Evidence map›Paper›PMID 41425086›Full record

ArticleAlzheimer's & dementia (New York, N. Y.)

Immediate reactions to amyloid PET disclosure in Japanese older adults without dementia.

Kenichiro Sato, Yoshiki Niimi, Ryoko Ihara, Takeshi Ikeuchi, Kenji Ishii, Kengo Ito, Atsushi Iwata, Kensaku Kasuga, Takashi Kato, Hisatomo Kowa and 7 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia (New York, N. Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

17 authors.

Kenichiro SatoDepartment of Neuropathology Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID https://orcid.org/0000-0003-4351-9526
Yoshiki NiimiUnit for Early and Exploratory Clinical Development The University of Tokyo Hospital Tokyo Japan.ORCID https://orcid.org/0000-0002-2556-8167
Ryoko IharaDepartment of Neurology Tokyo Metropolitan Institute for Geriatrics and Gerontology Tokyo Japan.
Takeshi IkeuchiDepartment of Molecular Genetics Brain Research Institute Niigata University Niigata-shi Japan.
Kenji IshiiIntegrated Research Initiative for Living Well with Dementia Tokyo Metropolitan Institute for Geriatrics and Gerontology Tokyo Japan.
Kengo ItoDepartment of Clinical and Experimental Neuroimaging National Center for Geriatrics and Gerontology Obu-shi Aichi Japan.
Atsushi IwataDepartment of Neurology Tokyo Metropolitan Institute for Geriatrics and Gerontology Tokyo Japan.
Kensaku KasugaDepartment of Molecular Genetics Brain Research Institute Niigata University Niigata-shi Japan.
Takashi KatoDepartment of Clinical and Experimental Neuroimaging National Center for Geriatrics and Gerontology Obu-shi Aichi Japan.
Hisatomo KowaGraduate School of Health Sciences Kobe University Kobe-shi Hyogo Japan.
Taizen NakaseDepartment of Geriatrics and Gerontology Institute of Development Aging and Cancer Tohoku University Sendai-shi Miyagi Japan.
Michio SendaDivision of Molecular Imaging Research Kobe City Medical Center General Hospital Kobe-shi Hyogo Japan.
Kazushi SuzukiDivision of Neurology Internal Medicine National Defense Medical College Tokorozawa-shi Saitama Japan.
Naoki TomitaDepartment of Geriatrics and Gerontology Institute of Development Aging and Cancer Tohoku University Sendai-shi Miyagi Japan.
Tadashi TsukamotoDepartment of Neurology National Center of Neurology and Psychiatry Kodaira-shi Tokyo Japan.
Kenji YoshiyamaDepartment of Psychiatry Graduate School of Medicine Osaka University Suita-shi Osaka Japan.
Takeshi IwatsuboDepartment of Neuropathology Graduate School of Medicine The University of Tokyo Tokyo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAmyloid positron emission tomography (PET) has become increasingly important for detection of early Alzheimer's disease (AD) and eligibility for emerging disease-modifying therapies. While North American and European studies report limited short-term psychological harm following disclosure of amyloid status in asymptomatic individuals, evidence in non-North American and European contexts is scarce. We evaluated the immediate psychological impact of amyloid PET disclosure in a large Japanese cohort without dementia.

methodsWe analyzed data from 630 cognitively unimpaired Clinical Dementia Rating global score (CDR-GS of 0, 70%) or mild cognitive impairment (CDR-GS of 0.5, 30%) participants 50-85 years of age enrolled in the Japanese Trial-Ready Cohort onsite study across seven centers between July 2020 and January 2024. Amyloid PET positivity was defined by visual read or Centiloid ≥12. Psychological outcomes-Future Time Perspective (FTP), and Concerns about AD-were assessed immediately before and after disclosure; Impact of Event Scale (IES) was also measured via telephone 1-3 days post-disclosure. Mixed-effects Poisson and linear regression models, adjusted for site, participant, and baseline covariates, evaluated the effects of PET positivity on post-disclosure outcomes.

resultsTwenty-six percent of participants were PET positive. PET-positive individuals experienced greater distress (median IES 8 vs 3) compared with PET-negative peers, whereas FTP improved similarly irrespective of PET status. Concerns about AD increased modestly in PET-positive participants (+4.8%) but decreased in PET-negative individuals (-5.5%; interaction DISCUSSION: Consistent with North American and European findings, amyloid PET disclosure in this Japanese cohort was generally well-tolerated, eliciting only modest increases in distress and concerns among PET-positive individuals. These results support the feasibility and ethical acceptability of structured disclosure protocols across cultural settings and highlight the importance of tailored counseling for at-risk subgroups. Highlights: Immediate impact of amyloid disclosure in a Japanese cohort without dementia.Amyloid-positive individuals had higher distress (Impact of Event Scale) after disclosure.Future Time Perspective improved similarly regardless of amyloid positron emission tomography (PET) results.Concerns about Alzheimer's disease slightly rose in PET-positive participants.Female sex and higher baseline depression and anxiety predicted larger distress.

Indexed as

Alzheimer's diseaseamyloid PETAsianJapanesemild cognitive impairmentpreclinicalpsychological distress

Identifiers

PMID41425086
PMCPMC12715704

What Socratic holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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 Socratic graph.