Furst Miriam, Levine Robert A
School of Electrical Engineering, Tel Aviv University, Tel Aviv, Israel.
Department of Ear, Nose and Throat and Head and Neck Surgery, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Handb Clin Neurol. 2015;129:649-65. doi: 10.1016/B978-0-444-62630-1.00036-6.
Multiple sclerosis (MS) is a disease that is both a focal inflammatory and a chronic neurodegenerative disease. The focal inflammatory component is characterized by destruction of central nervous system myelin, including the spinal cord; as such it can impair any central neural system, including the auditory system. While on the one hand auditory complaints in MS patients are rare compared to other senses, such as vision and proprioception, on the other hand auditory tests of precise neural timing are never "silent." Whenever focal MS lesions are detected involving the pontine auditory pathway, auditory tests requiring precise neural timing are always abnormal, while auditory functions not requiring such precise timing are often normal. Azimuth sound localization is accomplished by comparing the timing and loudness of the sound at the two ears. Hence tests of azimuth sound localization must obligatorily involve the central nervous system and particularly the brainstem. Whenever a focal lesion was localized to the pontine auditory pathway, timing tests were always abnormal, but loudness tests were not. Moreover, a timing test that included only high-frequency sounds was very often abnormal, even when there was no detectable focal MS lesion involving the pontine auditory pathway. This test may be a marker for the chronic neurodegenerative aspect of MS, and, as such could be used to complement the magnetic resonance imaging scan in monitoring the neurodegenerative aspect of MS. Studies of MS brainstem lesion location and auditory function have led to advances in understanding how the human brain processes sound. The brain processes binaural sounds independently for time and level in a two-stage process. The first stage is at the level of the superior olivary complex (SOC) and the second at a level rostral to the SOC.
多发性硬化症(MS)是一种兼具局灶性炎症和慢性神经退行性病变的疾病。局灶性炎症成分的特征是中枢神经系统髓鞘(包括脊髓)遭到破坏;因此它会损害任何中枢神经系统,包括听觉系统。一方面,与视觉和本体感觉等其他感官相比,MS患者的听觉主诉较为罕见;另一方面,精确神经定时的听觉测试并非毫无异常。每当检测到局灶性MS病变累及脑桥听觉通路时,需要精确神经定时的听觉测试总是异常,而不需要如此精确定时的听觉功能通常正常。方位声音定位是通过比较声音在双耳的定时和响度来完成的。因此,方位声音定位测试必然涉及中枢神经系统,尤其是脑干。每当局灶性病变定位于脑桥听觉通路时,定时测试总是异常,但响度测试则不然。此外,即使没有可检测到的累及脑桥听觉通路的局灶性MS病变,仅包含高频声音的定时测试也常常异常。该测试可能是MS慢性神经退行性病变方面的一个标志物,因此可用于在监测MS神经退行性病变方面补充磁共振成像扫描。对MS脑干病变位置和听觉功能的研究推动了对人类大脑如何处理声音的理解。大脑在一个两阶段过程中分别对双耳声音的时间和强度进行处理。第一阶段发生在上橄榄复合体(SOC)水平,第二阶段发生在SOC上方的水平。