The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration
Intervertebral disc degeneration (IVDD) is an important risk factor of low back pain. We previously found upregulated markers of fibrosis, the late stage of chronic inflammation, in degenerated IVD with a small number of clinical specimens. Here, we aimed to study on a larger scale the association o...
Saved in:
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2021-01-01
|
Series: | Mediators of Inflammation |
Online Access: | http://dx.doi.org/10.1155/2021/2933199 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832567682727149568 |
---|---|
author | Chang Liu Guoyan Liang Zhantao Deng Jing Tan Qiujian Zheng Feng-Juan Lyu |
author_facet | Chang Liu Guoyan Liang Zhantao Deng Jing Tan Qiujian Zheng Feng-Juan Lyu |
author_sort | Chang Liu |
collection | DOAJ |
description | Intervertebral disc degeneration (IVDD) is an important risk factor of low back pain. We previously found upregulated markers of fibrosis, the late stage of chronic inflammation, in degenerated IVD with a small number of clinical specimens. Here, we aimed to study on a larger scale the association of cyclooxygenase 2 (COX2), an inflammation and/or pain marker, with IVDD. This study involved 107 LBP participants. The IVD degeneration level was graded on a 1–5 scale according to the Pfirrmann classification system. Discs at grades 1-3 were further grouped as white discs with grades 4-5 as black discs. We recorded baseline information about age, gender, body mass index (BMI), diabetes history, smoking history, and magnetic resonance imaging (MRI). Their association with IVDD was statistically analyzed. The expression level of COX2 was investigated by immunohistochemistry. The total integrated COX2 optical density (IOD), number of COX2-positive cells, and total cell number of each image were counted and analyzed by Image-Pro Plus software. The IOD and number of COX2-positive cells were divided by the total cell number to obtain COX2 expression density (IOD/cell) and COX2 positivity (cell+/cell). As a result, among the baseline information investigated, only age was found to have a significant association with IVDD. The IOD/cell was found to be significantly increased from grade 2 to grade 5, as well as in black discs compared to white discs. The cell+/cell displayed the same trend that it increased in highly degenerative discs compared to their counterparts. In conclusion, the expression of COX2 is associated with IVDD, which highlights COX2 as a biomarker for IVD degeneration and indicates the involvement of inflammation and pain signaling in IVDD. |
format | Article |
id | doaj-art-c158e5ce8b8048048dbfe685340df26b |
institution | Kabale University |
issn | 0962-9351 1466-1861 |
language | English |
publishDate | 2021-01-01 |
publisher | Wiley |
record_format | Article |
series | Mediators of Inflammation |
spelling | doaj-art-c158e5ce8b8048048dbfe685340df26b2025-02-03T01:00:47ZengWileyMediators of Inflammation0962-93511466-18612021-01-01202110.1155/2021/29331992933199The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc DegenerationChang Liu0Guoyan Liang1Zhantao Deng2Jing Tan3Qiujian Zheng4Feng-Juan Lyu5Joint Center of South China University of Technology-The University of Western Australia for Regenerative Medicine Research, School of Medicine, South China University of Technology, Guangzhou 510006, ChinaDepartment of Orthopedics, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, ChinaDepartment of Orthopedics, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, ChinaJoint Center of South China University of Technology-The University of Western Australia for Regenerative Medicine Research, School of Medicine, South China University of Technology, Guangzhou 510006, ChinaDepartment of Orthopedics, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, ChinaJoint Center of South China University of Technology-The University of Western Australia for Regenerative Medicine Research, School of Medicine, South China University of Technology, Guangzhou 510006, ChinaIntervertebral disc degeneration (IVDD) is an important risk factor of low back pain. We previously found upregulated markers of fibrosis, the late stage of chronic inflammation, in degenerated IVD with a small number of clinical specimens. Here, we aimed to study on a larger scale the association of cyclooxygenase 2 (COX2), an inflammation and/or pain marker, with IVDD. This study involved 107 LBP participants. The IVD degeneration level was graded on a 1–5 scale according to the Pfirrmann classification system. Discs at grades 1-3 were further grouped as white discs with grades 4-5 as black discs. We recorded baseline information about age, gender, body mass index (BMI), diabetes history, smoking history, and magnetic resonance imaging (MRI). Their association with IVDD was statistically analyzed. The expression level of COX2 was investigated by immunohistochemistry. The total integrated COX2 optical density (IOD), number of COX2-positive cells, and total cell number of each image were counted and analyzed by Image-Pro Plus software. The IOD and number of COX2-positive cells were divided by the total cell number to obtain COX2 expression density (IOD/cell) and COX2 positivity (cell+/cell). As a result, among the baseline information investigated, only age was found to have a significant association with IVDD. The IOD/cell was found to be significantly increased from grade 2 to grade 5, as well as in black discs compared to white discs. The cell+/cell displayed the same trend that it increased in highly degenerative discs compared to their counterparts. In conclusion, the expression of COX2 is associated with IVDD, which highlights COX2 as a biomarker for IVD degeneration and indicates the involvement of inflammation and pain signaling in IVDD.http://dx.doi.org/10.1155/2021/2933199 |
spellingShingle | Chang Liu Guoyan Liang Zhantao Deng Jing Tan Qiujian Zheng Feng-Juan Lyu The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration Mediators of Inflammation |
title | The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration |
title_full | The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration |
title_fullStr | The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration |
title_full_unstemmed | The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration |
title_short | The Upregulation of COX2 in Human Degenerated Nucleus Pulposus: The Association of Inflammation with Intervertebral Disc Degeneration |
title_sort | upregulation of cox2 in human degenerated nucleus pulposus the association of inflammation with intervertebral disc degeneration |
url | http://dx.doi.org/10.1155/2021/2933199 |
work_keys_str_mv | AT changliu theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT guoyanliang theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT zhantaodeng theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT jingtan theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT qiujianzheng theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT fengjuanlyu theupregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT changliu upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT guoyanliang upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT zhantaodeng upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT jingtan upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT qiujianzheng upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration AT fengjuanlyu upregulationofcox2inhumandegeneratednucleuspulposustheassociationofinflammationwithintervertebraldiscdegeneration |