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Abstract #3211

Biophysical models on multi-parametric maps reveal brain tissue changes in molecular environments of iron and myelin in multiple sclerosis at 3T

Henri Trang1, Qianlan Chen1, Shir Filo2, Darius Mewes1,3,4, Claudia Chien1,3,5, Stefan Hetzer6, Lina Anderhalten1, Tanja Schmitz-Hübsch1,3, Alexander U. Brandt1, Aviv Mezer2, and Friedemann Paul1,3,7
1Experimental and Clinical Research Center, Max Delbrück Center for Molecular Medicine and Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany, 2The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel, 3Neuroscience Clinical Research Center, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany, 4Berlin Institute of Health at Charité – Universitätsmedizin Berlin, Biomedical Innovation Academy, Berlin, Germany, 5Department of Psychiatry and Neurosciences, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany, 6Berlin Center for Advanced Neuroimaging, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany, 7Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

Synopsis

Keywords: Biomarkers, Quantitative Imaging, brain, quantitative MRI, biophysical model

Motivation: Quantitative MRI is attractive for investigating pathological tissue changes, yet translation towards clinical research remains challenging.

Goal(s): Our goal was to explore sensitivity of a fast quantitative multi-parametric mapping protocol combined with biophysical models at 3T to multiple sclerosis subtypes.

Approach: We combined quantitative maps of magnetization transfer saturation, proton density, longitudinal and transverse relaxation rates with relaxivity approaches to disentangle water and macromolecular tissue driven changes and to identify MRI biomarkers of focal and diffuse demyelination or inflammation.

Results: We found significant alterations in white matter and lesions of surrogates for myelin and iron compared to controls and worsening with disease severity.

Impact: A fast quantitative multi-parameter mapping protocol combined with biophysical models based on in vivo relaxivity approaches in multiple sclerosis at 3T is sensitive to brain tissue alterations in patients, suggesting disease-specific demyelination and inflammation. An association with disability suggests disease-relevance.

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