Three-dimensional pseudocontinuous arterial spin labeling and susceptibility-weighted imaging associated with clinical progression in amnestic mild cognitive impairment and Alzheimer's disease

被引:10
|
作者
Huang, Qingling [1 ]
Cao, Xuan [2 ]
Chai, Xue [1 ]
Wang, Xiao [1 ]
Xu, Ligang [3 ]
Xiao, Chaoyong [1 ]
机构
[1] Nanjing Med Univ, Dept Radiol, Affiliated Nanjing Brain Hosp, 264 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[2] Univ Cincinnati, Dept Math Sci, Cincinnati, OH USA
[3] Nanjing Med Univ, Dept Neurol, Affiliated Nanjing Brain Hosp, Nanjing, Jiangsu, Peoples R China
关键词
3-dimensional pseudocontinuous arterial spin labeling; Alzheimer's disease; amnestic mild cognitive impairment; susceptibility-weighted imaging; CEREBRAL-BLOOD-FLOW; MRI; PREDICTION; PERFUSION; DEMENTIA; MCI; EVOLUTION; BIOMARKER; DECLINE; RISK;
D O I
10.1097/MD.0000000000015972
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
c Background: This study aimed to evaluate the value of 3-dimensional pseudocontinuous arterial spin labeling (3D-pcASL) and susceptibility-weighted imaging (SWI) for the early disease-sensitive markers of conversion from amnestic MCI (aMCI) to Alzheimer disease (AD) in this process. Methods: Forty patients with aMCI and AD respectively were recruited in the study, and 40 healthy subjects were taken as controls. Data were recorded using 3T MR scanner. We assessed the cerebral blood flow (CBF) in 11 different regions of interest, and counted number of microhemorrhages (MB) in 3 regions of brain lobes, bilateral basal ganglia/thalamus, and brain stem/cerebellum, and then investigated correlations between Montreal Cognitive Assessment (MoCA) scores, CBF, and susceptibility-weighted imaging (SWI) features in these 3 groups. Results: The results revealed that for AD patients, the MoCA scores and CBF values in frontal gray matter (FGM), occipital gray matter (OGM), temporal gray matter (TGM), parietal gray matter (PGM), hippocampus, anterior cingulate cortex (ACC), precuneus, posterior cingulate cortex (PCC), precuneus, basal ganglia and thalamus decreased compared with aMCI patients and control group, and significant difference was revealed among the 3 groups. While in cerebellum, statistical significance was only found between AD patients and control group. On SWI, the average numbers of hemorrhage in regions of lobes for AD patients were significantly higher than aMCI patients and control group. The same results occurred in the bilateral basal ganglia/thalamus. We further found the MoCA score was positively correlated with CBF, but negatively correlated with hypointense signal on SWI. Conclusion: 3D-pCASL and SWI have promising potential to be biomarkers for conversion from aMCI to AD in this process.
引用
收藏
页数:7
相关论文
共 50 条
  • [21] Pattern of cerebral hyperperfusion in Alzheimer's disease and amnestic mild cognitive impairment using voxel-based analysis of 3D arterial spin-labeling imaging: initial experience
    Ding, Bei
    Ling, Hua-wei
    Zhang, Yong
    Huang, Juan
    Zhang, Huan
    Wang, Tao
    Yan, Fu Hua
    CLINICAL INTERVENTIONS IN AGING, 2014, 9 : 493 - 500
  • [22] Fluency type index: A neuropsychological marker to predict amnestic mild cognitive impairment progression to Alzheimer's disease
    Gendarini, Claudia
    Cocuzza, Alessandro
    Romandini, Alessandra
    Mauri, Silvio
    Mercurio, Matteo
    Arighi, Andrea
    Scarpini, Elio
    Comi, Giacomo Pietro
    Saetti, Maria Cristina
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 429 : 99 - 99
  • [23] Comparison of 18F-FDG PET and arterial spin labeling MRI in evaluating Alzheimer’s disease and amnestic mild cognitive impairment using integrated PET/MR
    Sheng Bi
    Shaozhen Yan
    Zhigeng Chen
    Bixiao Cui
    Yi Shan
    Hongwei Yang
    Zhigang Qi
    Zhilian Zhao
    Ying Han
    Jie Lu
    EJNMMI Research, 14
  • [24] Comparison of 18F-FDG PET and arterial spin labeling MRI in evaluating Alzheimer's disease and amnestic mild cognitive impairment using integrated PET/MR
    Bi, Sheng
    Yan, Shaozhen
    Chen, Zhigeng
    Cui, Bixiao
    Shan, Yi
    Yang, Hongwei
    Qi, Zhigang
    Zhao, Zhilian
    Han, Ying
    Lu, Jie
    EJNMMI RESEARCH, 2024, 14 (01)
  • [25] Predicting pure amnestic mild cognitive impairment conversion to Alzheimer's disease using joint modeling of imaging and clinical data
    Kebets, V.
    Richiardi, J.
    van Assche, M.
    Goldstein, R.
    van der Meulen, M.
    Vuilleumier, P.
    Van de Ville, D.
    Assal, F.
    2015 INTERNATIONAL WORKSHOP ON PATTERN RECOGNITION IN NEUROIMAGING (PRNI) 2015, 2015, : 85 - 88
  • [26] Is semantic learning strategy an early clinical marker for amnestic mild cognitive impairment and Alzheimer's disease?
    Zhang, Nan
    INTERNATIONAL PSYCHOGERIATRICS, 2019, 31 (12) : 1695 - 1697
  • [27] Pattern of cerebral hypoperfusion in Alzheimer disease and mild cognitive impairment measured with arterial spin-labeling MR imaging: Initial experience
    Johnson, NA
    Jahng, GH
    Weiner, MW
    Miller, BL
    Chui, HC
    Jagust, WJ
    Gorno-Tempini, ML
    Schuff, N
    RADIOLOGY, 2005, 234 (03) : 851 - 859
  • [28] Early Microstructure Changes of White Matter Fiber Bundles in Patients with Amnestic Mild Cognitive Impairment Predicts Progression of Mild Cognitive Impairment to Alzheimer's Disease
    He, Fangmei
    Zhang, Yuchen
    Wu, Xiaofeng
    Li, Youjun
    Zhao, Jie
    Fang, Peng
    Fan, Liming
    Li, Chenxi
    Liu, Tian
    Wang, Jue
    JOURNAL OF ALZHEIMERS DISEASE, 2021, 84 (01) : 179 - 192
  • [29] Depression in Mild Cognitive Impairment is associated with Progression to Alzheimer's Disease: A Longitudinal Study
    Van der Mussele, Stefan
    Fransen, Erik
    Struyfs, Hanne
    Luyckx, Jill
    Marien, Peter
    Saerens, Jos
    Somers, Nore
    Goeman, Johan
    De Deyn, Peter P.
    Engelborghs, Sebastiaan
    JOURNAL OF ALZHEIMERS DISEASE, 2014, 42 (04) : 1239 - 1250
  • [30] Neuropsychiatric symptoms are associated with progression from mild cognitive impairment to Alzheimer's disease
    Teng, Edmond
    Lu, Po H.
    Cummings, Jeffrey L.
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2007, 24 (04) : 253 - 259