become neurotoxic, causing Aβ buildup, tau phosphorylation, protein misrouting, and apoptosis, which accelerate neuronal damage and cognitive decline.
View Article and Find Full Text PDFCureus
July 2025
Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, USA.
Background Alzheimer's disease (AD) is a progressive neurodegenerative disorder mainly characterized by progressive cognitive decline and memory loss. Identifying candidate biomarkers before the clinical onset of AD is crucial for enabling earlier diagnosis and timely therapeutic intervention. Among different molecular targets, N-acylsphingosine amidohydrolase 2 (ASAH2), a key enzyme in ceramide metabolism, has been linked to many neurodegenerative diseases, including AD.
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