File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1109/NER.2009.5109266
- Scopus: eid_2-s2.0-70350215741
Supplementary
-
Citations:
- Scopus: 0
- Appears in Collections:
Conference Paper: A rodent model of chronic compressive cervical myelopathy
Title | A rodent model of chronic compressive cervical myelopathy |
---|---|
Authors | |
Keywords | Cervical myelopathy Magnetic Resonance Imaging Rat Somatosensory-evoked potential Spinal cord compression |
Issue Date | 2009 |
Citation | The 4th International IEEE/EMBS Conference on Neural Engineering (NER '09), Antalya, Turkey, 29 April-2 May 2009. In Conference Proceedings, 2009, p. 191-194 How to Cite? |
Abstract | Degenerative chronic spinal cord compression induced cervical myelopathy is a common cause of spinal cord dysfunction. The disease generally leads to impairment of the sensory and motor function of the cord progressively and insidiously. However, the underlying pathophysiology and the precise mechanism of the disease are still uncertain and remain to be investigated. The establishment of an animal model which reproduces the clinical condition of cervical myelopathy would be helpful for better understanding to the disease. In this study, a rat model of chronic spinal cord compression was developed by implantation of water-absorbing polymer at the lateral side of the spinal canal. The structural and functional change of the spinal cord due to compression were then assessed with different techniques - Magnetic Resonance Imaging (MRI) for the structural assessment, and motor behavioral scoring and somatosensory-evoked potential (SSEP) for the functional evaluation. From the MR images the 1/4-lateral compression ratios are computed. The result shows that the compression is significant by compared with the compression ratios of the adjacent levels (p < 0.01). However, the severe changes of SSEP did not show a close correlation with the compression ratios, suggesting that MRI findings are not automatically associated with functional deficits in spinal cord. Further classification of animal based on SSEP response shows that latency delay was more severe with higher categories. It is suggested that changes in latency might be a prognosis for the surgical outcome, which animals in higher categories may have higher chance to have permanent loss of spinal cord function. ©2009 IEEE. |
Persistent Identifier | http://hdl.handle.net/10722/158599 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, DTH | en_HK |
dc.contributor.author | Hu, Y | en_HK |
dc.contributor.author | Wu, EX | en_HK |
dc.contributor.author | Luk, KDK | en_HK |
dc.date.accessioned | 2012-08-08T09:00:24Z | - |
dc.date.available | 2012-08-08T09:00:24Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | The 4th International IEEE/EMBS Conference on Neural Engineering (NER '09), Antalya, Turkey, 29 April-2 May 2009. In Conference Proceedings, 2009, p. 191-194 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/158599 | - |
dc.description.abstract | Degenerative chronic spinal cord compression induced cervical myelopathy is a common cause of spinal cord dysfunction. The disease generally leads to impairment of the sensory and motor function of the cord progressively and insidiously. However, the underlying pathophysiology and the precise mechanism of the disease are still uncertain and remain to be investigated. The establishment of an animal model which reproduces the clinical condition of cervical myelopathy would be helpful for better understanding to the disease. In this study, a rat model of chronic spinal cord compression was developed by implantation of water-absorbing polymer at the lateral side of the spinal canal. The structural and functional change of the spinal cord due to compression were then assessed with different techniques - Magnetic Resonance Imaging (MRI) for the structural assessment, and motor behavioral scoring and somatosensory-evoked potential (SSEP) for the functional evaluation. From the MR images the 1/4-lateral compression ratios are computed. The result shows that the compression is significant by compared with the compression ratios of the adjacent levels (p < 0.01). However, the severe changes of SSEP did not show a close correlation with the compression ratios, suggesting that MRI findings are not automatically associated with functional deficits in spinal cord. Further classification of animal based on SSEP response shows that latency delay was more severe with higher categories. It is suggested that changes in latency might be a prognosis for the surgical outcome, which animals in higher categories may have higher chance to have permanent loss of spinal cord function. ©2009 IEEE. | en_HK |
dc.language | eng | en_US |
dc.relation.ispartof | Proceedings of the 4th International IEEE/EMBS Conference on Neural Engineering, NER '09 | en_HK |
dc.subject | Cervical myelopathy | en_HK |
dc.subject | Magnetic Resonance Imaging | en_HK |
dc.subject | Rat | en_HK |
dc.subject | Somatosensory-evoked potential | en_HK |
dc.subject | Spinal cord compression | en_HK |
dc.title | A rodent model of chronic compressive cervical myelopathy | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Hu, Y:yhud@hku.hk | en_HK |
dc.identifier.email | Wu, EX:ewu1@hkucc.hku.hk | en_HK |
dc.identifier.email | Luk, KDK:hcm21000@hku.hk | en_HK |
dc.identifier.authority | Hu, Y=rp00432 | en_HK |
dc.identifier.authority | Wu, EX=rp00193 | en_HK |
dc.identifier.authority | Luk, KDK=rp00333 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1109/NER.2009.5109266 | en_HK |
dc.identifier.scopus | eid_2-s2.0-70350215741 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70350215741&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.spage | 191 | en_HK |
dc.identifier.epage | 194 | en_HK |
dc.identifier.scopusauthorid | Li, DTH=35746374500 | en_HK |
dc.identifier.scopusauthorid | Hu, Y=7407116091 | en_HK |
dc.identifier.scopusauthorid | Wu, EX=7202128034 | en_HK |
dc.identifier.scopusauthorid | Luk, KDK=7201921573 | en_HK |
dc.customcontrol.immutable | sml 170512 amended | - |