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纸质出版日期:2015
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王景红, 夏坤, 张志千, 等. 骨关节炎相关细胞因子及生物标志物的研究进展[J]. 中国实验方剂学杂志, 2015,21(10):225-230.
WANG Jing-hong, XIA Kun, ZHANG Zhi-qian, et al. Research Progress of Osteoarthritis-related Cytokines and Biomarkers[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(10): 225-230.
王景红, 夏坤, 张志千, 等. 骨关节炎相关细胞因子及生物标志物的研究进展[J]. 中国实验方剂学杂志, 2015,21(10):225-230. DOI: 10.13422/j.cnki.syfjx.2015100225.
WANG Jing-hong, XIA Kun, ZHANG Zhi-qian, et al. Research Progress of Osteoarthritis-related Cytokines and Biomarkers[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(10): 225-230. DOI: 10.13422/j.cnki.syfjx.2015100225.
骨关节炎(osteoarthritis
OA)是中老年常见的慢性关节疾病
以关节软骨的退行性变化、破坏及继发性骨质增生为特征
以关节反复发作疼痛、肿胀
逐渐加重
出现关节畸形、活动障碍为主要临床表现
其发病原因迄今尚不完全清楚.中医认为OA属于骨痹范畴
以肝肾亏虚为本
气滞血瘀、脉络痹阻为标
中医治疗亦多从此病机入手
以补肾活血为主
兼以祛湿止痛.各代医家在临床经验的基础上总结了许多治疗痹证的方药
有效地延缓了OA疾病的进程.此外
骨关节炎的临床诊断目前主要依靠症状体征以及影像学检查
但这些诊断方法对早期患者并不敏感
影响了骨关节炎患者的及时治疗.随着分子生物学的不断发展
越来越多的研究表明各种细胞因子在骨性关节炎的发生发展过程中起了重要作用
它们与滑膜、关节软骨、软骨下骨的功能改变密切相关
有较多的细胞因子及蛋白参与了 OA 的病理变化
如白细胞介素、肿瘤坏死因子-α、转化生长因子-β、胰岛素样生长因子、基质金属蛋白酶和骨桥骨蛋白等.同时
在 OA 患者的体液中也寻找出一些特异性生物标志物
如软骨代谢标志物、骨代谢标志物和滑膜代谢标志物等
这些生物标志物能够及时反映关节软骨早期退变的信息
能够对骨关节炎的早期诊断、治疗及预后评价
起到积极的指导作用.目前
有关细胞因子的研究已经深入到作用机制层面
如细胞因子与靶细胞表面受体的结合情况
细胞因子激活胞内信号转导通路等.在生物标志物研究方面
鉴于很多指标缺少专属性和特异性
寻找高灵敏性、高特异性生物标志物
开发简便、准确的多指标联合检测方法
来及时反映关节软骨早期退变等有关病理变化已是研究的热点问题.
Objective: Osteoarthritis (OA) is a common chronic joint disease in the elderly
characterized by degenerative changes
destruction of articular cartilage and secondary bone hyperplasia
with the main clinical manifestations of repeated episodes of pain
joint swelling
joint deformity and movement disorder. And its pathogenesis is still not clear.Traditional Chinese medicine believes that OA belongs to the bone rheumatism category
for the deficiency of the Ganshenxukui
Qizhixueyu
Mailuoizu as the representation
Chinese medicine treatment also from start to pathogenesis
invigorating the kidney and promoting blood circulation mainly
and concurrently to Qushi analgesic. Each generation of physicians summarizes prescription many treatment of Bi syndrome based on clinical experience
effectively delay the disease process of OA. In addition
the clinical diagnosis of osteoarthritis mainly relies on symptoms and imaging examination
but the diagnosis method is not sensitive to early patients
which hampers the timely treatment of early patients with osteoarthritis. With the development of molecular biology
more and more studies show that various cytokines play an important role in the occurrence and development of osteoarthritis
which are closely related to the articular cartilage
synovial membrane and the subchondral bone function. There are many cytokines and proteins involved in the pathological changes of OA
such as interleukin and tumor necrosis factor alpha
transforming growth factor
insulin-like growth factor
matrix metalloproteinase and bone bridge bone protein
etc. At the same time
some specific biomarkers have been discovered in OA patients with body fluids
such as cartilage metabolism markers
markers of bone metabolism and markers of synovial metabolism substance
which can reflect early articular cartilage degeneration to assist to evaluate the early diagnosis
treatment and prognosis of osteoarthritis. At present
the research on cytokines have been probed into the mechanism level
such as the combination of cytokines and receptors on the target cells
cytokines activating intracellular signal transduction pathway. In biomarker research
given the many indicators lacking specificity
it is necessary to develop biomarkers with high sensitivity and specificity
and develop a simple and accurate method to reflect the early articular cartilage degeneration and other relevant pathological changes.
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