Department of Neurology, Heidelberg University Hospital, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany.
Department of Neurology, Bonn University Hospital, Bonn, Germany.
Cerebellum. 2024 Feb;23(1):172-180. doi: 10.1007/s12311-023-01519-3. Epub 2023 Jan 30.
Brainstem degeneration is a prominent feature of spinocerebellar ataxia type 3 (SCA3), involving structures that execute binaural synchronization with microsecond precision. As a consequence, auditory processing may deteriorate during the course of disease. We tested whether the binaural "Huggins pitch" effect is suitable to study the temporal precision of brainstem functioning in SCA3 mutation carriers. We expected that they would have difficulties perceiving Huggins pitch at high frequencies, and that they would show attenuated neuromagnetic responses to Huggins pitch. The upper limit of Huggins pitch perception was psychoacoustically determined in 18 pre-ataxic and ataxic SCA3 mutation carriers and in 18 age-matched healthy controls. Moreover, the cortical N100 response following Huggins pitch onset was acquired by means of magnetoencephalography (MEG). MEG recordings were analyzed using dipole source modeling and comprised a monaural pitch condition and a no-pitch condition with simple binaural correlation changes. Compared with age-matched controls, ataxic but not pre-ataxic SCA3 mutation carriers had significantly lower frequency limits up to which Huggins pitch could be heard. Listeners with lower frequency limits also showed diminished MEG responses to Huggins pitch, but not in the two control conditions. Huggins pitch is a promising tool to assess brainstem functioning in ataxic SCA3 patients. Future studies should refine the psychophysiological setup to capture possible performance decrements also in pre-ataxic mutation carriers. Longitudinal observations will be needed to prove the potential of the assessment of Huggins pitch as a biomarker to track brainstem functioning during the disease course in SCA3.
脑干退化是脊髓小脑性共济失调 3 型(SCA3)的一个突出特征,涉及以微秒精度执行双耳同步的结构。因此,听觉处理可能会在疾病过程中恶化。我们测试了双耳“哈金斯音高”效应是否适合研究 SCA3 突变携带者中脑干功能的时间精度。我们预计他们在高频时难以感知哈金斯音高,并且对哈金斯音高的神经磁响应会减弱。在 18 名未共济失调和共济失调的 SCA3 突变携带者和 18 名年龄匹配的健康对照者中,通过心理声学确定了哈金斯音高感知的上限。此外,通过脑磁图(MEG)获得了哈金斯音高起始后的皮质 N100 反应。使用偶极子源建模分析了 MEG 记录,包括单耳音高条件和具有简单双耳相关变化的无音高条件。与年龄匹配的对照组相比,共济失调但不是未共济失调的 SCA3 突变携带者的频率上限明显较低,在这些频率上限内可以听到哈金斯音高。频率上限较低的听力者对哈金斯音高的 MEG 反应也减弱,但在两个对照条件下没有减弱。哈金斯音高是评估共济失调 SCA3 患者脑干功能的一种很有前途的工具。未来的研究应改进心理生理设置,以捕捉在未共济失调突变携带者中可能出现的表现下降。需要进行纵向观察,以证明评估哈金斯音高作为生物标志物在 SCA3 疾病过程中跟踪脑干功能的潜力。