Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1

Neuromuscul Disord. 2018 Nov;28(11):947-951. doi: 10.1016/j.nmd.2018.08.011. Epub 2018 Aug 31.

Abstract

We aimed to validate the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1 (DM1). Fifty patients with adult-onset, genetically confirmed DM1 were evaluated by Nine Hole Peg Test and re-evaluated at one week. Myotonia was not a limiting factor. The first test was compared with that performed by normal subjects (n = 28). Contextually, patients underwent handgrip and three-finger pinch assessments by handheld dynamometer. The Nine Hole Peg Test showed high intra-rater and inter-rater reliability in DM1 [ICC 0.86/0.83 for dominant and 0.90/0.88 for non-dominant hand, respectively]. Inverse correlation with handgrip and pinch strength values (r = -0.4; p < 0.01) and direct correlation with Muscular Impairment Rating Scale (r = 0.4; p < 0.01) were found for both DH and NDH. The test was able to differentiate severe DM1 patients, stratified by extent of muscle impairment, from mildly affected and normal controls, with a sensitivity of 97% and 95% for dominant hand and non-dominant hand, respectively (p < 0.0001). In conclusion, we showed that the Nine Hole Peg Test is a reliable, valid and sensitive test of dexterity in DM1, and that it can be considered as a candidate outcome measure to monitor natural history of disease and, possibly, therapeutic response in clinical trials.

Keywords: Dexterity; Myotonic Dystrophy type 1; Nine Hole Peg Test; Outcome measure; Quantitative muscle testing; Validation.

Publication types

  • Validation Study

MeSH terms

  • Adult
  • Aged
  • Female
  • Hand Strength / physiology*
  • Humans
  • Male
  • Middle Aged
  • Motor Skills / physiology*
  • Muscle Strength / physiology*
  • Muscle, Skeletal / physiopathology*
  • Myotonic Dystrophy / physiopathology*
  • Reproducibility of Results
  • Young Adult