艾洛比司他治疗帕金森病合并慢性便秘的疗效和安全性:CONST-PD 研究。
Efficacy and Safety of Elobixibat in Parkinson's Disease with Chronic Constipation: CONST-PD Study.
机构信息
Department of Neurology, Juntendo University Faculty of Medicine, Tokyo, Japan.
Department of Neurology, Juntendo Nerima Hospital, Tokyo, Japan.
出版信息
Mov Disord Clin Pract. 2024 Apr;11(4):352-362. doi: 10.1002/mdc3.13972. Epub 2024 Jan 24.
BACKGROUND
Chronic constipation is a common digestive complication of Parkinson's disease (PD).
OBJECTIVES
To verify the usefulness of elobixibat, an ileal bile acid transporter inhibitor, for chronic constipation in PD.
METHODS
This double-blind, placebo-controlled study consisted of a 2-week observation/washout period and a 4-week treatment period. All patients received a Bowel Movement Diary at Week -2 and were allocated to elobixibat (10 mg) or placebo at Week 0. Patients visited at Weeks 2 and 4 to report daily spontaneous bowel movements (SBM), stool form, drug use, quality of life (QOL), and safety. Changes in these parameters were assessed.
RESULTS
The study included 38 patients in the elobixibat group and 39 in the placebo group, and 37 each completed the study. SBM frequency/week (mean ± standard deviation) increased significantly from 4.2 ± 2.6 at baseline to 5.9 ± 3.2 at Week 4 in the elobixibat group (P = 0.0079), but not in the placebo group (4.5 ± 2.7 to 5.3 ± 3.5; P = 0.0889). On analysis of covariance, the between-group difference in frequency changes at Week 4 (primary endpoint) was not significant after adjustment by baseline and sex (point estimate = 0.8; 95% confidence interval = -0.57 to 2.09, P = 0.2601), although a significant difference (P = 0.0011) was evidenced at Week 1 by a similar analysis. Stool form and scores of satisfaction and stigma were improved by elobixibat. Adverse events were as previously reported.
CONCLUSIONS
Elobixibat improved the SBM frequency, though the defined primary endpoint was not evidenced. QOL parameters (stool consistency and treatment satisfaction) were also improved. Elobixibat may have therapeutic benefits in PD patients suffering from chronic constipation.
TRIAL REGISTRATION INFORMATION
Trial Registration Number: JPRN-jRCTs031200172 (submitted: October 26, 2020; first patient enrolment: December 23, 2020; https://jrct.niph.go.jp/en-latest-detail/jRCTs031200172).
背景
慢性便秘是帕金森病(PD)的一种常见消化道并发症。
目的
验证回肠胆汁酸转运体抑制剂依洛昔巴特治疗 PD 慢性便秘的有效性。
方法
这是一项为期 2 周的观察/洗脱期和 4 周治疗期的双盲、安慰剂对照研究。所有患者在 -2 周时均接受了排便日记,并在 0 周时被分配接受依洛昔巴特(10mg)或安慰剂。患者在第 2 周和第 4 周就诊时报告每日自发性排便(SBM)、粪便形态、药物使用、生活质量(QOL)和安全性。评估这些参数的变化。
结果
该研究纳入了 38 例依洛昔巴特组和 39 例安慰剂组患者,每组各有 37 例患者完成了研究。依洛昔巴特组每周 SBM 频率(均值±标准差)从基线时的 4.2±2.6 显著增加到第 4 周时的 5.9±3.2(P=0.0079),而安慰剂组则无显著变化(4.5±2.7 至 5.3±3.5;P=0.0889)。在协方差分析中,调整基线和性别后,第 4 周(主要终点)组间频率变化的差异无统计学意义(点估计值=0.8;95%置信区间=0.57 至 2.09,P=0.2601),尽管在第 1 周时通过类似分析证明存在显著差异(P=0.0011)。依洛昔巴特改善了粪便形态和满意度和耻辱感评分。不良反应与之前报道的相似。
结论
依洛昔巴特改善了 SBM 频率,但未达到既定的主要终点。QOL 参数(粪便一致性和治疗满意度)也得到了改善。依洛昔巴特可能对患有慢性便秘的 PD 患者具有治疗益处。
试验注册信息
试验注册号:JPRN-jRCTs031200172(提交日期:2020 年 10 月 26 日;首例患者入组日期:2020 年 12 月 23 日;https://jrct.niph.go.jp/en-latest-detail/jRCTs031200172)。