| Literature DB >> 28709641 |
Dominik Kentrup1, Philipp Bovenkamp2, Annika Busch2, Katharina Schuette-Nuetgen1, Helga Pawelski1, Hermann Pavenstädt1, Eberhard Schlatter1, Karl-Heinz Herrmann3, Jürgen R Reichenbach3, Bettina Löffler4, Barbara Heitplatz5, Veerle Van Marck5, Nirbhay N Yadav6, Guanshu Liu6, Peter C M van Zijl6, Stefan Reuter7, Verena Hoerr8.
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.Entities:
Keywords: acute rejection; glucoCEST MRI; inflammation; kidney transplantation
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Year: 2017 PMID: 28709641 DOI: 10.1016/j.kint.2017.04.015
Source DB: PubMed Journal: Kidney Int ISSN: 0085-2538 Impact factor: 10.612