Two for One—Combined Morphologic and Quantitative Knee Joint MRI Using a Versatile Turbo Spin-Echo Platform

Author:

Lemainque Teresa1ORCID,Pridöhl Nicola1,Huppertz Marc1,Post Manuel1ORCID,Yüksel Can1ORCID,Siepmann Robert1,Radke Karl Ludger2ORCID,Zhang Shuo34ORCID,Yoneyama Masami5ORCID,Prescher Andreas6,Kuhl Christiane1,Truhn Daniel1ORCID,Nebelung Sven1ORCID

Affiliation:

1. Department of Diagnostic and Interventional Radiology, Medical Faculty, RWTH Aachen University, 52074 Aachen, Germany

2. Department of Diagnostic and Interventional Radiology, University Hospital Düsseldorf, University Dusseldorf, 40225 Düsseldorf, Germany

3. Philips GmbH Market DACH, 22335 Hamburg, Germany

4. Philips Healthcare, 5684 PZ Best, The Netherlands

5. Philips Japan, Tokyo 108-8507, Japan

6. Institute of Molecular and Cellular Anatomy, Medical Faculty, RWTH Aachen University, 52074 Aachen, Germany

Abstract

Quantitative MRI techniques such as T2 and T1ρ mapping are beneficial in evaluating knee joint pathologies; however, long acquisition times limit their clinical adoption. MIXTURE (Multi-Interleaved X-prepared Turbo Spin-Echo with IntUitive RElaxometry) provides a versatile turbo spin-echo (TSE) platform for simultaneous morphologic and quantitative joint imaging. Two MIXTURE sequences were designed along clinical requirements: “MIX1”, combining proton density (PD)-weighted fat-saturated (FS) images and T2 mapping (acquisition time: 4:59 min), and “MIX2”, combining T1-weighted images and T1ρ mapping (6:38 min). MIXTURE sequences and their reference 2D and 3D TSE counterparts were acquired from ten human cadaveric knee joints at 3.0 T. Contrast, contrast-to-noise ratios, and coefficients of variation were comparatively evaluated using parametric tests. Clinical radiologists (n = 3) assessed diagnostic quality as a function of sequence and anatomic structure using five-point Likert scales and ordinal regression, with a significance level of α = 0.01. MIX1 and MIX2 had at least equal diagnostic quality compared to reference sequences of the same image weighting. Contrast, contrast-to-noise ratios, and coefficients of variation were largely similar for the PD-weighted FS and T1-weighted images. In clinically feasible scan times, MIXTURE sequences yield morphologic, TSE-based images of diagnostic quality and quantitative parameter maps with additional insights on soft tissue composition and ultrastructure.

Funder

Faculty of Medicine of the RWTH Aachen University

European Union’s Horizon Europe programme

Deutsche Forschungsgemeinschaft

German Federal Ministry of Education and Research

Publisher

MDPI AG

Reference32 articles.

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