Department of Biomedical and Neuromotor Science-DIBINEM, 1st Orthopaedic and Traumatologic Clinic, IRCCS Istituto Ortopedico Rizzoli, University of Bologna, Via Giulio Cesare Pupilli 1, 40136 Bologna, Italy.
Medicine and Rheumatology Unit, IRCCS Istituto Ortopedico Rizzoli, Via Giulio Cesare Pupilli 1, 40136 Bologna, Italy.
Int J Mol Sci. 2022 May 25;23(11):5914. doi: 10.3390/ijms23115914.
Adolescent idiopathic scoliosis (AIS) is a progressive deformity of the spine. Scoliotic curves progress until skeletal maturity leading, in rare cases, to a severe deformity. While the Cobb angle is a straightforward tool in initial curve magnitude measurement, assessing the risk of curve progression at the time of diagnosis may be more challenging. Epigenetic and genetic markers are potential prognostic tools to predict curve progression. The aim of this study is to review the available literature regarding the epigenetic and genetic factors associated with the risk of AIS curve progression. This review was carried out in accordance with Preferential Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. The search was carried out in January 2022. Only peer-reviewed articles were considered for inclusion. Forty studies were included; fifteen genes were reported as having SNPs with significant association with progressive AIS, but none showed sufficient power to sustain clinical applications. In contrast, nine studies reporting epigenetic modifications showed promising results in terms of reliable markers. Prognostic testing for AIS has the potential to significantly modify disease management. Most recent evidence suggests epigenetics as a more promising field for the identification of factors associated with AIS progression, offering a rationale for further investigation in this field.
青少年特发性脊柱侧凸(AIS)是脊柱的进行性畸形。脊柱侧凸曲线在骨骼成熟之前会持续进展,在极少数情况下会导致严重的畸形。虽然 Cobb 角是初始曲线幅度测量的直接工具,但在诊断时评估曲线进展的风险可能更具挑战性。表观遗传和遗传标志物是预测曲线进展的潜在预后工具。本研究旨在回顾与 AIS 曲线进展风险相关的表观遗传和遗传因素的现有文献。本综述按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行。搜索于 2022 年 1 月进行。仅考虑纳入同行评审的文章。共纳入 40 项研究;有 15 个基因被报道与具有显著相关性的 SNP 相关,但没有一个具有足够的效力来维持临床应用。相比之下,有 9 项报告表观遗传修饰的研究在可靠标志物方面显示出有希望的结果。AIS 的预后检测有可能显著改变疾病管理。最近的证据表明,表观遗传学作为识别与 AIS 进展相关因素的一个更有前途的领域,为该领域的进一步研究提供了依据。