Actigraphy Detects Greater Intra-Individual Variability During Gait in Non-Manifesting LRRK2 Mutation Carriers

被引:8
|
作者
van den Heuvel, Lieneke [1 ,2 ,7 ]
Lim, Andrew S. [2 ]
Visanji, Naomi P. [1 ,2 ]
Huang, Jana [1 ,2 ]
Ghate, Taneera [1 ,2 ]
Mestre, Tiago A. [3 ]
AlDakheel, Amaal [1 ,2 ]
Connolly, Barbara S. [1 ,2 ]
Gasca-Salas, Carmen [1 ,2 ]
Kern, Drew S. [4 ]
Jain, Jennifer [1 ,2 ]
Slow, Elizabeth J. [1 ,2 ]
Pondal, Margarita [1 ,2 ]
Faust-Socher, Achinoam [1 ,2 ]
Rogaeva, Ekaterina [5 ]
Tomlinson, George [6 ]
Lang, Anthony E. [1 ,2 ]
Marras, Connie [1 ,2 ,8 ]
机构
[1] Univ Toronto, Toronto Western Hosp, Morton & Gloria Shulman Movement Disorders Ctr, Toronto, ON, Canada
[2] Univ Toronto, Div Neurol, Sunnybrook Hlth Sci Ctr, Dept Med, Toronto, ON, Canada
[3] Ottawa Hosp Res Inst, Ottawa Brain & Mind Res Inst, Div Neurol, Dept Med,Parkinsons Dis & Movement Disorders Ctr, Ottawa, ON, Canada
[4] Univ Colorado, Movement Disorders Ctr, Dept Neurol, Anschutz Med Campus, Aurora, CO USA
[5] Univ Toronto, Tanz Ctr Res Neurodegenerat Dis, Toronto, ON, Canada
[6] Univ Toronto, Univ Hlth Network, Dept Med, Mt Sinai Hosp, Toronto, ON, Canada
[7] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[8] Hosp Madrid, HM Puerta Sur, CINAC, Madrid, Spain
关键词
Actigraphy; high risk Parkinson; LRRK2; mutation; non-manifesting LRRK2 carrier; Parkinson's disease; variability of gait; ARM SWING ASYMMETRY; PARKINSONS-DISEASE; G2019S MUTATION; PENETRANCE; PHENOTYPE; SYMPTOMS;
D O I
10.3233/JPD-171151
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: With recent advances in the search for disease-modifying therapies for Parkinson's disease (PD) the importance of identifying prodromal markers becomes greater. Non-manifesting LRRK2 mutation carriers (NMC) are at risk for developing PD, and provide a population in which to identify possible markers. Objective: The aim of this study was to test the hypothesis that NMC have differences in daily activity, fragmentation of sleep, arm swing asymmetry, and movement variability during walking, detectable by actigraphy, as compared to matched control subjects. Methods: Eleven NMC, fourteen PD patients (4 LRRK2-PD, 10 idiopathic PD (iPD)), and twenty-nine controls wore wristbands containing an accelerometer for seven days, and performed a daily walking task. Outcome measures included daily activity, fragmentation of activity, fragmentation of sleep, arm swing asymmetry during walking, and intra-individual variability. Results: Compared to healthy controls, both NMC and LRRK2/iPD showed higher intra-individual variability in activity during walking compared to healthy controls. Individuals with LRRK2-PD/iPD, but not NMC, tend to have lower activity levels, more arm swing asymmetry and less increase of arm swing with transition from slow to faster walking speed compared to healthy controls. Conclusion: Higher intra-individual variability of gait-associated movements might be a useful biomarker of prodromal PD. These results encourage replication in a larger sample and longitudinal analysis is warranted.
引用
收藏
页码:131 / 139
页数:9
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