Evidence map›Paper›PMID 39630731›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2024

Liver/spleen magnetic resonance elastography and T1/T2 mapping in chronic liver disease: a prospective study.

Gökhan Mert Özyurt, Kaan Esen, Enver Üçbilek, Feramuz Demir Apaydın

Erratum issuedAbstract read
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Article in Revista da Associacao Medica Brasileira (1992), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Gökhan Mert ÖzyurtMersin University, School of Medicine, Department of Radiology - Mersin, Turkey.ORCID http://orcid.org/0000-0002-5382-6696
Kaan EsenMersin University, School of Medicine, Department of Radiology - Mersin, Turkey.ORCID http://orcid.org/0000-0002-8404-7484
Enver ÜçbilekMersin University, School of Medicine, Department of Gastroenterology - Mersin, Turkey.ORCID http://orcid.org/0000-0002-2935-5580
Feramuz Demir ApaydınMersin University, School of Medicine, Department of Radiology - Mersin, Turkey.ORCID http://orcid.org/0000-0002-2989-1383

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aims to compare liver and spleen stiffness measurements using magnetic resonance elastography with T1 and T2 relaxation times in patients with chronic liver disease.

methodsA total of 75 chronic liver disease patients and 25 healthy volunteers underwent MR. Patients with significant liver fat and iron accumulation were excluded. Student's t-test was employed to compare magnetic resonance elastography and T1/T2 values. Pearson's correlation test was used to assess the relationship between magnetic resonance elastography and T1/T2 values.

resultsLiver magnetic resonance elastography showed a significant moderate positive correlation with liver T1 mapping (r=0.51, p<0.001) and liver T2 mapping (r=0.30, p=0.009) in patients. Spleen magnetic resonance elastography exhibited a significant moderate positive correlation with spleen T2 mapping (r=0.37, p=0.001). However, there was no significant correlation between spleen magnetic resonance elastography and spleen T1 mapping in patients. Spleen magnetic resonance elastography was moderately positively correlated with liver magnetic resonance elastography (r=0.30, p=0.01), and spleen volume showed positive correlations with spleen magnetic resonance elastography, spleen T1 mapping, and spleen T2 mapping. Cut-off values for liver magnetic resonance elastography, liver T1 mapping, and liver T2 mapping in patient and control groups were 2.6 kPa (AUC=0.97), 619 ms (AUC=0.90), and 52.5 ms (AUC=0.62), respectively.

conclusionRelaxation methods offer noninvasive imaging without additional equipment. Liver T1 mapping may serve as an alternative to magnetic resonance elastography for chronic liver patient follow-up, while spleen T1 mapping is not reliable.

Indexed as

Elasticity Imaging TechniquesLiverMagnetic Resonance ImagingSpleenAdultAgedCase-Control StudiesChronic DiseaseFemaleHumansLiver CirrhosisLiver DiseasesMaleMiddle AgedProspective StudiesReference Values

Identifiers

PMID39630731
PMCPMC11639558

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