Ferumoxytol-enhanced ultrashort TE MRA and quantitative morphometry of the human kidney vasculature.


Journal

Abdominal radiology (New York)
ISSN: 2366-0058
Titre abrégé: Abdom Radiol (NY)
Pays: United States
ID NLM: 101674571

Informations de publication

Date de publication:
07 2021
Historique:
received: 04 12 2020
accepted: 09 02 2021
revised: 28 01 2021
pubmed: 6 3 2021
medline: 25 6 2021
entrez: 5 3 2021
Statut: ppublish

Résumé

To evaluate the feasibility of Quantitative Ultrashort-Time-to-Echo Contrast-Enhanced (QUTE-CE) MRA using ferumoxytol as a contrast agent for abdominal angiography in the kidney. Four subjects underwent ferumoxytol-enhanced MRA with the 3D UTE Spiral VIBE WIP sequence at 3 T. Image quality metrics were quantified, specifically the blood Signal-to-Noise Ratio (SNR), blood-tissue Contrast-to-Noise Ratio (CNR) and Intraluminal Signal Heterogeneity (ISH) from both the aorta and inferior vena cava (IVC). Morphometric analysis of the vessels was performed using manual approach and semi-automatic approach using Vascular Modeling ToolKit (VMTK). Image quality and branching order were compared between QUTE-CE MRA and the Gadolinium (Gd) CEMRA reference image. QUTE-CE MRA provides a bright blood snapshot that delineates arteries and veins equally in the same scan. The maximum SNR and CNR values were 3,282 ± 1,218 and 1,295 ± 580, respectively - significantly higher than available literature values using other CEMRA techniques. QUTE-CE MRA had lower ISH and depicted higher vessel branching order (7th vs 3rd) within the kidney compared to a standard dynamic clinical Gd CEMRA scan. Morphometric analysis yielded quantitative results for the total kidney volume, total cyst volume and for diameters of the branching arterial network down to the 7 QUTE-CE MRA is feasible for kidney angiography, providing greater detail of kidney vasculature, enabling quantitative morphometric analysis of the abdominal and intra-renal vessels and yielding metrics relevant to vascular diseases while using a contrast agent ferumoxytol that is safe for CKD patients.

Identifiants

pubmed: 33666735
doi: 10.1007/s00261-021-02984-2
pii: 10.1007/s00261-021-02984-2
pmc: PMC8217117
mid: NIHMS1681651
doi:

Substances chimiques

Contrast Media 0
Gadolinium AU0V1LM3JT
Ferrosoferric Oxide XM0M87F357

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

3288-3300

Subventions

Organisme : NIDDK NIH HHS
ID : R21 DK118449
Pays : United States
Organisme : NIDA NIH HHS
ID : R41 DA043974
Pays : United States
Organisme : NIDA NIH HHS
ID : 1R41DA043974-01
Pays : United States

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Auteurs

Liam Timms (L)

Northeastern University, Boston, MA, USA.

Tianyi Zhou (T)

Northeastern University, Boston, MA, USA.

Yue Lyu (Y)

Northeastern University, Boston, MA, USA.

Ju Qiao (J)

Northeastern University, Boston, MA, USA.

Vishala Mishra (V)

Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.

Rita Maria Lahoud (RM)

Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.

Gayatri Veeramani Jayaraman (GV)

Department of Nephrology, Massachusetts General Hospital, Boston, MA, USA.
Department of Nephrology, Brigham and Women's Hospital, Boston, MA, USA.

Andrew S Allegretti (AS)

Department of Nephrology, Massachusetts General Hospital, Boston, MA, USA.

David Drew (D)

Tufts Medical Center, Boston, MA, USA.

Ravi T Seethamraju (RT)

Siemens Medical Solutions, Boston, MA, USA.

Mukesh Harisinghani (M)

Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.

Srinivas Sridhar (S)

Northeastern University, Boston, MA, USA. s.sridhar@northeastern.edu.
Theranano LLC, Newton, MA, USA. s.sridhar@northeastern.edu.
435 Egan Research Center, 120 Forsyth Street, Boston, MA, 02115, USA. s.sridhar@northeastern.edu.

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Classifications MeSH