Lin Shun-Hung, Chen Hsian-Min, Jiang Rong-San
Department of Otolaryngology, Taichung Veterans General Hospital, Taichung 407219, Taiwan.
Center for Quantitative Imaging in Medicine (CQUIM), Department of Medical Research, Taichung Veterans General Hospital, Taichung 407219, Taiwan.
Diagnostics (Basel). 2025 Jul 31;15(15):1927. doi: 10.3390/diagnostics15151927.
Congenital anosmia (CA) is a rare condition characterized by a lifelong inability to perceive odors, which significantly affects daily life and may be linked to broader neurodevelopmental alterations. This study aimed to investigate structural brain differences in patients with CA using MRI, focusing on gray matter (GM) and white matter (WM) changes and their implications for neurodevelopment. This retrospective study included 28 patients with CA and 28 age- and gender-matched healthy controls. Patients with CA were diagnosed at a single medical center between 1 January 2001 and 30 August 2024. Controls were randomly selected from an imaging database and had no history of olfactory dysfunction. Brain Magnetic Resonance Imaging (MRI)was analyzed using volumetric analysis in SPM12.GM and WM volumes were quantified across 11 anatomical brain regions based on theWFU_PickAtlas toolbox, including frontal, temporal, parietal, occipital, limbic, sub-lobar, cerebellum (anterior/posterior), midbrain, the pons, and the frontal-temporal junction. Left-right hemispheric comparisons were also conducted. Patients with CA exhibited significantly smaller GM volumes compared to healthy controls (560.6 ± 114.7 cc vs. 693.7 ± 96.3 cc, < 0.001) but larger WM volumes (554.2 ± 75.4 cc vs. 491.1 ± 79.7 cc, = 0.015). Regionally, GM reductions were observed in the frontal (131.9 ± 33.7 cc vs. 173.7 ± 27.0 cc, < 0.001), temporal (81.1 ± 18.4 cc vs. 96.5 ± 14.1 cc, = 0.001), parietal (52.4 ± 15.2 cc vs. 77.2 ± 12.4 cc, < 0.001), sub-lobar (57.8 ± 9.7 cc vs. 68.2 ± 10.2 cc, = 0.001), occipital (39.1 ± 13.0 cc vs. 57.8 ± 8.9 cc, < 0.001), and midbrain (2.0 ± 0.5 cc vs. 2.3 ± 0.4 cc, = 0.006) regions. Meanwhile, WM increases were notable in the frontal(152.0 ± 19.9 cc vs. 139.2 ± 24.0 cc, = 0.027), temporal (71.5 ± 11.5 cc vs. 60.8 ± 9.5 cc, = 0.001), parietal (75.8 ± 12.4 cc vs. 61.9 ± 11.5 cc, < 0.001), and occipital (58.7 ± 10.3 cc vs. 41.9 ± 7.9 cc, < 0.001) lobes. A separate analysis of the left and right hemispheres revealed similar patterns of reduced GM and increased WM volumes in patients with CA across both sides. An exception was noted in the right cerebellum-posterior, where patients with CA showed significantly greater WM volume (5.625 ± 1.667 cc vs. 4.666 ± 1.583 cc, = 0.026). This study demonstrates widespread structural brain differences in individuals with CA, including reduced GM and increased WM volumes across multiple cortical and sub-lobar regions. These findings suggest that congenital olfactory deprivation may impact brain maturation beyond primary olfactory pathways, potentially reflecting altered synaptic pruning and increased myelination during early neurodevelopment. The involvement of the cerebellum further implies potential adaptations beyond motor functions. These structural differences may serve as potential neuroimaging markers for monitoring CA-associated cognitive or emotional comorbidities.
先天性嗅觉缺失(CA)是一种罕见病症,其特征为终生无法感知气味,这对日常生活有显著影响,且可能与更广泛的神经发育改变有关。本研究旨在利用磁共振成像(MRI)调查CA患者的脑结构差异,重点关注灰质(GM)和白质(WM)的变化及其对神经发育的影响。这项回顾性研究纳入了28例CA患者以及28名年龄和性别匹配的健康对照者。CA患者于2001年1月1日至2024年8月30日期间在单一医疗中心被确诊。对照者从一个影像数据库中随机选取,且无嗅觉功能障碍病史。使用SPM12中的体积分析方法对脑磁共振成像(MRI)进行分析。基于WFU_PickAtlas工具箱,在11个脑解剖区域对GM和WM体积进行量化,包括额叶、颞叶、顶叶、枕叶、边缘叶、脑叶下区域、小脑(前/后)、中脑、脑桥以及额颞交界处。还进行了左右半球比较。与健康对照者相比,CA患者的GM体积显著更小(560.6±114.7立方厘米对693.7±96.3立方厘米,<0.0 < 0.001),但WM体积更大(554.2±75.4立方厘米对491.1±79.7立方厘米,= 0.015)。在区域上,额叶(131.9±33.7立方厘米对173.7±27.0立方厘米,<0.0 < 0.001)、颞叶(81.1±18.4立方厘米对96.5±14.1立方厘米,= 0.001)、顶叶(52.4±15.2立方厘米对77.2±12.4立方厘米,<0.0 < 0.001)、脑叶下区域(57.8±9.7立方厘米对68.2±10.2立方厘米,= 0.001)、枕叶(39.1±13.0立方厘米对57.8±8.9立方厘米,<0.0 < 0.001)和中脑(2.0±0.5立方厘米对2.3±0.4立方厘米,= 0.006)区域观察到GM减少。同时,额叶(152.0±19.9立方厘米对139.2±24.0立方厘米,= 0.027)、颞叶(71.5±11.5立方厘米对60.8±9.5立方厘米,= 0.001)、顶叶(75.8±12.4立方厘米对61.9±11.5立方厘米,<0.0 < 0.001)和枕叶(58.7±10.3立方厘米对41.9±7.9立方厘米,<0.0 < 0.001)脑叶中WM增加明显。对左右半球的单独分析显示,CA患者两侧的GM减少和WM体积增加模式相似。右小脑后部是个例外,CA患者在该区域的WM体积显著更大(5.625±1.667立方厘米对4.666±1.583立方厘米,= 0.026)。本研究表明,CA个体存在广泛的脑结构差异,包括多个皮质和脑叶下区域的GM减少和WM体积增加。这些发现表明,先天性嗅觉剥夺可能会影响超出初级嗅觉通路的脑成熟,可能反映了早期神经发育过程中突触修剪改变和髓鞘形成增加。小脑的参与进一步暗示了超出运动功能的潜在适应性变化。这些结构差异可能作为监测与CA相关的认知或情感共病的潜在神经影像标志物。