Burwell R Geoffrey, Dangerfield Peter H, Freeman Brian J C
Centre for Spinal Studies and Surgery, Nottingham University Hospitals Trust, Queen's Medical Centre Campus, Nottingham, UK.
Stud Health Technol Inform. 2008;135:3-52.
There is no generally accepted scientific theory for the causes of adolescent idiopathic scoliosis (AIS). Encouraging advances thought to be related to AIS pathogenesis have recently been made in several fields including anthropometry of bone growth, bone mass, spinal growth modulation, extra-spinal left-right skeletal length asymmetries and disproportions, magnetic resonance imaging of vertebral column, spinal cord, brain, skull, and molecular pathogenesis. These advances are leading to the evaluation of new treatments including attempts at minimally invasive surgery on the spine and peri-apical ribs. Several concepts of AIS are outlined indicating their clinical applications but not their research potential. The concepts, by derivation morphological, molecular and mathematical, are addressed in 15 sections: 1) initiating and progressive factors; 2) relative anterior spinal overgrowth; 3) dorsal shear forces that create axial rotational instability; 4) rotational preconstraint; 5) uncoupled, or asynchronous, spinal neuro-osseous growth; 6) brain, nervous system and skull; 7) a novel neuro-osseous escalator concept based on a putative abnormality of two normal polarized processes namely, a) increasing skeletal dimensions, and b) the CNS body schema - both contained within a neuro-osseous timing of maturation (NOTOM) concept; 8) transverse plane pelvic rotation, skeletal asymmetries and developmental theory; 9) thoraco-spinal concept; 10) origin in contracture at the hips; 11) osteopenia; 12) melatonin deficiency; 13) systemic melatonin-signaling pathway dysfunction; 14) platelet calmodulin dysfunction; and 15) biomechanical spinal growth modulation. From these concepts, a collective model for AIS pathogenesis is formulated. The central concept of this model includes the body schema of the neural systems, widely-studied in adults, that control normal posture and coordinated movements with frames of reference in the posterior parietal cortex. The escalator concept has implications for the normal development of upright posture, and the evolution in humans of neural control, the trunk and unique bipedal gait.
对于青少年特发性脊柱侧凸(AIS)的病因,目前尚无普遍接受的科学理论。最近,在包括骨骼生长人体测量学、骨量、脊柱生长调节、脊柱外左右骨骼长度不对称和比例失调、脊柱、脊髓、大脑、颅骨的磁共振成像以及分子发病机制等多个领域,都取得了与AIS发病机制相关的鼓舞人心的进展。这些进展正促使人们对新的治疗方法进行评估,包括尝试对脊柱和椎旁肋骨进行微创手术。本文概述了AIS的几个概念,阐述了它们的临床应用,但未涉及其研究潜力。这些概念从形态学、分子学和数学角度衍生而来,在15个部分进行了阐述:1)起始和进展因素;2)相对的脊柱前侧过度生长;3)产生轴向旋转不稳定的背侧剪切力;4)旋转预约束;5)未耦合或不同步的脊柱神经 - 骨生长;6)大脑、神经系统和颅骨;7)一种基于两个正常极化过程的假定异常的新型神经 - 骨自动扶梯概念,即a)骨骼尺寸增加,以及b)中枢神经系统身体模式——两者都包含在神经 - 骨成熟时间(NOTOM)概念中;8)冠状面骨盆旋转、骨骼不对称和发育理论;9)胸段 - 脊柱概念;10)起源于髋关节挛缩;11)骨质减少;12)褪黑素缺乏;13)全身褪黑素信号通路功能障碍;14)血小板钙调蛋白功能障碍;以及15)生物力学脊柱生长调节。基于这些概念,构建了一个AIS发病机制的综合模型。该模型的核心概念包括在成年人中广泛研究的神经系统身体模式,它控制正常姿势以及与后顶叶皮质中的参考框架协调运动。自动扶梯概念对直立姿势的正常发育以及人类神经控制、躯干和独特双足步态的进化具有启示意义。