Literature DB >> 16118170

Assessment of acute renal transplant rejection with blood oxygen level-dependent MR imaging: initial experience.

Elizabeth A Sadowski1, Sean B Fain, Sara K Alford, Frank R Korosec, Jason Fine, Rebecca Muehrer, Arjang Djamali, R Michael Hofmann, Bryan N Becker, Thomas M Grist.   

Abstract

PURPOSE: To prospectively assess the oxygenation state of renal transplants and determine the feasibility of using blood oxygen level-dependent (BOLD) magnetic resonance (MR) imaging to differentiate between acute tubular necrosis (ATN), acute rejection, and normal function.
MATERIALS AND METHODS: This HIPAA-compliant study had institutional human subjects review committee approval, and written informed consent was obtained from all patients. BOLD MR imaging was performed in 20 patients (age range, 21-70 years) who had recently received renal transplants. Six patients had clinically normal functioning transplants, eight had biopsy-proved rejection, and six had biopsy-proved ATN. R2* (1/sec) measurements were obtained in the medulla and cortex of transplanted kidneys. R2* is a measure of the rate of signal loss in a specific region and is related to the amount of deoxyhemoglobin present. Statistical analysis was performed by using a two-sample t test. Threshold R2* values were identified to discriminate between transplanted kidneys with ATN, those with acute rejection, and those with normal function.
RESULTS: R2* values for the medulla were significantly lower in the acute rejection group (R2* = 15.8/sec +/- 1.5) than in normally functioning transplants (R2* = 23.9/sec +/- 3.2) and transplants with ATN (R2* = 21.3/sec +/- 1.9). The differences between the acute rejection and normal function groups (P = .001), as well as between the acute rejection and ATN groups (P < .001), were significant. Acute rejection could be differentiated from normal function and ATN in all cases by using a threshold R2* value of 18/sec. R2* values for the cortex were higher in ATN (R2* = 14.2/sec +/- 1.4) than for normally functioning transplants (R2* = 12.7/sec +/- 1.6) and transplants with rejection (R2* = 12.4/sec +/- 1.2). The difference in R2* values in the cortex between ATN and rejection was statistically significant (P = .034), although there was no threshold value that enabled differentiation of all cases of ATN from cases of normal function or acute rejection.
CONCLUSION: R2* measurements in the medullary regions of transplanted kidneys with acute rejection were significantly lower than those in normally functioning transplants or transplants with ATN. These results suggest that marked changes in intrarenal oxygenation occur during acute transplant rejection.

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Year:  2005        PMID: 16118170     DOI: 10.1148/radiol.2363041080

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  41 in total

Review 1.  Noncontrast functional MRI of the kidneys.

Authors:  Lorenzo Mannelli; Jeffrey H Maki; Sherif F Osman; Hersh Chandarana; David J Lomas; William P Shuman; Ken F Linnau; Douglas E Green; Giacomo Laffi; Miriam Moshiri
Journal:  Curr Urol Rep       Date:  2012-02       Impact factor: 3.092

2.  [Functional magnetic resonance imaging for evaluation of radiation-induced renal damage].

Authors:  S Haneder; J Boda-Heggemann; S O Schoenberg; H J Michaely
Journal:  Radiologe       Date:  2012-03       Impact factor: 0.635

Review 3.  Targeting Endogenous Repair Pathways after AKI.

Authors:  Benjamin D Humphreys; Vincenzo Cantaluppi; Didier Portilla; Kai Singbartl; Li Yang; Mitchell H Rosner; John A Kellum; Claudio Ronco
Journal:  J Am Soc Nephrol       Date:  2015-11-18       Impact factor: 10.121

Review 4.  [Functional magnetic resonance imaging of the kidneys].

Authors:  R S Lanzman; M Notohamiprodjo; H J Wittsack
Journal:  Radiologe       Date:  2015-12       Impact factor: 0.635

5.  MR measures of renal perfusion, oxygen bioavailability and total renal blood flow in a porcine model: noninvasive regional assessment of renal function.

Authors:  Andrew L Wentland; Nathan S Artz; Sean B Fain; Thomas M Grist; Arjang Djamali; Elizabeth A Sadowski
Journal:  Nephrol Dial Transplant       Date:  2011-05-28       Impact factor: 5.992

Review 6.  Magnetic resonance imaging in the complications of kidney transplantation.

Authors:  M Onniboni; M De Filippo; R Averna; L Coco; M Zompatori; N Sverzellati; C Rossi
Journal:  Radiol Med       Date:  2012-10-22       Impact factor: 3.469

7.  Evaluation of renal allograft function early after transplantation with diffusion-weighted MR imaging.

Authors:  Ute Eisenberger; Harriet C Thoeny; Tobias Binser; Mathias Gugger; Felix J Frey; Chris Boesch; Peter Vermathen
Journal:  Eur Radiol       Date:  2009-12-16       Impact factor: 5.315

8.  Urinary oxygen tension measurement in humans using magnetic resonance imaging.

Authors:  Zhen J Wang; Bonnie N Joe; Fergus V Coakley; Greg Zaharchuk; Reed Busse; Benjamin M Yeh
Journal:  Acad Radiol       Date:  2008-11       Impact factor: 3.173

9.  Nox2 and Cyclosporine-Induced Renal Hypoxia.

Authors:  Arjang Djamali; Nancy A Wilson; Elizabeth A Sadowski; Wei Zha; David Niles; Omeed Hafez; Justin R Dorn; Thomas R Mehner; Paul C Grimm; F Michael Hoffmann; Weixiong Zhong; Sean B Fain; Shannon R Reese
Journal:  Transplantation       Date:  2016-06       Impact factor: 4.939

10.  Quantification of renal allograft perfusion using arterial spin labeling MRI: initial results.

Authors:  Rotem S Lanzman; Hans-Jörg Wittsack; Petros Martirosian; Panagiota Zgoura; Philip Bilk; Patric Kröpil; Fritz Schick; Adina Voiculescu; Dirk Blondin
Journal:  Eur Radiol       Date:  2009-12-01       Impact factor: 5.315

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