Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T

被引:0
|
作者
Lawless, Richard D. [1 ,2 ]
McNnight, Colin D. [3 ]
O'Grady, Kristin P. [1 ,2 ,3 ]
Combes, Anna J. E. [1 ]
Rogers, Baxter P. [1 ,3 ]
Witt, Atlee A. [1 ]
Visagie, Mereze [1 ]
Houston, Delaney C. [1 ]
Prock, Logan E. [1 ]
Bagnato, Francesca R. [4 ,5 ]
Smith, Seth A. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Inst Imaging Sci, Med Ctr, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Dept Radiol & Radiol Sci, Med Ctr, 1211 Medi Ctr Dr, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Neurol, Div Neuroimmunol, Med Ctr, Nashville, TN 37232 USA
[5] TN Valley Healthcare Syst, VA Hosp, Dept Neurol, Nashville, TN USA
关键词
Multiple sclerosis; cerebrospinal fluid; magnetic resonance imaging; spinal cord; magnetization transfer ratio; MAGNETIZATION-TRANSFER RATIO; CEREBROSPINAL-FLUID; RELAXATION; CONTRAST; TISSUE;
D O I
10.1177/20552173231211396
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundImaging investigation of cerebrospinal fluid (CSF) in multiple sclerosis (MS) is understudied. Development of noninvasive methods to detect pathological CSF changes would have a profound effect on MS diagnosis and would offer insight into MS pathophysiology and mechanisms of neurological impairment.ObjectiveWe propose magnetization transfer (MT) MRI as a tool to detect macromolecular changes in spinal CSF.MethodsMT and quantitative MT (qMT) data were acquired in the cervical region in 27 people with relapsing-remitting multiple sclerosis (pwRRMS) and 38 age and sex-matched healthy controls (HCs). MT ratio (MTR), the B1, B0, and R1 corrected qMT-derived pool size ratio (PSR) were quantified in the spinal cord and CSF of each group.ResultsBoth CSF MTR and CSF qMT-derived PSR were significantly increased in pwRRMS compared to HC (p = 0.027 and p = 0.020, respectively). CSF PSR of pwRRMS was correlated to Expanded Disability Status Scale Scores (p = 0.045, R = 0.352).ConclusionOur findings demonstrate increased CSF macromolecular content in pwRRMS and link CSF macromolecular content with clinical impairment. This highlights the potential role of CSF in processing products of demyelination.
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