Frontal neurodegeneration associated with Frontal Assessment Battery in early Alzheimer's disease

被引:2
作者
Terada, Tatsuhiro [1 ,2 ]
Kubota, Manabu [3 ,4 ]
Miyata, Jun [3 ,5 ]
Obi, Tomokazu [1 ]
Takashima, Hirotsugu [1 ,2 ]
Matsudaira, Takashi [1 ,2 ]
Bunai, Tomoyasu [2 ]
Ouchi, Yasuomi [2 ]
Murai, Toshiya [3 ]
机构
[1] Shizuoka Inst Epilepsy & Neurol Disorders, Dept Neurol, 886 Urushiyama,Aoi Ku, Shizuoka 4208688, Japan
[2] Hamamatsu Univ, Sch Med, Inst Photon Med, Preeminent Bioimaging Res,Dept Biofunct Imaging, 1-20-1 Handayama Higashi Ku, Hamamatsu 4313192, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Psychiat, 54 Shogoin-Kawahara Cho,Sakyo Ku, Kyoto 6068507, Japan
[4] Natl Inst Quantum & Radiol Sci & Technol, Natl Inst Radiol Sci, Dept Funct Brain Imaging, Brain Disorder Translat Res Grp, 4-9-1 Anagawa,Inage Ku, Chiba 2638555, Japan
[5] Aichi Med Univ, Dept Psychiat, 1-1 Karimata, Nagakute, Aichi 4801195, Japan
关键词
Alzheimer's disease (AD); Amnestic mild cognitive impairments (aMCI); Frontal Assessment Battery (FAB); Voxel-based morphometry (VBM); F-18]FDG; C-11]PiB; MILD COGNITIVE IMPAIRMENT; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; DEMENTIA; RECOMMENDATIONS; CONNECTIVITY; WORKGROUPS; VARIANT; SCALE; PET;
D O I
10.1016/j.jns.2024.123327
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The Frontal Assessment Battery (FAB) is widely used to assess executive dysfunction in patients with amnestic mild cognitive impairments due to Alzheimer's disease (aMCI-AD), but its neurobiological meaning is unclear. To elucidate this, we examined the relationship between the FAB score and three key imaging biomarkers: gray matter volume, amyloid-beta (A beta) deposition, and glucose metabolism. Methods: Twenty A beta- and tau-positive aMCI-AD patients and age-matched controls underwent structural magnetic resonance imaging and positron emission tomography with [C-11]PiB and [F-18]FDG. Voxel-based morphometry and statistical parametric mapping analyses were performed to elucidate the relationships between FAB scores and regional gray matter volume, [C-11]PiB uptake for A beta deposition, and [F-18]FDG uptake for glucose metabolism. Results: FAB scores were significantly lower in aMCI-AD than in controls (p < 0.001). In aMCI-AD, FAB was significantly correlated with right inferior frontal gray matter volume and right medial and left middle frontal glucose metabolism (family-wise error p < 0.05). However, there was no correlation between A beta deposition and FAB (family-wise error p < 0.05). Conclusions: The decreased FAB score is linked more with frontal-lobe neurodegeneration than with A beta pathology in aMCI-AD. The FAB could be an early marker for neurodegeneration related to frontal-lobe executive dysfunction.
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页数:10
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