不完善的临床前模型在青少年特发性脊柱侧凸中的重要性。

IF 3.3 3区 医学 Q2 CELL BIOLOGY
Disease Models & Mechanisms Pub Date : 2025-08-01 Epub Date: 2025-09-01 DOI:10.1242/dmm.052438
Diane S Sepich, Ryan S Gray, Nadav Ahituv, Christina A Gurnett, Jonathan J Rios, Lila Solnica-Krezel, Carol A Wise
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引用次数: 0

摘要

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的健康儿童身上。AIS影响全世界约3%的儿童,是儿科人群中最常见的肌肉骨骼诊断,给患者带来了重大的生理、社会心理和经济负担。遗传易感性是AIS的明确和主要贡献者,基因组发现的见解启发了最终旨在开发新型诊断和治疗的转化研究。AIS的临床前动物模型现在对于验证人类遗传发现、了解基因与环境的相互作用以及加速病因学和治疗发现至关重要。在这一观点中,我们强调了AIS临床前模型的现状,并讨论了该疾病的性质以及标准方法的局限性所带来的挑战。目前的研究表明,脊椎动物的同源AIS疾病基因的直接遗传靶向不一定会产生等效的生理表型,但可以用来了解疾病机制。需要长期的、适当复杂的模型来全面概括人类AIS表型,这些表型是由遗传、生理和机械相互作用引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The importance of imperfect pre-clinical models in adolescent idiopathic scoliosis.

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.

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来源期刊
Disease Models & Mechanisms
Disease Models & Mechanisms 医学-病理学
CiteScore
6.60
自引率
7.00%
发文量
203
审稿时长
6-12 weeks
期刊介绍: Disease Models & Mechanisms (DMM) is an online Open Access journal focusing on the use of model systems to better understand, diagnose and treat human disease.
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