| Literature DB >> 28974941 |
Elisabetta Groppo1, Francesca Baglio1, Davide Cattaneo1, Eleonora Tavazzi1, Niels Bergsland1,2, Sonia Di Tella1, Riccardo Parelli1, Ilaria Carpinella1, Cristina Grosso1, Ruggero Capra3, Marco Rovaris1.
Abstract
A 48-year-old woman with multiple sclerosis (MS), treated with natalizumab for more than one year without clinical and magnetic resonance imaging (MRI) signs of disease activity, was diagnosed with definite progressive multifocal leukoencephalopathy (PML). She presented with subacute motor deficit of the right upper limb (UL), followed by involvement of the homolateral leg and urinary urgency. The patient was treated with steroids and plasma exchange. On follow-up MRI scans, the PML lesion remained stable and no MS rebounds were observed, but the patient complained of a progressive worsening of the right UL motor impairment, becoming dependent in most activities of daily living. A cycle of multidisciplinary rehabilitation (MDR) was then started, including daily sessions of UL robot therapy and occupational therapy. Functional MRI (fMRI) was acquired before and at the end of the MDR cycle using a motor task which consisted of 2 runs: in one run the patient was asked to observe while the second one consisted of hand grasping movements. At the end of the rehabilitation period, both the velocity and the smoothness of arm trajectories during robot-based reaching movements were significantly improved. After MDR, compared with baseline, fMRI showed significantly increased functional activation within the sensory-motor network in the active, motor task, while no significant differences were found in the observational task. MDR in MS, including robot-assisted UL training, seems to be clinically efficacious and to have a significant impact on brain functional reorganization on a short-term, even in the presence of superimposed tissue damage provoked by PML.Entities:
Keywords: functional magnetic resonance imaging; multidisciplinary rehabilitation; multiple sclerosis; neuroplasticity; progressive multifocal leukoencephalopathy
Year: 2017 PMID: 28974941 PMCID: PMC5610687 DOI: 10.3389/fneur.2017.00491
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003
Figure 1FLAIR weighted image showing multiple sclerosis lesions distributed mainly periventricularly and a hyperintense lesion in the fronto-parietal region that extends to the cortex, suggestive of progressive multifocal leukoencephalopathy.
Patient performance on clinical and functional scales before and after MDR treatment.
| Before MDR | After MDR | ||
|---|---|---|---|
| EDSS | 5.5 | 4.5 | |
| Barthel Index | 81/100 | 89/100 | |
| Right UL MAS | Range: 0–4 | ||
| Biceps | 2 | 1 | |
| Triceps | 2 | 2 | |
| Wrist extensors | 2 | 2 | |
| Wrist flexors | 3 | 2 | |
| Fingers flexors | 3 | 2 | |
| ARAT (item 19, “hand to mouth”), s | 3.32 | 3.35 | |
| COPM-P | Range: 1–10 | 2.4 | 5.8 |
| COPM-S | Range: 1–10 | 3.8 | 8.0 |
EDSS, Expanded Disability Status Scale; MAS, Modified Ashworth Scale; ARAT, Action Research Arm Test; COPM-P, Canadian Occupational Performance Measure-Performance; COPM-S, Canadian Occupational Performance Measure-Satisfaction
Figure 2Robot output and functional MRI activation in pre (red) and post (blue) rehabilitation period. (A,B) on the left (red squared), the reaching trajectories before the robot-assisted rehabilitation; on the right (blue squared), the same trajectories after a 3-week period of robot-therapy. (C,D) Maxima of regions showing significant activations during the Observational task (C) and motor task (D) in pre—red areas—and post—blue areas—conditions. Transverse slice view (on a 152 T1 xjview template) of significant positive activation (thresholded at P FWE corrected <0.05 with k > 50 voxels).
MNI coordinate and Z-scores of the areas activated both during different task conditions, before and after MDR (BA, Brodmann area; L, left hemisphere; R, right hemisphere).
| PRE vs POST MDR | POST vs PRE MDR | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Cluster size | Peak MNI coordinate | Side | Brain region | BA | Cluster size | Peak MNI coordinate | Side | Brain region | BA | |||||||
| Run 1: movement vs rest | 208 | −8 | −90 | 8 | L | Calcarine/cuneus | 18/17 | 8.01 | 24,951 | 24 | −78 | 32 | R | Superior/middle occipital gyrus | 18/19 | 11.81 |
| −2 | −102 | 2 | L | Calcarine/cuneus | 5.70 | 44 | −62 | 18 | R | Middle temporal gyrus | 39 | 11.63 | ||||
| 620 | 32 | −88 | 0 | R | Middle occipital gyrus | 18 | 10.27 | 54 | −58 | 30 | R | Supramarginal gyrus/inferior parietal lobule | 40 | 11.00 | ||
| 34 | −64 | 0 | R | Middle occipital gyrus | 8.83 | 46 | −48 | 50 | R | Postcentral gyrus | 10.09 | |||||
| 34 | −76 | 0 | R | Inferior/middle occipital gyrus | 18/19 | 8.20 | 24 | −14 | 46 | R | Precentral gyrus | 6 | 9.24 | |||
| 211 | 34 | 6 | −36 | R | Middle temporal gyrus/temporal pole | 21/38 | 7.91 | |||||||||
| 1,333 | 16 | 52 | −4 | R | Medial frontal gyrus | 10 | 5.93 | |||||||||
| 12 | 36 | 32 | R | Anterior cingulate | 32 | 5.90 | ||||||||||
| 463 | −34 | 24 | 6 | L | Inferior frontal gyrus | 45 | 5.72 | |||||||||
| −24 | 12 | 0 | L | Putamen | 6.14 | |||||||||||
| 489 | −26 | −80 | −38 | L | Cerebellum posterior lobe | 6.69 | ||||||||||
| 309 | −42 | −60 | −46 | L | Cerebellum posterior lobe | 7.05 | ||||||||||
| 363 | 50 | −78 | −34 | R | Cerebellum posterior lobe | 7.72 | ||||||||||
| Run 2: observation vs rest | No suprathreshold clusters | No suprathreshold clusters | ||||||||||||||
Only regions that survived after FWE correction for multiple comparisons (.