Head and trunk stability during gait before and after levodopa intake in Parkinson's disease subtypes

被引:23
作者
Pelicioni, Paulo H. S. [1 ,2 ]
Brodie, Matthew A. [1 ]
Latt, Mark D. [3 ]
Menant, Jasmine C. [1 ,2 ]
Menz, Hylton B. [4 ]
Fung, Victor S. C. [5 ]
Lord, Stephen R. [1 ,2 ]
机构
[1] Neurosci Res Australia, Barker St, Sydney, NSW 2031, Australia
[2] Univ New South Wales, Sch Publ Hlth & Community & Med, Samuels Ave, Sydney, NSW 2033, Australia
[3] Royal Prince Alfred Hosp, Dept Aged Care, 50 Missenden Rd, Sydney, NSW 2050, Australia
[4] La Trobe Univ, Coll Sci Hlth & Engn, Sch Allied Hlth, Melbourne, Vic 1300, Australia
[5] Westmead Hosp, Dept Neurol, Hawkesbury Rd & Darcy Rd, Sydney, NSW 2145, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Parkinson's disease; Gait; Levodopa; Subtypes; ACCELERATION PATTERNS; POSTURAL INSTABILITY; PEOPLE; BALANCE; DYSFUNCTION; PROGRESSION; MEDICATION; DISORDERS; PHENOTYPE; COGNITION;
D O I
10.1016/j.exger.2018.06.031
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Introduction: People with Parkinson's disease (PD) can be classified into tremor dominant (TD) and postural instability and gait difficulty (PIGD) subtypes; the later group having more impaired gait and increased fall risk. While there is some evidence that anti-parkinsonian medication, levodopa, might not improve balance and gait control or reduce fall risk in the PIGD subtype, it is unclear whether the levodopa dosage intake affects gait stability. To address these issues, this study used accelerometry to compare gait stability: (i) during before and after levodopa intake between non-PIGD and PIGD subtypes; (ii) between individuals who took less or > 750 mg of levodopa/day. Methods: In 15 non-PIGD (Combination of 13 TD patients and 2 classified as indeterminate subtype) and 23 PIGD participants of similar mean (SD) age ((63.0 (7.6) versus 62.6 (10.0) years, respectively)) and disease-duration (8.9 (8.9) versus 11.3 (4.6) years, respectively), head and trunk stability during gait was examined using anteroposterior, vertical and mediolateral acceleration harmonic ratios (HRs). Participants were assessed before and after a levodopa dose, during typical "off" and "on" periods, respectively. Results: Two-way analyses of variance (group x medication status) revealed that compared to the non-PIGD subgroup, the PIGD subgroup showed significantly worse head stability (lower anteroposterior HR) in the "off" state, and significantly worse pelvis stability (significantly lower mediolateral and vertical HRs) in the "on" state (p < 0.05 for both). Levodopa was effective in treating most of the disease-related impairments (not bradykinesia) in both groups, (p < 0.05) but improved gait stability (lowered pelvis mediolateral and vertical HRs) only in people with the non-PIGD subtype (p < 0.05) and those taking < 750 mg of levodopa/day (p < 0.05). Conclusions: People with the PD PIGD subtype exhibit impaired gait stability that is not improved and frequently worsened by levodopa. New non-pharmaceutical approaches, technological (e.g. cueing) or exercise-based (e.g. balance training) are required to improve or compensate for mediolateral gait instability in this subtype and ultimately prevent falls.
引用
收藏
页码:78 / 85
页数:8
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