Intravoxel incoherent motion analysis of renal allograft diffusion with clinical and histopathological correlation in pediatric kidney transplant patients: A preliminary cross‐sectional observational study
The purpose of this study was to compare IVIM values in pediatric renal transplants with histopathology and clinical management change. Fifteen pediatric renal transplant recipients (mean 15.7±2.9 years) were prospectively scanned on a 3T MR scanner with multi‐b DTI, prior to same‐day transplant bio...
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Published in | Pediatric transplantation Vol. 21; no. 6 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
Wiley Subscription Services, Inc
01.09.2017
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Subjects | |
Online Access | Get full text |
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Summary: | The purpose of this study was to compare IVIM values in pediatric renal transplants with histopathology and clinical management change. Fifteen pediatric renal transplant recipients (mean 15.7±2.9 years) were prospectively scanned on a 3T MR scanner with multi‐b DTI, prior to same‐day transplant biopsy. IVIM maps from 14 subjects were analyzed (one excluded due to motion). Mean values were computed from cortical ROIs and medullary ROIs corresponding to the biopsy site. Subjects were also grouped according to whether or not the biopsy resulted in a change in clinical management. Cortico‐medullary IVIM estimates and histopathologic Banff scores were correlated with KT. Cortico‐medullary IVIM differences between the “change” and “no change” groups was compared with Mann‐Whitney U test. Cortical Dp showed significant moderate negative correlation with Banff t and ci scores (KT=−0.497, P=.035 and KT=−0.46, P=.046) and moderate positive correlation with Banff i score (KT=0.527, P=.028). Cortical Pf showed significant moderate correlation with ci and ct scores (KT=0.489, P=.035 and KT=0.457, P=.043). Tissue diffusivity, Dt, estimated with IVIM was significantly different between the “change” and “no change” groups in medullary ROIs (U=6, P=.021). IVIM analysis has potential as a noninvasive biomarker in assessment of pediatric renal allograft pathology. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Undefined-1 ObjectType-Feature-3 content type line 23 |
ISSN: | 1397-3142 1399-3046 |
DOI: | 10.1111/petr.12996 |