Sindhu Udeept, Sharma Akshay, Zawar Ifrah, Punia Vineet
Clinical Observer, Epilepsy Center, Cleveland Clinic, Cleveland, Ohio, USA.
Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Epilepsia Open. 2024 Dec;9(6):2528-2536. doi: 10.1002/epi4.13091. Epub 2024 Nov 2.
Newer glucose-lowering drugs (GLDs) protect against cerebrovascular, neurodegenerative, and neuroinflammatory pathologies. Therefore, we performed a meta-analysis of randomized controlled trials (RCTs) comparing newer GLDs to placebo that assessed long-term cardiovascular and renal outcomes to analyze their potential to prevent late-onset seizures and epilepsy, separately and as a combined outcome. A comprehensive MEDLINE and CENTRAL databases search for DPP-4 inhibitors, GLP-1 receptor agonists, and SGLT2 inhibitor RCTs, which reported adverse effects, including seizures and epilepsy on clinicaltrials.gov, yielded 413 studies. Of them, 27 studies with almost 200 000 patients (mean age 64.9 years, 65.6% males) were included. We calculated relative risk (RR) and odds ratio (OR) using the Mantel-Haenszel method and Peto's method. Patients taking newer GLDs had a 24% lower risk of late-onset seizures and epilepsy, combined, (RR: 0.76, 95% CI: 0.62-0.95) and 22% lower risk of late-onset seizures only (RR = 0.78; 95% CI = 0.60-1.00), compared to patients on placebo. This seizure and epilepsy prevention benefit was only noted among patients taking GLP-1 receptor agonists. Stroke incidence was comparable between newer GLDs and placebo group. GLP-1 receptor agonists like Semaglutide significantly reduce late-onset seizures and epilepsy, and their anti-epileptogenic potential in older adults needs further exploration. PLAIN LANGUAGE SUMMARY: Our analysis 27 clinical trials and nearly 200 000 patients evaluated the potential of newer glucose-lowering drugs (GLDs) to prevent late-onset seizures and epilepsy in older adults. The study found that newer GLDs, especially GLP-1 receptor agonists like Semaglutide, reduced the combined risk of seizures and epilepsy by 24% compared to placebo. These findings suggest that newer GLDs may offer prevention against the development of seizures and epilepsy in older adults. However, further research is needed to confirm their anti-epileptogenic effects.
新型降糖药物(GLDs)可预防脑血管、神经退行性和神经炎症性病变。因此,我们对随机对照试验(RCT)进行了荟萃分析,比较新型GLDs与安慰剂,评估长期心血管和肾脏结局,以分别分析其预防迟发性癫痫发作和癫痫的潜力,并将其作为综合结局进行分析。对MEDLINE和CENTRAL数据库进行全面检索,查找在clinicaltrials.gov上报告了包括癫痫发作和癫痫在内的不良反应的二肽基肽酶-4(DPP-4)抑制剂、胰高血糖素样肽-1(GLP-1)受体激动剂和钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂RCT,共获得413项研究。其中,纳入了27项研究,涉及近200000名患者(平均年龄64.9岁,男性占65.6%)。我们使用Mantel-Haenszel法和Peto法计算相对风险(RR)和比值比(OR)。与服用安慰剂的患者相比,服用新型GLDs的患者迟发性癫痫发作和癫痫的综合风险降低了24%(RR:0.76,95%置信区间:0.62-0.95),仅迟发性癫痫发作的风险降低了22%(RR = 0.78;95%置信区间 = 0.60-1.00)。这种癫痫发作和癫痫预防益处仅在服用GLP-1受体激动剂的患者中观察到。新型GLDs组和安慰剂组的中风发生率相当。司美格鲁肽等GLP-1受体激动剂可显著降低迟发性癫痫发作和癫痫的风险,其在老年人中的抗癫痫发生潜力有待进一步探索。
我们对27项临床试验和近200000名患者进行分析,评估了新型降糖药物(GLDs)预防老年人迟发性癫痫发作和癫痫的潜力。研究发现,与安慰剂相比,新型GLDs,尤其是司美格鲁肽等GLP-1受体激动剂,可使癫痫发作和癫痫的综合风险降低24%。这些发现表明,新型GLDs可能有助于预防老年人癫痫发作和癫痫的发生。然而,需要进一步研究来证实其抗癫痫发生作用。