Evidence map›Paper›PMID 41059714›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Novel differentially expressed genes and multiple biological pathways for Alzheimer's disease identified in brain tissue from African American donors.

Mark W Logue, Adam Labadorf, Nicholas K O'Neill, Dennis W Dickson, Brittany N Dugger, Margaret E Flanagan, Matthew P Frosch, Marla Gearing, Lee-Way Jin, Julia Kofler and 16 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. From correlation to causation: cell-type-specific gene regulatory networks in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  3. Article
  4. Article
  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Mark W LogueDepartment of Psychiatry, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Adam LabadorfDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Nicholas K O'NeillDepartment of Medicine (Biomedical Genetics), Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Dennis W DicksonDepartments of Neuroscience and Laboratory Medicine & Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Brittany N DuggerDepartments of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
Margaret E FlanaganNorthwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Matthew P FroschC.S. Kubik Laboratory for Neuropathology, Massachusetts General Hospital & Harvard Medical School, Boston, Massachusetts, USA.
Marla GearingGADRC and Departments of Pathology & Laboratory Medicine and Neurology, Emory University, Atlanta, Georgia, USA.
Lee-Way JinDepartments of Pathology and Laboratory Medicine, UC Davis School of Medicine, Sacramento, California, USA.
Julia KoflerDivision of Neuropathology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Richard MayeuxTaub Institute for Research on Alzheimer's Disease and the Aging Brain, Department of Neurology, Columbia University, New York, New York, USA.
Ann McKeeDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Carol A MillerDepartment of Pathology, University of Southern California, Los Angeles, California, USA.
Melissa E MurrayDepartments of Neuroscience and Laboratory Medicine & Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Peter T NelsonSanders-Brown Center on Aging and Department of Pathology & Laboratory Medicine, University of Kentucky, Lexington, Kentucky, USA.
Richard J PerrinDepartments of Neurology and Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA.
Julie A SchneiderDepartments of Pathology (Neuropathology) and Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA.
Thor D SteinDepartment of Pathology & Laboratory Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Andrew F TeichTaub Institute for Research on Alzheimer's Disease and the Aging Brain, Department of Neurology, Columbia University, New York, New York, USA.
Katarnut TobunluepopDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Juan C TroncosoDepartments of Pathology and Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Shih-Hsiu WangDuke University Medical Center, Durham, North Carolina, USA.
Zihan WangDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Benjamin WolozinDepartment of Anatomy & Neurobiology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Jesse MezDepartment of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Lindsay A FarrerDepartment of Medicine (Biomedical Genetics), Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.

Funding

Vascular Structure and Function in Cognitive AgingP01AG003949 · NIA · YESHIVA UNIVERSITY · PI CAROL A. DERBY · 1985 to 2026
$73.9M
Smartphone-Based "Burst" Cognitive AssessmentsP01AG003991 · NIA · WASHINGTON UNIVERSITY · PI JOHN MORRIS · 1985 to 2026
$69.5M
The natural history of AB accumulation in preclinical ADP01AG026276 · NIA · WASHINGTON UNIVERSITY · PI MORRIS, JOHN · 2005 to 2025
$49.5M
TBDU19AG068753 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Rhoda Au, Lindsay A. Farrer · 2020 to 2026
$42.4M
Research Education ComponentP30AG062421 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI MATTHEW P FROSCH · 2019 to 2026
$36.5M
Research Education ComponentP30AG062677 · NIA · MAYO CLINIC ROCHESTER · PI KEJAL KANTARCI · 2019 to 2026
$33.5M
Genome Center for Alzheimer's Disease (GCAD)U54AG052427 · NIA · UNIVERSITY OF PENNSYLVANIA · PI SCHELLENBERG, GERARD DAVID, WANG, LI-SAN · 2016 to 2025
$32.8M
The National Institute on Aging (NIA) Late Onset of Alzheimer's Disease (LOAD) Family-Based Study (FBS)U24AG056270 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Gary Wayne Beecham, TATIANA M. FOROUD · 2017 to 2026
$31.4M
Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Christiane Reitz · 2020 to 2026
$30.1M
Research Education ComponentP30AG066468 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI C. Elizabeth Shaaban · 2020 to 2026
$29.4M
Research Education ComponentP30AG066507 · NIA · JOHNS HOPKINS UNIVERSITY · PI Jinchong Xu · 2020 to 2026
$29.3M
The Goizueta Alzheimer's Disease Research CenterP30AG066511 · NIA · EMORY UNIVERSITY · PI Jonathan David Glass · 2020 to 2026
$29.0M
Florida Department of Health 20A22Florida Department of Health 8AZ06NIA NIH HHS P01 AG003949NIA NIH HHS P01 AG003991NIA NIH HHS P01 AG026276NIA NIH HHS P30 AG062421NIA NIH HHS P30 AG062677NIA NIH HHS P30 AG066444NIA NIH HHS P30 AG066462NIA NIH HHS P30 AG066468NIA NIH HHS P30 AG066507NIA NIH HHS P30 AG066511NIA NIH HHS P30 AG072946NIA NIH HHS P30 AG072958NIA NIH HHS P30 AG072972NIA NIH HHS P30 AG072978NIA NIH HHS R01 AG048927NIA NIH HHS R01 AG066107NIA NIH HHS R01 AG072474NIA NIH HHS R01 AG082339NIA NIH HHS RF1 AG066107NIA NIH HHS RF1 AG082339NIA NIH HHS U01 AG058654NIA NIH HHS U01 AG062602NIA NIH HHS U19 AG068753NIA NIH HHS U24 AG056270NIA NIH HHS U54 AG052427NIH HHS P01-AG003949NIH HHS P01-AG003991NIH HHS P01-AG026276NIH HHS P30-AG062421NIH HHS P30-AG062677NIH HHS P30-AG066444NIH HHS P30-AG066462NIH HHS P30-AG066468NIH HHS P30-AG 066507NIH HHS P30-AG066511NIH HHS P30-AG072946NIH HHS P30-AG072958NIH HHS P30-AG 072972NIH HHS P30-AG072978NIH HHS R01-AG048927NIH HHS R01-AG072474NIH HHS RF1-AG066107NIH HHS RF1-AG082339NIH HHS RF1-NS118584NIH HHS U01-081230NIH HHS U01-AG058654NIH HHS U01-AG062602NIH HHS U19-AG068753NIH HHS U24-AG056270NIH HHS U54-AG052427NINDS NIH HHS R01 NS118584NINDS NIH HHS R01 NS122854NINDS NIH HHS RF1 NS118584
6 · The paper itself

Abstract

introductionFew African American (AA) donors have been included in post mortem Alzheimer's disease (AD) studies compared to European-ancestry (EA) individuals.

methodsWe generated transcriptome-wide bulk pre-frontal cortex (PFC) gene expression data from 125 AA donors with neuropathologically determined AD and 82 AA controls.

resultsTranscriptome-wide significant differential expression was observed with 482 genes. The most significant, ADAMTS2, showed 1.52 times higher expression in AD cases (p = 2.96x10

conclusionThis first large-scale AA brain AD gene expression study identified many differentially expressed genes, including ADAMTS2, and supports gene expression as a molecular pathway underlying the impact of several AA AD risk variants. HIGHLIGHTS: We performed the largest African American brain tissue Alzheimer's disease (AD) gene expression study. Expression differences for 482 genes, notably ADAMTS2, were study-wide significant. Many significant differentially expressed genes are involved in energy metabolism. Several previously known AD-associated variants in African Americans are eQTLs. These results advance knowledge of the genetic basis of AD in the AA population.

Indexed as

Alzheimer DiseaseBlack or African AmericanBrainAgedAged, 80 and overFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedTissue DonorsTranscriptomeWhiteADAMTS2African AmericanAlzheimer diseasedifferential gene expressioneQTLgene network analysis

Identifiers

PMID41059714
PMCPMC12505200

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.