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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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