Abnormal involuntary movement scale in tardive dyskinesia: Minimal clinically important difference

Mov Disord. 2019 Aug;34(8):1203-1209. doi: 10.1002/mds.27769. Epub 2019 Jun 24.

Abstract

Background: A minimal clinically important difference has not been established for the Abnormal Involuntary Movement Scale in patients with tardive dyskinesia. Valbenazine is a vesicular monoamine transporter 2 inhibitor approved for the treatment of tardive dyskinesia in adults. Efficacy in randomized, double-blind, placebo-controlled trials was defined as the change from baseline in Abnormal Involuntary Movement Scale total score (sum of items 1-7).

Objectives: To estimate an minimal clinically important difference for the Abnormal Involuntary Movement Scale using valbenazine trial data and an anchor-based method.

Methods: Data were pooled from three 6-week double-blind, placebo-controlled trials: KINECT (NCT01688037), KINECT 2 (NCT01733121), and KINECT 3 (NCT02274558). Valbenazine doses were pooled for analyses as follows: "low dose," which includes 40 or 50 mg/day; and "high dose," which includes 75 or 80 mg/day. Mean changes from baseline in Abnormal Involuntary Movement Scale total score were analyzed in all participants (valbenazine- and placebo-treated) with a Clinical Global Impression of Change-Tardive Dyskinesia or Patient Global Impression of Change score of 1 (very much improved) to 3 (minimally improved).

Results: The least squares mean improvement from baseline to week 6 in Abnormal Involuntary Movement Scale total score was significantly greater with valbenazine (low dose: -2.4; high dose: -3.2; both, P < 0.001) versus placebo (-0.7). An minimal clinically important difference of 2 points was estimated based on least squares mean changes in Abnormal Involuntary Movement Scale total score in participants with a Clinical Global Impression of Change-Tardive Dyskinesia score ≤3 at week 6 (mean change: -2.2; median change: -2) or Patient Global Impression of Change score ≤3 at week 6 (mean change: -2.0; median change: -2).

Conclusions: Results from an anchor-based method indicate that a 2-point decrease in Abnormal Involuntary Movement Scale total score may be considered clinically important. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

Keywords: AIMS; MCID; clinical trial; tardive dyskinesia; valbenazine.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antipsychotic Agents / adverse effects
  • Female
  • Humans
  • Male
  • Middle Aged
  • Minimal Clinically Important Difference*
  • Mood Disorders / drug therapy
  • Psychotic Disorders / drug therapy
  • Schizophrenia / drug therapy
  • Tardive Dyskinesia / drug therapy*
  • Tardive Dyskinesia / etiology
  • Tardive Dyskinesia / physiopathology
  • Tetrabenazine / analogs & derivatives*
  • Tetrabenazine / therapeutic use
  • Treatment Outcome
  • Valine / analogs & derivatives*
  • Valine / therapeutic use
  • Vesicular Monoamine Transport Proteins / antagonists & inhibitors

Substances

  • Antipsychotic Agents
  • Vesicular Monoamine Transport Proteins
  • valbenazine
  • Valine
  • Tetrabenazine