Kapur Sachin, Vaughan Christina, Hawkins Jacob, Stebbins Glenn, Hall Deborah
Department of Neurological Sciences, Rush University, Department of Neurological Sciences, Chicago, IL.
Neurol Clin Pract. 2021 Dec;11(6):457-461. doi: 10.1212/CPJ.0000000000000958.
To determine whether varenicline is effective for the balance in Parkinson disease (PD).
This was an investigator-initiated, double-blind, placebo-controlled study. Participants with a clinical diagnosis of PD were randomized to receive varenicline or placebo for 8 weeks. After dose escalation, participants took 1 mg of drug twice daily until the end of the study. Patients with severe tremor were excluded. Primary outcome was a change on the Berg Balance Scale (BBS) from baseline to 8 weeks. The BBS is a 14-item measure consisting of basic balance tasks. The study had a secondary, exploratory outcome of a change in cognition, measured with the Frontal Assessment Battery (FAB) and the Mini-Mental State Exam (MMSE) from baseline to 8 weeks. The FAB is a 6-item measure of executive functioning.
Thirty-six participants were randomized (82% men, 100% White). Average age was 71.0 years (± 8.1). Average baseline motor Movement Disorder Society Unified Parkinson's Disease Rating Scale was 34.7 (± 11.6). There were no differences between treatment groups on the BBS (F[1,28] = 2.85, = 0.10) or FAB (d = 0.16, 95% confidence interval [CI] = [-1.39 to 1.53]) or MMSE (d = 0.81, 95% CI = [-0.40 to 1.40]).
The results did not suggest that varenicline had an effect on balance in patients with PD. Furthermore, varenicline did not seem to affect cognition. Perhaps, if an objective measure of balance had been used in place of the BBS, the analysis would show a difference between the groups. However, the authors do not recommend further study.
This study provides Class III evidence that in patients with PD with Hoehn and Yahr stages 2, 3, or 4, varenicline does not improve balance as assessed by the BBS.
确定伐尼克兰对帕金森病(PD)患者的平衡功能是否有效。
这是一项由研究者发起的、双盲、安慰剂对照研究。临床诊断为PD的参与者被随机分为接受伐尼克兰或安慰剂治疗8周。剂量递增后,参与者每日服用1毫克药物两次,直至研究结束。严重震颤患者被排除。主要结局是从基线到8周时伯格平衡量表(BBS)的变化。BBS是一项由14项基本平衡任务组成的测量指标。该研究的次要探索性结局是从基线到8周时用额叶评估量表(FAB)和简易精神状态检查表(MMSE)测量的认知变化。FAB是一项由6项组成的执行功能测量指标。
36名参与者被随机分组(82%为男性,100%为白人)。平均年龄为71.0岁(±8.1)。平均基线运动障碍协会统一帕金森病评定量表评分为34.7(±11.6)。治疗组在BBS(F[1,28]=2.85,P=0.10)、FAB(d=0.16,95%置信区间[CI]=[-1.39至1.53])或MMSE(d=0.81,95%CI=[-0.40至1.40])方面无差异。
结果未表明伐尼克兰对PD患者的平衡功能有影响。此外,伐尼克兰似乎也不影响认知功能。或许,如果使用客观的平衡测量指标代替BBS,分析可能会显示组间差异。然而,作者不建议进一步研究。
本研究提供了III类证据,即对于Hoehn和Yahr分期为2、3或4期的PD患者,伐尼克兰并不能改善BBS评估的平衡功能。