Literature DB >> 21531579

Osteopontin: a potential biomarker for heart failure and reverse remodeling after left ventricular assist device support.

Marguérite E I Schipper1, Maaike R Scheenstra, Joyce van Kuik, Dick F van Wichen, Petra van der Weide, Hub F J Dullens, Jaap Lahpor, Nicolaas de Jonge, Roel A De Weger.   

Abstract

BACKGROUND: Left ventricular assist device (LVAD) support in end-stage heart failure (HF) leads to recovery of the patient's condition, size reduction of cardiomyocytes, and also volume reduction and change in the composition of the extracellular matrix (ECM). Myocardial expression of ECM osteopontin (OPN) protein increases with the severity of HF. We analyzed whether OPN messenger RNA expression in heart tissue and/or OPN protein in plasma are associated with reverse remodeling during LVAD support.
METHODS: Plasma and heart tissue specimens of 22 end-stage HF patients before and after LVAD implantation and subsequent heart transplantation (HTx) were used to determine the concentrations of OPN protein (EIA) and OPN messenger RNA (mRNA) by quantitative polymerase chain reaction. Immunohistochemistry (IHC) and in situ hybridization (ISH) were performed to locate OPN protein and mRNA.
RESULTS: The high OPN protein levels in plasma of HF patients did not differ significantly before and after LVAD support in ischemic heart disease (IHD) (pre-LVAD 167 ± 32 ng/ml; post-LVAD 165 ± 28 ng/ml) and in dilated cardiomyopathy (DCM) (pre-LVAD 99 ± 12 ng/ml; post-LVAD (142 ± 6 ng/ml). The OPN plasma levels after HTx decreased to control levels (IHD, 48 ± 6; DCM, 40 ± 5; control, 31 ± 3 ng/ml). In contrast, expression of OPN mRNA in heart biopsy specimens decreased significantly after LVAD support (the relative quantity decreased > 90% in IHD and 50% in DCM). ISH and IHC revealed that OPN was present in cardiomyocytes and in the ECM.
CONCLUSIONS: Levels of OPN mRNA in the myocardium of HF patients showed a significant decrease after LVAD support but OPN protein expression did not. LVAD support only induced a decrease of OPN plasma levels in individual patients, whereas OPN plasma levels reduced significantly in all patients after HTx.
Copyright © 2011 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21531579     DOI: 10.1016/j.healun.2011.03.015

Source DB:  PubMed          Journal:  J Heart Lung Transplant        ISSN: 1053-2498            Impact factor:   10.247


  16 in total

Review 1.  Matricellular proteins in cardiac adaptation and disease.

Authors:  Nikolaos G Frangogiannis
Journal:  Physiol Rev       Date:  2012-04       Impact factor: 37.312

2.  Cellular, molecular, genomic changes occurring in the heart under mechanical circulatory support.

Authors:  Michele Gallo; Vincenzo Tarzia; Laura Iop; Jonida Bejko; Giacomo Bortolussi; Roberto Bianco; Tomaso Bottio; Gino Gerosa
Journal:  Ann Cardiothorac Surg       Date:  2014-09

Review 3.  Diagnosing destabilized heart failure in the emergency setting: current and future biomarker tests.

Authors:  Damien Gruson; Frédéric Thys; Franck Verschuren
Journal:  Mol Diagn Ther       Date:  2011-12-01       Impact factor: 4.074

4.  Serum osteopontin, but not OPN gene polymorphism, is associated with LVH in essential hypertensive patients.

Authors:  Xuwei Hou; Zhaohui Hu; Xiaohua Huang; Yan Chen; Xiuying He; Haiying Xu; Ningfu Wang
Journal:  J Mol Med (Berl)       Date:  2013-12-27       Impact factor: 4.599

5.  [Congestive heart failure: reverse cardiac remodeling mediated by left ventricular assist devices].

Authors:  J Wohlschläger; H Milting; J Stypmann; T Hager; C Schmid; B Levkau; H A Baba
Journal:  Pathologe       Date:  2012-05       Impact factor: 1.011

Review 6.  Osteopontin and Transplantation: Where Are We Now?

Authors:  Beata Kaleta
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2021-05-21       Impact factor: 4.291

7.  Transcriptional profiling of left ventricle and peripheral blood mononuclear cells in a rat model of postinfarction heart failure.

Authors:  Dorota Tulacz; Urszula Mackiewicz; Michal Maczewski; Agata Maciejak; Monika Gora; Beata Burzynska
Journal:  BMC Med Genomics       Date:  2013-11-08       Impact factor: 3.063

8.  Myocardial Expression Analysis of Osteopontin and Its Splice Variants in Patients Affected by End-Stage Idiopathic or Ischemic Dilated Cardiomyopathy.

Authors:  Manuela Cabiati; Benedetta Svezia; Marco Matteucci; Luca Botta; Angela Pucci; Mauro Rinaldi; Chiara Caselli; Vincenzo Lionetti; Silvia Del Ry
Journal:  PLoS One       Date:  2016-08-01       Impact factor: 3.240

9.  Osteopontin - a biomarker of disease, but also of stage stratification of the functional myocardial contractile deficit by chronic ischaemic heart disease.

Authors:  Bogdan-Ioan Coculescu; Gheorghe Manole; Gabi Valeriu Dincă; Elena Claudia Coculescu; Cristina Berteanu; Cristina Mariana Stocheci
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

10.  Assessment of brain-derived neurotrophic factor and osteopontin in a healthy pediatric population.

Authors:  Joshua D Chew; Larry Markham; Holly M Smith; Yan Ru Su; Kelsey Tomasek; James C Slaughter; Douglas Sawyer; Jonathan H Soslow
Journal:  J Circ Biomark       Date:  2018-10-18
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