In Myotonic Dystrophy Type 1 Head Repositioning Errors Suggest Impaired Cervical Proprioception

Stefano Scarano, A. Caronni, E. Carraro, C. R. Ferrari Aggradi, Viviana Rota, C. Malloggi, L. Tesio, V.A. Sansone
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Abstract

Background: Myotonic dystrophy type 1 (DM1) is a rare multisystemic genetic disorder with motor hallmarks of myotonia, muscle weakness and wasting. DM1 patients have an increased risk of falling of multifactorial origin, and proprioceptive and vestibular deficits can contribute to this risk. Abnormalities of muscle spindles in DM1 have been known for years. This observational cross-sectional study was based on the hypothesis of impaired cervical proprioception caused by alterations in the neck spindles. Methods: Head position sense was measured in 16 DM1 patients and 16 age- and gender-matched controls. A head-to-target repositioning test was requested from blindfolded participants. Their head was passively rotated approximately 30° leftward or rightward and flexed or extended approximately 25°. Participants had to replicate the imposed positions. An optoelectronic system was adopted to measure the angular differences between the reproduced and the imposed positions (joint position error, JPE, °) concerning the intended (sagittal, horizontal) and unintended (including the frontal) planar projections. In DM1 patients, JPEs were correlated with clinical and balance measures. Static balance in DM1 patients was assessed through dynamic posturography. Results: The accuracy and precision of head repositioning in the intended sagittal and horizontal error components did not differ between DM1 and controls. On the contrary, DM1 patients showed unintended side-bending to the left and the right: the mean [95%CI] of frontal JPE was −1.29° [−1.99°, −0.60°] for left rotation and 0.98° [0.28°, 1.67°] for right rotation. The frontal JPE of controls did not differ significantly from 0° (left rotation: 0.17° [−0.53°, 0.87°]; right rotation: −0.22° [−0.91°, 0.48°]). Frontal JPE differed between left and right rotation trials (p < 0.001) only in DM1 patients. No correlation was found between JPEs and measures from dynamic posturography and clinical scales. Conclusions: Lateral head bending associated with head rotation may reflect a latent impairment of neck proprioception in DM1 patients.
肌张力营养不良症 1 型患者的头部复位错误表明颈部运动能力受损
背景:1 型肌营养不良症(DM1)是一种罕见的多系统遗传性疾病,具有肌张力障碍、肌肉无力和消瘦等运动特征。由于多种原因,DM1 患者跌倒的风险增加,本体感觉和前庭功能障碍也会导致这种风险。DM1患者肌束异常已为人所知多年。本观察性横断面研究基于颈部肌束改变导致颈部本体感觉受损的假设。方法:对 16 名 DM1 患者和 16 名年龄与性别匹配的对照组患者的头部位置感进行测量。要求蒙上眼睛的参与者进行头部到目标的重新定位测试。参与者的头部被动向左或向右旋转约 30°,弯曲或伸展约 25°。参与者必须复制施加的位置。采用光电系统测量再现位置与施加位置之间的角度差(关节位置误差,JPE,°),涉及预期(矢状面、水平面)和非预期(包括正面)平面投影。在 DM1 患者中,JPE 与临床和平衡测量相关。DM1 患者的静态平衡通过动态体位测量法进行评估。结果显示DM1患者和对照组患者在预期矢状和水平误差成分中头部重新定位的准确性和精确度没有差异。相反,DM1 患者表现出了非预期的向左和向右侧弯:左旋转的额JPE平均值[95%CI]为-1.29° [-1.99°, -0.60°],右旋转的额JPE平均值为0.98° [0.28°, 1.67°]。对照组的额叶 JPE 与 0° 相比没有显著差异(左旋转:0.17° [-0.99°] ;右旋转:0.98° [0.28°, 1.67°] ):0.17°[-0.53°,0.87°];右旋转:-0.22° [-0.91°, 0.48°]).只有 DM1 患者的额叶 JPE 在左旋和右旋试验中存在差异(p < 0.001)。JPE与动态体位测量法和临床量表的测量结果之间没有相关性。结论与头部旋转相关的头部侧弯可能反映了DM1患者颈部本体感觉的潜在障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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