异维甲酸对颅颌面区骨动力学的影响:临床前证据的系统回顾。

IF 2
M Fernanda Ferreira, G Pereira Nunes, A Hernandes Chaves-Neto, A Henrique Reis-Prado, M Pagliusi Justo, C Ferreira-Baptista, N Amanda Gomes, A Carlos Botazzo Delbem, M Rogério de Mendonça
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引用次数: 0

摘要

目的:对异维甲酸对颅颌面骨影响的现有文献进行系统评价和综合。方法:遵循PRISMA指南并在PROSPERO注册,于2024年8月跨多个数据库进行综述。对符合条件的体内研究进行分析,以评估异维甲酸对颅颌面骨的影响。偏倚风险根据实验动物实验系统评价中心的动物研究RoB工具进行。结果:在3670项研究中,有8项符合条件。四项研究显示,异维甲酸治疗组特定牙根区域的透明化区域增加,同时成骨细胞和破骨细胞计数、毛细血管形成和新骨生长也存在显著差异,表明异维甲酸对骨组织的影响。两项研究报道骨小梁结构没有显著差异,但观察到胶原形成、根吸收和骨吸收频率的变化。关于异维甲酸对骨修复作用的研究揭示了截然不同的结果:高剂量(7.5 mg/kg/天)增强了颅骨缺损的骨形成,而低剂量(1 mg/kg/天)减缓了兔鼻整形模型的骨愈合,与对照组相比,愈合率降低。结论:本文综述的研究表明,异维甲酸对骨重塑具有剂量依赖性。高剂量促进骨形成和牙槽修复,但增加根吸收和改变骨形态,而低剂量减缓骨愈合。一些研究报告没有骨体积或移位的显著变化,但注意到牙龈愈合的改善。这些发现强调需要进一步的研究来指导异维甲酸对颅颌面骨健康的长期影响的临床决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of isotretinoin on bone dynamics in the craniomaxillofacial region: a systematic review of preclinical evidence.

Purpose: This systematic review provides a critical evaluation, synthesis of the existing literature on isotretinoin's effects on craniomaxillofacial bone.

Methods: Following the PRISMA guidelines and registered in PROSPERO, the review was conducted in August 2024 across various databases. Eligible in vivo studies were analysed for their assessment of isotretinoin's effects on craniomaxillofacial bone. Risk of bias was performed according to the Systematic Review Centre for Laboratory Animal Experimentation's RoB tool for animal studies.

Results: Out of 3670 studies, eight were eligible. Four studies revealed increased hyalinised areas in specific dental root regions amongst isotretinoin-treated groups, alongside significant differences in osteoblast and osteoclast counts, capillary formation, and new bone growth, indicating isotretinoin's impact on bone tissue. Two studies reported no significant disparities in trabecular bone structure but observed variations in collagen formation, root resorption, and bone resorption frequency. Studies on isotretinoin's effects on bone repair reveal contrasting outcomes: higher doses (7.5 mg/kg/day) enhanced bone formation in calvaria defects, whilst lower doses (1 mg/kg/day) slowed bone healing in a rabbit rhinoplasty model, showing reduced healing rates compared to controls.

Conclusions: The reviewed studies indicate that isotretinoin has dose-dependent effects on bone remodelling. Higher doses enhance bone formation and alveolar repair but increase root resorption and alter bone morphology, whilst lower doses slow bone healing. Some studies report no significant changes in bone volume or displacement but note improved gingival healing. These findings emphasise the need for further research to guide clinical decisions on isotretinoin's long-term impact on craniomaxillofacial bone health.

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