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Abstract #4462

Diagnosis of Fibrosis with Magnetization-Prepared Golden-angle RAdial Sparse Parallel (MP-GRASP) T1Mapping in Renal Allografts

Octavia Bane1,2, Li Feng3, Ding Xia1, Mira Liu1, Ian Bolger1, Sergio Calle1, Jonathan Dyke4, Madhav Menon5, Surya Seshan6, Steven Salvatore6, Isaac Stillman7, Thangamani Muthukumar8, Samira Farouk9, Bachir Taouli1,10, and Sara Lewis1
1Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States, 2BioMedical Engineering and Imaging Institute, Mount Sinai Hospital, New York, NY, United States, 3Radiology, New York University Grossman School of Medicine, New York, NY, United States, 4Weill Cornell Medicine, New York, NY, United States, 5Nephrology, Yale School of Medicine, New Haven, CT, United States, 6Pathology, Weill Cornell Medicine, New York, NY, United States, 7Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, United States, 8Nephrology and Kidney Transplantation Medicine, Weill Cornell Medicine, New York, NY, United States, 9Transplant Nephrology, Icahn School of Medicine at Mount Sinai, New York, NY, United States, 10BioMedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States

Synopsis

Keywords: Relaxometry, Acquisition Methods, renal transplant, fibrosis, preserved renal transplat function, T1, radial T1

Motivation: Inversion recovery T1 mapping methods with radial read-out can provide more reliable rapid renal T1 mapping compared to variable flip angle methods.

Goal(s): To compare T1 measurements and diagnostic performance for identification of renal fibrosis with novel 2D and 3D inversion-recovery radial acquisitions against variable flip angle acquisitions in patients with renal transplant.

Approach: 2D/3D GraspT1, and variable flip angle T1 maps were prospectively acquired in 61 renal transplant recipients and correlated with renal function and biopsy-proven renal allograft fibrosis.

Results: Medulla T1 measured with 2DGraspT1 identified patients with fibrotic, but functional allografts with very good diagnostic performance.

Impact: Renal T1 showed diagnostic sensitivity to the presence of renal allograft fibrosis, even in patients with preserved renal function, and thus can potentially be useful to select patients for biopsy or other interventions before serum eGFR decline.

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Keywords