评估长期抗癫痫治疗的癫痫患者的骨密度:试点数据

N. A. Sivakova, I. V. Abramova, V. P. Rybasova, O. D. Bolshunova, E. D. Kasyanov, G. V. Rukavishnikov, M. A. Khobeysh, M. Yu. Sorokin, L. V. Lukina, N. I. Ananyeva, R. F. Nasyrova, V. A. Mikhailov, G. E. Mazo
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All patients underwent general clinical, neurologic examination and densitometric study by quantitative computed tomography at three points (L1, L2 and femoral neck). Results. Decreased bone mineral density was found in 34.2% of the patients. Of them, 29% had osteopenia and 5.2% - osteoporosis. The change in mineral density was observed at a median duration of antiepileptic therapy of 8 years. ROC analysis showed that bone mineral density decreased statistically significantly with increasing duration of anitconvulsant therapy (SROC 0.929±0.052; 95% CI: 0.827-1.000). Correlation analysis revealed a markedly close association (ρ = -0.626, p < 0.001) between bone mineral density and duration of antiepileptic therapy. Conclusion. The results of the study confirm the effect of antiepileptic therapy on bone mineral density. And show that the probability of developing osteopenia and osteoprosis with longer duration of anticonvulsant therapy is higher than in the general population. 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引用次数: 0

摘要

目前,有许多抗惊厥药具有良好的药理学特征和高安全性。然而,在长期服用抗癫痫药物治疗期间,仍然存在药物诱导不良事件的风险。与使用抗惊厥药相关的骨组织最不利的变化之一是骨质疏松症,它导致骨密度下降,使骨骼更脆弱,容易骨折。癫痫患者骨密度降低和骨折频发的问题是一个重要但尚未得到充分研究的问题,它会显著降低癫痫患者的生活质量,并涉及到治疗和康复的重大经济成本。研究骨质疏松症与癫痫的相互作用,对于制定有效的方法及时诊断、治疗和预防骨代谢紊乱具有重要意义。本文介绍了一项探讨抗癫痫治疗对矿物质代谢和骨密度影响的初步研究结果。目的:评价长期接受抗癫痫药物治疗的成人癫痫患者的骨密度。材料和方法。对38例长期服用抗癫痫药物的成人癫痫患者进行了检查。所有患者均行一般临床、神经学检查和3点(L1、L2和股骨颈)定量计算机断层扫描密度测定。结果。34.2%的患者骨密度下降。其中29%为骨质减少,5.2%为骨质疏松。在抗癫痫治疗的中位持续时间为8年时观察到矿物质密度的变化。ROC分析显示,随着抗惊厥药治疗时间的延长,骨密度降低具有统计学意义(SROC 0.929±0.052;95% ci: 0.827-1.000)。相关分析显示,两者之间有显著的密切关系(ρ = -0.626, p <0.001)骨密度与抗癫痫治疗持续时间之间的关系。结论。本研究结果证实了抗癫痫治疗对骨密度的影响。结果表明,抗惊厥药物治疗时间越长,发生骨质减少和骨质疏松的概率高于一般人群。研究抗癫痫药物对骨代谢的影响对癫痫患者有效的抗癫痫治疗策略具有重要的临床意义,有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of bone mineral density in epileptic patients with long-term antiepileptic therapy: pilot data
Currently, there are numerous anticonvulsants with a favorable pharmacological profile and high safety are available. However, there is still a risk of drug-induced adverse events during long-term administration of antiepileptic therapy. One of the most unfavorable changes in bone tissue associated with anticonvulsant use is osteoporotic disorders, which result in a loss of bone density, making the bones more fragile and prone to fractures. The problem of decreased bone mineral density and frequent fractures in patients with epilepsy is an important and understudied issue that significantly reduces quality of life and involves significant economic costs for the treatment and rehabilitation of epileptic patients. Studying the interaction between osteoporosis and epilepsy is of great importance for the development of effective methods for timely diagnosis, treatment and prevention of bone metabolism disorders. This article presents pilot results of a study to investigate the effect of antiepileptic therapy on mineral metabolism and bone density. The aim of the study: to evaluate bone mineral density in adult patients with epilepsy long-term receiving antiepileptic therapy. Materials and methods. Thirty-eight adult patients with epilepsy taking antiepileptic drugs for a long time were examined. All patients underwent general clinical, neurologic examination and densitometric study by quantitative computed tomography at three points (L1, L2 and femoral neck). Results. Decreased bone mineral density was found in 34.2% of the patients. Of them, 29% had osteopenia and 5.2% - osteoporosis. The change in mineral density was observed at a median duration of antiepileptic therapy of 8 years. ROC analysis showed that bone mineral density decreased statistically significantly with increasing duration of anitconvulsant therapy (SROC 0.929±0.052; 95% CI: 0.827-1.000). Correlation analysis revealed a markedly close association (ρ = -0.626, p < 0.001) between bone mineral density and duration of antiepileptic therapy. Conclusion. The results of the study confirm the effect of antiepileptic therapy on bone mineral density. And show that the probability of developing osteopenia and osteoprosis with longer duration of anticonvulsant therapy is higher than in the general population. The study of the effects of antiepileptic drugs on bone metabolism has important clinical implications for effective strategies for prescribing antiepileptic therapy in epileptic patients and requires further research.
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