Evidence map›Paper›PMID 36939910›Full record

ArticleAbdominal radiology (New York)2023

Extracellular volume fraction obtained by dual-energy CT depicting the etiological differences of liver fibrosis.

Kumi Ozaki, Takashi Ohtani, Shota Ishida, Shohei Higuchi, Tomokazu Ishida, Kouki Takahashi, Yuki Matta, Hirohiko KImura, Toshifumi Gabata

Abstract read
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In one paragraph

Article in Abdominal radiology (New York), 2023. 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
2.8field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Kumi OzakiDepartment of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan. ozakik-rad@umin.org.ORCID http://orcid.org/0000-0002-1454-7512
Takashi OhtaniRadiological Center, University of Fukui Hospital, Eiheiji, Japan.
Shota IshidaRadiological Center, University of Fukui Hospital, Eiheiji, Japan.
Shohei HiguchiDepartment of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.
Tomokazu IshidaRadiological Center, University of Fukui Hospital, Eiheiji, Japan.
Kouki TakahashiRadiological Center, University of Fukui Hospital, Eiheiji, Japan.
Yuki MattaRadiological Center, University of Fukui Hospital, Eiheiji, Japan.
Hirohiko KImuraDepartment of Radiology, Faculty of Medical Sciences, University of Fukui, 23-3 Matsuoka-Shimoaizuki, Eiheiji, Fukui, 910-1193, Japan.
Toshifumi GabataDepartment of Radiology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.
University of Fukui Hospital · JPUniversity of Fukui · JPKanazawa University · JPKyoto College of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo assess etiological differences in extracellular volume fraction (ECV) and evaluate its influence on staging performance.

methodsA total of 166 patients with normal liver (n = 14) and chronic liver disease related to viral hepatitis (n = 71), alcohol (n = 44), and nonalcoholic steatohepatitis (NASH) (n = 37) underwent dual-energy CT (DECT) of the liver (5-min equilibrium-phase images) between January 2020 and July 2022. The iodine densities of the parenchyma and aorta were measured and ECV was calculated. Comparisons of ECV between each etiology and METAVIR fibrosis stage were statistically analyzed (p < 0.05).

resultsECV in each etiology and all patients significantly increased with higher fibrosis stage (p < 0.001) and showed a strong or moderate correlation with fibrosis stage (Spearman's ρ; all patients, 0.701; viral hepatitis, 0.638; alcoholic, 0.885; NASH, 0.791). In stages F2-F4, ECV in alcoholic liver disease was significantly larger than those for viral hepatitis and NASH (p < 0.05); however, no significant difference in stage F1 was found among the three etiologies. The cutoff values and areas under the receiver operating characteristic curve (AUC-ROCs) for discriminating fibrosis stage (≥ F1- ≥ F4) were higher for alcohol (cutoff values and AUC-ROC; 20.1% and 0.708 for ≥ F1, 23.8% and 0.990 for ≥ F2, 24.3% and 0.968 for ≥ F3, and 26.6% and 0.961 for ≥ F4, respectively) compared with those for the others.

conclusionECV in alcoholic liver disease is higher than that in other etiologies in the advanced stages of fibrosis, and etiological differences in ECV affect the staging performance of fibrosis.

Indexed as

Liver Diseases, AlcoholicNon-alcoholic Fatty Liver DiseaseEthanolFibrosisHumansLiverLiver CirrhosisRetrospective StudiesTomography, X-Ray ComputedEthanolAlcoholExtracellular volume fractionHepatitis virusLiver fibrosisNonalcoholic steatohepatitis

Identifiers

PMID36939910
OpenAlexW4327902096

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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.