Evidence map›Paper›PMID 41653394›Full record

ArticleAnnals of nuclear medicine2026

A new amyloid PET evaluation method using separated gray-matter histogram based on three-component model.

Chio Okuyama, Naoya Oishi, Koichi Ishizu, Hiroshi Hasegawa, Miki Ito, Yoshiharu Fujita, Kuninori Kusano, Tomoko Okina, Shinya Kagawa, Hiroyuki Watanabe and 3 more

Abstract read
In one paragraph

Article in Annals of nuclear medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Chio OkuyamaClinical Research Center , Shiga General Hospital , Moriyama, Japan. c-okuyama@res.med.shiga-pref.jp.ORCID http://orcid.org/0000-0002-9088-8917
Naoya OishiHuman Brain Research Center Graduate School of Medicine , Kyoto University , Kyoto, Japan.
Koichi IshizuClinical Research Center , Shiga General Hospital , Moriyama, Japan.
Hiroshi HasegawaDepartment of Neurology , Shiga General Hospital , Moriyama, Japan.
Miki ItoDepartment of Radiology , Shiga General Hospital , Moriyama, Japan.
Yoshiharu FujitaDepartment of Radiology , Shiga General Hospital , Moriyama, Japan.
Kuninori KusanoDepartment of Radiology , Shiga General Hospital , Moriyama, Japan.
Tomoko OkinaDepartment of Neurology , Shiga General Hospital , Moriyama, Japan.
Shinya KagawaClinical Research Center , Shiga General Hospital , Moriyama, Japan.
Hiroyuki WatanabeDepartment of Patho-Functional Bioanalysis Graduate School of Pharmaceutical Sciences , Kyoto University , Kyoto, Japan.
Tatsuya HigashiClinical Research Center , Shiga General Hospital , Moriyama, Japan.
Hiroshi YamauchiClinical Research Center , Shiga General Hospital , Moriyama, Japan.
Masahiro OnoDepartment of Patho-Functional Bioanalysis Graduate School of Pharmaceutical Sciences , Kyoto University , Kyoto, Japan.

Funding

Japan Society for the Promotion of Science KAKENHI (JSPS Grant Number JP21K07635).
6 · The paper itself

Abstract

objectiveWe have constructed a three-component model underlying amyloid PET accumulation and developed a new gray matter histogram evaluation method based on this model. This study aims to validate the utility of the new method compared with conventional visual and SUVR-based quantitative evaluation.

methodsA retrospective analysis was performed on amyloid PET/CT data from 63 participants (25 healthy volunteers, 38 patients with dementia or cognitive impairment) of previous study using 18F-FPYBF-2. Subjects were visually classified into three groups: negative, borderline, and positive, and quantitatively evaluated using composed standardized uptake value (comSUVR) with a reference to cerebellar cortex. Histograms were generated for the whole-brain, gray matter (GM-histogram), and white matter (WM-histogram) based on probability-tissue maps. The GM-histogram was further decomposed into two Gaussian components: G1 and G2 using statistical software. Parameters of whole-brain histogram: skewness, mode-to-mean ratio (MMR), and parameters of GM-histogram: GM-kurtosis, µG2 (mean of G2), and πG2 (proportion of G2), were compared among visual groups and the correlation with comSUVR was evaluated.

resultsThe GM-histogram was sharply unimodal in visually negative group but showed a wide shape to bimodal patterns in visually positive cases. Visually border group showed significantly higher πG2 than negative group, and positive group showed significantly higher µG2 than border group. GM-kurtosis and µG2 showed stronger negative (p < 0.0001, R2 = 0.7539) and positive (p < 0.0001, R2 = 0.8589) correlations with ComSUVR, respectively than the correlations between whole-brain histogram parameters and ComSUVR.

conclusionOur proposed GM-histogram provides a visually comprehensive morphology and quantitative indicators that match conventional visual and SUVR-based assessments and may potentially detect even subtle amyloid accumulation. This method is considered promising as a complementary tool for early diagnosis and treatment monitoring of Alzheimer’s disease.

Indexed as

AmyloidGray MatterImage Processing, Computer-AssistedPositron-Emission TomographyPositron Emission Tomography Computed TomographyAgedFemaleHumansMaleMiddle AgedRetrospective StudiesAmyloidAmyloid PETF-18-FPYBF-2Gray matterHistogramObjective evaluationThree-component model

Identifiers

PMID41653394
PMCPMC13124921

What Socratic holds

Textmetadata
LicenceCC BY
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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.