Baylor Institute for Rehabilitation, Dallas, Texas 75246, USA.
Mov Disord. 2011 Feb 1;26(2):209-15. doi: 10.1002/mds.23426. Epub 2010 Oct 19.
Clinical trials demonstrate that onabotulinumtoxinA reduces upper limb post-stroke spasticity, with therapeutic response influenced by injected dose. Individual studies provide limited insight regarding muscle group-specific dose-response relationships. Our objective was to characterize dose-response relationships between onabotulinumtoxinA and muscle tone in specific upper limb muscles. Individual patient data from seven multicenter, randomized, double-blind, placebo-controlled trials were pooled. Of 544 post-stroke patients enrolled, 362 received onabotulinumtoxinA and 182 received placebo, injected into the flexor carpi radialis (FCR), flexor carpi ulnaris (FCU), flexor digitorum superficialis (FDS), flexor digitorum profundus (FDP), and/or biceps brachii (BB). Ashworth Scale score change at week 6 (AshworthCBL) was the primary outcome measure for muscle tone. For a broader analysis of response, AshworthCBL/onabotulinumtoxinA dosage relationships were characterized using three techniques: (1) AshworthCBL plotted as a function of onabotulinumtoxinA dose in Units (U) [dose-response curve]; (2) mean AshworthCBL per onabotulinumtoxinA dose depicting the responses seen with specific dose injection clusters/groups for each specific muscle group; and (3) onabotulinumtoxinA dose estimated to produce a mean 1-point decrease in AshworthCBL as an indicator of clinically meaningful benefit of treatment. Increasing onabotulinumtoxinA doses produced greater AshworthCBLs (muscle tone improvements). The maximal week 6 response (E(max)) model indicated a saturating dose-response relationship, with mean E(max) AshworthCBL values of -1.48, -1.48, -0.63, -0.77, and -0.61 in the FCR, FCU, FDS, FDP, and BB, respectively. OnabotulinumtoxinA doses estimated to produce a mean 1-point decrease in AshworthCBL were: 22.5U, 18.4U, 66.3U, 42.5U in the FCR, FCU, FDS, and FDP, respectively, and not determinable in the BB. These analyses demonstrate a saturating effect of greater muscle tone improvements with increasing onabotulinumtoxinA doses in post-stroke spasticity patients. These findings suggest potentially effective onabotulinumtoxinA doses in selected muscle groups in this study population.
临床试验表明,肉毒毒素 A 可降低上肢卒中后痉挛,治疗反应受注射剂量影响。个别研究提供了关于肌肉群特异性剂量反应关系的有限见解。我们的目标是描述肉毒毒素 A 与特定上肢肌肉中肌肉张力之间的剂量反应关系。对来自七个多中心、随机、双盲、安慰剂对照试验的 544 名卒中后患者的个体患者数据进行了汇总。在入组的 544 名卒中后患者中,362 名患者接受了肉毒毒素 A 治疗,182 名患者接受了安慰剂治疗,药物分别注射至桡侧腕屈肌(FCR)、尺侧腕屈肌(FCU)、指浅屈肌(FDS)、指深屈肌(FDP)和/或肱二头肌(BB)。6 周时 Ashworth 量表评分变化(AshworthCBL)是肌肉张力的主要疗效指标。为了更广泛地分析反应,采用三种技术描述了 AshworthCBL/肉毒毒素 A 剂量关系:(1)以单位(U)表示的 AshworthCBL 作为肉毒毒素 A 剂量的函数绘制(剂量反应曲线);(2)每单位肉毒毒素 A 剂量的平均 AshworthCBL,描绘了每个特定肌肉群特定剂量注射簇/组的反应;(3)肉毒毒素 A 剂量估计可使 AshworthCBL 平均降低 1 点,作为治疗有临床意义获益的指标。增加肉毒毒素 A 剂量可产生更大的 AshworthCBL(肌肉张力改善)。最大第 6 周反应(E(max))模型表明存在饱和剂量反应关系,FCR、FCU、FDS、FDP 和 BB 的平均 E(max)AshworthCBL 值分别为-1.48、-1.48、-0.63、-0.77 和-0.61。肉毒毒素 A 剂量估计可使 AshworthCBL 平均降低 1 点,分别为 22.5U、18.4U、66.3U 和 42.5U,而在 BB 中则无法确定。这些分析表明,在卒中后痉挛患者中,随着肉毒毒素 A 剂量的增加,肌肉张力的改善呈饱和效应。这些发现表明,在该研究人群中,某些肌肉群可能有效使用肉毒毒素 A 剂量。