Odor Identification and Regional Gray Matter Atrophy in Patients with Alzheimer's Disease, Parkinson's Disease, and the Healthy Elderly: A Cross-Sectional Structural MRI Study

被引:6
作者
Jesmanas, Simonas [1 ]
Gleizniene, Rymante [1 ]
Baranauskas, Mindaugas [2 ]
Matijosaitis, Vaidas [3 ]
Rastenyte, Daiva [3 ]
机构
[1] Lithuanian Univ Hlth Sci, Med Acad, Dept Radiol, Mickeviciaus Str 9, LT-44307 Kaunas, Lithuania
[2] Kaunas Univ Technol, Biomed Engn Inst, K Barsausko Str 59-454, LT-44029 Kaunas, Lithuania
[3] Lithuanian Univ Hlth Sci, Med Acad, Dept Neurol, Mickeviciaus Str 9, LT-44307 Kaunas, Lithuania
关键词
odor identification; Alzheimer's disease; Parkinson's disease; gray matter atrophy; orbitofrontal cortex; HUMAN CEREBRAL-CORTEX; OLFACTORY DYSFUNCTION; CLINICAL-DIAGNOSIS; PERFORMANCE; SEGMENTATION; IMPAIRMENT; THICKNESS; ACCURATE; SYSTEM; STATE;
D O I
10.3390/brainsci11101296
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multiple associations between impaired olfactory performance and regional cortical and deep gray matter atrophy have been reported in separate studies of patients with Alzheimer's disease (AD), Parkinson's disease (PD), and of the healthy elderly. We aimed to evaluate such possible associations among these populations in a unified manner. Twenty AD, twenty PD patients' and twenty healthy age- and sex-matched controls' odor identification performance was assessed with the Lithuanian adaptation of the Sniffin' Sticks 12 odor identification test, followed by morphometric gray matter analysis by MRI using FreeSurfer. AD patients had significantly lower cognitive performance than both PD patients and the healthy elderly, as evaluated with the Mini-Mental State Examination (MMSE). Odor identification performance was significantly worse in AD and PD patients compared with the healthy elderly; AD patients performed slightly worse than PD patients, but the difference was not statistically significant. Among patients with AD, worse odor identification performance was initially correlated with atrophy of multiple cortical and deep gray matter regions known to be involved in olfactory processing, however, only two measures-decreased thicknesses of the right medial and left lateral orbitofrontal cortices-remained significant after adjustment for possible confounders (age, MMSE score, and global cortical thickness). Among patients with PD and the healthy elderly we found no similar statistically significant correlations. Our findings support the key role of the orbitofrontal cortex in odor identification among patients with AD, and suggest that correlations between impaired odor identification performance and regional gray matter atrophy may be relatively more pronounced in AD rather than in PD.
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页数:14
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