TY - JOUR
T1 - Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation
AU - Hocking, Darren R.
AU - Birch, Rachael C.
AU - Bui, Quang M.
AU - Menant, Jasmine C.
AU - Lord, Stephen R.
AU - Georgiou-Karistianis, Nellie
AU - Godler, David E.
AU - Wen, Wei
AU - Hackett, Anna
AU - Rogers, Carolyn
AU - Trollor, Julian N.
PY - 2017/2
Y1 - 2017/2
N2 - Recent evidence indicates that adults with a premutation (PM: 55–199 CGG repeats) expansion in the fragile X mental retardation 1 (FMR1) gene show postural control deficits that may reflect disruption to cerebellar motor regions. Less is known about the influence of reduced cerebellar volume and structural changes, and increase in CGG repeat and FMR1 mRNA levels on the attentional demands of step initiation in PM males. We investigated the effects of a concurrent cognitive task on choice stepping reaction time (CSRT) and explored the associations between CSRT performance, cerebellar volume, CGG size, and FMR1 mRNA levels in blood in PM males. We examined 19 PM males (ages 28–75) and 23 matched controls (CGG <44; ages 26–77), who performed a verbal fluency task during CSRT performance and single-task stepping without a secondary cognitive task. Our results provide preliminary evidence that smaller cerebellar volume (β = −2.73, p = 0.002) and increasing CGG repeat length (β = 1.69, p = 0.003) were associated with greater dual-task step initiation times in PM males, but not in controls. There was evidence of a mediating effect of cerebellar volume on the relationship between FMR1 mRNA levels and single-task CSRT performance in PM males (estimate coefficient = 8.69, standard error = 4.42, p = 0.049). These findings suggest increasing CGG repeat and FMR1 mRNA levels have neurotoxic effects on cerebellar regions underlying anticipatory postural responses during stepping. Cerebellar postural changes may be predictive of the increased risk of falls in older PM males.
AB - Recent evidence indicates that adults with a premutation (PM: 55–199 CGG repeats) expansion in the fragile X mental retardation 1 (FMR1) gene show postural control deficits that may reflect disruption to cerebellar motor regions. Less is known about the influence of reduced cerebellar volume and structural changes, and increase in CGG repeat and FMR1 mRNA levels on the attentional demands of step initiation in PM males. We investigated the effects of a concurrent cognitive task on choice stepping reaction time (CSRT) and explored the associations between CSRT performance, cerebellar volume, CGG size, and FMR1 mRNA levels in blood in PM males. We examined 19 PM males (ages 28–75) and 23 matched controls (CGG <44; ages 26–77), who performed a verbal fluency task during CSRT performance and single-task stepping without a secondary cognitive task. Our results provide preliminary evidence that smaller cerebellar volume (β = −2.73, p = 0.002) and increasing CGG repeat length (β = 1.69, p = 0.003) were associated with greater dual-task step initiation times in PM males, but not in controls. There was evidence of a mediating effect of cerebellar volume on the relationship between FMR1 mRNA levels and single-task CSRT performance in PM males (estimate coefficient = 8.69, standard error = 4.42, p = 0.049). These findings suggest increasing CGG repeat and FMR1 mRNA levels have neurotoxic effects on cerebellar regions underlying anticipatory postural responses during stepping. Cerebellar postural changes may be predictive of the increased risk of falls in older PM males.
KW - cerebellar motor networks
KW - choice stepping reaction time
KW - cognitive-motor interference
KW - FMR1 premutation carrier
KW - fragile X mental retardation gene 1 (FMR1)
KW - motor symptoms
KW - postural balance
KW - step initiation
UR - http://www.scopus.com/inward/record.url?scp=84994521865&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2016.10.017
DO - 10.1016/j.neurobiolaging.2016.10.017
M3 - Article
C2 - 27837676
AN - SCOPUS:84994521865
SN - 0197-4580
VL - 50
SP - 5
EP - 12
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -