Age and CGG-repeat length are associated with neuromotor impairments in at-risk females with the FMR1 premutation

Neurobiol Aging. 2014 Sep;35(9):2179.e7-13. doi: 10.1016/j.neurobiolaging.2014.03.018. Epub 2014 Mar 20.

Abstract

Recent studies report a higher risk of dementia and motor symptoms in females with the fragile X mental retardation 1 premutation (PM-carriers) than has hitherto been appreciated. Here, we use dual-task gait paradigms to identify potential markers of cognitive and motor decline in female PM-carriers. Spatiotemporal gait characteristics and variability of gait were assessed during single- and dual-task conditions in 28 female PM-carriers (mean age 41.32 ± 8.03 years) and 31 female controls with normal fragile X mental retardation 1 alleles (mean age 41.61 ± 8.30 years). Despite comparable gait characteristics at baseline, gait performance was significantly poorer for PM-carriers when performing concurrent working memory tasks (counting backwards by 3's or 7's) when compared with controls. Correlational analyses showed that low working memory capacity was significantly associated with dual-task interference for the gait domains of pace (speed, step length) and variability (step time, swing time) in PM-carriers. Multiple regression analyses further showed that the interaction between age and CGG repeat length was strongly predictive of gait variability during dual-task performance. These findings indicate for the first time that vulnerability in specific domains of gait control may act as sensitive surrogate markers of future decline in female PM-carriers.

Keywords: Alzheimer's disease; Cerebellar motor networks; Cognitive-motor interference; Dual-task paradigm; Fragile X mental retardation gene 1 (FMR1); Fragile X mental retardation protein (FMRP); Fragile X syndrome; Fragile X tremor ataxia syndrome (FXTAS); Gait variability; Working memory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aging*
  • Female
  • Fragile X Mental Retardation Protein / genetics*
  • Gait
  • Genetic Association Studies*
  • Heterozygote
  • Humans
  • Memory, Short-Term
  • Middle Aged
  • Mutation*
  • Psychomotor Disorders / genetics*
  • Psychomotor Disorders / physiopathology
  • Psychomotor Disorders / psychology
  • Psychomotor Performance
  • Regression Analysis
  • Risk
  • Trinucleotide Repeats*

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein