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使用注射用GLP-1激动剂减肥加重偏瘫性偏头痛。

Hemiplegic Migraines Exacerbated using an Injectable GLP-1 Agonist for Weight Loss.

作者信息

Modestino Edward J, Bowirrat Abdalla, Lewandrowski Kai-Uwe, Sharafshah Alireza, Badgaiyan Rajendra D, Thanos Panayotis K, Baron David, Dennen Catherine A, Elman Igor, Sunder Keerthy, Murphy Kevin T, Blum Kenneth

机构信息

Department of Psychology, Curry College, Milton, MA, USA.

Department of Molecular Biology, Adelson School of Medicine, Ariel University, Ariel, Israel.

出版信息

Acta Sci Neurol. 2024 May;7(5):12-18. doi: 10.31080/asne.2024.07.0731. Epub 2024 Apr 19.

Abstract

The widespread adoption of Glucagon-like peptide-1 (GLP-1) receptor agonists for the treatment of obesity and diabetes has raised concerns about their potential adverse effects, including the induction of depression and suicide ideation. We report on a male patient in his early 50s with a complex medical history, including adult Attention-Deficit/Hyperactive Disorder, narcolepsy with cataplexy, and major depressive disorder in remission, who experienced exacerbated hemiplegic migraines after initiating treatment with an injectable GLP-1 agonist (Saxenda) for weight loss. Despite a previous history of experiencing hemiplegic migraines once or twice a year, the patient reported daily occurrences of migraines, many of which were hemiplegic, during the 60 days of GLP-1 agonist treatment. The migraines abated only upon discontinuation of the medication. This case underscores the need to carefully consider patient history and potential genetic predispositions when prescribing GLP-1 agonists, highlighting the complex interactions between these medications, existing comorbidities, and the dopaminergic and calcitonin gene-related peptide pathways. Our findings suggest that GLP-1 agonists, while beneficial for some, may pose significant risks for patients with specific genetic backgrounds or neurological conditions, calling for personalized approaches to treatment and increased awareness of potential adverse effects.

摘要

胰高血糖素样肽-1(GLP-1)受体激动剂在肥胖症和糖尿病治疗中的广泛应用引发了人们对其潜在不良反应的担忧,包括诱发抑郁症和自杀念头。我们报告了一名50岁出头的男性患者,他有复杂的病史,包括成人注意力缺陷多动障碍、发作性睡病伴猝倒以及处于缓解期的重度抑郁症,在开始使用注射用GLP-1激动剂(司美格鲁肽)减肥治疗后,偏瘫性偏头痛加剧。尽管该患者既往有每年发作一两次偏瘫性偏头痛的病史,但在GLP-1激动剂治疗的60天内,他报告每天都有偏头痛发作,其中许多是偏瘫性的。偏头痛仅在停药后才减轻。该病例强调了在开具GLP-1激动剂处方时仔细考虑患者病史和潜在遗传易感性的必要性,突出了这些药物、现有合并症以及多巴胺能和降钙素基因相关肽途径之间复杂的相互作用。我们的研究结果表明,GLP-1激动剂虽然对某些人有益,但可能对具有特定遗传背景或神经系统疾病的患者构成重大风险,这就需要个性化的治疗方法,并提高对潜在不良反应的认识。

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