• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

吡仑帕奈对成年癫痫患者骨骼健康的影响。

Effects of perampanel on bone health in adult patients with epilepsy.

作者信息

Yu Mingxing, Zhang Nana, Chen Chunyan, He Yuxuan, Meng Jing, Luo Wen, Liang Yi, Guo Yi, Yu Liang

机构信息

Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Department of Neurology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

Epilepsia Open. 2025 Jun;10(3):822-830. doi: 10.1002/epi4.70038. Epub 2025 Apr 7.

DOI:10.1002/epi4.70038
PMID:40192489
Abstract

OBJECTIVE

The objective was to assess the effects of perampanel (PER) on bone metabolism and bone mineral density (BMD) in adult patients with epilepsy.

METHODS

This retrospective study included consecutive patients admitted to the Epilepsy Center of Sichuan Provincial People's Hospital from January 2023 to June 2024. A total of 39 patients who completed bone metabolism and BMD evaluations after 1 year of PER treatment were included in the PER group. The control group comprised 44 patients with newly diagnosed epilepsy. A cross-sectional analysis was conducted between the two groups. We conducted a subgroup analysis of patients stratified by seizure frequency and type. Patients in the PER group were further stratified according to their seizure frequency and seizure type. Finally, we performed a cohort study involving 10 PER-treated patients whose baseline data were available prior to initiating PER therapy.

RESULTS

No significant differences in bone mineral density were observed between the experimental groups and the control group. With respect to bone metabolism, minor alterations were observed only in thyroid hormone levels and serum magnesium concentrations relative to those of the controls. No significant differences in bone metabolism or BMD were observed before or after PER treatment.

SIGNIFICANCE

Short-term PER treatment did not significantly affect bone mineral density in adult patients with epilepsy.

PLAIN LANGUAGE SUMMARY

This study investigated how PER, a drug used to treat epilepsy, affects bone health in adult patients. Researchers compared 39 patients who were treated with PER for 1 year with 44 patients with newly diagnosed epilepsy. They did not observe significant differences in BMD between the two groups. Some minor changes were observed in thyroid hormone and magnesium levels in the blood, but overall, PER treatment did not have a major effect on bone metabolism or BMD. This study suggested that the short-term use of PER does not significantly affect bone health in people with epilepsy.

摘要

目的

评估吡仑帕奈(PER)对成年癫痫患者骨代谢和骨密度(BMD)的影响。

方法

这项回顾性研究纳入了2023年1月至2024年6月期间连续入住四川省人民医院癫痫中心的患者。PER组纳入了39例在接受PER治疗1年后完成骨代谢和BMD评估的患者。对照组包括44例新诊断的癫痫患者。对两组进行横断面分析。我们对按癫痫发作频率和类型分层的患者进行了亚组分析。PER组患者进一步根据其癫痫发作频率和发作类型进行分层。最后,我们进行了一项队列研究,涉及10例在开始PER治疗前有可用基线数据的接受PER治疗的患者。

结果

实验组和对照组之间未观察到骨密度的显著差异。关于骨代谢,相对于对照组,仅在甲状腺激素水平和血清镁浓度方面观察到微小变化。在PER治疗前后,骨代谢或BMD均未观察到显著差异。

意义

短期PER治疗对成年癫痫患者的骨密度没有显著影响。

通俗易懂的总结

本研究调查了用于治疗癫痫的药物PER如何影响成年患者的骨骼健康。研究人员将39例接受PER治疗1年的患者与44例新诊断的癫痫患者进行了比较。他们未观察到两组之间BMD的显著差异。在血液中的甲状腺激素和镁水平方面观察到了一些微小变化,但总体而言,PER治疗对骨代谢或BMD没有重大影响。这项研究表明,短期使用PER对癫痫患者的骨骼健康没有显著影响。

相似文献

1
Effects of perampanel on bone health in adult patients with epilepsy.吡仑帕奈对成年癫痫患者骨骼健康的影响。
Epilepsia Open. 2025 Jun;10(3):822-830. doi: 10.1002/epi4.70038. Epub 2025 Apr 7.
2
Effectiveness and safety of mono- and add-on perampanel in pediatric patients with epilepsy: Experience from a single-center retrospective study.单药及联合应用吡仑帕奈治疗小儿癫痫患者的有效性和安全性:一项单中心回顾性研究的经验
Epilepsia Open. 2024 Feb;9(1):268-277. doi: 10.1002/epi4.12865. Epub 2023 Nov 27.
3
Efficacy of perampanel by etiology in Japanese patients with epilepsy-subpopulation analysis of a prospective post-marketing observational study.依病因分层的日本癫痫患者中吡仑帕奈的疗效:一项前瞻性上市后观察性研究的亚人群分析。
Epilepsia Open. 2024 Oct;9(5):1772-1782. doi: 10.1002/epi4.13002. Epub 2024 Jul 4.
4
Clinical efficacy and safety of perampanel monotherapy as primary anti-seizure medication in the treatment of pediatric epilepsy: A single-center, prospective, observational study.吡仑帕奈单药治疗作为小儿癫痫主要抗癫痫药物的临床疗效和安全性:一项单中心、前瞻性、观察性研究。
Epilepsia Open. 2024 Dec;9(6):2209-2218. doi: 10.1002/epi4.13043. Epub 2024 Sep 18.
5
Efficacy and Safety of adjunctive Perampanel in a prospective, real-world, Phase IV study in Indian patients aged ≥12 years for Treatment of focal-onset Epilepsy: Study 508.在一项针对≥12 岁的印度局灶性癫痫患者的前瞻性、真实世界、四期研究中,附加用吡仑帕奈的疗效和安全性:研究 508。
Epilepsia Open. 2024 Jun;9(3):940-950. doi: 10.1002/epi4.12885. Epub 2024 Mar 16.
6
The effect of topiramate monotherapy on bone mineral density and markers of bone and mineral metabolism in premenopausal women with epilepsy.托吡酯单药治疗对绝经前女性癫痫患者骨密度及骨代谢标志物的影响。
Epilepsia. 2011 Oct;52(10):1884-9. doi: 10.1111/j.1528-1167.2011.03131.x. Epub 2011 Jun 21.
7
Effects of zonisamide monotherapy on bone health in drug-naive epileptic patients.左乙拉西坦单药治疗对初治癫痫患者骨健康的影响。
Epilepsia. 2020 Oct;61(10):2142-2149. doi: 10.1111/epi.16678. Epub 2020 Sep 18.
8
Adjunctive Perampanel in Older Patients With Epilepsy: A Multicenter Study of Clinical Practice.辅助性佩兰尼酮治疗老年癫痫患者:一项多中心临床实践研究。
Drugs Aging. 2021 Jul;38(7):603-610. doi: 10.1007/s40266-021-00865-3. Epub 2021 Jun 2.
9
A non-inferiority randomized controlled study of Perampanel versus Oxcarbazepine monotherapy for post-stroke epilepsy.吡仑帕奈与奥卡西平单药治疗卒中后癫痫的非劣效性随机对照研究。
Seizure. 2025 Feb;125:172-178. doi: 10.1016/j.seizure.2025.01.016. Epub 2025 Jan 11.
10
[Effect of carbamazepine and valproate on bone metabolism in children with epilepsy].[卡马西平和丙戊酸对癫痫患儿骨代谢的影响]
Zhonghua Er Ke Za Zhi. 2005 Oct;43(10):728-32.

本文引用的文献

1
The Effect of Antiseizure Medications on Thyroid Functions in Children With Epilepsy.抗癫痫药物对癫痫患儿甲状腺功能的影响。
Clin Pediatr (Phila). 2025 Mar;64(3):326-331. doi: 10.1177/00099228241262380. Epub 2024 Jun 19.
2
Prospective study of epilepsy with generalized tonic-clonic seizures alone: Clinical features, response to treatment, and likelihood of medication withdrawal.单纯全面性强直-阵挛发作癫痫的前瞻性研究:临床特征、治疗反应和停药可能性。
Epilepsia Open. 2024 Aug;9(4):1426-1436. doi: 10.1002/epi4.12981. Epub 2024 May 31.
3
Osteoporosis and depression in perimenopausal women: From clinical association to genetic causality.
围绝经期妇女的骨质疏松症和抑郁症:从临床关联到遗传因果关系。
J Affect Disord. 2024 Jul 1;356:371-378. doi: 10.1016/j.jad.2024.04.019. Epub 2024 Apr 10.
4
Effect of duration of sodium valproate therapy on bone mineral density and vitamin D levels.丙戊酸钠治疗时长对骨密度和维生素D水平的影响。
Epilepsy Behav. 2024 Apr;153:109733. doi: 10.1016/j.yebeh.2024.109733. Epub 2024 Mar 5.
5
Thyroid function and epilepsy: a two-sample Mendelian randomization study.甲状腺功能与癫痫:一项两样本孟德尔随机化研究。
Front Hum Neurosci. 2024 Jan 17;17:1295749. doi: 10.3389/fnhum.2023.1295749. eCollection 2023.
6
The impact of antiseizure medication on bone heath: A systematic review of animal studies.抗癫痫药物对骨骼健康的影响:动物研究的系统评价。
Epilepsy Res. 2024 Feb;200:107302. doi: 10.1016/j.eplepsyres.2024.107302. Epub 2024 Jan 17.
7
Both epilepsy and anti-seizure medications affect bone metabolism in children with self-limited epilepsy with centrotemporal spikes.癫痫和抗癫痫药物均会影响具有中央颞区棘波的自限性癫痫患儿的骨代谢。
Epilepsia. 2023 Oct;64(10):2667-2678. doi: 10.1111/epi.17733. Epub 2023 Aug 14.
8
Liver enzyme inducing anticonvulsant drug use is associated with prevalent vertebral fracture.肝酶诱导型抗癫痫药物的使用与普遍存在的椎体骨折有关。
Osteoporos Int. 2023 Oct;34(10):1793-1798. doi: 10.1007/s00198-023-06820-9. Epub 2023 Jun 28.
9
Fractures in people with epilepsy: A nationwide population-based cohort study.癫痫患者的骨折:一项全国范围内基于人群的队列研究。
Epilepsia Open. 2023 Sep;8(3):1028-1037. doi: 10.1002/epi4.12776. Epub 2023 Jun 25.
10
Association between Sensitivity to Thyroid Hormone Indices and Bone Mineral Density in US Males.美国男性甲状腺激素指标敏感性与骨密度之间的关联。
Int J Endocrinol. 2022 Oct 26;2022:2205616. doi: 10.1155/2022/2205616. eCollection 2022.