Department of Translational and Precision Medicine, "La Sapienza" University of Rome, 00161 Rome, Italy.
Department of Neuroscience, Imaging and Clinical Sciences, ITAB-Institute of Advanced Biomedical Technologies, "G. D'Annunzio" University, 66100 Chieti, Italy.
Int J Mol Sci. 2023 May 16;24(10):8844. doi: 10.3390/ijms24108844.
Gaucher disease (GD) has been increasingly recognized as a continuum of phenotypes with variable neurological and sensory involvement. No study has yet specifically explored the spectrum of neuropsychiatric and sensory abnormalities in GD patients through a multidisciplinary approach. Abnormalities involving the nervous system, including sensory abnormalities, cognitive disturbances, and psychiatric comorbidities, have been identified in GD1 and GD3 patients. In this prospective study, named SENOPRO, we performed neurological, neuroradiological, neuropsychological, ophthalmological, and hearing assessments in 22 GD patients: 19 GD1 and 3 GD3. First, we highlighted a high rate of parkinsonian motor and non-motor symptoms (including high rates of excessive daytime sleepiness), especially in GD1 patients harboring severe glucocerebrosidase variants. Secondly, neuropsychological evaluations revealed a high prevalence of cognitive impairment and psychiatric disturbances, both in patients initially classified as GD1 and GD3. Thirdly, hippocampal brain volume reduction was associated with impaired short- and long-term performance in an episodic memory test. Fourthly, audiometric assessment showed an impaired speech perception in noise in the majority of patients, indicative of an impaired central processing of hearing, associated with high rates of slight hearing loss both in GD1 and GD3 patients. Finally, relevant structural and functional abnormalities along the visual system were found both in GD1 and GD3 patients by means of visual evoked potentials and optical coherence tomography. Overall, our findings support the concept of GD as a spectrum of disease subtypes, and support the importance of in-depth periodic monitoring of cognitive and motor performances, mood, sleep patterns, and sensory abnormalities in all patients with GD, independently from the patient's initial classification.
戈谢病(GD)已被越来越多地认识为一种表型连续体,具有不同的神经和感觉受累。迄今为止,尚无研究通过多学科方法专门探讨 GD 患者的神经精神和感觉异常谱。在 GD1 和 GD3 患者中已发现涉及神经系统的异常,包括感觉异常、认知障碍和精神共病。在这项名为 SENOPRO 的前瞻性研究中,我们对 22 名 GD 患者进行了神经学、神经影像学、神经心理学、眼科和听力评估:19 名 GD1 和 3 名 GD3。首先,我们强调了帕金森运动和非运动症状(包括白天过度嗜睡的高发生率)的发生率很高,尤其是在携带严重葡萄糖脑苷脂酶变异的 GD1 患者中。其次,神经心理学评估显示认知障碍和精神障碍的患病率很高,无论是最初分类为 GD1 还是 GD3 的患者。第三,海马脑容量减少与情景记忆测试中短期和长期表现受损相关。第四,听力评估显示大多数患者在噪声中言语感知受损,表明听力中枢处理受损,与 GD1 和 GD3 患者的轻度听力损失率较高相关。最后,通过视觉诱发电位和光学相干断层扫描,在 GD1 和 GD3 患者中均发现了视觉系统的相关结构和功能异常。总之,我们的研究结果支持 GD 是一种疾病亚型谱的概念,并支持对所有 GD 患者进行认知和运动表现、情绪、睡眠模式和感觉异常的深入定期监测的重要性,而与患者的初始分类无关。