Imaging Mechanisms of Disease Progression in Multiple Sclerosis: Beyond Brain Atrophy

被引:28
作者
Bagnato, Francesca [1 ]
Gauthier, Susan A. [2 ,3 ]
Laule, Cornelia [4 ,5 ]
Moore, George R. Wayne [5 ,6 ]
Bove, Riley [7 ]
Cai, Zhengxin [8 ]
Cohen-Adad, Julien [9 ]
Harrison, Daniel M. [10 ]
Klawiter, Eric C. [11 ]
Morrow, Sarah A. [12 ]
Oz, Gulin [13 ]
Rooney, William D. [14 ,15 ,16 ]
Smith, Seth A. [17 ,18 ,19 ]
Calabresi, Peter A. [20 ]
Henry, Roland G. [21 ,22 ,23 ,24 ,25 ]
Oh, Jiwon [20 ,26 ]
Ontaneda, Daniel [27 ]
Pelletier, Daniel [28 ]
Reich, Daniel S. [29 ]
Shinohara, Russell T. [30 ]
Sicotte, Nancy L. [31 ]
机构
[1] Vanderbilt Univ, Dept Neurol, Med Ctr, Neuroimaging Unit,Neuroimmunol Div, 2201 Childrens Way,Suite 1222, Nashville, TN 37212 USA
[2] Weill Cornell Med, Feil Family Brain & Mind Inst, Dept Neurol, Judith Jaffe Multiple Sclerosis Ctr, New York, NY USA
[3] Weill Cornell Med, Dept Radiol, New York, NY USA
[4] Univ British Columbia, Dept Phys & Astron, Dept Radiol Pathol & Lab Med, Vancouver, BC, Canada
[5] Univ British Columbia, Int Collaborat Repair Discoveries ICORD, Vancouver, BC, Canada
[6] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC, Canada
[7] Univ Calif San Francisco, Dept Neurol, Weill Inst Neurosci, San Francisco, CA USA
[8] Yale Univ, PET Ctr, Dept Radiol & Biomed Imaging, New Haven, CT USA
[9] Univ Montreal, CRIUGM, Polytech Montreal & Funct Neuroimaging Unit, NeuroPoly Lab,Inst Biomed Engn, Montreal, PQ, Canada
[10] Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA
[11] Harvard Med Sch, Massachusetts Gen Hosp, Boston, MA 02115 USA
[12] Univ Western Ontario, Dept Clin Neurol Sci, London, ON, Canada
[13] Univ Minnesota, Ctr Magnet Resonance Res, Minneapolis, MN USA
[14] Oregon Hlth & Sci Univ, Adv Imaging Res Ctr, Dept Biomed Engn, Portland, OR 97201 USA
[15] Oregon Hlth & Sci Univ, Adv Imaging Res Ctr, Dept Neurol, Portland, OR 97201 USA
[16] Oregon Hlth & Sci Univ, Adv Imaging Res Ctr, Dept Behav Neurosci, Portland, OR 97201 USA
[17] Vanderbilt Univ, Med Ctr, Radiol & Radiol Sci, Nashville, TN 37212 USA
[18] Vanderbilt Univ, Med Ctr, Imaging Inst, Nashville, TN 37212 USA
[19] Vanderbilt Univ, Biomed Engn, Nashville, TN 37212 USA
[20] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[21] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[22] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
[23] Univ Calif San Francisco, Dept Biomed Imaging, San Francisco, CA 94143 USA
[24] Univ Calif San Francisco, UC San Francisco, San Francisco, CA 94143 USA
[25] Univ Calif San Francisco, Berkeley Bioengn Grad Grp, San Francisco, CA 94143 USA
[26] Univ Toronto, St Michaels Hosp, Div Neurol, Toronto, ON, Canada
[27] Cleveland Clin, Neurol Inst, Mellen Ctr Multiple Sclerosis, Cleveland, OH 44106 USA
[28] Univ Southern Calif, Keck Sch Med, Dept Neurol, Los Angeles, CA 90007 USA
[29] NINDS, Translat Neuroradiol Sect, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA
[30] Univ Penn, Penn Stat Imaging & Visualizat Ctr, Dept Biostat Epidemiol & Informat, Philadelphia, PA 19104 USA
[31] Cedars Sinai Med Ctr, Dept Neurol, Los Angeles, CA 90048 USA
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Axons; chronic inflammation; magnetic resonance imaging; multiple sclerosis; neurodegeneration; CERVICAL-SPINAL CORD; APPEARING WHITE-MATTER; AMINOBUTYRIC-ACID CONCENTRATION; STATE FUNCTIONAL CONNECTIVITY; TEST-RETEST REPRODUCIBILITY; DIGIT MODALITIES TEST; VESICLE PROTEIN 2A; IN-VIVO; AXONAL LOSS; MR SPECTROSCOPY;
D O I
10.1111/jon.12700
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Clinicians involved with different aspects of the care of persons with multiple sclerosis (MS) and scientists with expertise on clinical and imaging techniques convened in Dallas, TX, USA on February 27, 2019 at a North American Imaging in Multiple Sclerosis Cooperative workshop meeting. The aim of the workshop was to discuss cardinal pathobiological mechanisms implicated in the progression of MS and novel imaging techniques, beyond brain atrophy, to unravel these pathologies. Indeed, although brain volume assessment demonstrates changes linked to disease progression, identifying the biological mechanisms leading up to that volume loss are key for understanding disease mechanisms. To this end, the workshop focused on the application of advanced magnetic resonance imaging (MRI) and positron emission tomography (PET) imaging techniques to assess and measure disease progression in both the brain and the spinal cord. Clinical translation of quantitative MRI was recognized as of vital importance, although the need to maintain a relatively short acquisition time mandated by most radiology departments remains the major obstacle toward this effort. Regarding PET, the panel agreed upon its utility to identify ongoing pathological processes. However, due to costs, required expertise, and the use of ionizing radiation, PET was not considered to be a viable option for ongoing care of persons with MS. Collaborative efforts fostering robust study designs and imaging technique standardization across scanners and centers are needed to unravel disease mechanisms leading to progression and discovering medications halting neurodegeneration and/or promoting repair.
引用
收藏
页码:251 / 266
页数:16
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