TY - JOUR
T1 - MRI of the intraspinal nerve roots in patients with chronic inflammatory neuropathies
T2 - abnormalities correlate with clinical phenotypes
AU - van Rosmalen, Marieke H.J.
AU - Froeling, Martijn
AU - Mandija, Stefano
AU - Hendrikse, Jeroen
AU - van der Pol, W. Ludo
AU - Stephan Goedee, H.
N1 - Funding Information:
This work was supported by the Prinses Beatrix Spierfonds (W.OR17-21).
Funding Information:
M.H.J. van Rosmalen, S. Mandija and M. Froeling declare that they have no conflicts of interest. H.S. Goedee has received support from the Prinses Beatrix Spierfonds and a travel grant from Shire. W.L. van der Pol has received support from the Prinses Beatrix Spierfonds, Vriendenloterij and Stichting Spieren voor Spieren. J. Hendrikse has received research support from the Netherlands Organization for Scientific Research (NWO) under grant no. 91712322 and the European Research Council under grant agreements no. 637024.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.
PY - 2022/6
Y1 - 2022/6
N2 - Objective: Chronic inflammatory demyelinating polyneuropathy (CIDP) and multifocal motor neuropathy (MMN) are caused by inflammatory changes of peripheral nerves. It is unknown if the intra-spinal roots are also affected. This MRI study systematically visualized intra-spinal nerve roots, i.e., the ventral and dorsal roots, in patients with CIDP, MMN and motor neuron disease (MND). Methods: We performed a cross-sectional study in 40 patients with CIDP, 27 with MMN and 34 with MND. All patients underwent an MRI scan of the cervical intra-spinal roots. We systematically measured intra-spinal nerve root sizes bilaterally in the transversal plane at C5, C6 and C7 level. We calculated mean nerve root sizes and compared them between study groups and between different clinical phenotypes using a univariate general linear model. Results: Patients with MMN and CIDP with a motor phenotype had thicker ventral roots compared to patients with CIDP with a sensorimotor phenotype (p = 0.012), while patients with CIDP with a sensory phenotype had thicker dorsal roots compared to patients with a sensorimotor phenotype (p = 0.001) and with MND (p = 0.004). Conclusion: We here show changes in the morphology of intra-spinal nerve roots in patients with chronic inflammatory neuropathies, compatible with their clinical phenotype.
AB - Objective: Chronic inflammatory demyelinating polyneuropathy (CIDP) and multifocal motor neuropathy (MMN) are caused by inflammatory changes of peripheral nerves. It is unknown if the intra-spinal roots are also affected. This MRI study systematically visualized intra-spinal nerve roots, i.e., the ventral and dorsal roots, in patients with CIDP, MMN and motor neuron disease (MND). Methods: We performed a cross-sectional study in 40 patients with CIDP, 27 with MMN and 34 with MND. All patients underwent an MRI scan of the cervical intra-spinal roots. We systematically measured intra-spinal nerve root sizes bilaterally in the transversal plane at C5, C6 and C7 level. We calculated mean nerve root sizes and compared them between study groups and between different clinical phenotypes using a univariate general linear model. Results: Patients with MMN and CIDP with a motor phenotype had thicker ventral roots compared to patients with CIDP with a sensorimotor phenotype (p = 0.012), while patients with CIDP with a sensory phenotype had thicker dorsal roots compared to patients with a sensorimotor phenotype (p = 0.001) and with MND (p = 0.004). Conclusion: We here show changes in the morphology of intra-spinal nerve roots in patients with chronic inflammatory neuropathies, compatible with their clinical phenotype.
KW - Chronic inflammatory demyelinating polyneuropathy
KW - Intra-spinal nerve roots
KW - Intradural nerve roots
KW - Motor neuron disease
KW - MRI
KW - Multifocal motor neuropathy
UR - http://www.scopus.com/inward/record.url?scp=85122319481&partnerID=8YFLogxK
U2 - 10.1007/s00415-021-10864-4
DO - 10.1007/s00415-021-10864-4
M3 - Article
AN - SCOPUS:85122319481
SN - 0340-5354
VL - 269
SP - 3159
EP - 3166
JO - Journal of Neurology
JF - Journal of Neurology
IS - 6
ER -