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dc.contributor.authorBuchanan, Charlotte E
dc.contributor.authorMahmoud, Huda
dc.contributor.authorCox, Eleanor F
dc.contributor.authorPrestwich, Benjamin L
dc.contributor.authorNoble, Rebecca A
dc.contributor.authorSelby, Nicholas M
dc.contributor.authorTaal, Maarten W
dc.contributor.authorFrancis, Susan T
dc.date.accessioned2023-12-12T16:23:56Z
dc.date.available2023-12-12T16:23:56Z
dc.date.issued2023-11-24
dc.identifier.citationBuchanan CE, Mahmoud H, Cox EF, Prestwich BL, Noble RA, Selby NM, Taal MW, Francis ST. Multiparametric Renal Magnetic Resonance Imaging for Prediction and Annual Monitoring of the Progression of Chronic Kidney Disease over Two Years. J Clin Med. 2023 Nov 24;12(23):7282.en_US
dc.identifier.issn2077-0383
dc.identifier.eissn2077-0383
dc.identifier.doi10.3390/jcm12237282
dc.identifier.pmid38068333
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3198
dc.description.abstractBackground: 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 m2) were recruited. Annual 3T multiparametric renal MRI scans were performed, comprising total kidney volume (TKV), longitudinal relaxation time (T1), apparent diffusion coefficient (ADC), Arterial Spin Labelling, and Blood Oxygen Level Dependent relaxation time (T2*), with 15 patients completing a Year 2 scan. CKD progression over 2 years was defined as eGFR_slope ≥ -5 mL/min/1.73 m2/year. Results: At baseline, T1 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 T1 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 T2* at Year 1 or Year 2 for progressors or stable participants. Conclusion: Lower renal cortex perfusion and higher T1 in the cortex and medulla may predict CKD progression, while renal cortex T1, TKV, and ADC may be useful to monitor progression. This study provides pilot data for future large-scale studies.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.subjectNephrology/Renal medicineen_US
dc.titleMultiparametric renal magnetic resonance imaging for prediction and annual monitoring of the progression of chronic kidney disease over two yearsen_US
dc.typeArticle
dc.source.journaltitleJournal of Clinical Medicine
rioxxterms.versionNAen_US
dc.contributor.trustauthorMahmoud, Huda
dc.contributor.departmentNephrologyen_US
dc.contributor.roleMedical and Dentalen_US
dc.contributor.affiliationUniversity of Nottingham; Walsall Healthcare NHS Trust; Nottingham University Hospitals NHS Trusten_US
oa.grant.openaccessnaen_US


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