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Serum Cardiotrophin-1 as a novel biomarker for intracranial aneurysm
Weidong Men1, Xuehao Zhang1, Lijian Zhang1
1Department of Neurosurgery, Affiliated Hospital of Hebei University, Hebei University, Baoding, 071000, Hebei Province, China.
Insights
Cardiotrophin-1 (CT-1) shows promise as a non-invasive biomarker for detecting intracranial aneurysms (IAs) and assessing rupture risk. Elevated CT-1 levels in patients suggest its clinical utility for early screening.
Area of Science:
- Neurology
- Biomarker Discovery
- Vascular Medicine
Background:
- Intracranial aneurysms (IAs) pose a significant rupture risk, potentially causing subarachnoid hemorrhage.
- Current diagnostic methods for IAs are invasive and costly, necessitating the search for non-invasive alternatives.
Purpose of the Study:
- To evaluate serum inflammatory markers and cardiotrophin-1 (CT-1) as potential non-invasive biomarkers for IA presence.
- To assess the utility of these markers in stratifying the risk of IA rupture.
Main Methods:
- Serum levels of IL-6, IL-10, IL-33, S100B, E-selectin, and CT-1 were measured in 131 IA patients and 21 controls using ELISA.
- Statistical analyses included Kruskal-Wallis tests, ROC curve analysis, and logistic regression to identify risk factors.
Main Results:
- Serum CT-1 levels were significantly higher in IA patients compared to controls (p = 0.0002), with the highest levels observed in ruptured IAs.
- CT-1 demonstrated diagnostic potential for IA (AUC = 0.7801) and ruptured IA (AUC = 0.7911).
- Other tested markers (IL-6, IL-10, IL-33, S100B, E-selectin) showed no significant differences. Older age and smoking were identified as significant IA risk factors.
Conclusions:
- Cardiotrophin-1 (CT-1) is a promising serum biomarker for the detection of intracranial aneurysms.
- Elevated CT-1 levels, especially in ruptured cases, indicate its potential for non-invasive risk stratification.
- Further validation in larger patient cohorts is recommended to confirm clinical utility.
Background:
Intracranial aneurysms (IAs) carry a high risk of rupture leading to subarachnoid hemorrhage, yet current diagnostic methods are invasive and costly. This study aimed to evaluate the potential of serum inflammatory markers and cardiotrophin-1 (CT-1) as non-invasive biomarkers for IA presence and rupture risk.
Methods:
A total of 131 IA patients (33 unruptured, 98 ruptured) and 21 healthy controls were enrolled. Serum levels of IL-6, IL-10, IL-33, S100B, E-selectin, and CT-1 were measured by ELISA. Statistical analyses included Kruskal-Wallis tests, ROC curve evaluation, and logistic regression for risk factors.
Results:
Serum CT-1 levels were significantly elevated in IA patients versus controls (p = 0.0002), with the highest levels in ruptured IAs (p = 0.0001 vs controls). ROC analysis demonstrated CT-1's diagnostic potential for IA (AUC = 0.7801, sensitivity 75.57%) and ruptured IA (AUC = 0.7911, sensitivity 79.59%). No significant differences were observed for IL-6, IL-10, IL-33, S100B, or E-selectin. Older age (OR = 1.072) and smoking (OR = 9.659) were significant IA risk factors.
Conclusions:
CT-1 is a promising serum biomarker for IA detection and rupture risk stratification. Its elevation, particularly in ruptured cases, suggests potential clinical utility for non-invasive screening. Further validation in larger cohorts is warranted.
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