Evidence map›Paper›PMID 38629508›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2024

Racial and ethnic differences in plasma biomarker eligibility for a preclinical Alzheimer's disease trial.

Doris Patricia Molina-Henry, Rema Raman, Andy Liu, Oliver Langford, Keith Johnson, Leona K Shum, Crystal M Glover, Shobha Dhadda, Michael Irizarry, Gustavo Jimenez-Maggiora and 9 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04468659 (AHEAD 3-45 Study), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
13.1field-weighted citation impact, top 1% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04468659 phase3active not recruitingnot on this map

AHEAD 3-45 Study: A Placebo-Controlled, Double-Blind, Parallel-Treatment Arm, 216 Week Study With an Extension Phase to Evaluate Efficacy and Safety of Treatment With BAN2401 in Subjects With Preclinical Alzheimer's Disease and Elevated Amyloid (A45 Trial) and in Subjects With Early Preclinical Alzheimer's Disease and Intermediate Amyloid (A3 Trial)

TypeinterventionalSponsorEisai Inc.Ran2020 to 2031Enrolled1,400ConditionsPreclinical Alzheimer's Disease, Early Preclinical Alzheimer's DiseaseArmsLecanemab, Placebo
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Perspectives from Alzheimer's Disease Research Centers site directors on the early steps and the lasting impact.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. The roles of biomarkers in Alzheimer's disease clinical trials.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  11. Solving the 'Goldilocks problem' in dementia clinical trials with multimodal AI.The journal of prevention of Alzheimer's disease · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Comparison of plasma p-tau217/Aβ42, p-tau217, and Aβ42/Aβ40 biomarkers by race to detect Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  16. Review
  17. Evaluation of plasma p-tau217 for detecting amyloid pathology in a heterogeneous community-based cohort.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  18. Novel set of plasma proteins classifies Alzheimer's dementia in African American individuals with high accuracy.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  19. Impact of racialization on neuroimaging and plasma biomarkers of Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  20. Review
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

19 authors at 8 institutions in 1 country.

Doris Patricia Molina-HenryAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Rema RamanAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Andy LiuAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Oliver LangfordAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Keith JohnsonMassachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Leona K ShumAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Crystal M GloverRush Alzheimer's Disease Center, Chicago, Illinois, USA.
Shobha DhaddaEisai Inc., Nutley, New Jersey, USA.
Michael IrizarryEisai Inc., Nutley, New Jersey, USA.
Gustavo Jimenez-MaggioraAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Joel B BraunsteinC2N Diagnostics, St. Louis, Missouri, USA.
Kevin YarasheskiC2N Diagnostics, St. Louis, Missouri, USA.
Venky VenkateshC2N Diagnostics, St. Louis, Missouri, USA.
Tim WestC2N Diagnostics, St. Louis, Missouri, USA.
Philip B VergheseC2N Diagnostics, St. Louis, Missouri, USA.
Robert A RissmanDepartment of Physiology and Neuroscience, Alzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Paul AisenAlzheimer's Therapeutic Research Institute, Keck School of Medicine of the University of Southern California, San Diego, California, USA.
Joshua D GrillInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, USA.
Reisa A SperlingMassachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Autism Research Institute · USC2N Diagnostics (United States) · USUniversity of Southern California · USEisai (United States) · USHarvard University · USMassachusetts General Hospital · USRush University · USUniversity of California, Irvine · US

Funding

The Alzheimer's Clinical Trial Consortium - Down Syndrome Network (ACTC- DSN)U24AG057437 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Paul S. Aisen, RONALD C PETERSEN · 2018 to 2026
$198.4M
Combination anti-amyloid therapy for preclinical Alzheimer's diseaseR01AG061848 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AISEN, PAUL S., JOHNSON, KEITH A. · 2018 to 2024
$43.9M
Trial-Ready Cohort for Preclinical/Prodromal Alzheimer's DiseaseR01AG053798 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AISEN, PAUL S., CUMMINGS, JEFFREY L. · 2017 to 2022
$39.4M
USCADRC Diversity Supplement PachicanoP30AG066530 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HELENA Chang CHUI · 2020 to 2026
$27.8M
The A3 Study: Ante-Amyloid Prevention of Alzheimer's diseaseR01AG054029 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI AISEN, PAUL S., JOHNSON, KEITH A. · 2016 to 2023
$20.9M
Alzheimer's Association SG-22-877415-AHEADEisai Inc.Gerald and Henrietta Rauenhorst (GHR) FoundationNIA NIH HHS P30 AG066530NIA NIH HHS R01 AG053798NIA NIH HHS R01 AG054029NIA NIH HHS R01 AG061848NIH/NIA R01AG054029NIH/NIA R01AG061848NIH/NIA U24AG057437
6 · The paper itself

Abstract

introductionIn trials of amyloid-lowering drugs for Alzheimer's disease (AD), differential eligibility may contribute to under-inclusion of racial and ethnic underrepresented groups. We examined plasma amyloid beta 42/40 and positron emission tomography (PET) amyloid eligibility for the ongoing AHEAD Study preclinical AD program (NCT04468659).

methodsUnivariate logistic regression models were used to examine group differences in plasma and PET amyloid screening eligibility.

resultsOf 4905 participants screened at time of analysis, 1724 were plasma eligible to continue in screening: 13.3% Hispanic Black, 24.7% Hispanic White, 20.8% non-Hispanic (NH) Asian, 24.7% NH Black, and 38.9% NH White. Plasma eligibility differed across groups in models controlling for covariates (odds ratio from 1.9 to 4.0 compared to the NH White reference group, P < 0.001). Among plasma eligible participants, PET eligibility did not differ by group. DISCUSSION: These results suggest that prevalence of brain amyloid pathology differed, but that eligibility based on plasma was equally effective across racial and ethnic group members. HIGHLIGHTS: Plasma amyloid eligibility is lower in underrepresented racial and ethnic groups. In plasma eligible adults, positron emission tomography eligibility rates are similar across race and ethnicity. Plasma biomarker tests may be similarly effective across racial and ethnic groups.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBiomarkersPositron-Emission TomographyAgedBrainEthnicityFemaleHumansMaleRacial GroupsAmyloid beta-PeptidesBiomarkersamyloidbiomarkerethnicityplasmapositron emission tomographyrace

Identifiers

PMID38629508
PMCPMC11180863
OpenAlexW4394873360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.