Evidence map›Paper›PMID 37573451›Full record

ArticleScientific reports2023

Using AI and Gd-EOB-DTPA-enhanced MR imaging to assess liver function, comparing the MELIF score with the ALBI score.

Carolina Río Bártulos, Karin Senk, Ragnar Bade, Mona Schumacher, Nico Kaiser, Jan Plath, Mathis Planert, Christian Stroszczynski, Jan Woetzel, Philipp Wiggermann

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. 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
0.6field-weighted citation impact, top 28% of its field
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, 3 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Carolina Río Bártulos *Institut Für Röntgendiagnostik Und Nuklearmedizin, Städtisches Klinikum Braunschweig gGmbH, 38126, Braunschweig, Germany. c.rio@skbs.de.
Karin Senk *Institut Für Röntgendiagnostik, Universitätsklinikum Regensburg, 93053, Regensburg, Germany.
Ragnar BadeMeVis Medical Solutions AG, 28359, Bremen, Germany.
Mona SchumacherMeVis Medical Solutions AG, 28359, Bremen, Germany.
Nico KaiserMeVis Medical Solutions AG, 28359, Bremen, Germany.
Jan PlathMeVis Medical Solutions AG, 28359, Bremen, Germany.
Mathis PlanertInstitut Für Röntgendiagnostik Und Nuklearmedizin, Städtisches Klinikum Braunschweig gGmbH, 38126, Braunschweig, Germany.
Christian StroszczynskiInstitut Für Röntgendiagnostik, Universitätsklinikum Regensburg, 93053, Regensburg, Germany.
Jan WoetzelMeVis Medical Solutions AG, 28359, Bremen, Germany.
Philipp WiggermannInstitut Für Röntgendiagnostik Und Nuklearmedizin, Städtisches Klinikum Braunschweig gGmbH, 38126, Braunschweig, Germany.
MeVis Medical Solutions (Germany) · DEKlinikum Braunschweig · DEUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring disease progression is particularly important for determining the optimal treatment strategy in patients with liver disease. Especially for patients with diseases that have a reversible course, there is a lack of suitable tools for monitoring liver function. The development and establishment of such tools is very important, especially in view of the expected increase in such diseases in the future. Image-based liver function parameters, such as the T1 relaxometry-based MELIF score, are ideally suited for this purpose. The determination of this new liver function score is fully automated by software developed with AI technology. In this study, the MELIF score is compared with the widely used ALBI score. The ALBI score was used as a benchmark, as it has been shown to better capture the progression of less severe liver disease than the MELD and Child‒Pugh scores. In this study, we retrospectively determined the ALBI and MELIF scores for 150 patients, compared these scores with the corresponding MELD and Child‒Pugh scores (Pearson correlation), and examined the ability of these scores to discriminate between good and impaired liver function (AUC: MELIF 0.8; ALBI 0.77) and to distinguish between patients with and without cirrhosis (AUC: MELIF 0.83, ALBI 0.79). The MELIF score performed more favourably than the ALBI score and may also be suitable for monitoring mild disease progression. Thus, the MELIF score is promising for closing the gap in the available early-stage liver disease monitoring tools (i.e., identification of liver disease at a potentially reversible stage before chronic liver disease develops).

Indexed as

Contrast MediaLiver DiseasesDisease ProgressionGadolinium DTPAHumansMagnetic Resonance ImagingRetrospective StudiesContrast MediaGadolinium DTPAgadolinium ethoxybenzyl DTPA

Identifiers

PMID37573451
PMCPMC10423205
OpenAlexW4385783649

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.