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GLP-1 受体激动剂治疗与特发性颅内高压的显著体重减轻和有利头痛结局相关。

Treatment with GLP-1 receptor agonists is associated with significant weight loss and favorable headache outcomes in idiopathic intracranial hypertension.

机构信息

Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Comprehensive Center for Clinical Neurosciences, Medical University of Vienna, & Mental Health, Vienna, Austria.

出版信息

J Headache Pain. 2023 Jul 18;24(1):89. doi: 10.1186/s10194-023-01631-z.

DOI:10.1186/s10194-023-01631-z
PMID:37460968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10353241/
Abstract

BACKGROUND

In idiopathic intracranial hypertension (IIH), sustained weight loss is the main pillar in modifying disease course, whereby glucagon-like peptide-1 receptor agonists (GLP-1-RAs) could present an attractive treatment option.

METHODS

In this open-label, single-center, case-control pilot study, patients with IIH (pwIIH) and a body mass index (BMI) of ≥ 30 kg/m were offered to receive a GLP-1-RA (semaglutide, liraglutide) in addition to the usual care weight management (UCWM). Patients electing for UCWM only served as a control group matched for age-, sex- and BMI (1:2 ratio). The primary endpoint was the percentage weight loss at six months (M6) compared to baseline. Secondary endpoints included the rate of patients with a weight loss of ≥ 10%, monthly headache days (MHD), the rate of patients with a ≥ 30% and ≥ 50% reduction in MHD, visual outcome parameters, and adverse events (AEs).

RESULTS

We included 39 pwIIH (mean age 33.6 years [SD 8.0], 92.3% female, median BMI 36.3 kg/m [IQR 31.4-38.3]), with 13 patients being treated with GLP-1-RAs. At M6, mean weight loss was significantly higher in the GLP-1-RA group (-12.0% [3.3] vs. -2.8% [4.7]; p < 0.001). Accordingly, weight loss of ≥ 10% was more common in this group (69.2% vs. 4.0%; p < 0.001). Median reduction in MHD was significantly higher in the GLP-1-RA group (-4 [-10.5, 0.5] vs. 0 [-3, 1]; p = 0.02), and the 50% responder rate was 76.9% vs. 40.0% (p = 0.04). Visual outcome parameters did not change significantly from baseline to M6. Median reduction in acetazolamide dosage was significantly higher in the GLP-1-RA group (-16.5% [-50, 0] vs. 0% [-25, 50]; p = 0.04). AEs were mild or moderate and attributed to gastrointestinal symptoms in 9/13 patients. None of the AEs led to premature treatment discontinuation.

CONCLUSIONS

This open-label, single-center pilot study suggests that GLP-1-RAs are an effective and safe treatment option for achieving significant weight loss with a favorable effect on headache, leading to reduced acetazolamide dosage in pwIIH.

摘要

背景

在特发性颅内高压(IIH)中,持续减重是改变疾病进程的主要支柱,而胰高血糖素样肽-1 受体激动剂(GLP-1-RAs)可能是一种有吸引力的治疗选择。

方法

在这项开放标签、单中心、病例对照的初步研究中,患有 IIH(pwIIH)且体重指数(BMI)≥30 kg/m²的患者被提供 GLP-1-RA(司美格鲁肽、利拉鲁肽)联合常规体重管理(UCWM)。仅选择 UCWM 的患者作为年龄、性别和 BMI 匹配的对照组(1:2 比例)。主要终点是与基线相比,六个月时(M6)的体重减轻百分比。次要终点包括体重减轻≥10%的患者比例、每月头痛天数(MHD)、MHD 减少≥30%和≥50%的患者比例、视觉结果参数和不良事件(AE)。

结果

我们纳入了 39 名 pwIIH(平均年龄 33.6 岁[标准差 8.0],92.3%为女性,中位数 BMI 为 36.3 kg/m [IQR 31.4-38.3]),其中 13 名患者接受了 GLP-1-RA 治疗。在 M6 时,GLP-1-RA 组的平均体重减轻明显更高(-12.0%[3.3]与-2.8%[4.7];p<0.001)。因此,该组体重减轻≥10%的患者更为常见(69.2%与 4.0%;p<0.001)。GLP-1-RA 组 MHD 中位数降低更显著(-4[-10.5,0.5]与 0[-3,1];p=0.02),50%的应答率为 76.9%与 40.0%(p=0.04)。视觉结果参数从基线到 M6 没有显著变化。GLP-1-RA 组乙酰唑胺剂量中位数降低更显著(-16.5%[-50,0]与 0%[-25,50];p=0.04)。AE 为轻度或中度,归因于 13 名患者中的胃肠道症状。没有任何 AE 导致提前停药。

结论

这项开放标签、单中心的初步研究表明,GLP-1-RAs 是一种有效且安全的治疗选择,可实现显著的体重减轻,并对头痛有良好的影响,从而降低 pwIIH 的乙酰唑胺剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/87ce9f18fd0c/10194_2023_1631_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/1de8ceeae6fa/10194_2023_1631_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/88686e10e919/10194_2023_1631_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/c3b25f263b1c/10194_2023_1631_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/87ce9f18fd0c/10194_2023_1631_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/1de8ceeae6fa/10194_2023_1631_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/88686e10e919/10194_2023_1631_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/c3b25f263b1c/10194_2023_1631_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a1/10353241/87ce9f18fd0c/10194_2023_1631_Fig4_HTML.jpg

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