Burwell R Geoffrey, Dangerfield Peter H
Centre for Spinal Studies and Surgery, Nottingham University Hospitals Trust, Nottingham, NG7 2UH, UK.
Stud Health Technol Inform. 2012;176:3-19.
Although considerable progress had been made in the past two decades in understanding the etiopathogenesis of adolescent idiopathic scoliosis (AIS), it still lacks an agreed theory of etiopathogenesis. One problem may be that AIS results not from one cause, but several that interact with various genetic predisposing factors. There is a view there are two other pathogenic processes for idiopathic scoliosis namely, initiating (or inducing), and those that cause curve progression. Twin studies and observations of family aggregation have revealed significant genetic contributions to idiopathic scoliosis, that place AIS among other common disease or complex traits with a high heritability interpreted by the genetic variant hypothesis of disease. We summarize etiopathogenetic knowledge of AIS as theories of pathogenesis including recent multiple concepts, and blood tests for AIS based on predictive biomarkers and genetic variants that signify disease risk. There is increasing evidence for the possibility of an underlying neurological disorder for AIS, research which holds promise. Like brain research, most AIS workers focus on their own corner and there is a need for greater integration of research effort. Epigenetics, a relatively recent field, evaluates factors concerned with gene expression in relation to environment, disease, normal development and aging, with a complex regulation across the genome during the first decade of life. Research on the role of environmental factors, epigenetics and chronic non-communicable diseases (NCDs) including adiposity, after a slow start, has exploded in the last decade. Not so for AIS research and the environment where, except for monozygotic twin studies, there are only sporadic reports to suggest that environmental factors are at work in etiology. Here, we examine epigenetic concepts as they may relate to human development, normal life history phases and AIS pathogenesis. Although AIS is not regarded as an NCD, like them, it is associated with whole organism metabolic phenomena, including lower body mass index, lower circulating leptin levels and other systemic disorders. Some epigenetic research applied to Silver-Russell syndrome and adiposity is examined, from which suggestions are made for consideration of AIS epigenetic research, cross-sectional and longitudinal. The word scoliogeny is suggested to include etiology, pathogenesis and pathomechanism.
尽管在过去二十年里,人们对青少年特发性脊柱侧凸(AIS)的病因发病机制的理解取得了相当大的进展,但仍缺乏一个公认的病因发病理论。一个问题可能是,AIS并非由单一原因引起,而是由几个与各种遗传易感因素相互作用的原因导致。有一种观点认为,特发性脊柱侧凸还有另外两个致病过程,即起始(或诱导)过程和导致侧弯进展的过程。双胞胎研究和家族聚集观察表明,遗传因素对特发性脊柱侧凸有显著贡献,这使得AIS与其他具有高遗传度的常见疾病或复杂性状一样,符合疾病的遗传变异假说。我们将AIS的病因发病机制知识总结为发病机制理论,包括最近的多种概念,以及基于预测生物标志物和表示疾病风险的遗传变异的AIS血液检测。越来越多的证据表明AIS可能存在潜在的神经系统疾病,这一研究很有前景。与脑研究一样,大多数AIS研究人员专注于自己的领域,需要更大程度地整合研究工作。表观遗传学是一个相对较新的领域,它评估与基因表达相关的因素,涉及环境、疾病、正常发育和衰老,在生命的第一个十年中,基因组存在复杂的调控。对环境因素、表观遗传学和包括肥胖在内的慢性非传染性疾病(NCDs)作用的研究,在经历了缓慢的起步后,在过去十年中迅速发展。AIS研究和环境方面的情况并非如此,除了同卵双胞胎研究外,只有零星的报告表明环境因素在病因学中起作用。在这里,我们研究表观遗传学概念,因为它们可能与人类发育、正常生活史阶段和AIS发病机制相关。尽管AIS不被视为一种NCD,但与它们一样,它与整个生物体的代谢现象有关,包括较低的体重指数、较低的循环瘦素水平和其他全身疾病。我们研究了一些应用于Silver-Russell综合征和肥胖症的表观遗传学研究,并从中提出了一些建议,以供AIS表观遗传学的横断面和纵向研究参考。有人建议用“脊柱侧凸发生学”这个词来涵盖病因学、发病机制和病理机制。