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GlucoCEST magnetic resonance imaging in vivo may be diagnostic of acute renal allograft rejection.
Kentrup, Dominik; Bovenkamp, Philipp; Busch, Annika; Schuette-Nuetgen, Katharina; Pawelski, Helga; Pavenstädt, Hermann; Schlatter, Eberhard; Herrmann, Karl-Heinz; Reichenbach, Jürgen R; Löffler, Bettina; Heitplatz, Barbara; Van Marck, Veerle; Yadav, Nirbhay N; Liu, Guanshu; van Zijl, Peter C M; Reuter, Stefan; Hoerr, Verena.
Afiliação
  • Kentrup D; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Bovenkamp P; Department of Clinical Radiology, University Hospital Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Busch A; Department of Clinical Radiology, University Hospital Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Schuette-Nuetgen K; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Pawelski H; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Pavenstädt H; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Schlatter E; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Herrmann KH; Medical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich-Schiller-University Jena, Philosophenweg 3, 07743 Jena, Germany.
  • Reichenbach JR; Medical Physics Group, Institute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich-Schiller-University Jena, Philosophenweg 3, 07743 Jena, Germany.
  • Löffler B; Institute of Medical Microbiology, Jena University Hospital, Erlanger Allee 101, 07747 Jena, Germany.
  • Heitplatz B; Department of Pathology, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Van Marck V; Department of Pathology, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany.
  • Yadav NN; Russel H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, 1800 Orleans St., Baltimore, Maryland 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Research Institute, 707 N. Broadway, Baltimore, Maryland 21205, U
  • Liu G; Russel H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, 1800 Orleans St., Baltimore, Maryland 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Research Institute, 707 N. Broadway, Baltimore, Maryland 21205, U
  • van Zijl PCM; Russel H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, 1800 Orleans St., Baltimore, Maryland 21287, USA; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Research Institute, 707 N. Broadway, Baltimore, Maryland 21205, U
  • Reuter S; Medical Clinic D, University of Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany. Electronic address: Stefan.Reuter@ukmuenster.de.
  • Hoerr V; Department of Clinical Radiology, University Hospital Muenster, Albert-Schweitzer Campus 1, 48149 Muenster, Germany; Institute of Medical Microbiology, Jena University Hospital, Erlanger Allee 101, 07747 Jena, Germany. Electronic address: verena.hoerr@uni-jena.de.
Kidney Int ; 92(3): 757-764, 2017 09.
Article em En | MEDLINE | ID: mdl-28709641
ABSTRACT
Acute cellular renal allograft rejection (AR) frequently occurs after kidney transplantations. It is a sterile T-cell mediated inflammation leading to increased local glucose metabolism. Here we demonstrate in an allogeneic model of Brown Norway rat kidneys transplanted into uninephrectomized Lewis rats the successful implementation of the recently developed glucose chemical exchange saturation transfer (glucoCEST) magnetic resonance imaging. This technique is a novel method to assess and differentiate AR. Renal allografts undergoing AR showed significantly increased glucoCEST contrast ratios of cortex to medulla of 1.61 compared to healthy controls (1.02), syngeneic Lewis kidney to Lewis rat transplants without rejection (0.92), kidneys with ischemia reperfusion injury (0.99) and kidneys affected by cyclosporine A toxicity (1.10). Receiver operating characteristic curve analysis showed an area under the curve value of 0.92, and the glucoCEST contrast ratio predicted AR with a sensitivity of 100% and a specificity of 69% at a threshold level over 1.08. In defined animal models of kidney injuries, the glucoCEST contrast ratios of cortex to medulla correlated positively with mRNA expression levels of T-cell markers (CD3, CD4, CD8a/b), but did not correlate to impaired renal perfusion. Thus, the glucoCEST parameter may be valuable for the assessment and follow up treatment of AR.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Traumatismo por Reperfusão / Transplante de Rim / Aloenxertos / Rejeição de Enxerto / Rim Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Traumatismo por Reperfusão / Transplante de Rim / Aloenxertos / Rejeição de Enxerto / Rim Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article