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Plasma HGF and OPN as Potential Biomarkers of Pulmonary Arterial Hypertension in Congenital Heart Disease

Dongdong Zheng1,#, Chi Shen1,2,#, Wenshi Liu1, Wenjing Lv1, Xiaofei Li1,*
1 Department of Cardiovascular Internal Medicine, Affiliated Hospital of Nantong University, Nantong, 226001, China
2 Department of Cardiovascular Internal Medicine, Tongzhou People’s Hospital Affiliated to Nantong University, Nantong, 226300, China
* Corresponding Author: Xiaofei Li. Email:

Congenital Heart Disease 2021, 16(4), 373-381. https://doi.org/10.32604/CHD.2021.015260

Received 04 December 2020; Accepted 23 February 2021; Issue published 19 April 2021

Abstract

Objectives: Pulmonary arterial hypertension in congenital heart disease (PAH-CHD) is the most common type of PAH and increases morbidity and mortality in patients with CHD. Right heart catheterization (RHC) is the standard method to diagnose PAH. However, RHC is an invasive and complicated method with relatively high cost. Noninvasive, feasible, and cost-efficient methods are urgently needed. The objective of this study was to evaluate three potential biomarkers of PAH-CHD: Hepatocyte growth factor (HGF), osteopontin (OPN), and suppression of tumorigenicity 2 (ST2). Methods: Plasma samples were collected from patients with CHD (n = 46) and healthy individuals (n = 22) and divided into four groups according to the severity of PAH. The levels of HGF, OPN, and ST2 were then analyzed using an enzyme-linked immunosorbent assay. Correlations between HGF, OPN, ST2, and clinical parameters of PAH-CHD were analyzed. Results: The plasma HGF levels in the moderate to the severe group were significantly higher than those in the mild group, nonPAH group, and healthy control group (p < 0.05). Derived from a receiver operating characteristic (ROC) curve analysis, a cut-off value of 356.75 ng/ml for the HGF concentration was able to predict PAH-CHD with 53% sensitivity and 89% specificity. The HGF level was positively related to pulmonary arterial systolic pressure (PASP) (r = 0.36, p < 0.05) and pulmonary vascular resistance (PVR) (r = 0.36, p < 0.05). Plasma OPN levels in the mild group were significantly higher than other groups and positively correlated with the pulmonary-systemic shunt ratio (Qp/Qs) (r = 0.33, p < 0.05). There was no statistically significant between-group difference in plasma soluble ST2 (sST2) levels. Conclusion: The plasma HGF level was elevated in PAH-CHD patients and can be used as a potential biomarker. The plasma OPN level was positively correlated with the Qp/Qs.

Keywords

Congenital heart disease; pulmonary hypertension; hepatocyte growth factor; osteopontin; suppression of tumorigenicity 2; biomarker

Cite This Article

Zheng, D., Shen, C., Liu, W., Lv, W., Li, X. (2021). Plasma HGF and OPN as Potential Biomarkers of Pulmonary Arterial Hypertension in Congenital Heart Disease. Congenital Heart Disease, 16(4), 373–381.



This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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