Facial memory deficits in myotonic dystrophy type 1

Acta Neurol Scand. 2014 Nov;130(5):312-8. doi: 10.1111/ane.12228. Epub 2014 Feb 15.

Abstract

Objectives: To evaluate facial memory ability (FMA) in patients with myotonic dystrophy type 1 (DM1). We also explored the relationship between FMA and neuropsychological data, disease-related factors, and CTG repeat expansion size.

Materials and methods: Patients with DM1 (n = 33) and healthy subjects (n = 30) were tested with the faces task of the Rivermead Behavioural Memory Test - Extended version (RBMT-E) and an additional set of neuropsychological tests. Clinical data were collected, and CTG repeat size was quantified in blood lymphocytes.

Results: Low results on the faces task were more common in patients with DM1 compared with healthy subjects (P < 0.05), with 36% of the patients showing a poor/impaired performance. DM1 patients with deficits in FMA performed significantly worse on tests measuring visual-construction ability and memory. Furthermore, these patients more often falsely recognised unknown faces as known. Deficits in FMA were not associated with any disease-related factor, including CTG repeat expansion size.

Conclusions: These findings revealed deficits in FMA in the DM1 group, which was associated with reduced construction- and visual memory ability.

Keywords: CTG repeats; cognition; facial memory; myotonic dystrophy type 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Humans
  • Male
  • Memory Disorders / etiology*
  • Middle Aged
  • Myotonic Dystrophy / genetics
  • Myotonic Dystrophy / psychology*
  • Neuropsychological Tests
  • Trinucleotide Repeat Expansion