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利拉鲁肽与胰腺炎之间是否存在关联?对已完成的利拉鲁肽 2 型糖尿病临床试验的汇总和患者水平数据进行的事后回顾。

Is there a link between liraglutide and pancreatitis? A post hoc review of pooled and patient-level data from completed liraglutide type 2 diabetes clinical trials.

机构信息

UK Medical Affairs, Novo Nordisk Ltd., Gatwick, U.K.

Global Safety, Novo Nordisk A/S, Bagsværd, Copenhagen, Denmark.

出版信息

Diabetes Care. 2015 Jun;38(6):1058-66. doi: 10.2337/dc13-1210. Epub 2014 Dec 12.

DOI:10.2337/dc13-1210
PMID:25504028
Abstract

OBJECTIVE

To report the incidence of pancreatitis in type 2 diabetes trials of liraglutide and details of all pancreatitis cases.

RESEARCH DESIGN AND METHODS

Data from Novo Nordisk-sponsored trials with liraglutide (phase 2 and 3; NN2211 identifiers) completed by 19 April 2013 were pooled. All pancreatitis cases were reviewed.

RESULTS

Total exposure to liraglutide and active comparators was 5,021 and 1,354 patient-years, respectively (n = 6,345 and 1,846, respectively). Eight cases of acute pancreatitis (AP) with liraglutide and one with any comparator (glimepiride) were found. The incidence of AP was 1.6 cases/1,000 patient-years exposure (PYE) for liraglutide vs. 0.7 cases/1,000 PYE for total active comparators. One of the eight AP cases reported with liraglutide did not meet diagnostic criteria for AP. In six of these eight cases, recognized risk factors for AP were present and/or the onset of AP occurred >6 months after liraglutide initiation. All patients were receiving multiple medications. Four cases of chronic pancreatitis (CP) with liraglutide and none with comparators were found. One of these four cases fulfilled diagnostic criteria for CP; these criteria were not met or information was missing in the remaining three.

CONCLUSIONS

Based on the small number of cases observed, the incidences of reported AP and CP were numerically greater with liraglutide than with comparators. Not all cases fulfilled diagnostic criteria, and confounding variables were present in 75% of the AP cases with liraglutide therapy, precluding firm conclusions.

摘要

目的

报告利拉鲁肽治疗 2 型糖尿病试验中胰腺炎的发生率和所有胰腺炎病例的详细信息。

研究设计和方法

汇总了截至 2013 年 4 月 19 日由诺和诺德赞助的利拉鲁肽(2 期和 3 期;NN2211 标识符)试验的数据。对所有胰腺炎病例进行了回顾。

结果

利拉鲁肽和活性对照药物的总暴露量分别为 5021 和 1354 患者年(n=6345 和 1846,分别)。发现利拉鲁肽 8 例(1.6 例/1000 患者年暴露量)和任何对照药物(格列美脲)1 例(0.7 例/1000 患者年暴露量)发生急性胰腺炎(AP)。在这 8 例利拉鲁肽报告的 AP 病例中,有 1 例不符合 AP 的诊断标准。在这 8 例病例中,有 6 例存在 AP 的已知危险因素,并且/或者利拉鲁肽治疗后 6 个月以上发生了 AP。所有患者均接受了多种药物治疗。发现利拉鲁肽 4 例(0.6 例/1000 患者年暴露量)和对照药物无慢性胰腺炎(CP)病例。其中 1 例符合 CP 的诊断标准;其余 3 例未满足或信息缺失。

结论

基于观察到的少量病例,与对照药物相比,利拉鲁肽治疗报告的 AP 和 CP 的发生率在数值上更高。并非所有病例均符合诊断标准,并且在 75%的利拉鲁肽治疗的 AP 病例中存在混杂因素,无法得出明确的结论。

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