MRI of the central nervous system in MS patients with and without pain

Abstract Background Central pain (CP) is a common symptom in MS. Multiple theories are present about the mechanism of CP. Previous studies suggested that lesion of the spinothalamic tract is a necessary condition for development of CP. No previous study has in detail evaluated the association betwee...

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Veröffentlicht in:European journal of pain 2011-04, Vol.15 (4), p.395-401
Hauptverfasser: Svendsen, Kristina Bacher, Sørensen, Leif, Jensen, Troels Stahelin, Hansen, Hans Jacob, Bach, Flemming Winther
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Sprache:eng
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Zusammenfassung:Abstract Background Central pain (CP) is a common symptom in MS. Multiple theories are present about the mechanism of CP. Previous studies suggested that lesion of the spinothalamic tract is a necessary condition for development of CP. No previous study has in detail evaluated the association between the specific site of demyelinations and the presence of CP in MS. Objective The study aimed to evaluate the location of plaques in MS patients with CP including a group of MS patients without pain as a reference group. Methods All patients underwent a bedside sensory examination and MRI of the brain and spinal cord. MR imaging was acquired on an 1.5 Tesla MR equipment. A trained neuroradiologist, blinded to pain status, evaluated the MRI. Results Thirteen MS patients with CP and 10 MS patients without pain were included. Allodynia and/or dysesthesia were more frequent in pain patients (11/13 vs. 1/10, P < 0.01). No difference was found in the number of patients with plaques in spinothalamic tract, dorsal column-medial lemniscus, dorsolateral funiculus, grey substance, thalamus or capsula interna. A non-significantly lower number of pain patients had lesions in thalamo-cortical pathways (8/13 vs. 10/10, P = 0.027). Conclusions No association between CP and site of demyelinations was found, although a trend toward a higher prevalence of intact thalamo-cortical pathways was seen in pain patients. CP was associated with allodynia, suggesting central hyperexcitability.
ISSN:1090-3801
1532-2149
DOI:10.1016/j.ejpain.2010.09.006