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Jack, Clifford R

0000-0001-7916-622X

Mayo Clinic

Mayo Clinic

Citations 445

Clinicopathological and 123I‐FP‐CIT SPECT correlations in patients with dementia

Annals of Clinical and Translational Neurology | January 24, 2018 | Volume: 5 | Issue: 3 | Pages: 376-381

10.1002/acn3.521 | PMID 29560382

AbstractThe relationship between clinicopathologic diagnosis and 123I‐FP‐CIT SPECT in 18 patients with dementia (12 with Lewy body disease) from one center in the United States was assessed. The sensitivity and specificity of abnormal 123I‐FP‐CIT SPECT with reduced striatal uptake on visual inspection for predicting Lewy body disease were 91.7% and 83.3%, respectively. The mean calculated putamen to occipital ratio (mPOR) based on regions of interest was significantly reduced in Lewy body disease compared to non‐Lewy body disease cases (P = 0.002). In this study, abnormal 123I‐FP‐CIT SPECT was strongly associated with underlying Lewy body disease pathology, supporting the utility of 123I‐FP‐CIT SPECT in the clinical diagnosis of dementia with Lewy bodies.
Sex differences in cerebrovascular pathologies on FLAIR in cognitively unimpaired elderly

Neurology | January 17, 2018 | Volume: 90 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000004913 | PMID 29343465

[18F]AV‐1451 clustering of entorhinal and cortical uptake in Alzheimer's disease

Annals of Neurology | January 11, 2018 | Volume: 83 | Issue: 2 | Pages: 248-257

10.1002/ana.25142 | PMID 29323751

ObjectiveTo use a cluster analysis of [18F]AV‐1451 tau‐PET data to determine how subjects with Alzheimer's disease (AD) vary in the relative involvement of the entorhinal cortex and neocortex, and determine whether relative involvement of these two regions can help explain variability in age and clinical phenotype in AD.MethodsWe calculated [18F]AV‐1451 uptake in entorhinal cortex and neocortex in 62 amyloid‐positive AD patients (39 typical and 23 atypical presentation). tau‐PET (positron emission tomography) values were normalized to the cerebellum to create standard uptake value ratios (SUVRs). tau‐PET SUVRs were log‐transformed and clustered blinded to clinical information into three groups using K‐median cluster analysis. Demographics, clinical phenotype, cognitive performance, and apolipoprotein e4 frequency were compared across clusters.ResultsThe cluster analysis identified a cluster with low entorhinal and cortical uptake (ELo/CLo), one with low entorhinal but high cortical uptake (ELo/CHi), and one with high cortical and entorhinal uptake (EHi/CHi). Clinical phenotype differed across clusters, with typical AD most commonly observed in the ELo/CLo and EHi/CHi clusters, and atypical AD most commonly observed in the ELo/CHi cluster. The ELo/CLo cluster had an older age at PET and onset than the other clusters. Apolipoprotein e4 frequency was lower in the ELo/CHi cluster. The EHi/CHi cluster had the worst memory impairment, whereas the ELo/CHi cluster had the worst impairment in nonmemory domains.InterpretationThis study demonstrates considerable variability in [18F]AV‐1451 tau‐PET uptake in AD, but shows that a straightforward clustering based on entorhinal and cortical uptake maps well onto age and clinical presentation in AD. Ann Neurol 2018 Ann Neurol 2018;83:248–257
Novel GRN mutation presenting as an aphasic dementia and evolving into corticobasal syndrome

Neurology Genetics | December 13, 2017 | Volume: 3 | Issue: 6 | Pages: No page available

10.1212/nxg.0000000000000201 | PMID 29264393

Longitudinal Association Between Brain Amyloid-Beta and Gait in the Mayo Clinic Study of Aging

The Journals of Gerontology: Series A | December 9, 2017 | Volume: 73 | Issue: 9 | Pages: 1244-1250

10.1093/gerona/glx240 | PMID 29236984

Association Between Microinfarcts and Blood Pressure Trajectories

JAMA Neurology | December 4, 2017 | Volume: 75 | Issue: 2 | Pages: 212

10.1001/jamaneurol.2017.3392 | PMID 29204605

Widespread brain tau and its association with ageing, Braak stage and Alzheimer’s dementia

Brain | November 5, 2017 | Volume: 141 | Issue: 1 | Pages: 271-287

10.1093/brain/awx320 | PMID 29228201

Predicting clinical decline in progressive agrammatic aphasia and apraxia of speech

Neurology | November 1, 2017 | Volume: 89 | Issue: 22 | Pages: 2271-2279

10.1212/wnl.0000000000004685 | PMID 29093069

Quantitative magnetic resonance imaging phantoms: A review and the need for a system phantom

Magnetic Resonance in Medicine | October 30, 2017 | Volume: 79 | Issue: 1 | Pages: 48-61

10.1002/mrm.26982 | PMID 29083101

The MRI community is using quantitative mapping techniques to complement qualitative imaging. For quantitative imaging to reach its full potential, it is necessary to analyze measurements across systems and longitudinally. Clinical use of quantitative imaging can be facilitated through adoption and use of a standard system phantom, a calibration/standard reference object, to assess the performance of an MRI machine. The International Society of Magnetic Resonance in Medicine AdHoc Committee on Standards for Quantitative Magnetic Resonance was established in February 2007 to facilitate the expansion of MRI as a mainstream modality for multi‐institutional measurements, including, among other things, multicenter trials. The goal of the Standards for Quantitative Magnetic Resonance committee was to provide a framework to ensure that quantitative measures derived from MR data are comparable over time, between subjects, between sites, and between vendors. This paper, written by members of the Standards for Quantitative Magnetic Resonance committee, reviews standardization attempts and then details the need, requirements, and implementation plan for a standard system phantom for quantitative MRI. In addition, application‐specific phantoms and implementation of quantitative MRI are reviewed. Magn Reson Med 79:48–61, 2018. © 2017 International Society for Magnetic Resonance in Medicine.
Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry

The World Journal of Biological Psychiatry | October 27, 2017 | Volume: 19 | Issue: 4 | Pages: 244-328

10.1080/15622975.2017.1375556 | PMID 29076399