Department of Radiology, University of Michigan, Ann Arbor, MI, USA.
J Neural Transm (Vienna). 2013 Apr;120(4):571-6. doi: 10.1007/s00702-012-0956-y. Epub 2012 Dec 21.
Olfactory dysfunction is common in Parkinson's disease (PD) and has been attributed to early deposition of α-synuclein pathology in olfactory areas. The pathophysiology of olfactory dysfunction in PD, however, remains poorly understood. Changes in odor identification suggest in part impairment in odor memory, possibly due to hippocampal dysfunction. Olfactory dysfunction occurs also in Alzheimer's disease (AD) and increases with severity of dementia. Cholinergic degeneration is not only a feature of AD but can also occur in PD, at least in a subset of patients with cognitive changes. We reported previously that impaired odor identification in early PD is more closely correlated with hippocampal dopaminergic than nigrostriatal dopaminergic denervation. Results of our multi-tracer PET studies show that odor identification deficits in PD are best predicted by cholinergic denervation and to a lesser extent by dopaminergic denervation. These results suggest that olfactory dysfunction in PD may have multiple components including hippocampal dysfunction secondary to cholinergic and dopaminergic denervations. Olfactory dysfunction in PD may be the most marked in subjects at risk of incipient dementia, and may reflect the transition of PD toward a stage with more heterogeneous multi-system neurodegenerations. Our preliminary imaging data do not support a significant contribution of amyloidopathy or serotoninergic denervation to abnormal olfactory functions in PD, at least in the absence of dementia. We outline how progressive changes in olfaction may be used as a biomarker of cholinergic denervation and cognitive decline in PD patients. We will discuss also the utility of olfactory testing as an early screening test for neurodegeneration.
嗅觉功能障碍在帕金森病(PD)中很常见,其被归因于α-突触核蛋白病理学在嗅觉区域的早期沉积。然而,PD 中嗅觉功能障碍的病理生理学仍知之甚少。气味识别的变化部分提示嗅觉记忆受损,可能是由于海马功能障碍。嗅觉功能障碍也发生在阿尔茨海默病(AD)中,并随着痴呆的严重程度而增加。胆碱能退化不仅是 AD 的特征,而且在 PD 中也会发生,至少在一部分伴有认知变化的患者中会发生。我们之前报道过,早期 PD 中嗅觉识别受损与海马多巴胺能神经支配的损伤比黑质纹状体多巴胺能神经支配的损伤更为密切相关。我们的多示踪剂 PET 研究结果表明,PD 中嗅觉识别缺陷与胆碱能神经支配的相关性最强,与多巴胺能神经支配的相关性次之。这些结果表明,PD 中的嗅觉功能障碍可能有多个组成部分,包括海马功能障碍继发于胆碱能和多巴胺能神经支配的损伤。PD 中的嗅觉功能障碍在有早期痴呆风险的受试者中可能最为明显,可能反映了 PD 向具有更多异质性多系统神经退行性变的阶段转变。我们的初步影像学数据不支持淀粉样蛋白病或 5-羟色胺能神经支配对 PD 中异常嗅觉功能有重大贡献,至少在没有痴呆的情况下是这样。我们概述了嗅觉功能的进行性变化如何可作为 PD 患者胆碱能神经支配和认知下降的生物标志物。我们还将讨论嗅觉测试作为神经退行性变早期筛查测试的效用。