Multiparametric Renal Magnetic Resonance Imaging for Prediction and Annual Monitoring of the Progression of Chronic Kidney Disease over Two Years

被引:0
|
作者
Buchanan, Charlotte E. [1 ]
Mahmoud, Huda [2 ,3 ]
Cox, Eleanor F. [1 ,4 ,5 ]
Prestwich, Benjamin L. [1 ]
Noble, Rebecca A. [2 ]
Selby, Nicholas M. [2 ]
Taal, Maarten W. [2 ]
Francis, Susan T. [1 ,4 ,5 ]
机构
[1] Univ Nottingham, Sir Peter Mansfield Imaging Ctr, Sch Phys & Astron, Nottingham NG7 2RD, England
[2] Univ Nottingham, Ctr Kidney Res & Innovat, Royal Derby Hosp Campus, Derby DE2 3DT, England
[3] Manor Hosp, Walsall Healthcare NHS Trust, Moat Rd, Walsall WS2 9PS, England
[4] Nottingham Univ Hosp NHS Trust, NIHR Nottingham Biomed Res Ctr, Nottingham NG7 2QW, England
[5] Univ Nottingham, Nottingham NG7 2QW, England
基金
英国医学研究理事会;
关键词
chronic kidney disease; magnetic resonance imaging; multiparametric; progression; monitoring; INTRARENAL OXYGENATION; GFR DECLINE; END-POINT; FIBROSIS; PATHOLOGY; EQUATION; CKD;
D O I
10.3390/jcm12237282
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Multiparametric renal Magnetic Resonance Imaging (MRI) provides a non-invasive method to assess kidney structure and function, but longitudinal studies are limited. Methods: A total of 22 patients with CKD category G3-4 (estimated glomerular filtration rate (eGFR) 15-59 mL/min/1.73 m(2)) were recruited. Annual 3T multiparametric renal MRI scans were performed, comprising total kidney volume (TKV), longitudinal relaxation time (T-1), apparent diffusion coefficient (ADC), Arterial Spin Labelling, and Blood Oxygen Level Dependent relaxation time (T-2*), with 15 patients completing a Year 2 scan. CKD progression over 2 years was defined as eGFR_slope >= -5 mL/min/1.73 m(2)/year. Results: At baseline, T-1 was higher (cortex p = 0.05, medulla p = 0.03) and cortex perfusion lower (p = 0.015) in participants with subsequent progression versus stable eGFR. A significant decrease in TKV and ADC and an increase in cortex T-1 occurred in progressors at Year 1 and Year 2, with a significant decrease in perfusion in progressors only at Year 2. The only decline in the stable group was a reduction in TKV. There was no significant change in cortex or medulla T-2* at Year 1 or Year 2 for progressors or stable participants. Conclusion: Lower renal cortex perfusion and higher T-1 in the cortex and medulla may predict CKD progression, while renal cortex T-1, TKV, and ADC may be useful to monitor progression. This study provides pilot data for future large-scale studies.
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页数:13
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