Azzam Ahmed Y, Essibayi Muhammed Amir, Farkas Nathan, Azab Mohammed A, Morsy Mahmoud M, Elamin Osman, Elswedy Adam, Zomia Ahmed Saad Al, Alotaibi Hammam A, Alamoud Ahmed, Atallah Oday, Abukhadijah Hana J, Dmytriw Adam A, Baker Amanda, Khatri Deepak, Haranhalli Neil, Altschul David J
Montefiore-Einstein Cerebrovascular Research Lab, Albert Einstein College of Medicine, Bronx, NY, USA.
Department of Neurological Surgery, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
medRxiv. 2024 Nov 13:2024.11.12.24317193. doi: 10.1101/2024.11.12.24317193.
Idiopathic intracranial hypertension (IIH) is a neurological disorder characterized by elevated intracranial pressure, predominantly affecting obese women of reproductive age. While GLP-1 receptor agonists have shown promise in IIH management, the potential of dual GIP/GLP-1 receptor activation through tirzepatide remains unexplored. This study aimed to evaluate tirzepatide's efficacy as an adjunctive therapy in IIH management.
We conducted a retrospective cohort analysis using the TriNetX Global Health Research Network, analyzing data through November 2024. Through propensity score matching, we compared 193 tirzepatide-exposed IIH patients with 193 controls receiving standard care. Primary outcomes included papilledema severity, visual function, headache frequency, and treatment resistance, monitored at multiple follow-up timepoints.
Our analysis revealed significant improvements across all measured outcomes in the tirzepatide group. At 24 months, we observed a 68% reduction in papilledema risk (RR 0.320, 95% CI 0.189-0.542, p<0.001), a 73.9% reduction in visual disturbance and blindness risk (RR 0.261, 95% CI 0.143-0.477, p<0.001), and a 19.7% reduction in headache risk (RR 0.803, 95% CI 0.668-0.966, p=0.019). The tirzepatide group demonstrated significant body-mass index reductions, reaching -1.147 kg/m² (95% CI [-1.415, -0.879], p<0.001) at 24 months compared to controls.
Our results demonstrate that tirzepatide, when used as an adjunctive therapy, provides significant therapeutic benefits in IIH management, particularly in improving papilledema and visual outcomes. Our findings suggest that dual GIP/GLP-1 receptor activation may offer advantages over traditional single-receptor therapies, potentially through enhanced metabolic regulation and direct effects on intracranial pressure dynamics.
特发性颅内高压(IIH)是一种以颅内压升高为特征的神经系统疾病,主要影响育龄肥胖女性。虽然胰高血糖素样肽-1(GLP-1)受体激动剂在IIH治疗中已显示出前景,但通过替尔泊肽双重激活葡萄糖依赖性促胰岛素多肽(GIP)/GLP-1受体的潜力尚未得到探索。本研究旨在评估替尔泊肽作为IIH治疗辅助疗法的疗效。
我们使用TriNetX全球健康研究网络进行了一项回顾性队列分析,分析截至2024年11月的数据。通过倾向得分匹配,我们将193例接受替尔泊肽治疗的IIH患者与193例接受标准治疗的对照患者进行了比较。主要结局包括视乳头水肿严重程度、视觉功能、头痛频率和治疗抵抗,在多个随访时间点进行监测。
我们的分析显示,替尔泊肽组所有测量结局均有显著改善。在24个月时,我们观察到视乳头水肿风险降低68%(风险比[RR]0.320,95%置信区间[CI]0.189 - 0.542,p<0.001),视觉障碍和失明风险降低73.9%(RR 0.261,95% CI 0.143 - 0.477,p<0.001),头痛风险降低19.7%(RR 0.803,95% CI 0.668 - 0.966,p = 0.019)。与对照组相比,替尔泊肽组的体重指数显著降低,在24个月时达到-1.147kg/m²(95% CI [-1.415, -0.879],p<0.001)。
我们的结果表明,替尔泊肽作为辅助疗法在IIH治疗中具有显著的治疗益处,特别是在改善视乳头水肿和视觉结局方面。我们的研究结果表明,双重激活GIP/GLP-1受体可能比传统的单受体疗法具有优势,可能是通过增强代谢调节和对颅内压动态的直接作用。