Inflammatory biomarkers in sera of patients with intervertebral disc degeneration

被引:4
|
作者
Reis Rodrigues, Luciano Miller [1 ]
de Oliveira, Lilian Zerbinatti [2 ]
Ribeiro da Silva, Mariane de Barros [2 ]
Accardo, Camila de Melo [3 ]
Del Giglio, Adriana Braz [1 ]
da Silva Pinhal, Maria Aparecida [2 ]
机构
[1] Fac Med ABC, Santo Andre, SP, Brazil
[2] Univ Fed Sao Paulo, Sao Paulo, SP, Brazil
[3] Fac Americas, Sao Paulo, SP, Brazil
来源
EINSTEIN-SAO PAULO | 2019年 / 17卷 / 04期
关键词
Biomarkers; Proteoglycans; Glycosaminoglycans; Intervertebral disc degeneration; CATHEPSIN-B; HYALURONAN; CYTOKINES; PATHWAY;
D O I
10.31744/einstein_journal/2019AO4637
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate intervertebral disc levels of inflammatory factor (interleukin 6) and proteinase activity (cathepsin B) in patients with a degenerative disease and serum levels of interleukin 6, serum cathepsin B activity and hyaluronic acid biomarkers. Methods: We conducted immunohistochemistry studies of intervertebral discs to analyze interleukin 6 and cathepsin B levels of patients with degenerative disease and spine fracture (Control Group) and to measure hyaluronic acid, interleukin 6 and cathepsin B activity from sera of intervertebral disc degeneration patients, fracture patients, and healthy individuals. Results: Interleukin 6 and cathepsin B seem to be related with physiopathology of intervertebral disc degeneration, since the levels of both were higher in discs of patients with intervertebral disc degeneration. Interleukin 6 and cathepsin B do not represent good biomarkers of degenerative intervertebral disc disease, since the level of such compounds is increased in the plasma of patients with fractures. Conclusion: Hyaluronic acid can be a biomarker for intervertebral disc degeneration, because hyaluronic acid levels were higher only in sera of patients with intervertebral disc degeneration.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Models of Intervertebral Disc Degeneration
    Guclu, Bulent
    Naderi, Sait
    JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, 2011, 28 (03): : 417 - 426
  • [22] Imaging intervertebral disc degeneration
    Haughton, V
    JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A : 15 - 20
  • [23] Nanobacteria and intervertebral disc degeneration
    Eskandary, H
    Saba, M
    Yazdi, T
    MEDICAL HYPOTHESES, 2005, 65 (05) : 997 - 998
  • [24] Macrophages and Intervertebral Disc Degeneration
    Koroth, Jinsha
    Buko, Erick O.
    Abbott, Rebecca
    Johnson, Casey P.
    Ogle, Brenda M.
    Stone, Laura S.
    Ellingson, Arin M.
    Bradley, Elizabeth W.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (02)
  • [25] Genetics of Intervertebral Disc Degeneration
    David C. Ou-Yang
    Christopher J. Kleck
    Cheryl L. Ackert-Bicknell
    Current Osteoporosis Reports, 2023, 21 : 56 - 64
  • [26] Intervertebral disc degeneration and inflammatory microenvironment: expression, pathology, and therapeutic strategies
    Chen, Xin
    Wang, Zihan
    Deng, Rongrong
    Yan, Hongjie
    Liu, Xin
    Kang, Ran
    INFLAMMATION RESEARCH, 2023, 72 (09) : 1811 - 1828
  • [27] Intervertebral disc degeneration and inflammatory microenvironment: expression, pathology, and therapeutic strategies
    Xin Chen
    Zihan Wang
    Rongrong Deng
    Hongjie Yan
    Xin Liu
    Ran Kang
    Inflammation Research, 2023, 72 : 1811 - 1828
  • [28] Mechanobiology of the intervertebral disc and relevance to disc degeneration
    Setton, LA
    Chen, J
    JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A : 52 - 57
  • [29] The Immune Privilege of the Intervertebral Disc: Implications for Intervertebral Disc Degeneration Treatment
    Sun, Zhen
    Liu, Bing
    Luo, Zhuo-Jing
    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2020, 17 (05): : 685 - 692
  • [30] Gene expression profile identifies potential biomarkers for human intervertebral disc degeneration
    Guo, Wei
    Zhang, Bin
    Li, Yan
    Duan, Hui-Quan
    Sun, Chao
    Xu, Yun-Qiang
    Feng, Shi-Qing
    MOLECULAR MEDICINE REPORTS, 2017, 16 (06) : 8665 - 8672