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微小RNA作为生物标志物在异位骨化中的作用。

The role of miRNAs as biomarkers in heterotopic ossification.

作者信息

Xie Chen, Liu Xiao, Li Wenbao, Yao Zhaozhe, Men Hongyue, Li Zongyu

机构信息

Trauma center, The 960th Hospital of PLA, Jinan, Shandong, China.

Department of Basic Medical Sciences, The 960th Hospital of PLA, Jinan, Shandong, China.

出版信息

EFORT Open Rev. 2024 Dec 2;9(12):1120-1133. doi: 10.1530/EOR-22-0100.

Abstract

Fibrodysplasia ossificans progressiva and progressive osseous heteroplasia are genetic forms of heterotopic ossification (HO). Fibrodysplasia ossificans progressiva is caused by ACVR1 gene mutations, while progressive osseous heteroplasia is caused by GNAS gene mutations. Nongenetic HO typically occurs after trauma or surgery, with an occurrence rate of 20-60%. It can also be observed in conditions such as diffuse idiopathic skeletal hyperostosis, spinal ligament ossification, ankylosing spondylitis, and skeletal fluorosis. The exact cause of nongenetic HO is not entirely clear. More than 100 types of miRNAs have been identified as being linked to the development of HO. Some miRNAs are promising potential biomarkers for traumatic HO and ossification of the posterior longitudinal ligament. These findings further emphasize the significant role miRNAs play in the pathogenesis and progression of bone disorders. Repeated investigations into the function of a specific miRNA are infrequent and yield inconsistent results, possibly because of variable experimental conditions. It is hypothesized that miRNAs can enhance osteogenesis for the management of fractures and bone defects. However, further research is required to validate this hypothesis.

摘要

进行性骨化性纤维发育不良和进行性骨化性异位骨化是异位骨化(HO)的遗传形式。进行性骨化性纤维发育不良由ACVR1基因突变引起,而进行性骨化性异位骨化由GNAS基因突变引起。非遗传性HO通常发生在创伤或手术后,发生率为20%至60%。在弥漫性特发性骨肥厚、脊柱韧带骨化、强直性脊柱炎和氟骨症等病症中也可观察到。非遗传性HO的确切病因尚不完全清楚。已鉴定出100多种与HO发生相关的miRNA。一些miRNA有望成为创伤性HO和后纵韧带骨化的潜在生物标志物。这些发现进一步强调了miRNA在骨疾病发病机制和进展中的重要作用。对特定miRNA功能的反复研究并不常见,且结果不一致,这可能是由于实验条件不同所致。据推测,miRNA可增强成骨作用以治疗骨折和骨缺损。然而,需要进一步研究来验证这一假设。

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