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加兰他敏对阿尔茨海默病患者认知功能的长期影响与模拟疾病轨迹的对比:一项临床环境中的观察性研究

Long-term effect of galantamine on cognitive function in patients with Alzheimer's disease versus a simulated disease trajectory: an observational study in the clinical setting.

作者信息

Nakagawa Ryoko, Ohnishi Takashi, Kobayashi Hisanori, Yamaoka Toshio, Yajima Tsutomu, Tanimura Ai, Kato Toshiya, Yoshizawa Kazutake

机构信息

Evidence Generation Department, Medical Affairs Division.

Clinical Data Management Department, R&D Division.

出版信息

Neuropsychiatr Dis Treat. 2017 Apr 19;13:1115-1124. doi: 10.2147/NDT.S133145. eCollection 2017.

Abstract

BACKGROUND

Long-term maintenance of cognitive function is an important goal of treatment for Alzheimer's disease (AD), but evidence about the long-term efficacy of cholinesterase inhibitors is sparse. To evaluate the long-term efficacy and safety of galantamine for AD in routine clinical practice, we conducted a 72-week post-marketing surveillance study. The effect of galantamine on cognitive function was estimated in comparison with a simulated disease trajectory.

PATIENTS AND METHODS

Patients with mild-to-moderate AD received flexible dosing of galantamine (16-24 mg/day) during this study. Cognitive function was assessed by the mini mental state examination (MMSE) and the clinical status was determined by the Clinical Global Impression-Improvement (CGI-I). Changes of the MMSE score without treatment were estimated in each patient using Mendiondo's model. Generalized linear mixed model analysis was performed to compare the simulated MMSE scores with the actual scores.

RESULTS

Of the 661 patients who were enrolled, 642 were evaluable for safety and 554 were assessed for efficacy. The discontinuation rate was 46.73%. Cognitive decline indicated by the mean change of actual MMSE scores was significantly smaller than the simulated decline. Individual analysis demonstrated that >70% of patients had better actual MMSE scores than their simulated scores. Significant improvement of CGI-I was also observed during the observation period. Adverse events occurred in 28.5% of patients and were serious in 8.41%. The reported events generally corresponded with the safety profile of galantamine in previous studies.

CONCLUSION

These findings support the long-term efficacy of galantamine for maintaining cognitive function and the clinical state in AD patients. Treatment with galantamine was generally safe. Importantly, this study revealed that galantamine improved cognitive function above the predicted level in >70% of the patients.

摘要

背景

认知功能的长期维持是阿尔茨海默病(AD)治疗的一个重要目标,但关于胆碱酯酶抑制剂长期疗效的证据稀少。为了评估加兰他敏在常规临床实践中治疗AD的长期疗效和安全性,我们开展了一项为期72周的上市后监测研究。将加兰他敏对认知功能的影响与模拟疾病轨迹进行比较来评估。

患者与方法

在本研究中,轻至中度AD患者接受灵活剂量的加兰他敏(16 - 24毫克/天)治疗。通过简易精神状态检查(MMSE)评估认知功能,通过临床总体印象改善量表(CGI - I)确定临床状态。使用门迪奥多模型估计每位患者未治疗时MMSE评分的变化。进行广义线性混合模型分析以比较模拟的MMSE评分与实际评分。

结果

在纳入的661例患者中,642例可进行安全性评估,554例进行了疗效评估。停药率为46.73%。实际MMSE评分的平均变化所表明的认知衰退明显小于模拟衰退。个体分析表明,超过70%的患者实际MMSE评分优于模拟评分。在观察期内还观察到CGI - I有显著改善。28.5%的患者发生了不良事件,严重不良事件发生率为8.41%。报告的事件总体上与加兰他敏在既往研究中的安全性特征相符。

结论

这些发现支持加兰他敏在维持AD患者认知功能和临床状态方面的长期疗效。加兰他敏治疗总体安全。重要的是,本研究显示超过70%的患者加兰他敏改善认知功能的程度高于预测水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42b2/5402999/3d4c02fac2ac/ndt-13-1115Fig1.jpg

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