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1990 - 2021年全球、区域和国家的癫痫负担:2021年全球疾病负担研究的系统分析

Global, regional, and national burden of epilepsy, 1990-2021: a systematic analysis for the Global Burden of Disease Study in 2021.

作者信息

Sun Tianqi, Yu Tianfu, Liu Pengcheng

机构信息

School of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, China.

Department of Neurosurgery, The Affiliated Drum Tower Hospital, School of Medicine, Nanjing University, Nanjing, China.

出版信息

Cost Eff Resour Alloc. 2025 Jun 11;23(1):28. doi: 10.1186/s12962-025-00635-7.

Abstract

BACKGROUND

Idiopathic epilepsy is a serious neurological disorder that can lead to premature death and severe disability. We aimed to assess the global burden of idiopathic epilepsy, to provide a comprehensive understanding of the current dynamics and trends in idiopathic epilepsy, and to gain insight into its epidemiological attributes.

METHODS

This study assessed the global, regional, and national impact of idiopathic epilepsy through incidence and disability-adjusted life year (DALY) based on the Global Burden of Disease Study 2021 (GBD 2021). After statistically summarizing the global incidence rates and disability-adjusted life years (DALYs), we performed Estimating Average Percent Change (EAPC) correlation analyses and Joinpoint regression analyses to further derive global trends in idiopathic epilepsy incidence rates and DALYs. Furthermore, through decomposition analysis, we determined which factors significantly influence the change in incidence and DALYs and the extent of their contribution. In addition, this study quantified the disparities in the burden of idiopathic epilepsy across countries through cross-country social inequality analyses, and finally predicted the future burden of idiopathic epilepsy based on Bayesian Age-Period-Cohort Model (BAPC).

RESULTS

From 1990 to 2021, the incidence of idiopathic epilepsy increased generally, whereas DALY decreased. In terms of age and gender, the burden of idiopathic epilepsy is more severe in children and older age groups, with males bearing a higher burden than females. In terms of geographical distribution, the incidence was significantly higher in high Socio-Demographic Index (SDI) regions, while the burden of idiopathic epilepsy was heavier in low SDI areas. Decomposition analyses showed that the increase in incidence of idiopathic epilepsy and DALY in high SDI regions was mainly driven by epidemiological changes, whereas the increase in low SDI areas was more due to population growth. Cross-country social inequality analyses showed that despite improvements in the burden of idiopathic epilepsy, the burden and inequalities in low SDI countries remains significant. Projections indicated an increase in the incidence of idiopathic epilepsy globally, particularly in the 85 + age group, while global DALY was anticipated to continue declining.

CONCLUSIONS

Although global health is improving in line with population growth and age structure, the burden of idiopathic epilepsy remains significant. This study provides an important basis for prevention and care strategies for idiopathic epilepsy in different regions. Future work should focus on integrating idiopathic epilepsy into public health priorities, promoting effective measures, and narrowing treatment gaps.

摘要

背景

特发性癫痫是一种严重的神经系统疾病,可导致过早死亡和严重残疾。我们旨在评估特发性癫痫的全球负担,全面了解特发性癫痫的当前动态和趋势,并深入洞察其流行病学特征。

方法

本研究基于《2021年全球疾病负担研究》(GBD 2021),通过发病率和伤残调整生命年(DALY)评估特发性癫痫对全球、区域和国家的影响。在对全球发病率和伤残调整生命年进行统计汇总后,我们进行了平均百分比变化估计(EAPC)相关分析和Joinpoint回归分析,以进一步得出特发性癫痫发病率和伤残调整生命年的全球趋势。此外,通过分解分析,我们确定了哪些因素对发病率和伤残调整生命年的变化有显著影响及其贡献程度。此外,本研究通过跨国社会不平等分析量化了各国特发性癫痫负担的差异,最后基于贝叶斯年龄-时期-队列模型(BAPC)预测了特发性癫痫的未来负担。

结果

从1990年到2021年,特发性癫痫的发病率总体上升,而伤残调整生命年下降。在年龄和性别方面,特发性癫痫在儿童和老年人群中的负担更为严重,男性负担高于女性。在地理分布方面,社会人口指数(SDI)高的地区发病率显著更高,而SDI低的地区特发性癫痫负担更重。分解分析表明,SDI高的地区特发性癫痫发病率和伤残调整生命年的增加主要由流行病学变化驱动,而SDI低的地区增加更多是由于人口增长。跨国社会不平等分析表明,尽管特发性癫痫负担有所改善,但SDI低的国家的负担和不平等现象仍然显著。预测表明全球特发性癫痫发病率将上升,特别是在85岁以上年龄组,而全球伤残调整生命年预计将继续下降。

结论

尽管全球健康状况随着人口增长和年龄结构的变化而改善,但特发性癫痫的负担仍然很重。本研究为不同地区特发性癫痫的预防和护理策略提供了重要依据。未来的工作应侧重于将特发性癫痫纳入公共卫生优先事项,推广有效措施,并缩小治疗差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0da/12160428/2be4f4dc58f7/12962_2025_635_Fig1_HTML.jpg

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