The Genetic and Biological Basis of Pseudoarthrosis in Fractures: Current Understanding and Future Directions.

IF 2.9 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Amalia Kotsifaki, Georgia Kalouda, Sousanna Maroulaki, Athanasios Foukas, Athanasios Armakolas
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引用次数: 0

Abstract

Pseudoarthrosis-the failure of normal fracture healing-remains a significant orthopedic challenge affecting approximately 10-15% of long bone fractures, and is associated with significant pain, prolonged disability, and repeated surgical interventions. Despite extensive research into the pathophysiological mechanisms of bone healing, diagnostic approaches remain reliant on clinical findings and radiographic evaluations, with little innovation in tools to predict or diagnose non-union. The present review evaluates the current understanding of the genetic and biological basis of pseudoarthrosis and highlights future research directions. Recent studies have highlighted the potential of specific molecules and genetic markers to serve as predictors of unsuccessful fracture healing. Alterations in mesenchymal stromal cell (MSC) function, including diminished osteogenic potential and increased cellular senescence, are central to pseudoarthrosis pathogenesis. Molecular analyses reveal suppressed bone morphogenetic protein (BMP) signaling and elevated levels of its inhibitors, such as Noggin and Gremlin, which impair bone regeneration. Genetic studies have uncovered polymorphisms in BMP, matrix metalloproteinase (MMP), and Wnt signaling pathways, suggesting a genetic predisposition to non-union. Additionally, the biological differences between atrophic and hypertrophic pseudoarthrosis, including variations in vascularity and inflammatory responses, emphasize the need for targeted approaches to management. Emerging biomarkers, such as circulating microRNAs (miRNAs), cytokine profiles, blood-derived MSCs, and other markers (B7-1 and PlGF-1), have the potential to contribute to early detection of at-risk patients and personalized therapeutic approaches. Advancing our understanding of the genetic and biological underpinnings of pseudoarthrosis is essential for the development of innovative diagnostic tools and therapeutic strategies.

骨折假关节的遗传和生物学基础:目前的认识和未来的方向。
假关节——骨折正常愈合的失败——仍然是骨科的一个重大挑战,影响了大约10-15%的长骨骨折,并与明显的疼痛、长期残疾和反复手术干预有关。尽管对骨愈合的病理生理机制进行了广泛的研究,但诊断方法仍然依赖于临床表现和影像学评估,在预测或诊断骨不连的工具方面几乎没有创新。本文综述了目前对假关节的遗传和生物学基础的认识,并指出了未来的研究方向。最近的研究强调了特定分子和遗传标记作为骨折愈合失败的预测因素的潜力。间充质间质细胞(MSC)功能的改变,包括成骨潜能的降低和细胞衰老的增加,是假关节发病的核心。分子分析显示骨形态发生蛋白(BMP)信号被抑制,其抑制剂(如Noggin和Gremlin)水平升高,从而损害骨再生。遗传学研究揭示了BMP、基质金属蛋白酶(MMP)和Wnt信号通路的多态性,提示不愈合的遗传易感。此外,萎缩性和肥厚性假关节之间的生物学差异,包括血管和炎症反应的差异,强调需要有针对性的治疗方法。新兴的生物标志物,如循环microrna (mirna)、细胞因子谱、血液来源的MSCs和其他标志物(B7-1和PlGF-1),有可能有助于早期发现高危患者和个性化治疗方法。推进我们对假关节的遗传和生物学基础的理解对于创新诊断工具和治疗策略的发展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
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0.00%
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审稿时长
6 weeks
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