Evidence map›Paper›PMID 24434295›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2014

Evaluation of frame-based and event-by-event motion-correction methods for awake monkey brain PET imaging.

Xiao Jin, Tim Mulnix, Christine M Sandiego, Richard E Carson

Registry-linked trialAbstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05105542 (Muscarinic M1 Receptor Availability and Cognition in Schizophrenia), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

NCT05105542 phase1completednot on this mapstarted 2021, after this paper: background citation

Muscarinic M1 Receptor Availability and Cognition in Schizophrenia

TypeinterventionalSponsorYale UniversityRan2021 to 2023Enrolled18ConditionsSchizophrenia, Schizoaffective Disorder, HealthyArms11C-EMO - A Novel PET Radiotracer for Muscarinic M1 Receptor, PET Scan
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Performance Characteristics of the NeuroEXPLORER, a Next-Generation Human Brain PET/CT Imager.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
    Article
  4. Fast Reconstruction for Deep Learning PET Head Motion Correction.Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention · 2023
    Article
  5. Supervised Deep Learning for Head Motion Correction in PET.Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

4 authors.

Xiao JinDepartment of Biomedical Engineering, Yale University, New Haven, Connecticut; and.
Tim Mulnix
Christine M Sandiego
Richard E Carson

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
Quantitative High Resolution Human Brain PET ImagingR01NS058360 · NINDS · YALE UNIVERSITY · PI CARSON, RICHARD E. · 2007 to 2010
$1.4M
NCRR NIH HHS UL1 RR024139NINDS NIH HHS R01 NS058360
6 · The paper itself

Abstract

unlabelledPET imaging of nonhuman primates (NHPs) requires correction of head motion if the subjects are scanned awake and their heads are unrestrained, because the NHPs move their heads faster and more frequently than human subjects. This work focuses on designing and validating 2 motion-correction algorithms for awake NHP brain PET imaging.

methodsTwo motion-correction methods were implemented for awake NHP brain PET imaging: multiacquisition frame (MAF) and event-by-event (EBE). Motion data were acquired from an external motion-tracking device. The MAF method divides scan data into short subframes, reconstructs each subframe individually, and registers them to a reference orientation. This method suffers from residual intraframe motion and data loss when motion is large because a minimum frame duration is often required. The EBE method, previously implemented for a human brain scanner and adapted for a small-animal PET scanner in this work, eliminates intraframe motion and should have a best accuracy. We first evaluated the accuracy of both motion-correction methods with moving phantom scans. Both motion-correction methods were then applied to awake NHP brain PET studies with a gamma-aminobutyric acid A-benzodiazepine receptor ligand, (11)C-flumazenil, and the reconstructed images were compared with those from a motion-free anesthetized study.

resultsThe phantom studies showed that EBE motion correction recovers the contrast (within 3%) similarly to the static study, whereas MAF motion correction using the standard algorithm setting showed a 25% reduction in contrast from the static case. In awake NHP brain PET imaging, EBE motion correction better recovers the fine structures than the MAF method, as compared with anesthetized studies.

conclusionThe large magnitude and frequency of NHP head motion suggests that EBE motion correction with accurate externally measured motion data can noticeably alleviate image blurring due to the intraframe motion in the MAF motion-correction method.

Indexed as

AlgorithmsAnimalsArtifactsBrainFlumazenilgamma-Aminobutyric AcidImage Processing, Computer-AssistedLigandsMacaca mulattaModels, StatisticalMotionPhantoms, ImagingPositron-Emission TomographyReproducibility of ResultsTime FactorsWakefulnessFlumazenilgamma-Aminobutyric AcidLigandsawakemonkeymotion correctionPET

Identifiers

PMID24434295
PMCPMC4157052

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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.