Circulating transforming growth factor-beta levels and myocardial remodeling in young adults with mitral valve prolapse patients
Left ventricular (LV) remodeling could be found in a range of connective tissue disorders with involvement of transforming growth factor (TGF)-β pathway. Only rare data are available on it in patients with mitral valve prolapse (MVP). The aim of the study is to assess mechanisms of myocardial remode...
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Published in | Progress in pediatric cardiology Vol. 62; p. 101347 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.09.2021
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ISSN | 1058-9813 1558-1519 |
DOI | 10.1016/j.ppedcard.2021.101347 |
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Abstract | Left ventricular (LV) remodeling could be found in a range of connective tissue disorders with involvement of transforming growth factor (TGF)-β pathway. Only rare data are available on it in patients with mitral valve prolapse (MVP).
The aim of the study is to assess mechanisms of myocardial remodeling and diastolic dysfunction in asymptomatic young patients without mitral regurgitation.
78 asymptomatic young subjects with MVP were consecutively enrolled in our observational, single-center study. Concentrations of TGF-β1 and -β2 in serum were determined by enzyme-linked immunosorbent assay. Standard echocardiography extended with speckle-tracking echocardiography was performed in all patients.
Levels of TGF-β1 (15.2 ± 12.3 ng/ml vs. 9.3 ± 7.7 ng/ml; р = 0.004) and -β2 (3.0 ± 1.9 ng/ml vs. 2.5 ± 1.2 ng/ml; р = 0.04) in serum were significantly higher in patients with MVP. LV myocardial mass index in patients with MVP did not differ from the controls but in MVP group there were more patients with concentric and eccentric hypertrophy. Significant deterioration of longitudinal early diastolic strain rate (SRe) was found in patients with MVP in the region of the interventricular septum (1.38 ± 0.22 s-1 vs. 1.54 ± 0.25 s-1; p = 0.00001) and anterior wall (1.44 ± 0.23 s-1 vs. 1.56 ± 0.22 s-1; p = 0.0007). In MVP group level of TGF-β2 correlated with LV mass index and SRe. Multivariate regression analysis between such factors as age and sex detected influence TGF-β2 concentration on SRe (OR 1.95; 95% CI 1.3–4.1; р = 0.01).
A circulating TGF-β is involved in the LV remodeling and deterioration of the diastolic function in MVP patients without significant mitral regurgitation, apparently due to the profibrotic nature of this cytokine.
•Levels of TGF-β1 and TGF-β2 in the blood serum elevated in MVP patients.•Abnormal geometry of LV is more common in MVP patients then in controls.•Deterioration of regional diastolic SR was found in the IVS and anterior wall.•A circulating TGF-β is involved in the LV remodeling and diastolic disfunction in MVP. |
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AbstractList | Left ventricular (LV) remodeling could be found in a range of connective tissue disorders with involvement of transforming growth factor (TGF)-β pathway. Only rare data are available on it in patients with mitral valve prolapse (MVP).
The aim of the study is to assess mechanisms of myocardial remodeling and diastolic dysfunction in asymptomatic young patients without mitral regurgitation.
78 asymptomatic young subjects with MVP were consecutively enrolled in our observational, single-center study. Concentrations of TGF-β1 and -β2 in serum were determined by enzyme-linked immunosorbent assay. Standard echocardiography extended with speckle-tracking echocardiography was performed in all patients.
Levels of TGF-β1 (15.2 ± 12.3 ng/ml vs. 9.3 ± 7.7 ng/ml; р = 0.004) and -β2 (3.0 ± 1.9 ng/ml vs. 2.5 ± 1.2 ng/ml; р = 0.04) in serum were significantly higher in patients with MVP. LV myocardial mass index in patients with MVP did not differ from the controls but in MVP group there were more patients with concentric and eccentric hypertrophy. Significant deterioration of longitudinal early diastolic strain rate (SRe) was found in patients with MVP in the region of the interventricular septum (1.38 ± 0.22 s-1 vs. 1.54 ± 0.25 s-1; p = 0.00001) and anterior wall (1.44 ± 0.23 s-1 vs. 1.56 ± 0.22 s-1; p = 0.0007). In MVP group level of TGF-β2 correlated with LV mass index and SRe. Multivariate regression analysis between such factors as age and sex detected influence TGF-β2 concentration on SRe (OR 1.95; 95% CI 1.3–4.1; р = 0.01).
A circulating TGF-β is involved in the LV remodeling and deterioration of the diastolic function in MVP patients without significant mitral regurgitation, apparently due to the profibrotic nature of this cytokine.
•Levels of TGF-β1 and TGF-β2 in the blood serum elevated in MVP patients.•Abnormal geometry of LV is more common in MVP patients then in controls.•Deterioration of regional diastolic SR was found in the IVS and anterior wall.•A circulating TGF-β is involved in the LV remodeling and diastolic disfunction in MVP. |
ArticleNumber | 101347 |
Author | Malev, Eduard Luneva, Ekaterina Omelchenko, Marina Reeva, Svetlana Zemtsovsky, Eduard Timofeev, Eugeny |
Author_xml | – sequence: 1 givenname: Eduard surname: Malev fullname: Malev, Eduard email: malev@almazovcentre.ru organization: Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia – sequence: 2 givenname: Ekaterina surname: Luneva fullname: Luneva, Ekaterina organization: Almazov National Medical Research Centre, Saint-Petersburg, Russia – sequence: 3 givenname: Svetlana surname: Reeva fullname: Reeva, Svetlana organization: Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia – sequence: 4 givenname: Eugeny surname: Timofeev fullname: Timofeev, Eugeny organization: Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia – sequence: 5 givenname: Marina surname: Omelchenko fullname: Omelchenko, Marina organization: Almazov National Medical Research Centre, Saint-Petersburg, Russia – sequence: 6 givenname: Eduard surname: Zemtsovsky fullname: Zemtsovsky, Eduard organization: Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia |
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Cites_doi | 10.1016/j.amjcard.2011.12.029 10.1371/journal.pone.0129353 10.1093/ejechocard/jer021 10.1016/S0002-8703(99)70151-1 10.1590/S0066-782X2000000500007 10.1152/ajpheart.00484.2008 10.1093/ejechocard/jen323 10.1136/heartjnl-2016-309303 10.1038/nrcardio.2011.154 10.1161/CIRCULATIONAHA.108.841981 10.1056/NEJM199907013410101 10.1093/cvr/cvr337 10.1016/j.carpath.2015.07.009 10.1111/j.1540-8175.2010.01359.x 10.1017/S1047951113001042 10.1002/clc.22320 10.1111/j.1540-8175.2011.01544.x 10.1172/JCI0214190 10.1093/eurjhf/hfq127 10.1111/j.1365-2567.2006.02336.x 10.1038/s41598-020-65983-1 10.1093/ejechocard/jeq012 10.1016/j.jacc.2018.06.048 10.1152/ajpheart.00578.2001 10.1016/j.tcm.2009.01.001 10.1093/ejechocard/jep110 10.1016/j.echo.2016.01.011 10.1016/j.jacc.2016.12.012 |
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Keywords | Diastolic function Mitral valve prolapse Left ventricular remodeling Transforming growth factor-β |
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SubjectTerms | Diastolic function Left ventricular remodeling Mitral valve prolapse Transforming growth factor-β |
Title | Circulating transforming growth factor-beta levels and myocardial remodeling in young adults with mitral valve prolapse patients |
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