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青少年特发性脊柱侧凸中脊髓的相对缩短和功能受限——神经与骨骼生长不同步的结果,国际脊柱侧凸研究学会电子焦点小组辩论总结

Relative shortening and functional tethering of spinal cord in adolescent scoliosis - Result of asynchronous neuro-osseous growth, summary of an electronic focus group debate of the IBSE.

作者信息

Chu Winnie Cw, Lam Wynnie Mw, Ng Bobby Kw, Tze-Ping Lam, Lee Kwong-Man, Guo Xia, Cheng Jack Cy, Burwell R Geoffrey, Dangerfield Peter H, Jaspan Tim

机构信息

The Centre for Spinal Studies & Surgery, Nottingham University Hospitals Trust, Queen's Medical Centre Campus, Nottingham NG7 2UH, UK.

出版信息

Scoliosis. 2008 Jun 27;3:8. doi: 10.1186/1748-7161-3-8.

Abstract

There is no generally accepted scientific theory for the causes of adolescent idiopathic scoliosis (AIS). As part of its mission to widen understanding of scoliosis etiology, the International Federated Body on Scoliosis Etiology (IBSE) introduced the electronic focus group (EFG) as a means of increasing debate on knowledge of important topics. This has been designated as an on-line Delphi discussion. The Statement for this debate was written by Dr WCW Chu and colleagues who examine the spinal cord to vertebral growth interaction during adolescence in scoliosis. Using the multi-planar reconstruction technique of magnetic resonance imaging they investigated the relative length of spinal cord to vertebral column including ratios in 28 girls with AIS (mainly thoracic or double major curves) and 14 age-matched normal girls. Also evaluated were cerebellar tonsillar position, somatosensory evoked potentials (SSEPs), and clinical neurological examination. In severe AIS compared with normal controls, the vertebral column is significantly longer without detectable spinal cord lengthening. They speculate that anterior spinal column overgrowth relative to a normal length spinal cord exerts a stretching tethering force between the two ends, cranially and caudally leading to the initiation and progression of thoracic AIS. They support and develop the Roth-Porter concept of uncoupled neuro-osseous growth in the pathogenesis of AIS which now they prefer to term 'asynchronous neuro-osseous growth'. Morphological evidence about the curve apex suggests that the spinal cord is also affected, and a 'double pathology' is suggested. AIS is viewed as a disorder with a wide spectrum and a common neuroanatomical abnormality namely, a spinal cord of normal length but short relative to an abnormally lengthened anterior vertebral column. Neuroanatomical changes and/or abnormal neural function may be expressed only in severe cases. This asynchronous neuro-osseous growth concept is regarded as one component of a larger concept. The other component relates to the brain and cranium of AIS subjects because abnormalities have been found in brain (infratentorial and supratentorial) and skull (vault and base). The possible relevance of systemic melatonin-signaling pathway dysfunction, platelet calmodulin levels and putative vertebral vascular biology to the asynchronous neuro-osseous growth concept is discussed. A biomechanical model to test the spinal component of the concept is in hand. There is no published research on the biomechanical properties of the spinal cord for scoliosis specimens. Such research on normal spinal cords includes movements (kinematics), stress-strain responses to uniaxial loading, and anterior forces created by the stretched cord in forward flexion that may alter sagittal spinal shape during adolescent growth. The asynchronous neuro-osseous growth concept for the spine evokes controversy. Dr Chu and colleagues respond to five other concepts of pathogenesis for AIS and suggest that relative anterior spinal overgrowth and biomechanical growth modulation may also contribute to AIS pathogenesis.

摘要

对于青少年特发性脊柱侧凸(AIS)的病因,目前尚无被广泛接受的科学理论。作为扩大对脊柱侧凸病因理解使命的一部分,国际脊柱侧凸病因联合组织(IBSE)引入了电子焦点小组(EFG),作为增加对重要主题知识辩论的一种方式。这被指定为在线德尔菲讨论。本次辩论的声明由WCW Chu博士及其同事撰写,他们研究了脊柱侧凸青少年期脊髓与椎体生长的相互作用。他们使用磁共振成像的多平面重建技术,调查了28名AIS女孩(主要是胸段或双主弯)和14名年龄匹配的正常女孩的脊髓与脊柱的相对长度,包括比例。还评估了小脑扁桃体位置、体感诱发电位(SSEP)和临床神经学检查。与正常对照组相比,重度AIS患者的脊柱明显更长,而脊髓没有明显延长。他们推测,相对于正常长度脊髓,脊柱前柱过度生长在两端(头侧和尾侧)之间施加了拉伸束缚力,导致胸段AIS的发生和进展。他们支持并发展了AIS发病机制中神经 - 骨生长解耦的Roth - Porter概念,现在他们更喜欢称之为“异步神经 - 骨生长”。关于侧弯顶点的形态学证据表明脊髓也受到影响,提示存在“双重病理”。AIS被视为一种具有广泛谱系和常见神经解剖学异常(即正常长度但相对于异常延长的前脊柱短的脊髓)的疾病。神经解剖学变化和/或异常神经功能可能仅在严重病例中表现出来。这种异步神经 - 骨生长概念被视为一个更大概念的一个组成部分。另一个组成部分与AIS患者的大脑和颅骨有关,因为在大脑(幕下和幕上)和颅骨(穹窿和颅底)中发现了异常。讨论了全身褪黑素信号通路功能障碍、血小板钙调蛋白水平和假定的椎体血管生物学与异步神经 - 骨生长概念的可能相关性。一个测试该概念脊柱成分的生物力学模型正在研究中。目前尚无关于脊柱侧凸标本脊髓生物力学特性的已发表研究。关于正常脊髓的此类研究包括运动(运动学)、对单轴加载的应力 - 应变反应,以及在青少年生长期间向前屈曲时拉伸脊髓产生的前向力,这可能会改变脊柱矢状面形状。脊柱的异步神经 - 骨生长概念引发了争议。Chu博士及其同事回应了AIS发病机制的其他五个概念,并表明相对的脊柱前柱过度生长和生物力学生长调节也可能导致AIS发病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee9d/2474583/843c17df4ae3/1748-7161-3-8-1.jpg

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