加巴喷丁依卡倍特对中重度原发性不宁腿综合征成人国际不宁腿研究组评分量表单项及睡眠后问卷的影响:3项随机试验的汇总分析
Effect of Gabapentin Enacarbil on Individual Items of the International Restless Legs Study Group Rating Scale and Post-sleep Questionnaire in Adults with Moderate-to-Severe Primary Restless Legs Syndrome: Pooled Analysis of 3 Randomized Trials.
作者信息
Ahmed Mansoor, Hays Ryan, Steven Poceta J, Jaros Mark J, Kim Richard, Shang Gwendoline
机构信息
Cleveland Sleep Research Center, Middleburg Heights, Ohio.
University of Texas Southwestern Medical Center, Dallas, Texas.
出版信息
Clin Ther. 2016 Jul;38(7):1726-1737.e1. doi: 10.1016/j.clinthera.2016.05.008. Epub 2016 Jun 7.
PURPOSE
Few studies have investigated restless legs syndrome (RLS) treatment effects on individual International RLS Study Group Rating Scale (IRLS) items. We assessed the effects of gabapentin enacarbil (GEn) on individual IRLS items and their correlation with sleep disturbances in adults with moderate-to-severe primary RLS.
METHODS
Data were pooled from the randomized, double-blind, placebo-controlled, 12-week studies of XP052, XP053, and XP081 for adults who received GEn (600 or 1200 mg) or placebo once daily. Adults had primary RLS, IRLS total score ≥15, and RLS symptoms >15 days during the month before screening and for ≥4 of the 7 consecutive evenings at baseline. End points included mean change from baseline to week 12 in individual IRLS and post-sleep questionnaire (PSQ) items. For IRLS items, least squares mean treatment differences were calculated from a mixed model for repeated measures. For PSQ items, Cochran-Mantel-Haenszel row mean scores tests with integer scoring were used. Correlations between IRLS and PSQ items were assessed by Spearman's rank coefficients. Safety profile outcomes included treatment-emergent adverse events (TEAEs) and serious TEAEs.
FINDINGS
The modified intent-to-treat population included 671 patients (GEn 600 mg = 161; GEn 1200 mg = 266; placebo = 244). GEn significantly improved mean [SE] differences versus placebo for all IRLS items at week 12, including severity of sleep disturbance (GEn 600 mg, -0.4 [0.10]; GEn 1200 mg, -0.4 [0.09]), daytime tiredness (-0.4 [0.09]; -0.4 [0.08]), RLS severity (-0.4 [0.10]; -0.3 [0.08]), impact on daily affairs (-0.3 [0.07]; -0.3 [0.07]), and mood disturbance (-0.2 [0.07]; -0.3 [0.06]); all P<0.001). For PSQ items, significant (P<0.01) improvements occurred with both GEn doses versus placebo at week 12. The correlations between IRLS and PSQ items for change from baseline to week 12 were moderate to strong, and all correlations were significant (P<0.001). The most frequent TEAEs were somnolence (GEn 600 mg, 20%; GEn 1200 mg, 23%; placebo, 5%) and dizziness (GEn 600 mg, 14%; GEn 1200 mg, 22%; placebo, 5%).
IMPLICATIONS
GEn significantly improved individual IRLS items and sleep disturbance versus placebo. Correlations between IRLS and PSQ items were moderate to strong. This was not a formal meta-analysis and was not powered to compare the GEn doses. Nevertheless, our study finds that the benefits of GEn extend to individual IRLS items and supports the importance of sleep quality in RLS treatment. ClinicalTrials.gov identifiers: NCT00298623, NCT00365352, and NCT01332305.
目的
很少有研究调查不安腿综合征(RLS)治疗对国际RLS研究组评分量表(IRLS)各个项目的影响。我们评估了加巴喷丁依卡倍特(GEn)对中度至重度原发性RLS成人患者IRLS各个项目的影响及其与睡眠障碍的相关性。
方法
数据来自XP052、XP053和XP081的随机、双盲、安慰剂对照、为期12周的研究,研究对象为每日接受一次GEn(600或1200mg)或安慰剂的成人。成人患有原发性RLS,IRLS总分≥15,且在筛查前一个月内RLS症状出现>15天,且在基线时连续7个晚上中至少有4个晚上出现症状。终点包括从基线到第12周IRLS和睡眠后问卷(PSQ)各个项目的平均变化。对于IRLS项目,通过重复测量的混合模型计算最小二乘均数治疗差异。对于PSQ项目,使用具有整数评分的 Cochr an-Mantel-Haenszel行均数得分检验。通过Spearman等级系数评估IRLS和PSQ项目之间的相关性。安全性概况结果包括治疗中出现的不良事件(TEAE)和严重TEAE。
结果
改良意向性治疗人群包括671名患者(GEn 600mg组 = 161人;GEn 1200mg组 = 266人;安慰剂组 = 244人)。在第12周时,与安慰剂相比,GEn显著改善了所有IRLS项目的平均[标准误]差异,包括睡眠障碍严重程度(GEn 600mg组,-0.4[0.10];GEn 1200mg组,-0.4[0.09])、白天疲劳感(-0.4[0.09];-0.4[0.08])、RLS严重程度(-0.4[0.10];-0.3[0.08])、对日常事务的影响(-0.3[0.07];-0.3[0.07])和情绪障碍(-0.2[0.07];-0.3[0.06]);所有P<0.001)。对于PSQ项目,在第12周时,两种GEn剂量与安慰剂相比均有显著(P<0.01)改善。从基线到第12周的变化中,IRLS和PSQ项目之间的相关性为中度至高度,且所有相关性均显著(P<0.001)。最常见的TEAE是嗜睡(GEn 600mg组,20%;GEn 1200mg组,23%;安慰剂组,5%)和头晕(GEn 600mg组,14%;GEn 1200mg组,22%;安慰剂组,5%)。
结论
与安慰剂相比,GEn显著改善了IRLS各个项目和睡眠障碍。IRLS和PSQ项目之间的相关性为中度至高度。这不是一项正式的荟萃分析,也没有能力比较GEn的剂量。尽管如此,我们的研究发现GEn的益处扩展到了IRLS各个项目,并支持了睡眠质量在RLS治疗中的重要性。ClinicalTrials.gov标识符:NCT00298623、NCT00365352和NCT01332305。