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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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in Cooperation with on an Cooperation-Score of 37%

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Publications (1/1 displayed)

  • 2023Alpha-cardiac Actin Serum Expression Levels Detect Acute Cellular Rejection in Heart Transplant Patients4citations

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Chart of shared publication
González-Juanatey, José Ramón
1 / 1 shared
Lago, Francisca
1 / 2 shared
Feijóo-Bandín, Sandra
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Triviño, Juan Carlos
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Tarazón, Estefanía
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Portolés, Manuel
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Martínez-Dolz, Luis
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Roselló-Lletí, Esther
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Sánchez-Lázaro, Ignacio
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Pérez-Carrillo, Lorena
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2023

Co-Authors (by relevance)

  • González-Juanatey, José Ramón
  • Lago, Francisca
  • Feijóo-Bandín, Sandra
  • Triviño, Juan Carlos
  • Tarazón, Estefanía
  • Portolés, Manuel
  • Martínez-Dolz, Luis
  • Roselló-Lletí, Esther
  • Sánchez-Lázaro, Ignacio
  • Pérez-Carrillo, Lorena
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article

Alpha-cardiac Actin Serum Expression Levels Detect Acute Cellular Rejection in Heart Transplant Patients

  • González-Juanatey, José Ramón
  • Lago, Francisca
  • Feijóo-Bandín, Sandra
  • Triviño, Juan Carlos
  • Tarazón, Estefanía
  • Portolés, Manuel
  • Martínez-Dolz, Luis
  • Roselló-Lletí, Esther
  • Sánchez-Lázaro, Ignacio
  • Giménez-Escamilla, Isaac
  • Pérez-Carrillo, Lorena
Abstract

<jats:sec><jats:title>Background.</jats:title><jats:p>Given the central role of sarcomeric dysfunction in cardiomyocyte biology and sarcomere alterations described in endomyocardial biopsies of transplant patients with rejection, we hypothesized that the serum expression levels of genes encoding sarcomeric proteins were altered in acute cellular rejection (ACR). The aim of this study is to identify altered sarcomere-related molecules in serum and to evaluate their diagnostic accuracy for detecting rejection episodes.</jats:p></jats:sec><jats:sec><jats:title>Methods.</jats:title><jats:p>Serum samples from transplant recipients undergoing routine endomyocardial biopsies were included in an RNA sequencing analysis (n = 40). Protein concentrations of alpha-cardiac actin were determined using a specific enzyme-linked immunoassay (n = 80).</jats:p></jats:sec><jats:sec><jats:title>Results.</jats:title><jats:p>We identified 17 sarcomeric genes differentially expressed in patients with clinically relevant rejection (grade ≥2R ACR). A receiver operating characteristic curve was done to assess their accuracy for ACR detection and found that 6 relevant actins, myosins, and other sarcomere-related genes showed great diagnostic capacity with an area under the curve (AUC) &gt; 0.800. Specifically, the gene encoding alpha-cardiac actin (<jats:italic toggle="yes">ACTC1</jats:italic>) showed the best results (AUC = 1.000, <jats:italic toggle="yes">P</jats:italic> &lt; 0.0001). We determine ACTC1 protein levels in a larger patient cohort, corroborating its overexpression and obtaining a significant diagnostic capacity for clinically relevant rejection (AUC = 0.702, <jats:italic toggle="yes">P</jats:italic> &lt; 0.05).</jats:p></jats:sec><jats:sec><jats:title>Conclusions.</jats:title><jats:p>Sarcomeric alterations are reflected in peripheral blood of patients with allograft rejection. Because of their precision to detect ACR, we propose sarcomere ACTC1 serum expression levels as potential candidate for to be included in the development of molecular panel testing for noninvasive ACR detection.</jats:p></jats:sec>

Topics
  • impedance spectroscopy
  • size-exclusion chromatography