Evidence mapPaperPMID 40596172Full record

ArticleScientific reports2025

Predictive value of asprosin combined with LAP for metabolic dysfunction associated steatotic liver disease in the physical examination population.

Dan Lv, Zepu Wang, Yan Li, Shuchun Chen, Letian Li

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Dan LvUltrasound Department, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.
Zepu WangDepartment of Hepatobiliary Surgery, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.
Yan LiUltrasound Department, Hebei General Hospital, Shijiazhuang City, Hebei Province, China.
Shuchun ChenEndocrinology Department, Hebei General Hospital, 348 Heping West Road, Shijiazhuang City, Hebei Province, China. chenshuc2014@163.com.
Letian LiEmergency Department, The Second Affiliated Hospital of Xingtai Medical College, Xingtai City, Hebei Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To combine two indicators, asprosin and lipid accumulation product (LAP), to assess their predictive value for metabolic dysfunction-associated steatotic liver disease (MASLD) and to provide a more convenient and accurate option for mass screening of the MASLD population. Data were collected from 1249 adult subjects who underwent physical examination, LAP was calculated and serum asprosin was measured. Statistical analyses were performed and ROC curves were constructed to assess the predictive value of asprosin, LAP and their combination for MASLD. Asprosin and LAP levels were significantly higher in the MASLD group than in the non-MASLD group (P < 0.001), and asprosin and LAP were independent risk factors for the development of MASLD (P < 0.05).The combination of asprosin and LAP had the highest predictive efficacy for MASLD, and the AUCs were 0.841, 0.821 and 0.871 in the total, male and female populations, respectively. Asprosin and LAP are both good predictors of MASLD, and their combined performance is better than either indicator alone, and better in women than in men.The combination of asprosin and LAP may be an ideal marker for MASLD screening and individualised monitoring and management.

Indexed as

Fatty LiverFibrillin-1Lipid Accumulation ProductAdipokinesAdultAgedBiomarkersFemaleHumansMaleMiddle AgedPredictive Value of TestsRisk FactorsROC CurveAdipokinesBiomarkersFBN1 protein, humanFibrillin-1AsprosinLipid accumulation productMetabolic dysfunction-associated steatotic liver diseasePrediction effectivenessScreening

Identifiers

PMID40596172
PMCPMC12215385

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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 Socratic graph.