Lee Hsun-Hua, Ma Hon-Ping, Ou Ju-Chi, Ong Jiann Ruey, Chen Kai-Yun, Wu Chung-Che, Chiu Wen-Ta, Liao Kuo-Hsing, Lin Chien-Min, Lin Shu-Yu, Wu Dean, Huang Yao-Hsien, Wang Yuan-Hung, Hu Chaur-Jong, Hong Chien-Tai
College of Medicine, Graduate Institute of Clinical Medicine, Taipei Medical University, Taipei, Taiwan.
Department of Neurology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Front Neurol. 2019 Feb 11;10:88. doi: 10.3389/fneur.2019.00088. eCollection 2019.
Dizziness and balance impairment are common symptoms of mild traumatic brain injury (mTBI). Acid-sensing ion channel 3 (ASIC3) is expressed in the vestibular and proprioceptive systems and associated with balance functions. However, whether the genetic variants of are associated with people who suffer dizziness and balance impairment after mTBI remained unknown. A total of 200 people with mTBI and 109 non-mTBI controls were recruited. Dizziness, balance functions, and the ability to perform daily activities were assessed by Dizziness Handicap Inventory (DHI), and objective balance functions were investigated by the postural stability test. Three diseases-related genetic variants of were determined through polymerase chain reaction and followed by restriction fragment length polymorphism. The Student's -test and Mann-Whitney -test were used for normal and abnormal distributed data, respectively. The regression was applied to adjust gender and age. The normality of continuous data was evaluated by Shapiro-Wilk test. In the mTBI people, the rs2288645-A allele carriers exhibited a significantly worse physical domain DHI score (A-allele carriers: 11.39 ± 8.42, non-A carriers: 8.76 ± 7.87, = 0.03). The rs4148855-GTC deletion carriers an exhibited significantly worse overall postural stability (GTC deletion carriers: 0.53 ± 0.33, non-carriers: 0.46 ± 0.20, = 0.03). In the controls, rs2288646-A allele carriers were significant worse in the medial-to-lateral postural stability (A-allele carriers: 0.31 ± 0.17, non-A carriers: 0.21 ± 0.10, = 0.01). The present study demonstrated that genetic variants were associated with certain aspects of balance functions and dizziness questionnaires in people of mTBI and non-mTBI. It provides a possible evidence that could be a new target for the management of the balancing disorders. However, further investigations are warranted to elucidate the underlying mechanisms and clinical significance.
头晕和平衡功能障碍是轻度创伤性脑损伤(mTBI)的常见症状。酸敏感离子通道3(ASIC3)在前庭和本体感觉系统中表达,并与平衡功能相关。然而,ASIC3的基因变异是否与mTBI后出现头晕和平衡功能障碍的人群有关尚不清楚。共招募了200名mTBI患者和109名非mTBI对照者。通过头晕残障量表(DHI)评估头晕、平衡功能和日常活动能力,并通过姿势稳定性测试研究客观平衡功能。通过聚合酶链反应确定了三种与疾病相关的ASIC3基因变异,随后进行限制性片段长度多态性分析。分别使用Student's t检验和Mann-Whitney U检验处理正态分布和非正态分布的数据。应用回归分析调整性别和年龄。通过Shapiro-Wilk检验评估连续数据的正态性。在mTBI患者中,rs2288645-A等位基因携带者的身体领域DHI评分明显更差(A等位基因携带者:11.39±8.42,非A携带者:8.76±7.87,P = 0.03)。rs4148855-GTC缺失携带者的整体姿势稳定性明显更差(GTC缺失携带者:0.53±0.33,非携带者:0.46±0.20,P = 0.03)。在对照者中,rs2288646-A等位基因携带者的左右姿势稳定性明显更差(A等位基因携带者:0.31±0.17,非A携带者:0.21±0.10,P = 0.01)。本研究表明,ASIC3基因变异与mTBI患者和非mTBI对照者的某些平衡功能方面和头晕问卷有关。它提供了一个可能的证据,表明ASIC3可能是平衡障碍管理的新靶点。然而,需要进一步研究以阐明其潜在机制和临床意义。