Sepich Diane S, Gray Ryan S, Ahituv Nadav, Gurnett Christina A, Rios Jonathan J, Solnica-Krezel Lila, Wise Carol A
Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Pediatrics, Dell Pediatric Research Institute, University of Texas at Austin Dell Medical School, Austin, TX 78723, USA.
Dis Model Mech. 2025 Aug 1;18(8). doi: 10.1242/dmm.052438. Epub 2025 Sep 1.
Adolescent idiopathic scoliosis (AIS) is a twisting spinal deformity that occurs in otherwise healthy children at the time of rapid pre-pubescent growth. AIS affects ∼3% of children worldwide and is the most common musculoskeletal diagnosis in pediatric populations, posing a significant physiological, psychosocial and financial burden to patients. Genetic predisposition is a clear and major contributor to AIS, and insights from genomic discoveries are inspiring translational studies ultimately aimed at developing novel diagnostics and therapies. Pre-clinical animal models of AIS are now essential to validate human genetic findings, understand gene-by-environment interactions, and speed etiologic and therapeutic discovery. In this Perspective, we highlight the current status of pre-clinical models of AIS and discuss the challenges posed by the nature of the disorder combined with the limitations of standard approaches. Current research suggests that straightforward genetic targeting of orthologous AIS disease genes in vertebrates may not necessarily yield equivalent physiological phenotypes but nevertheless can be utilized to understand disease mechanisms. Longer-term, appropriately complex models are needed to fully recapitulate the human AIS phenotype arising from genetic, physiological and mechanical interactions.
青少年特发性脊柱侧凸(AIS)是一种脊柱扭曲畸形,发生在青春期前快速生长阶段的健康儿童中。AIS影响全球约3%的儿童,是儿科人群中最常见的肌肉骨骼疾病诊断,给患者带来了巨大的生理、心理社会和经济负担。遗传易感性是AIS的一个明确且主要的促成因素,基因组发现的见解正在推动转化研究,最终目标是开发新的诊断方法和治疗手段。AIS的临床前动物模型现在对于验证人类遗传研究结果、理解基因与环境的相互作用以及加速病因和治疗方法的发现至关重要。在这篇观点文章中,我们强调了AIS临床前模型的现状,并讨论了该疾病的性质与标准方法的局限性所带来的挑战。目前的研究表明,在脊椎动物中直接针对直系同源AIS疾病基因进行基因靶向操作不一定会产生等效的生理表型,但仍然可以用于理解疾病机制。从长远来看,需要更复杂的模型来全面再现由遗传、生理和机械相互作用产生的人类AIS表型。