ASAF: altered spontaneous activity fingerprinting in Alzheimer's disease based on multisite fMRI
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  • 英文篇名:ASAF: altered spontaneous activity fingerprinting in Alzheimer's disease based on multisite fMRI
  • 作者:Jiachen ; Li ; Dan ; Jin ; Ang ; Li ; Bing ; Liu ; Chengyuan ; Song ; Pan ; Wang ; Dawei ; Wang ; Kaibin ; Xu ; Hongwei ; Yang ; Hongxiang ; Yao ; Bo ; Zhou ; Alexandre ; Bejanin ; Gael ; Chetelat ; Tong ; Han ; Jie ; Lu ; Qing ; Wang ; Chunshui ; Yu ; Xinqing ; Zhang ; Yuying ; Zhou ; Xi ; Zhang ; Tianzi ; Jiang ; Yong ; Liu ; Ying ; Han
  • 英文作者:Jiachen Li;Dan Jin;Ang Li;Bing Liu;Chengyuan Song;Pan Wang;Dawei Wang;Kaibin Xu;Hongwei Yang;Hongxiang Yao;Bo Zhou;Alexandre Bejanin;Gael Chetelat;Tong Han;Jie Lu;Qing Wang;Chunshui Yu;Xinqing Zhang;Yuying Zhou;Xi Zhang;Tianzi Jiang;Yong Liu;Ying Han;Department of Neurology,Xuanwu Hospital of Capital Medical University;Brainnetome Center & National Laboratory of Pattern Recognition,Institute of Automation,Chinese Academy of Sciences;School of Artificial Intelligence,University of Chinese Academy of Sciences;Center for Excellence in Brain Science and Intelligence Technology,Institute of Automation,Chinese Academy of Sciences;Department of Neurology,Qilu Hospital of Shandong University;Department of Neurology,Tianjin Huanhu Hospital;Institute of Geriatrics and Gerontology,Chinese PLA General Hospital;Department of Radiology,Qilu Hospital;Department of Radiology,Xuanwu Hospital of Capital Medical University;Department of Radiology,Chinese PLA General Hospital;Université Normandie,Inserm,Université de Caen-Normandie;Department of Radiology,Tianjin Huanhu Hospital;Department of Radiology,Tianjin Medical University General Hospital;Center of Alzheimer’s Disease,Beijing Institute for Brain Disorders;Beijing Institute of Geriatrics;National Clinical Research Center for Geriatric Disorders;
  • 英文关键词:Brain spontaneous activity;;Multisite;;Biomarkers;;Leave-one-site-out cross-validation;;Alzheimer's disease
  • 中文刊名:JXTW
  • 英文刊名:科学通报(英文版)
  • 机构:Department of Neurology,Xuanwu Hospital of Capital Medical University;Brainnetome Center & National Laboratory of Pattern Recognition,Institute of Automation,Chinese Academy of Sciences;School of Artificial Intelligence,University of Chinese Academy of Sciences;Center for Excellence in Brain Science and Intelligence Technology,Institute of Automation,Chinese Academy of Sciences;Department of Neurology,Qilu Hospital of Shandong University;Department of Neurology,Tianjin Huanhu Hospital;Institute of Geriatrics and Gerontology,Chinese PLA General Hospital;Department of Radiology,Qilu Hospital;Department of Radiology,Xuanwu Hospital of Capital Medical University;Department of Radiology,Chinese PLA General Hospital;Université Normandie,Inserm,Université de Caen-Normandie;Department of Radiology,Tianjin Huanhu Hospital;Department of Radiology,Tianjin Medical University General Hospital;Center of Alzheimer’s Disease,Beijing Institute for Brain Disorders;Beijing Institute of Geriatrics;National Clinical Research Center for Geriatric Disorders;
  • 出版日期:2019-07-25
  • 出版单位:Science Bulletin
  • 年:2019
  • 期:v.64
  • 基金:supported by the National Key Research and Development Program of China (2016YFC1305904, 2016YFC1306300);; the National Natural Science Foundation of China (81871438, 61633018, 81571062, 81471120, 61431012, 81430037);; the Strategic Priority Research Program (B) of Chinese Academy of Sciences (XDB32020200);; the Beijing Municipal Commission of Health and Family Planning (PXM2019_026283_000002)
  • 语种:英文;
  • 页:JXTW201914009
  • 页数:13
  • CN:14
  • ISSN:10-1298/N
  • 分类号:50-62
摘要
Several monocentric studies have noted alterations in spontaneous brain activity in Alzheimer's disease(AD), although there is no consensus on the altered amplitude of low-frequency fluctuations in AD patients. The main aim of the present study was to identify a reliable and reproducible abnormal brain activity pattern in AD. The amplitude of local brain activity(AM), which can provide fast mapping of spontaneous brain activity across the whole brain, was evaluated based on multisite rs-fMRI data for688 subjects(215 normal controls(NCs), 221 amnestic mild cognitive impairment(aMCI) 252 AD).Two-sample t-tests were used to detect group differences between AD patients and NCs from the same site. Differences in the AM maps were statistically analyzed via the Stouffer's meta-analysis. Consistent regions of lower spontaneous brain activity in the default mode network and increased activity in the bilateral hippocampus/parahippocampus, thalamus, caudate nucleus, orbital part of the middle frontal gyrus and left fusiform were observed in the AD patients compared with those in NCs. Significant correlations(P < 0.05, Bonferroni corrected) between the normalized amplitude index and Mini-Mental State Examination scores were found in the identified brain regions, which indicates that the altered brain activity was associated with cognitive decline in the patients. Multivariate analysis and leave-one-siteout cross-validation led to a 78.49% prediction accuracy for single-patient classification. The altered activity patterns of the identified brain regions were largely correlated with the FDG-PET results from another independent study. These results emphasized the impaired brain activity to provide a robust and reproducible imaging signature of AD.
        Several monocentric studies have noted alterations in spontaneous brain activity in Alzheimer's disease(AD), although there is no consensus on the altered amplitude of low-frequency fluctuations in AD patients. The main aim of the present study was to identify a reliable and reproducible abnormal brain activity pattern in AD. The amplitude of local brain activity(AM), which can provide fast mapping of spontaneous brain activity across the whole brain, was evaluated based on multisite rs-fMRI data for688 subjects(215 normal controls(NCs), 221 amnestic mild cognitive impairment(aMCI) 252 AD).Two-sample t-tests were used to detect group differences between AD patients and NCs from the same site. Differences in the AM maps were statistically analyzed via the Stouffer's meta-analysis. Consistent regions of lower spontaneous brain activity in the default mode network and increased activity in the bilateral hippocampus/parahippocampus, thalamus, caudate nucleus, orbital part of the middle frontal gyrus and left fusiform were observed in the AD patients compared with those in NCs. Significant correlations(P < 0.05, Bonferroni corrected) between the normalized amplitude index and Mini-Mental State Examination scores were found in the identified brain regions, which indicates that the altered brain activity was associated with cognitive decline in the patients. Multivariate analysis and leave-one-siteout cross-validation led to a 78.49% prediction accuracy for single-patient classification. The altered activity patterns of the identified brain regions were largely correlated with the FDG-PET results from another independent study. These results emphasized the impaired brain activity to provide a robust and reproducible imaging signature of AD.
引文
[1]Albert MS,DeKosky ST,Dickson D,et al.The diagnosis of mild cognitive impairment due to Alzheimer’s disease:recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease.Alzheimers Dement 2011;7:270-9.
    [2]Albert M,Zhu Y,Moghekar A,et al.Predicting progression from normal cognition to mild cognitive impairment for individuals at 5 years.Brain2018;141:877-87.
    [3]Mc Khann GM,Knopman DS,Chertkow H,et al.The diagnosis of dementia due to Alzheimer’s disease:recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease.Alzheimers Dement 2011;7:263-9.
    [4]Chan KY,Wang W,Wu JJ,et al.Epidemiology of Alzheimer’s disease and other forms of dementia in China,1990-2010:a systematic review and analysis.Lancet 2013;381:2016-23.
    [5]Prince M,Comas-Herrera A,Knapp M,et al.World Alzheimer report 2016:improving healthcare for people living with dementia.Alzheimer’s Disease International 2016.
    [6]Ikonomovic MD,Klunk WE,Abrahamson EE,et al.Post-mortem correlates of in vivo PiB-PET amyloid imaging in a typical case of Alzheimer’s disease.Brain2008;131:1630-45.
    [7]Dubois B,Feldman HH,Jacova C,et al.Advancing research diagnostic criteria for Alzheimer’s disease:the IWG-2 criteria.Lancet Neurol 2014;13:614-29.
    [8]Wang L,Benzinger TL,Su Y,et al.Evaluation of tau imaging in staging Alzheimer disease and revealing interactions between beta-amyloid and tauopathy.JAMA Neurol 2016;73:1070-7.
    [9]Gordon BA,Blazey T,Su Y,et al.Longitudinal beta-amyloid deposition and hippocampal volume in preclinical Alzheimer disease and suspected nonAlzheimer disease pathophysiology.JAMA Neurol 2016;73:1192-200.
    [10]Sperling RA,Aisen PS,Beckett LA,et al.Toward defining the preclinical stages of Alzheimer’s disease:recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease.Alzheimers Dement 2011;7:280-92.
    [11]Jack Jr CR,Bennett DA,Blennow K,et al.NIA-AA research framework:toward a biological definition of Alzheimer’s disease.Alzheimers Dement2018;14:535-62.
    [12]Barkhof F,Haller S,Rombouts SA.Resting-state functional MR imaging:a new window to the brain.Radiology 2014;272:29-49.
    [13]Brier MR,Gordon B,Friedrichsen K,et al.Tau and Ab imaging,CSF measures,and cognition in Alzheimer’s disease.Sci Transl Med 2016;8:338ra66.
    [14]Zang YF,He Y,Zhu CZ,et al.Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI.Brain Dev 2007;29:83-91.
    [15]Bijsterbosch J,Harrison S,Duff E,et al.Investigations into within-and between-subject resting-state amplitude variations.Neuroimage.2017;159:57-69.
    [16]de Vos F,Koini M,Schouten TM,et al.A comprehensive analysis of resting state fMRI measures to classify individual patients with Alzheimer’s disease.Neuroimage 2017;167:62-72.
    [17]Zhou Y,Yu F,Duong TQ,et al.White matter lesion load is associated with resting state functional MRI activity and amyloid PET but not FDG in mild cognitive impairment and early Alzheimer’s disease patients.J Magn Reson Imaging 2015;41:102-9.
    [18]He Y,Wang L,Zang Y,et al.Regional coherence changes in the early stages of Alzheimer’s disease:a combined structural and resting-state functional MRIstudy.Neuroimage 2007;35:488-500.
    [19]Wang Z,Yan C,Zhao C,et al.Spatial patterns of intrinsic brain activity in mild cognitive impairment and Alzheimer’s disease:a resting-state functional MRIstudy.Hum Brain Mapp 2011;32:1720-40.
    [20]Song J,Qin W,Liu Y,et al.Aberrant functional organization within and between resting-state networks in AD.PLoS One 2013;8:e63727.
    [21]Liu Y,Yu C,Zhang X,et al.Impaired long distance functional connectivity and weighted network architecture in Alzheimer’s disease.Cereb Cortex2014;24:1422-35.
    [22]Liu X,Wang S,Zhang X,et al.Abnormal amplitude of low-frequency fluctuations of intrinsic brain activity in Alzheimer’s disease.J Alzheimers Dis2014;40:387-97.
    [23]Weiler M,Teixeira CV,Nogueira MH,et al.Differences and the relationship in default mode network intrinsic activity and functional connectivity in mild Alzheimer’s disease and amnestic mild cognitive impairment.Brain Connect2014;4:567-74.
    [24]Liang P,Xiang J,Liang H,et al.Altered amplitude of low-frequency fluctuations in early and late mild cognitive impairment and Alzheimer’s disease.Curr Alzheimer Res 2014;11:389-98.
    [25]Cha J,Hwang JM,Jo HJ,et al.Assessment of functional characteristics of amnestic mild cognitive impairment and Alzheimer’s disease using various methods of resting-state FMRI analysis.Biomed Res Int 2015;2015:907464.
    [26]Wen X,Wu X,Li R,et al.Alzheimer’s disease-related changes in regional spontaneous brain activity levels and inter-region interactions in the default mode network.Brain Res 2013;1509:58-65.
    [27]Mascali D,DiNuzzo M,Gili T,et al.Intrinsic patterns of coupling between correlation and amplitude of low-frequency fMRI fluctuations are disrupted in degenerative dementia mainly due to functional disconnection.PLoS One2015;10:e0120988.
    [28]Dai Z,Yan C,Wang Z,et al.Discriminative analysis of early Alzheimer’s disease using multi-modal imaging and multi-level characterization with multi-classifier(M3).Neuroimage 2012;59:2187-95.
    [29]Wang X,Wang J,He Y,et al.Apolipoprotein E epsilon4 modulates cognitive profiles,hippocampal volume,and resting-state functional connectivity in Alzheimer’s disease.J Alzheimers Dis 2015;45:781-95.
    [30]Poldrack RA,Poline JB.The publication and reproducibility challenges of shared data.Trends Cogn Sci 2015;19:59-61.
    [31]Biswal BB,Mennes M,Zuo XN,et al.Toward discovery science of human brain function.Proc Natl Acad Sci USA 2010;107:4734-9.
    [32]Wang X,Jiao Y,Tang T,et al.Investigating univariate temporal patterns for intrinsic connectivity networks based on complexity and low-frequency oscillation:a test-retest reliability study.Neuroscience 2013;254:404-26.
    [33]Button KS,Ioannidis JP,Mokrysz C,et al.Power failure:why small sample size undermines the reliability of neuroscience.Nat Rev Neurosci2013;14:365-76.
    [34]Dillen KNH,Jacobs HIL,Kukolja J,et al.Aberrant functional connectivity differentiates retrosplenial cortex from posterior cingulate cortex in prodromal Alzheimer’s disease.Neurobiol Aging 2016;44:114-26.
    [35]Teipel SJ,Wohlert A,Metzger C,et al.Multicenter stability of resting state fMRI in the detection of Alzheimer’s disease and amnestic MCI.Neuroimage Clin 2017;14:183-94.
    [36]Borenstein M,Hedges LV,Higgins JPT,et al.Introduction to metaanalysis.West Sussex:John Wiley&Sons,Ltd;2009.
    [37]Nellessen N,Rottschy C,Eickhoff SB,et al.Specific and disease stagedependent episodic memory-related brain activation patterns in Alzheimer’s disease:a coordinate-based meta-analysis.Brain Struct Funct2015;220:1555-71.
    [38]Jacobs HI,Gronenschild EH,Evers EA,et al.Visuospatial processing in early Alzheimer’s disease:a multimodal neuroimaging study.Cortex 2015;64:394-406.
    [39]Browndyke JN,Giovanello K,Petrella J,et al.Phenotypic regional functional imaging patterns during memory encoding in mild cognitive impairment and Alzheimer’s disease.Alzheimers Dement 2013;9:284-94.
    [40]Li HJ,Hou XH,Liu HH,et al.Toward systems neuroscience in mild cognitive impairment and Alzheimer’s disease:a meta-analysis of 75 fMRI studies.Hum Brain Mapp 2015;36:1217-32.
    [41]Pan P,Zhu L,Yu T,et al.Aberrant spontaneous low-frequency brain activity in amnestic mild cognitive impairment:a meta-analysis of resting-state f MRIstudies.Ageing Res Rev 2017;35:12-21.
    [42]Lau WK,Leung MK,Lee TM,et al.Resting-state abnormalities in amnestic mild cognitive impairment:a meta-analysis.Transl Psychiatry 2016;6:e790.
    [43]Xing XX,Zuo XN.The anatomy of reliability:a must read for future human brain mapping.Sci Bull 2018;63:1606-7.
    [44]Zuo XN,Biswal BB,Poldrack RA.Editorial:reliability and reproducibility in functional connectomics.Front Neurosci 2019;13:117.
    [45]Kublbock M,Woletz M,Hoflich A,et al.Stability of low-frequency fluctuation amplitudes in prolonged resting-state fMRI.Neuroimage 2014;103:249-57.
    [46]Chen X,Lu B,Yan CG.Reproducibility of R-fMRI metrics on the impact of different strategies for multiple comparison correction and sample sizes.Hum Brain Mapp 2018;39:300-18.
    [47]Zou Q,Miao X,Liu D,et al.Reliability comparison of spontaneous brain activities between BOLD and CBF contrasts in eyes-open and eyes-closed resting states.Neuroimage 2015;121:91-105.
    [48]Zuo XN,Xing XX.Test-retest reliabilities of resting-state FMRI measurements in human brain functional connectomics:a systems neuroscience perspective.Neurosci Biobehav Rev 2014;45:100-18.
    [49]Costafreda SG.Pooling FMRI data:meta-analysis,mega-analysis and multicenter studies.Front Neuroinform 2009;3:33.
    [50]Xu K,Liu Y,Zhan Y,et al.BRANT:a versatile and extendable resting-state fMRI toolkit.Front Neuroinform 2018;12:52.
    [51]Zhan Y,Ma J,Alexander-Bloch AF,et al.Longitudinal study of impaired intraand inter-network brain connectivity in subjects at high risk for Alzheimer’s disease.J Alzheimers Dis 2016;52:913-27.
    [52]Zhan YF,Yao HX,Wang P,et al.Network-based statistic show aberrant functional connectivity in Alzheimer’s disease.IEEE J Sel Top Signal Process2016;10:1182-8.
    [53]Power JD,Barnes KA,Snyder AZ,et al.Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion.Neuroimage2012;59:2142-54.
    [54]Satterthwaite TD,Wolf DH,Loughead J,et al.Impact of in-scanner head motion on multiple measures of functional connectivity:relevance for studies of neurodevelopment in youth.Neuroimage 2012;60:623-32.
    [55]Van Dijk KR,Sabuncu MR,Buckner RL.The influence of head motion on intrinsic functional connectivity MRI.Neuroimage 2012;59:431-8.
    [56]Li T,Wang Q,Zhang J,et al.Brain-wide analysis of functional connectivity in first-episode and chronic stages of schizophrenia.Schizophr Bull2017;43:436-48.
    [57]Zaykin DV.Optimally weighted Z-test is a powerful method for combining probabilities in meta-analysis.J Evol Biol 2011;24:1836-41.
    [58]Zhang J,Cheng W,Liu Z,et al.Neural,electrophysiological and anatomical basis of brain-network variability and its characteristic changes in mental disorders.Brain 2016;139:2307-21.
    [59]Glahn DC,Laird AR,Ellison-Wright I,et al.Meta-analysis of gray matter anomalies in schizophrenia:application of anatomic likelihood estimation and network analysis.Biol Psychiatry 2008;64:774-81.
    [60]Stouffer SA,Suchman EA,Evinney LC,et al.The American soldier:adjustment during Army life.(Studies in social psychology in World War II,Vol.I).Princeton,NJ:Princeton University Press;1949.
    [61]Hedges LV,Vevea JL.Fixed-and random-effects models in meta-analysis.Psychol Methods 1998;3:486-504.
    [62]Beheshti I,Demirel H.Alzheimer’s disease neuroimaging I.Feature-rankingbased Alzheimer’s disease classification from structural MRI.Magn Reson Imaging 2016;34:252-63.
    [63]Feng F,Wang P,Zhao K,et al.Radiomic features of hippocampal subregions in Alzheimer’s disease and amnestic mild cognitive impairment.Front Aging Neurosci 2018;10:290.
    [64]Abraham A,Milham MP,Di Martino A,et al.Deriving reproducible biomarkers from multi-site resting-state data:an autism-based example.Neuroimage 2017;147:736-45.
    [65]Varoquaux G,Raamana PR,Engemann DA,et al.Assessing and tuning brain decoders:cross-validation,caveats,and guidelines.Neuroimage2017;145:166-79.
    [66]Nunes A,Schnack HG,Ching CRK,et al.Using structural MRI to identify bipolar disorders-13 site machine learning study in 3020 individuals from the ENIGMA Bipolar Disorders Working Group.Mol Psychiatry 2018.https://doi.org/10.1038/s41380-018-0228-9.
    [67]Rozycki M,Satterthwaite TD,Koutsouleris N,et al.Multisite machine learning analysis provides a robust structural imaging signature of schizophrenia detectable across diverse patient populations and within individuals.Schizophr Bull 2018;44:1035-44.
    [68]Mutlu J,Landeau B,Gaubert M,et al.Distinct influence of specific versus global connectivity on the different Alzheimer’s disease biomarkers.Brain2017;140:3317-28.
    [69]Bejanin A,La Joie R,Landeau B,et al.Distinct interplay between atrophy and hypometabolism in Alzheimer’s versus semantic dementia.Cereb Cortex2018;5:1889-99.
    [70]Greicius MD,Srivastava G,Reiss AL,et al.Default-mode network activity distinguishes Alzheimer’s disease from healthy aging:evidence from functional MRI.Proc Natl Acad Sci USA 2004;101:4637-42.
    [71]Greicius MD,Kimmel DL.Neuroimaging insights into network-based neurodegeneration.Curr Opin Neurol 2012;25:727-34.
    [72]Buckner RL,Sepulcre J,Talukdar T,et al.Cortical hubs revealed by intrinsic functional connectivity:mapping,assessment of stability,and relation to Alzheimer’s disease.J Neurosci 2009;29:1860-73.
    [73]Buckner RL,Andrews-Hanna JR,Schacter DL.The brain’s default network:anatomy,function,and relevance to disease.Ann N Y Acad Sci2008;1124:1-38.
    [74]Raichle ME.The brain’s default mode network.Annu Rev Neurosci2015;38:433-47.
    [75]Sorg C,Grothe MJ.The complex link between amyloid and neuronal dysfunction in Alzheimer’s disease.Brain 2015;138:3472-5.
    [76]Villain N,Fouquet M,Baron JC,et al.Sequential relationships between grey matter and white matter atrophy and brain metabolic abnormalities in early Alzheimer’s disease.Brain 2010;133:3301-14.
    [77]Shima K,Matsunari I,Samuraki M,et al.Posterior cingulate atrophy and metabolic decline in early stage Alzheimer’s disease.Neurobiol Aging2012;33:2006-17.
    [78]Minoshima S,Giordani B,Berent S,et al.Metabolic reduction in the posterior cingulate cortex in very early Alzheimer’s disease.Ann Neurol1997;42:85-94.
    [79]Grothe MJ,Teipel SJ.Alzheimer’s disease neuroimaging I.Spatial patterns of atrophy,hypometabolism,and amyloid deposition in Alzheimer’s disease correspond to dissociable functional brain networks.Hum Brain Mapp2016;37:35-53.
    [80]Pereira JB,Strandberg TO,Palmqvist S,et al.Amyloid network topology characterizes the progression of Alzheimer’s Disease during the predementia stages.Cereb Cortex 2018;28:340-9.
    [81]Wang WY,Yu JT,Liu Y,et al.Voxel-based meta-analysis of grey matter changes in Alzheimer’s disease.Transl Neurodegener 2015;4:6.
    [82]Yang J,Pan P,Song W,et al.Voxelwise meta-analysis of gray matter anomalies in Alzheimer’s disease and mild cognitive impairment using anatomic likelihood estimation.J Neurol Sci 2012;316:21-9.
    [83]Badhwar A,Tam A,Dansereau C,et al.Resting-state network dysfunction in Alzheimer’s disease:a systematic review and meta-analysis.Alzheimers Dement(Amst).2017;8:73-85.
    [84]Zeidman P,Maguire EA.Anterior hippocampus:the anatomy of perception,imagination and episodic memory.Nat Rev Neurosci 2016;17:173-82.
    [85]Bast T,Pezze M,McGarrity S.Cognitive deficits caused by prefrontal cortical and hippocampal neural disinhibition.Br J Pharmacol 2017;174:3211-25.
    [86]Pasquini L,Scherr M,Tahmasian M,et al.Link between hippocampus’raised local and eased global intrinsic connectivity in AD.Alzheimers Dement2015;11:475-84.
    [87]Tahmasian M,Pasquini L,Scherr M,et al.The lower hippocampus global connectivity,the higher its local metabolism in Alzheimer disease.Neurology2015;84:1956-63.
    [88]Scheltens P,Blennow K,Breteler MMB,et al.Alzheimer’s disease.The Lancet2016;388:505-17.
    [89]Nugent AC,Martinez A,D’Alfonso A,et al.The relationship between glucose metabolism,resting-state fMRI BOLD signal,and GABAA-binding potential:a preliminary study in healthy subjects and those with temporal lobe epilepsy.J Cereb Blood Flow Metab 2015;35:583-91.
    [90]Marchitelli R,Aiello M,Cachia A,et al.Simultaneous resting-state FDG-PET/fMRI in Alzheimer disease:relationship between glucose metabolism and intrinsic activity.Neuroimage 2018;176:246-58.
    [91]Abi-Dargham A,Horga G.The search for imaging biomarkers in psychiatric disorders.Nat Med 2016;22:1248-55.
    [92]Bateman RJ,Xiong C,Benzinger TL,et al.Clinical and biomarker changes in dominantly inherited Alzheimer’s disease.N Engl J Med 2012;367:795-804.
    [93]Woo CW,Chang LJ,Lindquist MA,et al.Building better biomarkers:brain models in translational neuroimaging.Nat Neurosci 2017;20:365-77.
    [94]Varoquaux G.Cross-validation failure:small sample sizes lead to large error bars.Neuroimage 2018;180:68-77.
    [95]Salimi-Khorshidi G,Smith SM,Keltner JR,et al.Meta-analysis of neuroimaging data:a comparison of image-based and coordinate-based pooling of studies.Neuroimage 2009;45:810-23.
    [96]Zhang Z,Liu Y,Jiang T,et al.Altered spontaneous activity in Alzheimer’s disease and mild cognitive impairment revealed by regional homogeneity.Neuroimage 2012;59:1429-40.
    [97]He X,Qin W,Liu Y,et al.Abnormal salience network in normal aging and in amnestic mild cognitive impairment and Alzheimer’s disease.Hum Brain Mapp 2014;35:3446-64.
    [98]Li Y,Wang X,Li Y,et al.Abnormal resting-state functional connectivity strength in mild cognitive impairment and its conversion to Alzheimer’s disease.Neural Plast 2016;2016:4680972.
    [99]Guo Y,Zhang Z,Zhou B,et al.Grey-matter volume as a potential feature for the classification of Alzheimer’s disease and mild cognitive impairment:an exploratory study.Neurosci Bull 2014;30:477-89.
    [100]Wang P,Zhou B,Yao H,et al.Aberrant intra-and inter-network connectivity architectures in Alzheimer’s disease and mild cognitive impairment.Sci Rep2015;5:14824.
    [101]Li S,Yuan X,Pu F,et al.Abnormal changes of multidimensional surface features using multivariate pattern classification in amnestic mild cognitive impairment patients.J Neurosci 2014;34:10541-53.
    [102]Jin D,Li A,Liu B,et al.Impaired whole brain functional connectivity in Alzheimer’s disease:a multicenter study(N=688).Singapore:Organization of Human Brain Mapping Annual Meeting 2018;2018.
    [103]Jin D,Xu J,Zhao K,et al.Attention-based 3D convolutional network for Alzheimer’s disease diagnosis and biomarkers exploration.In:2019 IEEEInternational Symposium on Biomedical Imaging(ISBI)2019 April 8-11,2019;Venice,Italy.p.1047-51.
    [104]Zhou HH,Singh V,Johnson SC,et al.Statistical tests and identifiability conditions for pooling and analyzing multisite datasets.Proc Natl Acad Sci USA 2018;115:1481-6.

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