Riera-Punet N, Martinez-Gomis J, Willaert E, Povedano M, Peraire M
Department of Prosthodontics, School of Dentistry, Faculty of Medicine and Health Sciences, University of Barcelona, L'Hospitalet de llobregat, Barcelona, Spain.
Oral Health and Masticatory System Group (Bellvitge Biomedical Research Institute), IDIBELL, L'Hospitalet de llobregat, Barcelona, Spain.
J Oral Rehabil. 2018 Mar;45(3):204-210. doi: 10.1111/joor.12597. Epub 2017 Dec 30.
Amyotrophic lateral sclerosis (ALS) with bulbar dysfunction affects the motor neurons responsible for controlling the muscles in the jaw, face, soft palate, pharynx, larynx and tongue. This cross-sectional study aimed to determine the functional limitation of the jaw in patients with ALS and bulbar dysfunction who had upper motor neuron (UMN), lower motor neuron (LMN) or balanced involvement. One hundred and fifty-three patients with ALS and 23 controls were included. All participants answered using the 8-item Jaw Functional Limitation Scale (JFLS-8). Patients with ALS were grouped by neurologic examination as follows: non-bulbar ALS, bulbar UMN-predominant ALS; bulbar LMN-predominant ALS; and bulbar balanced (UMN + LMN) ALS. Jaw limitation between the different groups was compared using the Kruskal-Wallis test. Patients with non-bulbar ALS had similar mandibular limitations to healthy participants. Only patients with balanced UMN and LMN bulbar manifestations reported greater difficulties in chewing soft food or in jaw mobility compared to the non-bulbar ALS group. Patients with bulbar involvement also had greater difficulties in chewing tough food or chicken and in swallowing and talking compared to the non-bulbar group, regardless of whether UMN or LMN predominant. No significant differences were found between the groups in smiling and yawning difficulties. Bulbar involvement in patients with ALS is associated with functional limitation of the masticatory system. However, balanced bulbar UMN and LMN involvement is associated with the worst impairments in chewing soft food and in opening the jaw widely.
伴有延髓功能障碍的肌萎缩侧索硬化症(ALS)会影响负责控制颌部、面部、软腭、咽部、喉部和舌部肌肉的运动神经元。这项横断面研究旨在确定患有上运动神经元(UMN)、下运动神经元(LMN)受累或两者均衡受累的伴有延髓功能障碍的ALS患者的颌部功能限制。研究纳入了153例ALS患者和23名对照者。所有参与者均使用8项颌部功能限制量表(JFLS - 8)进行回答。ALS患者根据神经学检查分组如下:非延髓性ALS、延髓UMN为主型ALS、延髓LMN为主型ALS以及延髓均衡(UMN + LMN)型ALS。使用Kruskal - Wallis检验比较不同组之间的颌部限制情况。非延髓性ALS患者的下颌限制与健康参与者相似。与非延髓性ALS组相比,只有UMN和LMN延髓表现均衡的患者在咀嚼软食或颌部活动方面报告有更大困难。与非延髓性组相比,延髓受累的患者在咀嚼硬食或鸡肉以及吞咽和说话方面也有更大困难,无论UMN还是LMN占主导。各组在微笑和打哈欠困难方面未发现显著差异。ALS患者的延髓受累与咀嚼系统的功能限制有关。然而,延髓UMN和LMN均衡受累与咀嚼软食和张大嘴巴方面的最差损害有关。