Burwell R G
University of Nottingham, UK.
Pediatr Rehabil. 2003 Jul-Dec;6(3-4):137-70. doi: 10.1080/13638490310001642757.
The aetiology of the three-dimensional spinal deformity of idiopathic scoliosis (IS) is unknown. Progressive adolescent idiopathic scoliosis (AIS) that mainly affects girls is generally attributed to relative anterior spinal overgrowth from a mechanical mechanism (torsion) during the adolescent growth spurt. Established biological risk factors to AIS are growth velocity and potential residual spinal growth assessed by maturity indicators. Spine slenderness and ectomorphy in girls are thought to be risk factors for AIS. Claimed biomechanical susceptibilities are (1) a fixed lordotic area and hypokyphosis and (2) concave periapical rib overgrowth. MRI has revealed neuroanatomical abnormalities in approximately 20% of younger children with IS. A neuromuscular cause for AIS is probable but not established. Possible susceptibilities to AIS in tissues relate to muscles, ligaments, discs, skeletal proportions and asymmetries, the latter also affecting soft tissues (e.g. dermatoglyphics). AIS is generally considered to be multi-factorial in origin. The many anomalies detected, particularly left-right asymmetries, have led to spatiotemporal aetiologic concepts involving chronomics and the genome altered by nurture without the necessity for a disease process. Genetic susceptibilities defined in twins are being evaluated in family studies; polymorphisms in the oestrogen receptor gene are associated with curve severity. A neurodevelopmental concept is outlined for the aetiology of progressive AIS. This concept involves lipid peroxidation and, if substantiated, has initial therapeutic potential by dietary anti-oxidants. Growth saltations have not been evaluated in IS.
特发性脊柱侧凸(IS)三维脊柱畸形的病因尚不清楚。主要影响女孩的进行性青少年特发性脊柱侧凸(AIS)通常归因于青少年生长突增期间机械机制(扭转)导致的相对脊柱前方过度生长。AIS已确定的生物学危险因素是生长速度和通过成熟度指标评估的潜在脊柱剩余生长。女孩的脊柱细长和瘦长体型被认为是AIS的危险因素。所谓的生物力学易感性包括:(1)固定的前凸区域和后凸减少;(2)凹侧根尖肋骨过度生长。MRI显示约20%的年幼IS患儿存在神经解剖学异常。AIS可能存在神经肌肉病因,但尚未确定。组织对AIS的可能易感性与肌肉、韧带、椎间盘、骨骼比例和不对称性有关,后者也会影响软组织(如皮纹)。AIS通常被认为是多因素起源。检测到的许多异常,尤其是左右不对称,导致了涉及时间组学和由后天培养改变的基因组的时空病因学概念,而无需疾病过程。双胞胎中定义的遗传易感性正在家族研究中进行评估;雌激素受体基因的多态性与侧弯严重程度相关。本文概述了进行性AIS病因的神经发育概念。这一概念涉及脂质过氧化,如果得到证实,通过饮食抗氧化剂具有初步治疗潜力。生长突变在IS中尚未得到评估。