Program in Physical Therapy, Washington University in St, Louis, Campus Box 8502, 4444 Forest Park Blvd, Stb Louis, MO 63108, USA.
Orphanet J Rare Dis. 2012 Dec 8;7:92. doi: 10.1186/1750-1172-7-92.
Classically characterized by early onset insulin-dependent diabetes mellitus, optic atrophy, deafness, diabetes insipidus, and neurological abnormalities, Wolfram syndrome (WFS) is also associated with atypical brainstem and cerebellar findings in the first decade of life. As such, we hypothesized that gait differences between individuals with WFS and typically developing (TD) individuals may be detectable across the course of the disease.
Gait was assessed for 13 individuals with WFS (min 6.4 yrs, max 25.8 yrs) and 29 age-matched, typically developing individuals (min 5.6 yrs, max 28.5 yrs) using a GAITRite ® walkway system. Velocity, cadence, step length, base of support and double support time were compared between groups.
Across all tasks, individuals with WFS walked slower (p = 0.03), took shorter (p ≤ 0.001) and wider (p ≤ 0.001) steps and spent a greater proportion of the gait cycle in double support (p = 0.03) compared to TD individuals. Cadence did not differ between groups (p = 0.62). Across all tasks, age was significantly correlated with cadence and double support time in the TD group but only double support time was correlated with age in the WFS group and only during preferred pace forward (rs = 0.564, p = 0.045) and dual task forward walking (rs = 0.720, p = 0.006) tasks. Individuals with WFS also had a greater number of missteps during tandem walking (p ≤ 0.001). Within the WFS group, spatiotemporal measures of gait did not correlate with measures of visual acuity. Balance measures negatively correlated with normalized gait velocity during fast forward walking (rs = -0.59, p = 0.03) and percent of gait cycle in double support during backward walking (rs = -0.64, p = 0.03).
Quantifiable gait impairments can be detected in individuals with WFS earlier than previous clinical observations suggested. These impairments are not fully accounted for by the visual or balance deficits associated with WFS, and may be a reflection of early cerebellar and/or brainstem abnormalities. Effective patient-centered treatment paradigms could benefit from a more complete understanding of the progression of motor and other neurological symptom presentation in individuals with WFS.
Wolfram 综合征(WFS)的特征为发病早、需依赖胰岛素的糖尿病、视神经萎缩、耳聋、尿崩症和神经异常,也与儿童早期的非典型脑干和小脑异常有关。因此,我们假设 WFS 患者和典型发育(TD)个体之间的步态差异可能在疾病过程中是可检测到的。
使用 GAITRite ® 步态分析系统评估了 13 名 WFS 患者(最小年龄 6.4 岁,最大年龄 25.8 岁)和 29 名年龄匹配的 TD 个体(最小年龄 5.6 岁,最大年龄 28.5 岁)的步态。比较两组之间的速度、步频、步长、支撑基础和双支撑时间。
在所有任务中,WFS 患者的行走速度较慢(p = 0.03),步长较短(p ≤ 0.001)且较宽(p ≤ 0.001),双支撑时间占步态周期的比例较大(p = 0.03)与 TD 个体相比。两组之间的步频没有差异(p = 0.62)。在所有任务中,年龄与 TD 组的步频和双支撑时间显著相关,但仅在 WFS 组中,仅在双支撑时间与年龄相关,且仅在自由步态时(rs = 0.564,p = 0.045)和双重任务前进行走(rs = 0.720,p = 0.006)任务。WFS 患者在并足行走时也有更多的错误步(p ≤ 0.001)。在 WFS 组中,步态的时空测量与视力测量值不相关。平衡测量值与快速前进行走时的归一化步态速度(rs = -0.59,p = 0.03)和后退行走时双支撑时间的百分比(rs = -0.64,p = 0.03)呈负相关。
与之前的临床观察相比,WFS 患者的可量化步态障碍可以更早被发现。这些障碍不能完全归因于 WFS 相关的视觉或平衡缺陷,可能反映了早期小脑和/或脑干异常。有效的以患者为中心的治疗方案可能会受益于对 WFS 患者运动和其他神经症状表现进展的更全面理解。