Shill Holly A, Zhang Nan, Driver-Dunckley Erika, Mehta Shyamal, Adler Charles H, Beach Thomas G
Department of Neurology, Barrow Neurological Institute, Phoenix, Arizona, USA.
Department of Neurology, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona, USA.
Mov Disord. 2021 Jul;36(7):1700-1704. doi: 10.1002/mds.28568. Epub 2021 Mar 23.
Hyposmia is characteristic of idiopathic Parkinson's disease (PD) and dementia with Lewy bodies (DLBs), whereas progressive supranuclear palsy (PSP) typically has normal sense of smell. However, there is a lack of pathologically confirmed data.
The objective is to study hyposmia in pathologically confirmed PSP patients and compare to PD patients and nondegenerative controls.
We studied autopsied subjects in the Arizona Study of Aging and Neurodegenerative Disorders who had antemortem olfactory testing and a neuropathological diagnosis of either PD, PSP, or control.
This study included 281 cases. Those with neuropathologically confirmed PSP (N = 24) and controls (N = 174) had significantly better sense of smell than those with PD (N = 76). Although most PSP patients had normal olfaction, there were some with hyposmia, resulting in an overall reduced sense of smell in PSP compared to controls. The sensitivity of having PSP pathologically in those presenting with parkinsonism and normosmia was 93.4% with a specificity of 64.7%. Cases with both PSP and PD pathologically had reduced sense of smell similar to PD alone (N = 7). Hyposmic PSP patients had significantly higher Lewy body burden not meeting criteria for additional PD/DLB diagnosis.
Pathologically confirmed PD had reduced olfaction compared with PSP or controls. In the setting of parkinsonism in this sample, the presence of normosmia had high sensitivity for PSP. Hyposmia in PSP suggests the presence of additional Lewy body pathology. © 2021 International Parkinson and Movement Disorder Society.
嗅觉减退是特发性帕金森病(PD)和路易体痴呆(DLB)的特征,而进行性核上性麻痹(PSP)通常嗅觉正常。然而,缺乏病理证实的数据。
研究经病理证实的PSP患者的嗅觉减退情况,并与PD患者和非退行性对照进行比较。
我们研究了参与亚利桑那州衰老与神经退行性疾病研究的尸检对象,这些对象生前进行了嗅觉测试,并经神经病理学诊断为PD、PSP或对照。
本研究包括281例病例。经神经病理学证实的PSP患者(N = 24)和对照(N = 174)的嗅觉明显优于PD患者(N = 76)。虽然大多数PSP患者嗅觉正常,但也有一些嗅觉减退,导致PSP患者的总体嗅觉较对照降低。帕金森综合征伴嗅觉正常的患者中,病理诊断为PSP的敏感性为93.4%,特异性为64.7%。病理诊断为PSP和PD的病例嗅觉减退程度与单独PD患者相似(N = 7)。嗅觉减退的PSP患者路易体负担明显更高,但不符合额外的PD/DLB诊断标准。
经病理证实,与PSP或对照相比,PD患者嗅觉减退。在本样本的帕金森综合征患者中,嗅觉正常对PSP具有较高的敏感性。PSP患者嗅觉减退提示存在额外的路易体病理改变。© 2021国际帕金森和运动障碍协会