Assessing the reliability to detect cerebral hypometabolism in probable Alzheimer's disease and amnestic mild cognitive impairment
▶ Measure hypometabolism reliability for FDG-PET using Bootstrap resampling. ▶ Discuss this reliability with the hypometabolism consistency over multi-datasets. ▶ Characterize this reliability relation to the parametric type-I error. ▶ Propose its use for longitudinal study and for multiple comparis...
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Published in | Journal of neuroscience methods Vol. 192; no. 2; pp. 277 - 285 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
15.10.2010
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Abstract | ▶ Measure hypometabolism reliability for FDG-PET using Bootstrap resampling. ▶ Discuss this reliability with the hypometabolism consistency over multi-datasets. ▶ Characterize this reliability relation to the parametric type-I error. ▶ Propose its use for longitudinal study and for multiple comparison correction.
Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD neuroimaging initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap-based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap-based reliability index and the type-I error. For threshold p=0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG-PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques. |
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AbstractList | Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD neuroimaging initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap-based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap-based reliability index and the type-I error. For threshold p=0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG-PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques. ▶ Measure hypometabolism reliability for FDG-PET using Bootstrap resampling. ▶ Discuss this reliability with the hypometabolism consistency over multi-datasets. ▶ Characterize this reliability relation to the parametric type-I error. ▶ Propose its use for longitudinal study and for multiple comparison correction. Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD neuroimaging initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap-based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap-based reliability index and the type-I error. For threshold p=0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG-PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques. Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD neuroimaging initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap-based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap-based reliability index and the type-I error. For threshold p=0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG-PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques.Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD neuroimaging initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap-based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap-based reliability index and the type-I error. For threshold p=0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG-PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques. Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease (pAD) and amnestic mild cognitive impairment (aMCI). This study aims to characterize the consistency of regional hypometabolism in pAD and aMCI patients enrolled in the AD Neuroimaging Initiative (ADNI) using statistical parametric mapping (SPM) and bootstrap resampling, and to compare bootstrap based reliability index to the commonly used type-I error approach with or without correction for multiple comparisons. Batched SPM5 was run for each of 1,000 bootstrap iterations to compare FDG-PET images from 74 pAD and 142 aMCI patients, respectively, to 82 normal controls. Maps of the hypometabolic voxels detected for at least a specific percentage of times over the 1000 runs were examined and compared to an overlap of the hypometabolic maps obtained from 3 randomly partitioned independent sub-datasets. The results from the bootstrap derived reliability of regional hypometabolism in the overall data set were similar to that observed in each of the three non-overlapping sub-sets using family-wise error. Strong but non-linear association was found between the bootstrap based reliability index and the type-I error. For threshold p =0.0005, pAD was associated with extensive hypometabolic voxels in the posterior cingulate/precuneus and parietotemporal regions with reliability between 90% and 100%. Bootstrap analysis provides an alternative to the parametric family-wise error approach used to examine consistency of hypometabolic brain voxels in pAD and aMCI patients. These results provide a foundation for the use of bootstrap analysis characterize statistical ROIs or search regions in both cross-sectional and longitudinal FDG PET studies. This approach offers promise in the early detection and tracking of AD, the evaluation of AD-modifying treatments, and other biologically or clinical important measurements using brain images and voxel-based data analysis techniques. |
Author | Fleisher, Adam Alexander, Gene E. Jagust, William J. Ayutyanont, Napatkamon Harvey, Danielle J. Chen, Kewei Reschke, Cole Langbaum, Jessica B.S. Foster, Norman L. Reiman, Eric M. Yao, Li Bandy, Dan Liu, Xiaofen Koeppe, Robert A. Weiner, Michael W. Thompson, Paul M. Wu, Xia Lee, Wendy |
AuthorAffiliation | k Division of Nuclear Medicine, Department of Radiology, University of Michigan, USA o Arizona Alzheimer's Consortium, Phoenix, AZ, USA i Department of Medicine, Radiology, Psychiatry, and Neurology, University of California San Francisco, USA c Departments of Radiology, University of Arizona, Tucson, AZ, USA g Department of Psychology and Evelyn F. McKnight Brain Institute, University of Arizona, Phoenix, AZ, USA n University of California, Davis, USA b Banner Alzheimer's Institute, Phoenix, AZ, USA l Helen Wills Neuroscience Institute, School of Public Health, University of California Berkeley, USA f School of Medicine, University of California, Los Angeles, USA j Center for Imaging and Neurodegenerative Diseases, San Francisco Veterans Affairs Medical Center, USA d School of Mathematics and Statistics, Arizona State University, Tempe, AZ, USA m State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China PR a School of Information Science and Technology |
AuthorAffiliation_xml | – name: c Departments of Radiology, University of Arizona, Tucson, AZ, USA – name: e Department of Neurosciences, University of California, San Diego, USA – name: l Helen Wills Neuroscience Institute, School of Public Health, University of California Berkeley, USA – name: h Center for Alzheimer's Care, Imaging and Research and Department of Neurology, University of Utah – name: j Center for Imaging and Neurodegenerative Diseases, San Francisco Veterans Affairs Medical Center, USA – name: k Division of Nuclear Medicine, Department of Radiology, University of Michigan, USA – name: n University of California, Davis, USA – name: d School of Mathematics and Statistics, Arizona State University, Tempe, AZ, USA – name: m State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China PR – name: i Department of Medicine, Radiology, Psychiatry, and Neurology, University of California San Francisco, USA – name: g Department of Psychology and Evelyn F. McKnight Brain Institute, University of Arizona, Phoenix, AZ, USA – name: b Banner Alzheimer's Institute, Phoenix, AZ, USA – name: a School of Information Science and Technology, Beijing Normal University, Beijing, China PR – name: f School of Medicine, University of California, Los Angeles, USA – name: o Arizona Alzheimer's Consortium, Phoenix, AZ, USA |
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CitedBy_id | crossref_primary_10_1093_arclin_acs093 crossref_primary_10_1016_j_jalz_2013_05_1769 crossref_primary_10_9758_cpn_2023_21_2_359 crossref_primary_10_1007_s12013_014_0138_7 crossref_primary_10_4061_2011_490140 crossref_primary_10_1177_0891988714524629 crossref_primary_10_1016_j_nic_2011_11_008 crossref_primary_10_1212_WNL_0b013e318295d6cf crossref_primary_10_1016_j_jalz_2011_09_172 crossref_primary_10_1016_j_jalz_2014_11_001 crossref_primary_10_1016_j_jalz_2015_04_005 crossref_primary_10_1016_j_neurobiolaging_2017_04_016 |
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Copyright | 2010 Elsevier B.V. Copyright © 2010 Elsevier B.V. All rights reserved. |
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CorporateAuthor | the Alzheimer's Disease Neuroimaging Initiative Alzheimer's Disease Neuroimaging Initiative |
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Keywords | FDG-PET SPM MCI Reproducibility of results Family-wise error Reliability Alzheimer's disease Bootstrap resampling |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 Data used in the preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (www.loni.ucla.edu/ADNI). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in the analyses or writing of this report. The complete listing of ADNI investigators is available at www.loni.ucla.edu\ADNI\Collaboration\ADNI_Authorship_list.pdf. |
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Snippet | ▶ Measure hypometabolism reliability for FDG-PET using Bootstrap resampling. ▶ Discuss this reliability with the hypometabolism consistency over... Fluorodeoxyglucose positron emission tomography (FDG-PET) studies report characteristic patterns of cerebral hypometabolism in probable Alzheimer's disease... |
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SubjectTerms | Aged Aged, 80 and over Alzheimer Disease - diagnostic imaging Alzheimer Disease - metabolism Alzheimer's disease Amnesia - diagnostic imaging Amnesia - metabolism Bootstrap resampling Brain - diagnostic imaging Brain - metabolism Brain Mapping - methods Cognition Disorders - diagnostic imaging Cognition Disorders - metabolism Family-wise error FDG-PET Female Humans Image Processing, Computer-Assisted Male MCI Middle Aged Positron-Emission Tomography - methods Reliability Reproducibility of Results SPM |
Title | Assessing the reliability to detect cerebral hypometabolism in probable Alzheimer's disease and amnestic mild cognitive impairment |
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