Evidence map›Paper›PMID 40885779›Full record

ArticleScientific reports2025

Quantification of liver steatosis of metabolic dysfunction-associated steatotic liver disease based on body composition analysis.

Toshikazu Kohira, Satoshi Oeda, Erina Eto, Yoshihito Kubotsu, Misa Norita, Kaori Inoue, Nagisa Hara, Shotaro Noge, Kenichi Tanaka, Shigenobu Yoshimura and 11 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

21 authors.

Toshikazu KohiraLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Satoshi OedaLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Erina EtoDiabetes and Endocrinology, Saga-Ken Medical Centre Koseikan, Saga, Japan.
Yoshihito KubotsuDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Misa NoritaDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Kaori InoueLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Nagisa HaraLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Shotaro NogeDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Kenichi TanakaDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Shigenobu YoshimuraDepartment of Advanced Medicine for Biliary and Pancreatic Disease, Faculty of Medicine, Saga University, Saga, Japan.
Noriko OzaLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Keizo AnzaiDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Yuichiro EguchiLoco Medical General Institute, Ogi, Saga, Japan.
Cheng Han NgDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Daniel Q HuangDivision of Gastroenterology and Hepatology, Department of Medicine, National University Hospital, Singapore, Singapore.
Mark D MuthiahDivision of Gastroenterology and Hepatology, Department of Medicine, National University Hospital, Singapore, Singapore.
Atsushi KawaguchiEducation and Research Center for Community Medicine, Faculty of Medicine, Saga Medical School, Saga, Japan.
Shinichi AishimaDepartment of Scientific Pathology Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Hiroshi IsodaLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan.
Takuya KuwashiroDivision of Metabolism and Endocrinology, Faculty of Medicine, Saga University, Saga, Japan.
Hirokazu TakahashiLiver Center, Saga University Hospital, Nabeshima 5-1-1, Saga City, 8498501, Saga, Japan. takahas2@cc.saga-u.ac.jp.ORCID http://orcid.org/0000-0003-1900-4389

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver steatosis can be measured with ultrasound techniques such as the controlled attenuation parameter (CAP) on an equipped FibroScan. For more widespread screening and quantitative evaluation of liver steatosis, a predictive model using body composition data obtained by body bioelectrical impedance analysis (BIA) was developed. In the training cohort including 365 patients suspected of having metabolic dysfunction-associated steatotic liver disease, a stepwise selection method was used to determine the BIA-related variables associated with CAP. Using the significant variables, a predictive formula was developed, and the estimated CAP (eCAP) was obtained. The diagnostic performance of eCAP was tested to predict liver steatosis with receiver operating characteristic (ROC) curve analysis in the training, validation (n = 408) and liver biopsy (n = 158) cohorts. The body fat mass of the trunk, skeletal muscle index and age were significant variables associated with CAP. eCAP was obtained as 219.1 - 0.4479 × age + 3.476 × BFM of trunk + 7.045 × SMI. The area under the ROC curve was 0.814 in the training cohort and 0.808 in the validation cohort. The sensitivity and specificity were 72.5% and 82.1% with a cut-off value of eCAP = 281 dB/m. For sensitivity ≥ 90%, the cut-off of eCAP was 266 dB/m. In the liver biopsy cohort, the presence of pathological steatosis was predicted with eCAP as an area under the ROC curve = 0.826, which was not statistically different from CAP (0.871). Completely non-invasive BIA-based eCAP could predict liver steatosis.

Indexed as

Body CompositionFatty LiverAdultAgedElectric ImpedanceFemaleHumansLiverMaleMiddle AgedROC CurveUltrasonographyBioelectrical impedance analysisBody compositionControlled attenuation parameterMetabolic dysfunction-associated steatotic liver disease

Identifiers

PMID40885779
PMCPMC12398518

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.