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The cellular pathobiology of the degenerate intervertebral disc and discogenic back pain

机译:椎间盘退变和椎间盘源性腰痛的细胞病理生物学

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摘要

In 2007, three times as many peer reviewed publications covering the biology and biotherapeutics of intervertebral disc (IVD) disease appeared in the literature than in 1997. This is testimony to the upsurge in interest in the IVD, mainly driven by the openings that modern molecular pathology has generated to investigate mechanisms of human disease and the potential offered by novel therapeutic technologies to use data coming from these studies to positively influence chronic discogenic back pain and sciatica. Molecular pathology has shown IVD degeneration, a major cause of low back pain, to be a complex, active disorder in which disturbed cytokine biology, cellular dysfunction and altered load responses play key roles. This has translated into a search for target molecules and disease processes that might be the focus of future, evidence-based therapies for back pain. It is not possible to describe the totality of advances that have been made in understanding the biology of the IVD in recent years, but in this review those areas of biology that are currently influencing, or could conceivably soon impinge on, clinical thinking or practice around IVD degeneration and discogenic back pain are described and discussed.
机译:2007年,涉及椎间盘(IVD)疾病的生物学和生物治疗学的同行评审出版物的数量是1997年的三倍。这证明了对IVD的兴趣激增,这主要是由于现代分子生物学的开放病理学已经开始研究人类疾病的机制,以及新型治疗技术提供的潜力,利用这些研究中的数据积极影响慢性盘源性背痛和坐骨神经痛。分子病理学表明,IVD变性是下背痛的主要原因,是一种复杂的活动性疾病,其中细胞因子生物学异常,细胞功能障碍和负荷反应改变均起关键作用。这已经转化为对目标分子和疾病过程的搜索,这可能是未来基于证据的腰痛治疗的重点。不可能描述近年来在理解IVD生物学方面取得的全部进展,但是在本综述中,目前正在影响或可能很快影响到临床思维或实践的生物学领域描述和讨论了IVD变性和椎间盘源性背痛。

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  • 来源
    《Rheumatology 》 |2009年第1期| p.5-10| 共6页
  • 作者

    A. J. Freemont1;

  • 作者单位

    1Tissue Injury and Repair Research Group, Research School of Clinical and Laboratory Sciences, University of Manchester, Manchester, UK.;

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