Angiostatic Peptide, Endostatin, Predicts Severity in Pediatric Congenital Heart Disease-Associated Pulmonary Hypertension

被引:7
|
作者
Daly, Caroline M. [1 ]
Griffiths, Megan [2 ]
Simpson, Catherine E. [3 ]
Yang, Jun [2 ]
Damico, Rachel L. [3 ]
Vaidya, R. Dhananjay [4 ]
Williams, Monica [5 ]
Brandal, Stephanie [2 ]
Jone, Pei-Ni [6 ]
Polsen, Cassandra [6 ]
Ivy, D. Dunbar [6 ]
Austin, Eric D. [7 ]
Nichols, William C. [8 ]
Pauciulo, Michael W. [8 ]
Lutz, Katie [8 ]
Nies, Melanie K. [2 ]
Rosenzweig, Erika B. [10 ]
Hirsch, Russel [9 ]
Yung, Delphine [11 ]
Everett, Allen D. [2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Dept Pediat, Div Pediat Cardiol, 1800 Orleans St Room M2303, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Div Pulm & Crit Care Med, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Dept Internal Med, Baltimore, MD 21287 USA
[5] Johns Hopkins Univ, Dept Anesthesia & Crit Care Med, Baltimore, MD 21287 USA
[6] Univ Colorado, Childrens Hosp Colorado, Dept Pediat Cardiol, Aurora, CO USA
[7] Vanderbilt Univ, Med Ctr, Dept Pediat, Div Allergy Immunol & Pulm Med, Nashville, TN 37232 USA
[8] Univ Cincinnati, Coll Med, Dept Pediat, Div Human Genet, Cincinnati, OH USA
[9] Univ Cincinnati, Coll Med, Dept Pediat, Div Pediat Cardiol, Cincinnati, OH USA
[10] Columbia Univ, Dept Pediat, Div Pediat Cardiol, New York, NY 10027 USA
[11] Univ Washington, Dept Pediat, Div Pediat Cardiol, Seattle, WA 98195 USA
来源
基金
美国国家卫生研究院;
关键词
angiogenesis; biomarkers; children; proteomics; pulmonary vascular disease; ARTERIAL-HYPERTENSION; SERUM ENDOSTATIN; RIGHT VENTRICLE; ANGIOGENESIS; GROWTH;
D O I
10.1161/JAHA.120.021409
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Endostatin, an angiogenic inhibitor, is associated with worse pulmonary arterial hypertension (PAH) outcomes in adults and poor lung growth in children. This study sought to assess whether endostatin is associated with disease severity and outcomes in pediatric PAH. Methods and Results Serum endostatin was measured in cross-sectional (N=160) and longitudinal cohorts (N=64) of pediatric subjects with PAH, healthy pediatric controls and pediatric controls with congenital heart disease (CHD) (N=54, N=15), and adults with CHD associated PAH (APAH-CHD, N=185). Outcomes, assessed by regression and Kaplan-Meier analysis, included hemodynamics, change in endostatin over time, and transplant-free survival. Endostatin secretion was evaluated in pulmonary artery endothelial and smooth muscle cells. Endostatin was higher in those with PAH compared with healthy controls and controls with CHD and was highest in those with APAH-CHD. In APAH-CHD, endostatin was associated with a shorter 6-minute walk distance and increased mean right atrial pressure. Over time, endostatin was associated with higher pulmonary artery pressure and pulmonary vascular resistance index, right ventricular dilation, and dysfunction. Endostatin decreased with improved hemodynamics over time. Endostatin was associated with worse transplant-free survival. Addition of endostatin to an NT-proBNP (N-terminal pro-B-type natriuretic peptide) based survival analysis improved risk stratification, reclassifying subjects with adverse outcomes. Endostatin was secreted primarily by pulmonary artery endothelial cells. Conclusions Endostatin is associated with disease severity, disease improvement, and worse survival in APAH-CHD. Endostatin with NT-proBNP improves risk stratification, better predicting adverse outcomes. The association of elevated endostatin with shunt lesions suggests that endostatin could be driven by both pulmonary artery flow and pressure. Endostatin could be studied as a noninvasive prognostic marker, particularly in APAH-CHD.
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页数:24
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