Evidence map›Paper›PMID 24335879›Full record

Trial reportNuclear medicine communications2014

Calibrated image-derived input functions for the determination of the metabolic uptake rate of glucose with [18F]-FDG PET.

Anders N Christensen, Michala H Reichkendler, Rasmus Larsen, Pernille Auerbach, Liselotte Højgaard, Henning B Nielsen, Thorkil Ploug, Bente Stallknecht, Søren Holm

Abstract readClinical Trial
In one paragraph

Trial report in Nuclear medicine communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  6. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Anders N ChristensenDepartments of aClinical Physiology, Nuclear Medicine and PET bAnesthesiology, Rigshospitalet cDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen dDepartment of Applied Mathematics and Computer Science, Technical University of Denmark, Kongens Lyngby, Denmark.
Michala H Reichkendler
Rasmus Larsen
Pernille Auerbach
Liselotte Højgaard
Henning B Nielsen
Thorkil Ploug
Bente Stallknecht
Søren Holm

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe investigated the use of a simple calibration method to remove bias in previously proposed approaches to image-derived input functions (IDIFs) when used to calculate the metabolic uptake rate of glucose (K(m)) from dynamic [(18)F]-FDG PET scans of the thigh. Our objective was to obtain nonbiased, low-variance K(m) values without blood sampling. MATERIALS AND

methodsWe evaluated eight previously proposed IDIF methods. K(m) values derived from these IDIFs were compared with Km values calculated from the arterial blood samples (gold standard). We used linear regression to extract calibration parameters to remove bias. Following calibration, cross-validation and bootstrapping were used to estimate the mean square error and variance.

resultsThree of the previously proposed methods failed mainly because of zero-crossings of the IDIF. The remaining five methods were improved by calibration, yielding unbiased Km values. The method with the lowest SD yielded an SD of 0.0017/min--that is, below 10% of the muscle K(m) value in this study.

conclusionPreviously proposed IDIF methods can be improved by using a simple calibration procedure. The calibration procedure may be used in other studies, thus obviating the need for arterial blood sampling, once the calibration parameters have been established in a subgroup of participants. The method has potential for use in other parts of the body as it is robust with regard to partial volume effects.

Indexed as

Fluorodeoxyglucose F18Image Processing, Computer-AssistedPositron-Emission TomographyArea Under CurveBiological TransportBrainCalibrationGlucoseHumansMaleFluorodeoxyglucose F18Glucose

Identifiers

PMID24335879
PMCPMC3940375

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Registered trials

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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.