Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India; Centre of Excellence in Unani Medicine (Pharmacognosy & Pharmacology), Bioactive Natural Product Laboratory, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India.
Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India; Centre of Excellence in Unani Medicine (Pharmacognosy & Pharmacology), Bioactive Natural Product Laboratory, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India.
Epilepsy Res. 2024 Feb;200:107302. doi: 10.1016/j.eplepsyres.2024.107302. Epub 2024 Jan 17.
Antiseizure medications (ASMs) are known to potentially impact bone health, but existing literature presents conflicting results regarding their specific effects on bone mineralization, metabolism, and quality.
This systematic review aims to establish a consensus regarding the influence of ASMs on bone health based on existing preclinical studies.
Following SYRCLE and PRISMA guidelines, we conducted a systematic search in PubMed, Science Direct, and Google Scholar to identify relevant studies. Ultimately, 21 articles were selected for inclusion in this review.
Among the chosen studies, approximately half involved Wistar rats as experimental subjects. Levetiracetam and sodium valproate were the most frequently investigated drugs, with a typical treatment duration of 10-12 weeks. These studies exhibited a low risk of bias in aspects like sequence generation, random housing, random outcome assessment, and reporting bias. However, blinding in performance, allocation concealment, and detection were often rated as having a high risk of bias. The collective findings suggest that prolonged ASM use leads to reduced bone mineral density, altered bone turnover marker levels (including hypovitaminosis D, hypocalcemia, and secondary hyperparathyroidism), deterioration of bone microarchitecture, and decreased mechanical strength.
The adverse effects on bone associated with ASMs are not limited to enzyme-inducing drugs, as newer generation ASMs may also contribute to these effects. Hypovitaminosis D alone may not be solely responsible for ASM-induced bone issues, suggesting the involvement of other mechanisms. Furthermore, substantial variations were observed in the results of different preclinical studies on individual ASMs, highlighting the need to standardize animal study methodologies to enhance reproducibility and reduce variation.
抗癫痫药物(ASMs)已知可能会影响骨骼健康,但现有文献对于它们对骨矿化、代谢和质量的具体影响存在相互矛盾的结果。
本系统评价旨在根据现有临床前研究,就 ASMs 对骨骼健康的影响达成共识。
根据 SYRCLE 和 PRISMA 指南,我们在 PubMed、Science Direct 和 Google Scholar 中进行了系统搜索,以确定相关研究。最终,有 21 篇文章被纳入本综述。
在所选择的研究中,大约一半涉及 Wistar 大鼠作为实验对象。左乙拉西坦和丙戊酸钠是研究最多的两种药物,典型的治疗持续时间为 10-12 周。这些研究在序列生成、随机分组、随机结果评估和报告偏倚方面的偏倚风险较低。然而,在操作、分配隐匿和检测方面的盲法往往被评为具有高偏倚风险。综合研究结果表明,长期使用 ASM 会导致骨密度降低、骨转换标志物水平改变(包括维生素 D 缺乏、低钙血症和继发性甲状旁腺功能亢进)、骨微结构恶化和机械强度降低。
与 ASMs 相关的骨骼不良影响不仅限于酶诱导药物,因为新一代 ASMs 也可能导致这些影响。维生素 D 缺乏症本身可能不是 ASM 引起的骨骼问题的唯一原因,这表明涉及其他机制。此外,不同临床前研究中个别 ASM 的结果存在很大差异,这突出表明需要标准化动物研究方法,以提高重现性并减少变异性。