Scarano Stefano, Caronni Antonio, Carraro Elena, Ferrari Aggradi Carola Rita, Rota Viviana, Malloggi Chiara, Tesio Luigi, Sansone Valeria Ada
Department of Biomedical Sciences for Health, University of Milan, 20133 Milan, Italy.
IRCCS Istituto Auxologico Italiano, Department of Neurorehabilitation Sciences, Ospedale San Luca, 20122 Milan, Italy.
J Clin Med. 2024 Aug 9;13(16):4685. doi: 10.3390/jcm13164685.
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. 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. 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 ( < 0.001) only in DM1 patients. No correlation was found between JPEs and measures from dynamic posturography and clinical scales. Lateral head bending associated with head rotation may reflect a latent impairment of neck proprioception in DM1 patients.
1型强直性肌营养不良(DM1)是一种罕见的多系统遗传性疾病,具有肌强直、肌肉无力和萎缩等运动特征。DM1患者因多种因素导致跌倒风险增加,本体感觉和前庭功能障碍会增加这种风险。多年来已知DM1患者的肌梭存在异常。这项观察性横断面研究基于颈部肌梭改变导致颈部本体感觉受损的假设。对16例DM1患者和16例年龄及性别匹配的对照者进行头部位置感测量。要求蒙眼参与者进行头部到目标的重新定位测试。他们的头部被被动向左或向右旋转约30°,并向前或向后弯曲约25°。参与者必须重现施加的位置。采用光电系统测量重现位置与施加位置之间在预期(矢状面、水平面)和非预期(包括额面)平面投影上的角度差异(关节位置误差,JPE,°)。在DM1患者中,JPE与临床和平衡测量结果相关。通过动态姿势描记法评估DM1患者的静态平衡。DM1患者和对照组在预期矢状面和水平面误差分量上头部重新定位的准确性和精确性没有差异。相反,DM1患者表现出向左和向右的非预期侧弯:左侧旋转时额面JPE的平均值[95%置信区间]为-1.29°[-1.99°,-0.60°],右侧旋转时为0.98°[0.28°,1.67°]。对照组的额面JPE与0°无显著差异(左侧旋转:0.17°[-0.53°,0.87°];右侧旋转:-0.22°[-0.91°,0.48°])。仅在DM1患者中,左侧和右侧旋转试验的额面JPE存在差异(<0.001)。未发现JPE与动态姿势描记法测量结果和临床量表之间存在相关性。与头部旋转相关的侧向头部弯曲可能反映了DM1患者颈部本体感觉的潜在损害。