Department of Food Science and Human Nutrition, University of Illinois at Urbana Champaign, Urbana, IL, USA.
Department of Psychiatry, School of Medicine, Washington University, St. Louis, MO, USA.
Orphanet J Rare Dis. 2020 Feb 22;15(1):57. doi: 10.1186/s13023-020-1335-7.
Wolfram syndrome is a rare genetic disease characterized by insulin-dependent diabetes, optic nerve atrophy, sensorineural hearing loss and neurodegeneration. Although olfactory dysfunction, a classical clinical marker of neurodegenerative processes, has been reported in Wolfram syndrome, its use as a clinical marker in Wolfram is limited due to data scarcity. In addition, it is unknown whether Wolfram syndrome affects the sense of taste.
Smell and taste perception were assessed in participants with Wolfram syndrome (n = 40) who were 15.1 ± 6.0 years of age (range: 5.1-28.7 years) and two sex- and age-matched control groups: one group with type 1 diabetes mellitus (T1D; n = 25) and a healthy control group (HC; n = 29). Smell sensitivity was assessed by measuring n-butanol detection thresholds and smell identification by using the University of Pennsylvania Smell Identification Test (UPSIT). Taste function was assessed using NIH Toolbox, which includes the assessment of sucrose (sweet) taste preference, and perceived intensity of sucrose, sodium chloride (salty), and quinine hydrochloride (bitter) both in the tip of the tongue (regional test) and the whole mouth.
Smell sensitivity was not significantly different among groups; however, smell identification was impaired in Wolfram syndrome, as reflected by significantly lower UPSIT scores in Wolfram syndrome compared to HC and T1D (P < 0.001). Compared to participants in the control groups, participants with Wolfram syndrome had a blunted perception of sweetness and saltiness when taste stimuli were applied regionally (P < 0.05), but differences in perceived intensity were no longer significant among groups when taste stimuli were tasted with the whole mouth. Groups preferred similar sucrose concentrations.
Wolfram syndrome was associated with olfactory dysfunction. However, the olfactory dysfunction was qualitative (related to smell identification) and not secondary to olfactory insensitivity or diabetes, suggesting is arising from dysfunction in central olfactory brain regions. In contrast to olfaction, and despite decreased perception of taste intensity in the anterior tongue, the sense of taste was overall well-conserved in individuals with Wolfram syndrome. Future longitudinal studies of taste and smell perception in Wolfram syndrome will be important to determine the use of the chemical senses as clinical markers of disease progression.
Wolfram 综合征是一种罕见的遗传性疾病,其特征为胰岛素依赖型糖尿病、视神经萎缩、感觉神经性听力损失和神经退行性变。尽管嗅觉功能障碍是神经退行性过程的经典临床标志物,但由于数据有限,Wolfram 综合征中嗅觉功能障碍的应用受到限制。此外,Wolfram 综合征是否影响味觉尚不清楚。
研究纳入 40 名年龄为 15.1±6.0 岁(范围:5.1-28.7 岁)的 Wolfram 综合征患者,并将其与 2 个年龄和性别匹配的对照组进行比较,对照组分别为 1 型糖尿病组(n=25)和健康对照组(n=29)。通过测量正丁醇检测阈值评估嗅觉敏感性,采用宾夕法尼亚大学嗅觉识别测试(UPSIT)评估嗅觉识别能力。采用 NIH 工具包评估味觉功能,包括蔗糖(甜)味觉偏好评估以及舌尖(区域测试)和整个口腔(整体口腔测试)中蔗糖、氯化钠(咸)和盐酸奎宁(苦)感知强度的评估。
各组之间的嗅觉敏感性无显著差异;然而,Wolfram 综合征患者的嗅觉识别能力受损,与健康对照组和 1 型糖尿病组相比,Wolfram 综合征患者的 UPSIT 评分显著降低(P<0.001)。与对照组参与者相比,Wolfram 综合征患者在区域味觉刺激时对甜味和咸味的感知减弱(P<0.05),但当味觉刺激通过整个口腔品尝时,各组之间的感知强度差异不再显著。各组对相似的蔗糖浓度表现出相似的偏好。
Wolfram 综合征与嗅觉功能障碍有关。然而,这种嗅觉功能障碍是定性的(与嗅觉识别有关),而不是嗅觉不敏感或糖尿病引起的,这表明嗅觉功能障碍源于中枢嗅觉脑区的功能障碍。与嗅觉不同的是,尽管在前舌部味觉强度的感知降低,但 Wolfram 综合征患者的整体味觉仍保持良好。未来对 Wolfram 综合征味觉和嗅觉感知的纵向研究对于确定化学感觉作为疾病进展的临床标志物非常重要。