Evidence map›Paper›PMID 42455403›Full record

ArticleEJNMMI physics2026

MLPET: a localized neural network approach for probabilistic post-reconstruction PET image analysis using informed priors.

Thomas Mejer Hansen, Nana Louise Christensen, Mikkel Holm Vendelbo

Abstract read
In one paragraph

Article in EJNMMI physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Thomas Mejer HansenDepartment of Geoscience, Aarhus University, Høgh-Guldbergs Gade 2, 8000, Aarhus C, Denmark. tmeha@geo.au.dk.ORCID http://orcid.org/0000-0003-4529-0112
Nana Louise ChristensenDepartment of Nuclear Medicine and PET-center, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-9936-1636
Mikkel Holm VendelboDepartment of Nuclear Medicine and PET-center, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0003-0431-2522

Funding

Beta.Health Denmark 2024-1792
6 · The paper itself

Abstract

purposePET images often make small lesions difficult to identify because of noise and system blur. We address this by developing and evaluating MLPET , a fast localized machine-learning method that approximates a computationally expensive probabilistic sampling approach while reducing noise and increasing spatial resolution.

methodsBuilding on a probabilistic deconvolution framework with informed priors, MLPET replaces computationally demanding Markov chain Monte Carlo sampling with a localized neural network trained to directly estimate the posterior mean of voxel activity from small image neighborhoods. The method incorporates scanner-specific point spread functions (PSF), spatially correlated noise modeling, and flexible prior information. Performance was evaluated on NEMA phantom data acquired on three PET systems (GE Discovery MI, Siemens Biograph Vision 600, and Siemens Biograph Vision Quadra Edge) under varying reconstruction settings and acquisition times.

resultsOn NEMA IEC phantom data, MLPET produced contrast-recovery coefficients consistently higher than PET and frequently close to 1.0 (including the 10 mm sphere in several settings), while simultaneously reducing background noise and improving spatial definition. The effective point-spread function (PSF) full width at half maximum (FWHM) was on average reduced from about 2 mm in PET to below 1 mm with MLPET , corresponding to roughly a 2.5× decrease in effective blur. Comparable image quality was obtained at 40-80 s acquisition time using MLPET versus 900 s with conventional PET. A clinical example in a breast cancer patient illustrates potential clinical applicability.

conclusionsMLPET provides a computationally efficient approach for quantitative probabilistic post-reconstruction PET image analysis. By combining informed priors with the speed of a neural network, it achieves both noise suppression and resolution enhancement. The method shows promise for improved small-lesion detectability and quantitative reliability in clinical PET imaging. Future clinical studies will evaluate its performance on patient data and quantify effects under realistic prior uncertainty.

Indexed as

Medical imagingNEMA phantomNeural networksPET imagingPost-reconstruction analysisProbabilisticResolution

Identifiers

PMID42455403
PMCPMC13677664

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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.