Intravoxel incoherent imaging of renal fibrosis induced in a murine model of unilateral ureteral obstruction.

Abstract:

PURPOSE:To evaluate non-invasive imaging biomarkers for assessing renal fibrosis. DWI is used to assess renal function; intravoxel incoherent motion (IVIM) provides additional measures of perfusion-related diffusion (D*, blood flow; f, perfusion fraction). We aim to determine if reduced ADC seen in renal fibrosis is attributable to perfusion-related diffusion changes or to known reduction in tissue diffusivity (D). MATERIALS AND METHODS:Unilateral ureteral obstruction (UUO) was created in six mice to induce renal fibrosis. DWI was performed the day before and 7 days post-UUO. A range of b-values from 0 to 1200 s/mm(2) were used. IVIM parameters were obtained using region of interests drawn over the renal parenchyma. Histopathological analysis of both kidneys was performed in all mice. Results were analyzed using the paired t-test with P<0.05 considered statistically significant. RESULTS:D and f were significantly lower in the ligated kidneys at Day 7 compared to before ligation and no significant difference was found for D*. Comparing non-ligated and ligated kidneys within the same mouse at Day 7, significantly lower D values were observed in the ligated kidneys, while no significant difference was found for f and D*, although the values of f were generally lower. Histopathological analysis confirmed development of fibrosis and reduction in glomeruli in all the ligated kidneys at Day 7. CONCLUSION:Our study shows that the reduction in ADC seen in renal fibrosis is attributable not only to reduced D as previously encountered but also a decrease in vascularity as assessed by f. Reduction in f is possibly related to a reduction in glomeruli.

journal_name

Magn Reson Imaging

authors

Hennedige T,Koh TS,Hartono S,Yan YY,Song IC,Zheng L,Lee WS,Rumpel H,Martarello L,Khoo JB,Koh DM,Chuang KH,Thng CH

doi

10.1016/j.mri.2015.07.012

subject

Has Abstract

pub_date

2015-12-01 00:00:00

pages

1324-1328

issue

10

eissn

0730-725X

issn

1873-5894

pii

S0730-725X(15)00188-5

journal_volume

33

pub_type

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