Eric McDade

ORCID: 0000-0002-6764-3866
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About
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Research Areas
  • Alzheimer's disease research and treatments
  • Dementia and Cognitive Impairment Research
  • Functional Brain Connectivity Studies
  • Bioinformatics and Genomic Networks
  • Advanced Neuroimaging Techniques and Applications
  • Health, Environment, Cognitive Aging
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Neurological Disease Mechanisms and Treatments
  • Health Systems, Economic Evaluations, Quality of Life
  • Statistical Methods in Clinical Trials
  • Parkinson's Disease Mechanisms and Treatments
  • Cholinesterase and Neurodegenerative Diseases
  • Genomics and Rare Diseases
  • Tryptophan and brain disorders
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Medical Imaging Techniques and Applications
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Down syndrome and intellectual disability research
  • Statistical Methods and Inference
  • Frailty in Older Adults
  • Advanced MRI Techniques and Applications
  • Diet and metabolism studies
  • Ginkgo biloba and Cashew Applications
  • Cardiovascular Health and Disease Prevention
  • Cancer-related cognitive impairment studies

Washington University in St. Louis
2016-2025

Prevent Alzheimer’s Disease 2020
2016-2024

University of Pittsburgh
2011-2023

University of Missouri–St. Louis
2023

Alzheimer’s Disease Neuroimaging Initiative
2015-2023

Hope Center for Neurological Disorders
2022-2023

John Wiley & Sons (United States)
2023

Hudson Institute
2023

Liechtenstein Institute
2023

Clinical Trial Investigators
2023

The order and magnitude of pathologic processes in Alzheimer's disease are not well understood, partly because the develops over many years. Autosomal dominant has a predictable age at onset provides an opportunity to determine sequence changes that culminate symptomatic disease.

10.1056/nejmoa1202753 article EN New England Journal of Medicine 2012-07-11

White matter hyperintensities (WMHs) are areas of increased signal on T2-weighted magnetic resonance imaging (MRI) scans that most commonly reflect small vessel cerebrovascular disease. Increased WMH volume is associated with risk and progression Alzheimer's disease (AD). These observations typically interpreted as evidence vascular abnormalities play an additive, independent role contributing to symptom presentation, but not core features AD. We examined the severity distribution in...

10.1002/ana.24647 article EN Annals of Neurology 2016-03-26

Abstract The National Institute on Aging and the Alzheimer's Association convened three separate work groups in 2011 single 2012 2018 to create recommendations for diagnosis characterization of disease (AD). present document updates research framework response several recent developments. Defining diseases biologically, rather than based syndromic presentation, has long been standard many areas medicine (e.g., oncology), is becoming a unifying concept common all neurodegenerative diseases,...

10.1002/alz.13859 article EN cc-by-nc-nd Alzheimer s & Dementia 2024-06-27

To investigate age-related default mode network (DMN) connectivity in a large cognitively normal elderly cohort and patients with Alzheimer disease (AD) compared age-, gender-, education-matched controls.We analyzed task-free-fMRI data both independent component analysis seed-based to identify anterior posterior DMNs. We investigated changes sample of 341 subjects. then 28 AD 56 noncarriers the APOE ε4 allele matched for age, education, gender.The DMN shows age-associated increases decreases...

10.1212/wnl.0b013e318233b33d article EN Neurology 2011-10-06

Significance Beta-amyloid plaque accumulation, glucose hypometabolism, and neuronal atrophy are hallmarks of Alzheimer’s disease. However, the regional ordering these biomarkers prior to dementia remains untested. In a cohort with disease mutations, we performed an integrated whole-brain analysis three major imaging techniques: amyloid PET, [ 18 F]fluro-deoxyglucose structural MRI. We found that most gray-matter structures plaques later have hypometabolism followed by atrophy. Critically,...

10.1073/pnas.1317918110 article EN Proceedings of the National Academy of Sciences 2013-11-05

<h3>Objective</h3> To assess the onset, sequence, and rate of progression comprehensive biomarker clinical measures across spectrum Alzheimer disease (AD) using Dominantly Inherited Network (DIAN) study compare these to cross-sectional estimates. <h3>Methods</h3> We conducted longitudinal clinical, cognitive, CSF, neuroimaging assessments (mean 2.7 [±1.1] visits) in 217 DIAN participants. Linear mixed effects models were used changes each measure relative individuals9 estimated years symptom...

10.1212/wnl.0000000000006277 article EN Neurology 2018-09-14

Abstract Introduction The Dominantly Inherited Alzheimer Network Trials Unit (DIAN‐TU) trial is an adaptive platform testing multiple drugs to slow or prevent the progression of Alzheimer's disease in autosomal dominant (ADAD) families. With completion enrollment first two drug arms, DIAN‐TU now plans add new platform, designated as Next Generation (NexGen) prevention trial. Methods In collaboration with ADAD families, philanthropic organizations, academic leaders, Pharma Consortium,...

10.1016/j.jalz.2016.07.005 article EN Alzheimer s & Dementia 2016-08-29

Abstract Background Lecanemab, a humanized IgG1 monoclonal antibody that targets soluble aggregated Aβ species (protofibrils), has demonstrated robust brain fibrillar amyloid reduction and slowing of clinical decline in early AD. The objective this analysis is to report results from study 201 blinded period (core), the open-label extension (OLE), gap (between core OLE) supporting effectiveness lecanemab. Methods lecanemab was double-blind, randomized, placebo-controlled 856 patients...

10.1186/s13195-022-01124-2 article EN cc-by Alzheimer s Research & Therapy 2022-12-21
Antoine Drieu Siling Du Steffen E. Storck Justin Rustenhoven Zachary Papadopoulos and 95 more Taitea Dykstra Fenghe Zhong Kyungdeok Kim Susan Blackburn Tornike Mamuladze Oscar Harari Celeste M. Karch Randall J. Bateman Richard J. Perrin Martin R. Farlow Jasmeer P. Chhatwal Jared R. Brosch Jill Buck Marty Farlow Bernardino Ghetti Sarah Adams Nicolas R. Barthélemy Tammie L.S. Benzinger Susan E. Brandon Virginia Buckles Lisa Cash Charlie Chen Jasmin Chua Carlos Cruchaga Darcy Denner Aylin Dincer Tamara Donahue Anne M. Fagan Becca Feldman Shaney Flores Erin Franklin Nelly Joseph‐Mathurin Alyssa Gonzalez Brian A. Gordon Julia Gray Emily Gremminger Alex Groves Jason Hassenstab Cortaiga Hellm Elizabeth Herries Laura Hoechst-Swisher David M. Holtzman Russ C. Hornbeck Gina Jerome Sarah Keefe Deb Koudelis Yan Li Jacob I. Marsh Rita Martinez Kwasi G. Mawuenyega Austin McCullough Eric McDade John Morris Joanne Norton Kristine Shady Wendy Sigurdson Jennifer A. Smith Peter Wang Qing Wang Chengjie Xiong Jinbin Xu Xu Xiong Ricardo Allegri Patricio Chrem Méndez Noelia Egido Aki Araki Takeshi Ikeuchi Kenji Ishii Kensaku Kasuga Jacob Bechara W. K. Brooks Peter R. Schofield Sarah Berman Sarah B. Goldberg Snežana Ikonomović William E. Klunk Oscar L. López James M. Mountz Neelesh K. Nadkarni Riddhi Patira Lori Smith Beth E. Snitz Sarah Thompson Elise A. Weamer Courtney Bodge Stephen Salloway Kathleen Carter Duc M. Duong Erik C. B. Johnson Allan I. Levey Lingyan Ping Nicholas T. Seyfried Colleen Fitzpatrick Helena C. Chui John M. Ringman

Macrophages are important players in the maintenance of tissue homeostasis1. Perivascular and leptomeningeal macrophages reside near central nervous system (CNS) parenchyma2, their role CNS physiology has not been sufficiently well studied. Given continuous interaction with cerebrospinal fluid (CSF) strategic positioning, we refer to these cells collectively as parenchymal border (PBMs). Here demonstrate that PBMs regulate CSF flow dynamics. We identify a subpopulation express high levels...

10.1038/s41586-022-05397-3 article EN cc-by Nature 2022-11-09

Tauopathy is a hallmark pathology of Alzheimer's disease with strong relationship cognitive impairment. As such, understanding tau may be key to clinical interventions. In vivo tauopathy has been measured using cerebrospinal fluid assays, but these do not provide information about where in the brain. The introduction PET ligands that bind paired helical filaments provides ability measure amount and distribution pathology. heritability age dementia onset tied specific mutations found...

10.1093/brain/awz019 article EN Brain 2019-01-29
Estrella Morenas‐Rodríguez Yan Li Brigitte Nuscher Nicolai Franzmeier Chengjie Xiong and 95 more Marc Suárez‐Calvet Anne M. Fagan Stephanie A. Schultz Brian A. Gordon Tammie L.S. Benzinger Jason Hassenstab Eric McDade Regina Feederle Celeste M. Karch Kai Schlepckow John C. Morris Gernot Kleinberger Bengt Nellgård Jonathan Vöglein Kaj Blennow Henrik Zetterberg Michael Ewers Mathias Jucker Johannes Levin Randall J. Bateman Christian Haass Sarah Adams Ricardo Allegri Aki Araki Nicolas R. Barthélemy Jacob Bechara Sarah Berman Courtney Bodge Susan E. Brandon William S. Brooks Jared R. Brosch Jill Buck Virginia Buckles Kathleen Carter Lisa Cash Charlie Chen Jasmeer P. Chhatwal Patricio Chrem Jasmin Chua Helena Chui Carlos Cruchaga Gregory S. Day Chrismary De La Cruz Darcy Denner Anna Diffenbacher Aylin Dincer Tamara Donahue Jane Douglas Duc M. Duong Noelia Egido Bianca Esposito Marty Farlow Becca Feldman Colleen Fitzpatrick Shaney Flores Nick C. Fox Erin Franklin Nelly Friedrichsen Hisako Fujii Samantha L. Gardener Bernardino Ghetti Alison Goate Sarah B. Goldberg Jill Goldman Alyssa Gonzalez Susanne Gräber‐Sultan Neill Graff-Radford Morgan Graham Julia Gray Emily Gremminger Miguel L. Grilo Alex Groves Lisa M. Häsler Cortaiga Hellm Elizabeth Herries Laura Hoechst-Swisher Anna Hofmann David M. Holtzman Russ C. Hornbeck Yakushev Igor Ryoko Ihara Takeshi Ikeuchi Snežana Ikonomović Kenji Ishii Clifford Jack Gina Jerome Erik C. B. Johnson Stephan Käser Kensaku Kasuga Sarah Keefe William E. Klunk Robert A. Koeppe Deb Koudelis Elke Kuder-Buletta Christoph Laske

Therapeutic modulation of TREM2-dependent microglial function might provide an additional strategy to slow the progression Alzheimer's disease. Although studies in animal models suggest that TREM2 is protective against pathology, its effect on tau pathology and potential beneficial role people with disease still unclear. Our aim was study associations between dynamics soluble TREM2, as a biomarker signalling, amyloid β (Aβ) deposition, tau-related neuroimaging markers, cognitive decline,...

10.1016/s1474-4422(22)00027-8 article EN cc-by-nc-nd The Lancet Neurology 2022-03-16
Erik C. B. Johnson Shijia Bian Rafi U. Haque Kathleen Carter Caroline M. Watson and 95 more Brian A. Gordon Lingyan Ping Duc M. Duong Michael P. Epstein Eric McDade Nicolas R. Barthélemy Celeste M. Karch Chengjie Xiong Carlos Cruchaga Richard J. Perrin Aliza P. Wingo Thomas S. Wingo Jasmeer P. Chhatwal Gregory S. Day James M. Noble Sarah Berman Ralph N. Martins Neill R. Graff‐Radford Peter R. Schofield Takeshi Ikeuchi Hiroshi Mori Johannes Levin Martin R. Farlow James J. Lah Christian Haass Mathias Jucker John C. Morris Tammie L.S. Benzinger Blaine R. Roberts Randall J. Bateman Anne M. Fagan Nicholas T. Seyfried Allan I. Levey Jonathan Vöglein Ricardo Allegri Patricio Chrem Méndez Ezequiel Surace Sarah Berman Snežana Ikonomović Neelesh K. Nadkarni Francisco Lopera Laura Ramírez David Aguillón Yudy Milena Leon Cláudia Ramos Diana Alzate Ana Baena Natalia Padilla Sonia Moreno Christoph Laske Elke Kuder-Buletta Susanne Gräber‐Sultan Oliver Preische Anna Hofmann Kensaku Kasuga Yoshiki Niimi Kenji Ishii Michio Senda Raquel Sánchez‐Valle Pedro Rosa‐Neto Nick C. Fox David M. Cash Jae‐Hong Lee Jee Hoon Roh Meghan Riddle William Menard Courtney Bodge Mustafa Surti Leonel Tadao Takada Víctor Javier Sánchez-González Maribel Orozco-Barajas Alison Goate Alan E. Renton Bianca Esposito Jacob Marsh Carlos Cruchaga María Victoria Fernández Gina Jerome Elizabeth Herries Jorge J. Llibre‐Guerra William S. Brooks Jacob Bechara Jason Hassenstab Erin Franklin Allison Chen Charles D. Chen Shaney Flores Nelly Friedrichsen Nancy Hantler Russ C. Hornbeck Steve Jarman Sarah Keefe Deborah Koudelis Parinaz Massoumzadeh Austin McCullough

Abstract Alzheimer’s disease (AD) pathology develops many years before the onset of cognitive symptoms. Two pathological processes—aggregation amyloid-β (Aβ) peptide into plaques and microtubule protein tau neurofibrillary tangles (NFTs)—are hallmarks disease. However, other brain processes are thought to be key mediators Aβ plaque NFT pathology. How these additional pathologies evolve over course is currently unknown. Here we show that proteomic measurements in autosomal dominant AD...

10.1038/s41591-023-02476-4 article EN cc-by Nature Medicine 2023-08-01

Genetic studies of Alzheimer disease (AD) have prioritized variants in genes related to the amyloid cascade, lipid metabolism, and neuroimmune modulation. However, cell-specific effect these is not fully understood. Here, we perform single-nucleus RNA-sequencing (snRNA-seq) on nearly 300,000 nuclei from parietal cortex AD autosomal dominant (APP PSEN1) risk-modifying variant (APOE, TREM2 MS4A) carriers. Within individual cell types, capture commonly dysregulated across groups. specific...

10.1038/s41467-023-37437-5 article EN cc-by Nature Communications 2023-04-21
Jorge J. Llibre‐Guerra María Victoria Fernández Nelly Joseph‐Mathurin Shijia Bian Kathleen Carter and 95 more Yan Li Andrew J. Aschenbrenner Cyril Pottier Wendy Sigurdson Eric McDade Brian A. Gordon Alan E. Renton Tammie L.S. Benzinger Laura Ibáñez Nicole Barthélémy Matthew P. Johnson Jason Hassenstab Guoqiao Wang Alison Goate Daniel Western Ciyang Wang Diana A. Hobbs Alisha Daniels Celeste M. Karch John C. Morris Carlos Cruchaga Erik C. B. Johnson Randall J. Bateman David Aguillón Ricardo Allegri Ana Baena Bryce Baker Jessica Banks Nicolas R. Barthélemy Jamie Bartzel Randall J. Bateman Jacob Bechara Sarah Berman Yamile Bocanegra William S. Brooks David M. Cash Allison Chen Charles Chen Jasmeer P. Chhatwal Patricio Chrem Méndez Laura Courtney Alisha Daniels Gregory S. Day Emma Devenney Anne M. Fagan Martin R. Farlow Shaney Flores Nick C. Fox Erin Franklin Brian Fulton‐Howard Manu S. Goyal Susanne Gräber‐Sultan Neill R. Graff‐Radford Emily Gremminger Cortaiga Hellm David M. Holtzman Russ C. Hornbeck Edward D. Huey Laura Ibáñez Takeshi Ikeuchi Snežana Ikonomović Takanobu Ishiguro Kenji Ishii Kelley Jackson Gina Jerome Mathias Jucker Celeste M. Karch Kensaku Kasuga Sarah Keefe Deborah Koudelis Elke Kuder-Buletta Christian la Fougère Christoph Laske Jae Hong Lee Allan I. Levey Johannes Levin Yudy Milena Leon Francisco Lopera Ruijin Lu Courtney Maa Jacob Marsh Mariana Martin Ralph N. Martins Parinaz Massoumzadeh Colin L. Masters Austin McCullough Nicole S. McKay Matthew Minton Hiroshi Mori Joyce Nicklaus Yu-zheng Nie Yoshiki Niimi James M. Noble Ulrike Obermueller Richard J. Perrin

10.1038/s41591-025-03494-0 article EN Nature Medicine 2025-02-10

Objective To examine default mode and salience network functional connectivity as a function of APOE ε4 status in group cognitively normal age-, sex-, education-matched older adults. Design Case-control study. Subjects Fifty-six carriers 56 sex- noncarriers. Main Outcome Measure Alterations in-phase compared with noncarriers ranging from 63 to 91 years age. Results A posterior cingulate seed revealed decreased regions the that included left inferior parietal lobe, middle temporal gyrus,...

10.1001/archneurol.2011.108 article EN Archives of Neurology 2011-05-10
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