Department of Neurology and Neurobiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Eur Neurol. 2011;66(2):98-105. doi: 10.1159/000329371. Epub 2011 Aug 12.
The mechanism underlying olfactory dysfunction in Parkinson's disease (PD) remains unknown. The current study aims to investigate the relationship between sequential changes of volume change of cortex associated with olfactory function and degree of deficiency of olfactory performance in PD.
Based on the arbitrary cut-off score of olfactory performance measured by 'five odors olfactory detection arrays', subjects were classified into three groups: PD patients with olfactory impairment (OPD, n = 12), PD without olfactory impairment (NPD, n = 14), and healthy controls without olfactory impairment (NC, n = 26). A morphometric analysis of magnetic resonance images (voxel-based morphometry; VBM) was used to investigate cortical volume change.
The scores of olfactory performance were higher in both NPD and OPD groups than in the NC group independent of age and disease duration, indicating that NPD subjects did have board line deficiency of olfaction though not meet the cut-off score for abnormal olfactory function. Both NPD and OPD had cortical atrophy in the parahippocampal gyrus (PCG), but only OPD also had change in orbitofrontal cortex (OFC). Correlation analysis revealed that decrement of volumes of PCG and right OFC was associated with decreased olfactory detection sensitivity, and the right OFC was also correlated to olfactory identification. However, no correlation was found between structural changes and the severity of the disease measured by UPDRS score.
The results confirmed that atrophy in piriform cortex and orbitofrontal cortex is associated with olfactory dysfunction in early PD. Atrophy of the orbitofrontal cortex becomes significant as olfactory damage progresses. Volume measurement of olfaction-associated areas together with the assessment of olfactory function may be a sensitive indicator for the early diagnosis of PD.
帕金森病(PD)嗅觉功能障碍的发病机制尚不清楚。本研究旨在探讨与嗅觉功能相关的皮质体积变化与 PD 患者嗅觉功能缺失程度的关系。
根据“五气味觉检测数组”测量的嗅觉功能的任意截止评分,将受试者分为三组:嗅觉障碍的 PD 患者(OPD,n=12)、无嗅觉障碍的 PD 患者(NPD,n=14)和无嗅觉障碍的健康对照组(NC,n=26)。使用磁共振成像(基于体素的形态测量学;VBM)形态分析来研究皮质体积变化。
NPD 和 OPD 组的嗅觉功能评分均高于 NC 组,与年龄和疾病持续时间无关,表明 NPD 患者确实有嗅觉缺陷,但未达到异常嗅觉功能的截止评分。NPD 和 OPD 均有海马旁回(PCG)皮质萎缩,但只有 OPD 也有眶额皮质(OFC)改变。相关分析显示,PCG 和右侧 OFC 体积的减少与嗅觉检测敏感性下降有关,右侧 OFC 也与嗅觉识别有关。然而,结构变化与 UPDRS 评分测量的疾病严重程度之间没有相关性。
结果证实,梨状皮质和眶额皮质的萎缩与早期 PD 的嗅觉功能障碍有关。随着嗅觉损伤的进展,眶额皮质的萎缩变得更加明显。嗅觉相关区域的体积测量以及嗅觉功能的评估可能是 PD 早期诊断的敏感指标。