Non-arteritic anterior ischaemic optic neuropathy incidence in placebo-controlled clinical trials of liraglutide or semaglutide.

IF 3.5 2区 医学 Q1 OPHTHALMOLOGY
Tina Vilsbøll,Dikshit Arun Kumar,Lloyd Paul Aiello,Cecilia Rönnbäck,Michael Stellfeld,Lars Michael Larsen
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引用次数: 0

Abstract

BACKGROUND Risk of non-arteritic anterior ischaemic optic neuropathy (NAION) following exposure to glucagon-like peptide-1 receptor agonists (GLP-1RAs) in people with type 2 diabetes and/or obesity remains unclear. The aim of this study was to investigate NAION incidence across randomised placebo-controlled trials evaluating the GLP-1RAs liraglutide and semaglutide. METHODS Pooled safety evaluation of NAION incidence from completed phase II, III and IV randomised placebo-controlled trials that evaluated the six Novo Nordisk-manufactured GLP-1RA products (active ingredients: liraglutide and semaglutide) in people with type 2 diabetes and/or overweight/obesity. Potential NAION cases were identified and categorised based on the likelihood of NAION occurrence (definite, probable, unlikely or not assessable). Definite or probable NAION cases were considered confirmed. RESULTS This pooled analysis included 96 829 participants (GLP-1RA-treated: n=64 917; placebo-treated: n=31 912) with 205 777 participant-years of observation (PYO) (GLP-1RA-treated: 119 393 PYO; placebo-treated: 86 384 PYO). Across all trials, three confirmed NAION cases were identified in three GLP-1RA-treated participants and five confirmed cases were identified in four placebo-treated participants. In GLP-1RA-treated participants, the incidence of confirmed NAION cases was approximately three cases per 100 000 PYO, while in placebo-treated participants, the incidence was approximately six cases per 100 000 PYO. All ophthalmologist-confirmed cases reported one or more associated risk factors (eg, age >50 years, obesity, smoking, dyslipidaemia, hypertension). CONCLUSION Data from randomised placebo-controlled trials with semaglutide and liraglutide do not show an increased incidence of NAION in participants receiving GLP-1RA treatment versus those receiving placebo and, thus, do not suggest a relationship between GLP-1RA use and NAION. SUMMARY Based on data from randomised placebo-controlled trials, exposure to the glucagon-like peptide-1 receptor agonists (GLP-1RA) semaglutide and liraglutide was not associated with an increased incidence of non-arteritic anterior ischaemic optic neuropathy (NAION) relative to placebo.
利拉鲁肽或半马鲁肽安慰剂对照临床试验中的非动脉性前缺血性视神经病变发生率。
背景:2型糖尿病和/或肥胖患者暴露于胰高血糖素样肽-1受体激动剂(GLP-1RAs)后发生非动脉性前缺血性视神经病变(NAION)的风险尚不清楚。本研究的目的是在评估GLP-1RAs利拉鲁肽和semaglutide的随机安慰剂对照试验中调查NAION的发生率。方法:已完成的II期、III期和IV期随机安慰剂对照试验评估了6种诺和诺德生产的GLP-1RA产品(有效成分:利拉鲁肽和西马鲁肽)在2型糖尿病和/或超重/肥胖患者中的发生率。根据NAION发生的可能性(确定、可能、不太可能或不可评估)对潜在的NAION病例进行识别和分类。确定或可能的国家感染病例被认为是确诊的。结果该合并分析包括96 829名参与者(glp - 1ra治疗组:n=64 917;安慰剂治疗组:n=31 912),有205 777参与者年的观察(PYO) (glp - 1ra治疗组:119 393 PYO;安慰剂治疗组:86 384 PYO)。在所有试验中,3名glp - 1ra治疗的参与者中发现了3例确诊的NAION病例,4名安慰剂治疗的参与者中发现了5例确诊病例。在glp - 1ra治疗的参与者中,确诊的NAION病例的发生率约为每10万PYO 3例,而在安慰剂治疗的参与者中,发生率约为每10万PYO 6例。所有眼科确诊病例均报告了一个或多个相关危险因素(例如,年龄50 - 50岁、肥胖、吸烟、血脂异常、高血压)。结论:来自西马鲁肽和利拉鲁肽随机对照试验的数据显示,接受GLP-1RA治疗的受试者与接受安慰剂的受试者相比,NAION的发生率没有增加,因此,不表明GLP-1RA的使用与NAION之间存在关系。基于随机安慰剂对照试验的数据,与安慰剂相比,暴露于胰高血糖素样肽-1受体激动剂(GLP-1RA) semaglutide和liraglutide与非动脉性前缺血性视神经病变(NAION)发生率增加无关。
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来源期刊
CiteScore
10.30
自引率
2.40%
发文量
213
审稿时长
3-6 weeks
期刊介绍: The British Journal of Ophthalmology (BJO) is an international peer-reviewed journal for ophthalmologists and visual science specialists. BJO publishes clinical investigations, clinical observations, and clinically relevant laboratory investigations related to ophthalmology. It also provides major reviews and also publishes manuscripts covering regional issues in a global context.
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