TY - JOUR
T1 - Noninvasive assessment of renal fibrosis with magnetization transfer MR imaging
T2 - Validation and evaluation in murine renal artery stenosis
AU - Jiang, Kai
AU - Ferguson, Christopher M.
AU - Ebrahimi, Behzad
AU - Tang, Hui
AU - Kline, Timothy L.
AU - Burningham, Tyson A.
AU - Mishra, Prassana K.
AU - Grande, Joseph P.
AU - Macura, Slobodan I.
AU - Lerman, Lilach O.
N1 - Funding Information:
Supported by the National Heart, Lung, and Blood Institute (HL123160), the National Institute of Diabetes and Digestive and Kidney Diseases (DK102325, DK104273, DK73608), and the National Institute of Allergy and Infectious Diseases (AI-100911).
Publisher Copyright:
© 2017 RSNA.
PY - 2017/4
Y1 - 2017/4
N2 - Purpose: To test the utility of magnetization transfer imaging in detecting and monitoring the progression of renal fibrosis in mice with unilateral renal artery stenosis. Materials and Methods: This prospective study was approved by the Institutional Animal Care and Use Committee. Renal artery stenosis surgery (n = 10) or sham surgery (n = 5) was performed, and the stenotic and contralateral kidneys were studied longitudinally in vivo at baseline and 2, 4, and 6 weeks after surgery. After a 16.4-T magnetic resonance imaging examination, magnetization transfer ratio was measured as an index of fibrosis (guided by parameters selected in preliminary phantom studies). In addition, renal volume, perfusion, blood flow, and oxygenation were assessed. Fibrosis was subsequently measured ex vivo by means of histologic analysis and hydroxyproline assay. The Wilcoxon rank sum or signed rank test was used for statistical comparisons between or within groups, and Pearson and Spearman rank correlation was used to compare fibrosis measured in vivo and ex vivo. Results: In the stenotic kidney, the median magnetization transfer ratio showed progressive increases from baseline to 6 weeks after surgery (increases of 13.7% [P = .0006] and 21.3% [P = .0005] in cortex and medulla, respectively), which were accompanied by a progressive loss in renal volume, perfusion, blood flow, and oxygenation. The 6-week magnetization transfer ratio map showed good correlation with fibrosis measured ex vivo (Pearson r = 0.9038 and Spearman ρ = 0.8107 [P = .0002 vs trichrome staining]; r = 0.9540 and r = 0.8821 [P < .0001 vs Sirius red staining]; and r = 0.8429 and r = 0.7607 [P = .001 vs hydroxyproline assay]). Conclusion: Magnetization transfer imaging was used successfully to measure and longitudinally monitor the progression of renal fibrosis in mice with unilateral renal artery stenosis.
AB - Purpose: To test the utility of magnetization transfer imaging in detecting and monitoring the progression of renal fibrosis in mice with unilateral renal artery stenosis. Materials and Methods: This prospective study was approved by the Institutional Animal Care and Use Committee. Renal artery stenosis surgery (n = 10) or sham surgery (n = 5) was performed, and the stenotic and contralateral kidneys were studied longitudinally in vivo at baseline and 2, 4, and 6 weeks after surgery. After a 16.4-T magnetic resonance imaging examination, magnetization transfer ratio was measured as an index of fibrosis (guided by parameters selected in preliminary phantom studies). In addition, renal volume, perfusion, blood flow, and oxygenation were assessed. Fibrosis was subsequently measured ex vivo by means of histologic analysis and hydroxyproline assay. The Wilcoxon rank sum or signed rank test was used for statistical comparisons between or within groups, and Pearson and Spearman rank correlation was used to compare fibrosis measured in vivo and ex vivo. Results: In the stenotic kidney, the median magnetization transfer ratio showed progressive increases from baseline to 6 weeks after surgery (increases of 13.7% [P = .0006] and 21.3% [P = .0005] in cortex and medulla, respectively), which were accompanied by a progressive loss in renal volume, perfusion, blood flow, and oxygenation. The 6-week magnetization transfer ratio map showed good correlation with fibrosis measured ex vivo (Pearson r = 0.9038 and Spearman ρ = 0.8107 [P = .0002 vs trichrome staining]; r = 0.9540 and r = 0.8821 [P < .0001 vs Sirius red staining]; and r = 0.8429 and r = 0.7607 [P = .001 vs hydroxyproline assay]). Conclusion: Magnetization transfer imaging was used successfully to measure and longitudinally monitor the progression of renal fibrosis in mice with unilateral renal artery stenosis.
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U2 - 10.1148/radiol.2016160566
DO - 10.1148/radiol.2016160566
M3 - Article
C2 - 27697008
AN - SCOPUS:85017157876
SN - 0033-8419
VL - 283
SP - 77
EP - 86
JO - Radiology
JF - Radiology
IS - 1
ER -