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迟发性癫痫(LOE)与痴呆之间的双向关系:队列研究的系统评价和荟萃分析。

Bidirectional relationship between late-onset epilepsy (LOE) and dementia: A systematic review and meta-analysis of cohort studies.

机构信息

Department of Neurology, Hefei Hospital Affiliated to Anhui Medical University (The Second People's Hospital of Hefei), Hefei, Anhui 230011, China; The Fifth Clinical Medical College of Anhui Medical University, Hefei, Anhui 230032, China.

Department of Pharmacy, The Second People's Hospital of Hefei, Hefei, Anhui 230011, China.

出版信息

Epilepsy Behav. 2024 Apr;153:109723. doi: 10.1016/j.yebeh.2024.109723. Epub 2024 Mar 14.

Abstract

OBJECTIVE

To explore the bidirectional relationship of late-onset epilepsy (LOE) with dementia and Alzheimer's disease (AD).

METHODS

Using the common electronic databases, including PubMed, Cochrane Library databases and EMBASE, we systematically reviewed published cohort studies that assessed the risk of LOE in individuals comorbid with dementia or AD, and those with dementia or AD comorbid with LOE that had been published up to 31 March 2023. The data extraction process was carried out independently by two authors. The summary adjusted relative ratio (aRR) was calculated by employing Rev Man 5.3 for the inclusion of studies. To investigate the origins of heterogeneity, we conducted both subgroup and sensitivity analyses. In the presence of heterogeneity, a random-effects model was employed. To evaluate potential publication bias, we utilized the funnel plot and conducted Begg's and Egger's tests.

RESULTS

We included 20 eligible studies in the final analysis after a rigorous screening process. Pooled results indicated that LOE was association with an increased risk of all-cause dementia (aRR: 1.34, 95% confidence interval [CI]: 1.13-1.59) and AD (aRR: 2.49, 95% CI: 1.16-5.32). In addition, the pooled effect size for LOE associated with baseline AD and all-cause dementia were 3.51 (95% CI: 3.47-3.56) and 2.53 (95% CI: 2.39-2.67), respectively. Both sensitivity and subgroup analyses showed that these positive correlations persisted. According to the results of the Egger's and Begg's tests, as well as visual inspection of funnel plots, none of the studies appeared to be biased by publication.

CONCLUSION

The findings suggested that LOE is a potential risk factor for dementia and AD, and vice versa, dementia and AD are both potential risk indicators for LOE. Since there is substantial heterogeneity among the cohorts analyzed and more cohort studies should be conducted to confirm the correlations found in the current study.

摘要

目的

探讨迟发性癫痫(LOE)与痴呆和阿尔茨海默病(AD)之间的双向关系。

方法

使用常见的电子数据库,包括 PubMed、Cochrane Library 数据库和 EMBASE,我们系统地回顾了截至 2023 年 3 月 31 日发表的评估 LOE 风险的队列研究,这些研究评估了 LOE 与痴呆或 AD 共病患者以及痴呆或 AD 与 LOE 共病患者的风险。数据提取过程由两名作者独立进行。采用 RevMan 5.3 计算纳入研究的调整后的相对比值(aRR)。为了探讨异质性的来源,我们进行了亚组和敏感性分析。存在异质性时,采用随机效应模型。为了评估潜在的发表偏倚,我们使用漏斗图和 Begg 和 Egger 检验。

结果

经过严格筛选,我们最终纳入了 20 项符合条件的研究。汇总结果表明,LOE 与全因痴呆(aRR:1.34,95%置信区间[CI]:1.13-1.59)和 AD(aRR:2.49,95% CI:1.16-5.32)的风险增加相关。此外,LOE 与基线 AD 和全因痴呆相关的汇总效应大小分别为 3.51(95% CI:3.47-3.56)和 2.53(95% CI:2.39-2.67)。敏感性分析和亚组分析的结果均表明,这些正相关关系仍然存在。根据 Egger 和 Begg 检验的结果以及漏斗图的直观检查,没有研究显示受到发表偏倚的影响。

结论

研究结果表明,LOE 是痴呆和 AD 的潜在危险因素,反之亦然,痴呆和 AD 也是 LOE 的潜在危险因素。由于分析的队列之间存在大量异质性,需要进行更多的队列研究来证实当前研究中发现的相关性。

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