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Population Study Confirms Serum Proteins' Change and Reveals Diagnostic Values in Congenital Ventricular Septal
Jinghua Long1, Shun Liu1, Xiaoyun Zeng1
1Department of Epidemiology School of Public Health, Guangxi Medical University, Shuangyong Road 22, Nanning, 530021, Guangxi, China.
Insights
Thrombospondin 1 (TSP-1), vascular endothelial-cadherin (VE-cad), and insulin-like growth factor 2 (IGF-2) show diagnostic value for ventricular septal defect (VSD). Elevated levels of these proteins in children indicate an increased risk and potential for early VSD diagnosis.
Area of Science:
- Biomarkers
- Cardiovascular Research
- Pediatric Cardiology
Background:
- Ventricular septal defect (VSD) is a common congenital heart anomaly.
- Identifying reliable biomarkers for VSD diagnosis and risk assessment is crucial.
- Current diagnostic methods may have limitations in early detection.
Purpose of the Study:
- To validate thrombospondin 1 (TSP-1), vascular endothelial-cadherin (VE-cad), insulin-like growth factor 2 (IGF-2), and amyloid precursor protein (APP) as potential biomarkers for VSD.
- To assess the diagnostic value of these proteins in a pediatric VSD cohort.
- To explore the association between protein levels and VSD risk.
Main Methods:
- A hospital-based case-control study involving 40 VSD children and 40 healthy controls.
- Serum protein levels measured using enzyme-linked immunosorbent assay (ELISA).
- Statistical analyses included logistic regression and receiver operating characteristic (ROC) curve analysis.
Main Results:
- Serum levels of TSP-1, VE-cad, and IGF-2 were significantly elevated in VSD patients compared to controls (p < 0.05).
- High TSP-1, VE-cad, and IGF-2 levels were strongly associated with increased VSD risk (p < 0.001 for TSP-1 and VE-cad, p = 0.015 for IGF-2).
- ROC curve analysis indicated significant diagnostic value for TSP-1 (AUC 0.985), VE-cad (AUC 0.838), and IGF-2 (AUC 0.658).
Conclusions:
- TSP-1, VE-cad, and IGF-2 are significantly associated with VSD risk.
- These proteins demonstrate diagnostic potential for VSD.
- Findings may contribute to understanding VSD etiology and improving early diagnosis and prevention strategies.
Abstract:
This study was designed to validate thrombospondin 1 (TSP-1), vascular endothelial-cadherin complex (VE-cad), insulin-like growth factor 2 (IGF-2), and amyloid precursor protein (APP) and assess their diagnostic value in ventricular septal defect (VSD). We investigated the serum levels of TSP-1, VE-cad, IGF-2, and APP by enzyme-linked immunosorbent assay in a hospital-based case-control study that included 40 VSD children and 40 healthy controls. Logistic regression analysis was applied to evaluate the relationship of the proteins and VSD, and receiver operating characteristic (ROC) curve was used to assess the diagnostic value of the significant proteins. The serum levels of TSP-1, VE-cad, and IGF-2 were significantly higher in VSD patients than those in healthy controls (p < 0.05). Multivariate logistic regression analysis demonstrated that high levels of TSP-1, VE-cad, and IGF-2 were significantly associated with an increased risk of VSD [TSP-1 (OR 26.91, 95% CI 6.60-72.66, p < 0.001), VE-cad (OR 11.91, 95% CI 3.90-36.36, p < 0.001), IGF-2 (OR 3.25, 95% CI 1.25-8.43, p = 0.015)]. Areas under the ROC curve for TSP-1, VE-cad, and IGF-2 were 0.985, 0.838, and 0.658, respectively. These data demonstrated that TSP-1, VE-cad, and IGF-2 were significantly associated with risk of VSD and manifested diagnostic values, which may provide new evidence for understanding the etiology and promote the early diagnosis and prevention of VSD.
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