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      Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

      research-article
      1 , 2 , , 1 , 2 , 1 , 2 , 3 , 3 , 1 , 2 , 1 , 3 ,   4 , 5 , 3 , 1 , 3 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 3 , 3 , 3 , 1 , 3 , 4 , 6 , 3 , 3 , 1 , 2 , The Genetic FTD Initiative (GENFI), The Alzheimer’s Disease Neuroimaging Initiative (ADNI)
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          Abstract

          The heterogeneity of neurodegenerative diseases is a key confound to disease understanding and treatment development, as study cohorts typically include multiple phenotypes on distinct disease trajectories. Here we introduce a machine-learning technique—Subtype and Stage Inference (SuStaIn)—able to uncover data-driven disease phenotypes with distinct temporal progression patterns, from widely available cross-sectional patient studies. Results from imaging studies in two neurodegenerative diseases reveal subgroups and their distinct trajectories of regional neurodegeneration. In genetic frontotemporal dementia, SuStaIn identifies genotypes from imaging alone, validating its ability to identify subtypes; further the technique reveals within-genotype heterogeneity. In Alzheimer’s disease, SuStaIn uncovers three subtypes, uniquely characterising their temporal complexity. SuStaIn provides fine-grained patient stratification, which substantially enhances the ability to predict conversion between diagnostic categories over standard models that ignore subtype ( p = 7.18 × 10 −4) or temporal stage ( p = 3.96 × 10 −5). SuStaIn offers new promise for enabling disease subtype discovery and precision medicine.

          Abstract

          Progressive diseases tend to be heterogeneous in their underlying aetiology mechanism, disease manifestation, and disease time course. Here, Young and colleagues devise a computational method to account for both phenotypic heterogeneity and temporal heterogeneity, and demonstrate it using two neurodegenerative disease cohorts.

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          Most cited references15

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          Genetics of Alzheimer disease.

          Alzheimer disease (AD) is the most common causes of neurodegenerative disorder in the elderly individuals. Clinically, patients initially present with short-term memory loss, subsequently followed by executive dysfunction, confusion, agitation, and behavioral disturbances. Three causative genes have been associated with autosomal dominant familial AD (APP, PSEN1, and PSEN2) and 1 genetic risk factor (APOEε4 allele). Identification of these genes has led to a number of animal models that have been useful to study the pathogenesis underlying AD. In this article, we provide an overview of the clinical and genetic features of AD.
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            Neuroimaging correlates of pathologically defined subtypes of Alzheimer's disease: a case-control study.

            Three subtypes of Alzheimer's disease (AD) have been pathologically defined on the basis of the distribution of neurofibrillary tangles: typical AD, hippocampal-sparing AD, and limbic-predominant AD. Compared with typical AD, hippocampal-sparing AD has more neurofibrillary tangles in the cortex and fewer in the hippocampus, whereas the opposite pattern is seen in limbic-predominant AD. We aimed to determine whether MRI patterns of atrophy differ between these subtypes and whether structural neuroimaging could be a useful predictor of pathological subtype at autopsy. We identified patients who had been followed up in the Mayo Clinic Alzheimer's Disease Research Center (Rochester, MN, USA) or in the Alzheimer's Disease Patient Registry (Rochester, MN, USA) between 1992 and 2005. To be eligible for inclusion, participants had to have had dementia, AD pathology at autopsy (Braak stage ≥IV and intermediate to high probability of AD), and an ante-mortem MRI. Cases were assigned to one of three pathological subtypes--hippocampal-sparing, limbic-predominant, and typical AD--on the basis of neurofibrillary tangle counts in hippocampus and cortex and ratio of hippocampal to cortical burden, without reference to neuronal loss. Voxel-based morphometry and atlas-based parcellation were used to compare patterns of grey matter loss between groups and with age-matched control individuals. Neuroimaging was obtained at the time of first presentation. To summarise pair-wise group differences, we report the area under the receiver operator characteristic curve (AUROC). Of 177 eligible patients, 125 (71%) were classified as having typical AD, 33 (19%) as having limbic-predominant AD, and 19 (11%) as having hippocampal-sparing AD. Most patients with typical (98 [78%]) and limbic-predominant AD (31 [94%]) initially presented with an amnestic syndrome, but fewer patients with hippocampal-sparing AD (eight [42%]) did. The most severe medial temporal atrophy was recorded in patients with limbic-predominant AD, followed by those with typical disease, and then those with hippocampal-sparing AD. Conversely, the most severe cortical atrophy was noted in patients with hippocampal-sparing AD, followed by those with typical disease, and then limbic-predominant AD. The ratio of hippocampal to cortical volumes allowed the best discrimination between subtypes (p<0·0001; three-way AUROC 0·52 [95% CI 0·47-0·52]; ratio of AUROC to chance classification 3·1 [2·8-3·1]). Patients with typical AD and non-amnesic initial presentation had a significantly higher ratio of hippocampal to cortical volumes (median 0·045 [IQR 0·035-0·056]) than did those with an amnesic presentation (0·041 [0·031-0·057]; p=0·001). Patterns of atrophy on MRI differ across the pathological subtypes of AD. MRI regional volumetric analysis can reliably track the distribution of neurofibrillary tangle pathology and can predict pathological subtype of AD at autopsy. US National Institutes of Health (National Institute on Aging). Copyright © 2012 Elsevier Ltd. All rights reserved.
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              • Article: not found

              Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers.

              Repeat expansions in chromosome 9 open reading frame 72 (C9ORF72) are an important cause of both motor neuron disease (MND) and frontotemporal dementia (FTD). Currently, little is known about factors that could account for the phenotypic heterogeneity detected in C9ORF72 expansion carriers. In this study, we investigated 4 genes that could represent genetic modifiers: ataxin-2 (ATXN2), non-imprinted in Prader-Willi/Angelman syndrome 1 (NIPA1), survival motor neuron 1 (SMN1), and survival motor neuron 2 (SMN2). Assessment of these genes, in a unique cohort of 331 C9ORF72 expansion carriers and 376 control subjects, revealed that intermediate repeat lengths in ATXN2 possibly act as disease modifier in C9ORF72 expansion carriers; no evidence was provided for a potential role of NIPA1, SMN1, or SMN2. The effects of intermediate ATXN2 repeats were most profound in probands with MND or FTD/MND (2.1% vs. 0% in control subjects, p = 0.013), whereas the frequency in probands with FTD was identical to control subjects. Though intermediate ATXN2 repeats were already known to be associated with MND risk, previous reports did not focus on individuals with clear pathogenic mutations, such as repeat expansions in C9ORF72. Based on our present findings, we postulate that intermediate ATXN2 repeat lengths may render C9ORF72 expansion carriers more susceptible to the development of MND; further studies are needed, however, to validate our findings. Copyright © 2014 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                alexandra.young@ucl.ac.uk
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                15 October 2018
                15 October 2018
                2018
                : 9
                : 4273
                Affiliations
                [1 ]ISNI 0000000121901201, GRID grid.83440.3b, Centre for Medical Image Computing, , University College London, ; London, WC1E 6BT UK
                [2 ]ISNI 0000000121901201, GRID grid.83440.3b, Department of Computer Science, , University College London, ; London, WC1E 6BT UK
                [3 ]ISNI 0000000121901201, GRID grid.83440.3b, Dementia Research Centre, Institute of Neurology, , University College London, ; London, WC1N 3BG UK
                [4 ]ISNI 0000000121901201, GRID grid.83440.3b, Leonard Wolfson Experimental Neurology Centre, UCL Institute of Neurology, , University College London, ; London, WC1N 3BG UK
                [5 ]ISNI 0000000121901201, GRID grid.83440.3b, Neuroradiological Academic Unit, Department of Brain Repair and Rehabilitation, UCL Institute of Neurology, , University College London, ; London, WC1N 3BG UK
                [6 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, School of Biomedical Engineering and Imaging Sciences, , King′s College London, ; London, WC2R 2LS UK
                [7 ]ISNI 000000040459992X, GRID grid.5645.2, Erasmus Medical Center, ; 3000 CA Rotterdam, The Netherlands
                [8 ]ISNI 0000000417571846, GRID grid.7637.5, Neurology Unit, Department of Clinical and Experimental Sciences, University of Brescia, ; 25121 Brescia, Italy
                [9 ]ISNI 0000 0004 1757 2822, GRID grid.4708.b, Dept. of Physiopathology and Transplantation, , University of Milan, Centro Dino Ferrari, ; 20122 Milan, Italy
                [10 ]Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, via F. Sforza, 35, 20122 Milan, Italy
                [11 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Sunnybrook Health Sciences Centre, University of Toronto, ; ON, M4N 3M5 Canada
                [12 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Centre for Research in Neurodegenerative Diseases, University of Toronto, ON, ; Toronto, M5T 0S8 Canada
                [13 ]ISNI 0000000121885934, GRID grid.5335.0, University of Cambridge, Department of Clinical Neurosciences, ; Cambridge, CB2 0SZ UK
                [14 ]GRID grid.465198.7, Karolinska Institutet, ; 171 77 Solna, Sweden
                [15 ]ISNI 0000 0001 0707 5492, GRID grid.417894.7, Istituto Neurologico Carlo Besta, ; 20133 Milan, Italy
                [16 ]ISNI 0000 0001 2322 4988, GRID grid.8591.5, University Hospitals and University of Geneva, ; Geneva, Switzerland
                [17 ]ISNI 0000 0004 1936 8390, GRID grid.23856.3a, Université Laval, ; Quebec, QC G1V 0A6 Canada
                [18 ]ISNI 0000 0004 1936 8884, GRID grid.39381.30, University of Western Ontario, ; London, ON N6A 3K7 Canada
                [19 ]ISNI 0000 0001 2181 4263, GRID grid.9983.b, Faculdade de Medicina, Universidade de Lisboa, ; 1649-028 Lisboa, Portugal
                [20 ]ISNI 0000 0004 1757 2304, GRID grid.8404.8, Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, ; 50121 Florence, Italy
                [21 ]IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy
                [22 ]GRID grid.465198.7, Department of Clinical Neuroscience, , Karolinska Institutet, ; 171 77 Solna, Sweden
                [23 ]GRID grid.412725.7, Biotechnology Laboratory, Department of Diagnostics, , Civic Hospital of Brescia, ; 25123 Brescia, Italy
                [24 ]GRID grid.419422.8, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Centro San Giovanni di Dio Fatebenefratelli, ; 25125 Brescia, Italy
                [25 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, LC Campbell Cognitive Neurology Research Unit, , Sunnybrook Research Institute, ; Toronto, ON M4N 3M5 Canada
                [26 ]ISNI 0000000417571846, GRID grid.7637.5, Centre of Brain Aging, , University of Brescia, ; 25121 Brescia, Italy
                [27 ]ISNI 0000 0000 9241 5705, GRID grid.24381.3c, Department of Geriatric Medicine, , Karolinska University Hospital, ; 171 77 Solna, Sweden
                [28 ]ISNI 0000 0000 9511 4342, GRID grid.8051.c, Instituto Ciências Nucleares Aplicadas à Saúde, , Universidade de Coimbra, ; 3000-548 Coimbra, Portugal
                [29 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Division of Neurology, Baycrest Centre for Geriatric Care, , University of Toronto, ; Toronto, ON M5S 3H7 Canada
                [30 ]ISNI 0000000417571846, GRID grid.7637.5, Centre of Brain Aging, Neurology Unit, Department of Clinical and Experimental Sciences, , University of Brescia, ; 25121 Brescia, Italy
                [31 ]ISNI 0000 0001 0707 5492, GRID grid.417894.7, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Istituto Neurologico Carlo Besta, ; 20133 Milan, Italy
                [32 ]GRID grid.465198.7, Division of Clinical Geriatrics, , Karolinska Institutet, ; 171 77 Solna, Sweden
                [33 ]ISNI 000000040459992X, GRID grid.5645.2, Department of Neurology, , Erasmus Medical Center, ; 3000 CA Rotterdam, The Netherlands
                [34 ]ISNI 0000 0001 0012 4167, GRID grid.417188.3, University Health Network Memory Clinic, , Toronto Western Hospital, ; Toronto, ON M5T 2S8 Canada
                [35 ]Lisbon Faculty of Medicine, Language Research Laboratory, 1649-028 Lisbon, Portugal
                [36 ]ISNI 0000000121901201, GRID grid.83440.3b, MRC Prion Unit, Department of Neurodegenerative Disease, , UCL Institute of Neurology, ; Queen Square, London, WC1N 3BG UK
                [37 ]ISNI 000000040459992X, GRID grid.5645.2, Department of Clinical Genetics, , Erasmus Medical Center, ; Rotterdam, 3000 CA The Netherlands
                [38 ]GRID grid.465198.7, Division of Neurogeriatrics, , Karolinska Institutet, ; 171 77 Solna, Sweden
                [39 ]ISNI 0000000417571846, GRID grid.7637.5, Neurology Unit, Department of Medical and Experimental Sciences, , University of Brescia, ; 25121 Brescia, Italy
                [40 ]ISNI 0000 0004 1757 2304, GRID grid.8404.8, Department of Clinical Pathophysiology, , University of Florence, ; 50121 Florence, Italy
                [41 ]ISNI 0000000417571846, GRID grid.7637.5, Centre for Ageing Brain and Neurodegenerative Disorders, Neurology Unit, , University of Brescia, ; 25121 Brescia, Italy
                [42 ]ISNI 0000 0004 0443 9942, GRID grid.417467.7, Department of Neurosciences, , Mayo Clinic, ; Jacksonville, FL 32224 USA
                [43 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Tanz Centre for Research in Neurodegenerative Diseases, , University of Toronto, ; Toronto, ON M5S 3H7 Canada
                [44 ]GRID grid.465198.7, Center for Alzheimer Research, Division of Neurogeriatrics, , Karolinska Institutet, ; 171 77 Solna, Sweden
                [45 ]ISNI 0000 0001 2181 4263, GRID grid.9983.b, Department of Neurosciences, Santa Maria Hospital, , University of Lisbon, ; 1649-035 Lisbon, Portugal
                [46 ]ISNI 0000 0001 2297 6811, GRID grid.266102.1, UC San Francisco, ; San Francisco, CA 94143 USA
                [47 ]ISNI 0000 0001 2107 4242, GRID grid.266100.3, UC San Diego, ; San Diego, CA 92093 USA
                [48 ]ISNI 0000 0004 0459 167X, GRID grid.66875.3a, Mayo Clinic, ; Rochester, NY 14603 USA
                [49 ]ISNI 0000 0001 2181 7878, GRID grid.47840.3f, UC Berkeley, ; Berkeley, CA 94720 USA
                [50 ]ISNI 0000 0004 1936 8972, GRID grid.25879.31, UPenn, ; Philadelphia, PA 9104 USA
                [51 ]ISNI 0000 0001 2156 6853, GRID grid.42505.36, USC, ; Los Angeles, CA 90089 USA
                [52 ]ISNI 0000 0004 1936 9684, GRID grid.27860.3b, UC Davis, ; Davis, CA 95616 USA
                [53 ]ISNI 0000 0004 0378 8294, GRID grid.62560.37, Brigham and Women’s Hospital/Harvard Medical School, ; Boston, MA 02115 USA
                [54 ]ISNI 0000 0001 0790 959X, GRID grid.411377.7, Indiana University, ; Bloomington, IN 47405 USA
                [55 ]ISNI 0000 0001 2355 7002, GRID grid.4367.6, Washington University in St Louis, ; St Louis, MI 63130 USA
                [56 ]GRID grid.468171.d, Prevent Alzheimer’s Disease 2020, ; Rockville, MD 20850 USA
                [57 ]ISNI 000000012178835X, GRID grid.5406.7, Siemens, ; Munich, 80333 Germany
                [58 ]ISNI 0000 0004 1936 9000, GRID grid.21925.3d, University of Pittsburgh, ; Pittsburgh, PA 15260 USA
                [59 ]ISNI 000000041936877X, GRID grid.5386.8, Cornell University, , Weill Cornell Medical College, ; New York City, NY 10065 USA
                [60 ]ISNI 0000000121791997, GRID grid.251993.5, Albert Einstein College of Medicine of Yeshiva University, ; Bronx, NY 10461 USA
                [61 ]AD Drug Discovery Foundation, New York City, NY 10019 USA
                [62 ]GRID grid.427650.2, Acumen Pharmaceuticals, ; Livermore, CA 94551 USA
                [63 ]ISNI 0000 0001 2299 3507, GRID grid.16753.36, Northwestern University, ; Evanston and Chicago, IL 60208 USA
                [64 ]ISNI 0000 0004 0464 0574, GRID grid.416868.5, National Institute of Mental Health, ; Rockville, MD 20852 USA
                [65 ]ISNI 0000 0004 1936 9094, GRID grid.40263.33, Brown University, ; Providence, RI 02912 USA
                [66 ]ISNI 0000 0000 2220 2544, GRID grid.417540.3, Eli Lilly, ; Indianapolis, IN 46225 USA
                [67 ]ISNI 0000000122986657, GRID grid.34477.33, University of Washington, ; Seattle, WA 98195 USA
                [68 ]ISNI 0000 0000 9632 6718, GRID grid.19006.3e, UCLA, ; Los Angeles, CA 90095 USA
                [69 ]ISNI 0000000086837370, GRID grid.214458.e, University of Michigan, ; Ann Arbor, MI 48109 USA
                [70 ]ISNI 0000 0001 2193 0096, GRID grid.223827.e, University of Utah, ; Salt Lake City, UT 84112 USA
                [71 ]ISNI 0000 0004 0406 4925, GRID grid.418204.b, Banner Alzheimer’s Institute, ; Phoenix, AZ 85006 USA
                [72 ]ISNI 0000 0001 0668 7243, GRID grid.266093.8, UC Irvine, ; Irvine, CA 92697 USA
                [73 ]ISNI 0000 0000 9372 4913, GRID grid.419475.a, National Institute on Aging, ; Bethesda, MD 20892 USA
                [74 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Johns Hopkins University, ; Baltimore, MD 21218 USA
                [75 ]Richard Frank Consulting, Washington, DC 20001 USA
                [76 ]ISNI 0000 0000 9758 5690, GRID grid.5288.7, Oregon Health and Science University, ; Portland, OR 97239 USA
                [77 ]ISNI 0000 0001 2160 926X, GRID grid.39382.33, Baylor College of Medicine, ; Houston, TX 77030 USA
                [78 ]ISNI 0000000106344187, GRID grid.265892.2, University of Alabama, ; Birmingham, AL 35233 USA
                [79 ]ISNI 0000 0001 0670 2351, GRID grid.59734.3c, Mount Sinai School of Medicine, ; New York City, NY 10029 USA
                [80 ]ISNI 0000 0001 0705 3621, GRID grid.240684.c, Rush University Medical Center, ; Chicago, IL 60612 USA
                [81 ]Wien Center, Miami, FL 33140 USA
                [82 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, New York University, ; New York City, NY 10003 USA
                [83 ]ISNI 0000000100241216, GRID grid.189509.c, Duke University Medical Center, ; Durham, NC 27710 USA
                [84 ]ISNI 0000 0004 1936 8438, GRID grid.266539.d, University of Kentucky, ; Lexington, KY 0506 USA
                [85 ]ISNI 0000 0004 1936 9166, GRID grid.412750.5, University of Rochester Medical Center, ; Rochester, NY 14642 USA
                [86 ]ISNI 0000 0000 9482 7121, GRID grid.267313.2, University of Texas Southwestern Medical School, ; Dallas, TX 75390 USA
                [87 ]ISNI 0000 0001 0941 6502, GRID grid.189967.8, Emory University, ; Atlanta, GA 30322 USA
                [88 ]ISNI 0000 0001 2177 6375, GRID grid.412016.0, University of Kansas, Medical Center, ; Kansas City, KS 66103 USA
                [89 ]ISNI 0000 0004 0443 9942, GRID grid.417467.7, Mayo Clinic, ; Jacksonville, FL 32224 USA
                [90 ]ISNI 0000000419368710, GRID grid.47100.32, Yale University School of Medicine, ; New Haven, CT 06510 USA
                [91 ]ISNI 0000 0000 9401 2774, GRID grid.414980.0, McGill University/Montreal-Jewish General Hospital, ; Montreal, QC H3T 1E2 Canada
                [92 ]ISNI 0000 0001 2288 9830, GRID grid.17091.3e, University of British Columbia Clinic for AD & Related Disorders, ; Vancouver, BC V6T 1Z3 Canada
                [93 ]ISNI 0000 0000 9674 4717, GRID grid.416448.b, Cognitive Neurology, , St Joseph’s Health Care, ; London, ON N6A 4V2 Canada
                [94 ]ISNI 0000 0001 0675 4725, GRID grid.239578.2, Cleveland Clinic Lou Ruvo Center for Brain Health, ; Las Vegas, NV 89106 USA
                [95 ]ISNI 0000 0000 9674 4717, GRID grid.416448.b, St Joseph’s Health Care, ; London, ON N6A 4V2 Canada
                [96 ]ISNI 0000 0004 0371 6506, GRID grid.489127.1, Premiere Research Institute, , Palm Beach Neurology, ; Miami, FL 33407 USA
                [97 ]ISNI 0000 0001 2186 0438, GRID grid.411667.3, Georgetown University Medical Center, ; Washington, DC 20007 USA
                [98 ]ISNI 0000 0004 0619 8759, GRID grid.414208.b, Banner Sun Health Research Institute, ; Sun City, AZ 85351 USA
                [99 ]ISNI 0000 0004 1936 7558, GRID grid.189504.1, Boston University, ; Boston, MA 02215 USA
                [100 ]ISNI 0000 0001 0547 4545, GRID grid.257127.4, Howard University, ; Washington, DC 20059 USA
                [101 ]ISNI 0000 0001 2164 3847, GRID grid.67105.35, Case Western Reserve University, ; Cleveland, OH 20002 USA
                [102 ]Neurological Care of CNY, Liverpool, NY 13088 USA
                [103 ]GRID grid.491177.d, Parkwood Hospital, ; London, ON N6C 0A7 Canada
                [104 ]ISNI 0000 0001 0701 8607, GRID grid.28803.31, University of Wisconsin, ; Madison, WI 53706 USA
                [105 ]GRID grid.417854.b, Dent Neurologic Institute, ; Amherst, NY 14226 USA
                [106 ]ISNI 0000 0001 2285 7943, GRID grid.261331.4, Ohio State University, ; Columbus, OH 43210 USA
                [107 ]ISNI 0000 0001 0427 8745, GRID grid.413558.e, Albany Medical College, ; Albany, NY 12208 USA
                [108 ]Hartford Hospital, Olin Neuropsychiatry Research Center, Hartford, CT 06114 USA
                [109 ]ISNI 0000 0004 0440 749X, GRID grid.413480.a, Dartmouth-Hitchcock Medical Center, ; Lebanon, NH 03766 USA
                [110 ]ISNI 0000 0004 0459 1231, GRID grid.412860.9, Wake Forest University Health Sciences, ; Winston-Salem, NC 27157 USA
                [111 ]ISNI 0000 0001 0557 9478, GRID grid.240588.3, Rhode Island Hospital, ; Providence, RI 02903 USA
                [112 ]ISNI 0000 0000 8593 9332, GRID grid.273271.2, Butler Hospital, ; Providence, RI 02906 USA
                [113 ]ISNI 0000 0001 2189 3475, GRID grid.259828.c, Medical University South Carolina, ; Charleston, SC 29425 USA
                [114 ]ISNI 0000 0001 2189 4777, GRID grid.250263.0, Nathan Kline Institute, ; Orangeburg, NY 10962 USA
                [115 ]ISNI 0000 0004 1936 8294, GRID grid.214572.7, University of Iowa College of Medicine, ; Iowa City, IA 52242 USA
                [116 ]ISNI 0000 0001 2353 285X, GRID grid.170693.a, University of South Florida: USF Health Byrd Alzheimer’s Institute, ; Tampa, FL 33613 USA
                [117 ]ISNI 0000 0004 0478 6223, GRID grid.420391.d, Department of Defense, ; Arlington, VA 22350 USA
                [118 ]ISNI 0000000419368956, GRID grid.168010.e, Stanford University, ; Stanford, CA 94305 USA
                Author information
                http://orcid.org/0000-0002-7772-781X
                http://orcid.org/0000-0003-4042-8493
                http://orcid.org/0000-0003-0203-3909
                http://orcid.org/0000-0001-7833-616X
                http://orcid.org/0000-0003-1491-1641
                http://orcid.org/0000-0003-1284-2558
                http://orcid.org/0000-0002-2031-490X
                http://orcid.org/0000-0003-2059-024X
                http://orcid.org/0000-0003-2439-350X
                Article
                5892
                10.1038/s41467-018-05892-0
                6189176
                29317637
                cb3e64b6-1f86-4990-877e-b26ef04c7c1f
                © The Author(s) 2018

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                : 20 July 2018
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