Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect

Uncorrected atrial septal defect undergoes right ventricle chronic volume overload which may lead to pulmonary hypertension and Eisenmenger Syndrome. The soluble suppression of tumorigenicity-2 is a left ventricle strain biomarker; however, its role in right ventricle strain is unclear. This study a...

Full description

Bibliographic Details
Main Authors: Reza S. Pratama, Anggoro B. Hartopo, Dyah W. Anggrahini, Vera C. Dewanto, Lucia K. Dinarti
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:Pulmonary Circulation
Online Access:https://doi.org/10.1177/2045894020915832
_version_ 1817978157314080768
author Reza S. Pratama
Anggoro B. Hartopo
Dyah W. Anggrahini
Vera C. Dewanto
Lucia K. Dinarti
author_facet Reza S. Pratama
Anggoro B. Hartopo
Dyah W. Anggrahini
Vera C. Dewanto
Lucia K. Dinarti
author_sort Reza S. Pratama
collection DOAJ
description Uncorrected atrial septal defect undergoes right ventricle chronic volume overload which may lead to pulmonary hypertension and Eisenmenger Syndrome. The soluble suppression of tumorigenicity-2 is a left ventricle strain biomarker; however, its role in right ventricle strain is unclear. This study aimed to investigate the implication of serum soluble suppression of tumorigenicity-2 in adult uncorrected atrial septal defect. This was a cross-sectional study. We enrolled 81 adult uncorrected secundum atrial septal defect patients. Clinical and hemodynamic data were collected. Serum samples were withdrawn from the pulmonary artery during right heart catheterization. Serum soluble suppression of tumorigenicity-2 and NT-proBNP levels were measured. Subjects were divided into three groups based on clinical and hemodynamic severity. The correlation of soluble suppression of tumorigenicity-2 with patients' data and comparison among groups were analyzed. A p value <0.05 was considered statistically significant. Results showed that, there were significant correlations between serum soluble suppression of tumorigenicity-2 and mean pulmonary artery pressure ( r  = 0.203, p  = 0.035) and right ventricle end-diastolic diameter ( r  = 0.203, p <0.05). Median serum soluble suppression of tumorigenicity-2 level was incrementally increased from group I (atrial septal defect and no-pulmonary hypertension), group II (left-to-right atrial septal defect and pulmonary hypertension), to group III (Eisenmenger Syndrome): (17.4 ng/mL, 21.8 ng/mL, and 29.4 ng/mL, respectively). A post-hoc analysis showed that serum soluble suppression of tumorigenicity-2 level was significantly different between groups I and III ( p  = 0.01). Serum N terminal pro brain natriuretic peptide (NT-proBNP) level was consistently associated with worse clinical and hemodynamic parameters. No correlation was found between serum soluble suppression of tumorigenicity-2 and NT-proBNP level. In conclusion, serum soluble suppression of tumorigenicity-2 level had significant positive correlation with mean pulmonary artery pressure and right ventricle end-diastolic diameter in uncorrected secundum atrial septal defect patients. Higher serum soluble suppression of tumorigenicity-2 level was associated with the presence of pulmonary hypertension and Eisenmenger Syndrome in uncorrected secundum atrial septal defect patients.
first_indexed 2024-04-13T22:26:38Z
format Article
id doaj.art-275e112224664818a3a6481c203d52d9
institution Directory Open Access Journal
issn 2045-8940
language English
last_indexed 2024-04-13T22:26:38Z
publishDate 2020-05-01
publisher Wiley
record_format Article
series Pulmonary Circulation
spelling doaj.art-275e112224664818a3a6481c203d52d92022-12-22T02:27:03ZengWileyPulmonary Circulation2045-89402020-05-011010.1177/2045894020915832Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defectReza S. PratamaAnggoro B. HartopoDyah W. AnggrahiniVera C. DewantoLucia K. DinartiUncorrected atrial septal defect undergoes right ventricle chronic volume overload which may lead to pulmonary hypertension and Eisenmenger Syndrome. The soluble suppression of tumorigenicity-2 is a left ventricle strain biomarker; however, its role in right ventricle strain is unclear. This study aimed to investigate the implication of serum soluble suppression of tumorigenicity-2 in adult uncorrected atrial septal defect. This was a cross-sectional study. We enrolled 81 adult uncorrected secundum atrial septal defect patients. Clinical and hemodynamic data were collected. Serum samples were withdrawn from the pulmonary artery during right heart catheterization. Serum soluble suppression of tumorigenicity-2 and NT-proBNP levels were measured. Subjects were divided into three groups based on clinical and hemodynamic severity. The correlation of soluble suppression of tumorigenicity-2 with patients' data and comparison among groups were analyzed. A p value <0.05 was considered statistically significant. Results showed that, there were significant correlations between serum soluble suppression of tumorigenicity-2 and mean pulmonary artery pressure ( r  = 0.203, p  = 0.035) and right ventricle end-diastolic diameter ( r  = 0.203, p <0.05). Median serum soluble suppression of tumorigenicity-2 level was incrementally increased from group I (atrial septal defect and no-pulmonary hypertension), group II (left-to-right atrial septal defect and pulmonary hypertension), to group III (Eisenmenger Syndrome): (17.4 ng/mL, 21.8 ng/mL, and 29.4 ng/mL, respectively). A post-hoc analysis showed that serum soluble suppression of tumorigenicity-2 level was significantly different between groups I and III ( p  = 0.01). Serum N terminal pro brain natriuretic peptide (NT-proBNP) level was consistently associated with worse clinical and hemodynamic parameters. No correlation was found between serum soluble suppression of tumorigenicity-2 and NT-proBNP level. In conclusion, serum soluble suppression of tumorigenicity-2 level had significant positive correlation with mean pulmonary artery pressure and right ventricle end-diastolic diameter in uncorrected secundum atrial septal defect patients. Higher serum soluble suppression of tumorigenicity-2 level was associated with the presence of pulmonary hypertension and Eisenmenger Syndrome in uncorrected secundum atrial septal defect patients.https://doi.org/10.1177/2045894020915832
spellingShingle Reza S. Pratama
Anggoro B. Hartopo
Dyah W. Anggrahini
Vera C. Dewanto
Lucia K. Dinarti
Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
Pulmonary Circulation
title Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
title_full Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
title_fullStr Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
title_full_unstemmed Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
title_short Serum soluble suppression of tumorigenicity-2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
title_sort serum soluble suppression of tumorigenicity 2 level associates with severity of pulmonary hypertension associated with uncorrected atrial septal defect
url https://doi.org/10.1177/2045894020915832
work_keys_str_mv AT rezaspratama serumsolublesuppressionoftumorigenicity2levelassociateswithseverityofpulmonaryhypertensionassociatedwithuncorrectedatrialseptaldefect
AT anggorobhartopo serumsolublesuppressionoftumorigenicity2levelassociateswithseverityofpulmonaryhypertensionassociatedwithuncorrectedatrialseptaldefect
AT dyahwanggrahini serumsolublesuppressionoftumorigenicity2levelassociateswithseverityofpulmonaryhypertensionassociatedwithuncorrectedatrialseptaldefect
AT veracdewanto serumsolublesuppressionoftumorigenicity2levelassociateswithseverityofpulmonaryhypertensionassociatedwithuncorrectedatrialseptaldefect
AT luciakdinarti serumsolublesuppressionoftumorigenicity2levelassociateswithseverityofpulmonaryhypertensionassociatedwithuncorrectedatrialseptaldefect