Evidence map›Paper›PMID 40281626›Full record

ArticlePopulation health metrics2025

NPR is an independent risk factor for predicting all-cause mortality in patients with metabolic dysfunction-associated steatotic liver disease: evidence from NHANES 2007-2020.

Dan Ye, Xueying Ji, Yiming Ma, Jiaheng Shi, Jiaofeng Wang, Jie Chen, Xiaona Hu, Zhijun Bao

Abstract read
In one paragraph

Article in Population health metrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. 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

8 authors.

Dan Ye *Department of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China.
Xueying Ji *Department of General Practice, Huadong Hospital Affiliated With Fudan University, Shanghai, China.
Yiming Ma *Department of General Practice, Huadong Hospital Affiliated With Fudan University, Shanghai, China.
Jiaheng ShiDepartment of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China.
Jiaofeng WangDepartment of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China.
Jie ChenDepartment of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China. laughchen@126.com.
Xiaona HuDepartment of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China. huxn06@163.com.
Zhijun BaoDepartment of Gastroenterology, Huadong Hospital Affiliated With Fudan University, Shanghai, China. zhijunbao@fudan.edu.cn.

Funding

Key Discipline Projects of Huadong Hospital LCZX2202Key Specialization Diseases Construction of Huadong Hospital ZDZB2225National Key R&D Program of China 2018YFC2002000National Natural Science Foundation of China 82071581Shanghai Municipal Health Commission JKKPYL-2022-15Shanghai Outstanding Young Medical Personnel Training Program & Excellence Project of the Shanghai Municipal Health Commission 20224Z0009
6 · The paper itself

Abstract

backgroundNeutrophil-associated inflammatory markers (NPR, NHR, SII, and SIRI) have been implicated in various metabolic diseases. However, studies on these markers with metabolic dysfunction-associated steatotic liver disease (MASLD) and advanced liver fibrosis (ALF), as well as their impact on all-cause mortality, remain limited.

methodsIn this historical cohort study, data from 8051 adults aged 20 years and older were analysed. Weighted logistic regression was used to investigate the associations of neutrophil-associated inflammatory markers with MASLD and ALF. Nonlinear associations were described via restricted cubic spline regression. The diagnostic utility was assessed via receiver operating characteristic (ROC) curves. Furthermore, weighted Kaplan‒Meier survival curves and Cox proportional hazards models were employed to assess all-cause mortality risk. Sensitivity analyses were employed to guarantee the robustness of the findings.

resultsFollowing adjustment for confounding factors, there was a significant positive association between the ln-transformed NPR, NHR, SII, and SIRI and the risk of MASLD (P < 0.001). Conversely, an inverse association was noted between the ln-transformed SII, SIRI and ALF (P < 0.05). Nonlinear relationships were identified between ln-transformed NPR, NHR, and SIRI and the risk of MASLD (P < 0.001), as well as between ln-transformed NPR, SII, and SIRI and the risk of ALF (P < 0.001). Furthermore, the ln-transformed NHR (cut-off value: - 2.571) exhibited the highest diagnostic accuracy for MASLD (AUC 0.71, 95% CI = 0.70, 0.72), whereas the NPR (cut-off value: - 3.857) demonstrated the highest diagnostic value for ALF (AUC 0.73, 95% CI = 0.70, 0.75). The results of the present study revealed an independent association between the ln-transformed NPR and an elevated risk of all-cause mortality in subjects diagnosed with MASLD. Subgroup analyses highlighted the underrepresentation of neutrophil-associated inflammatory markers in lean individuals with MASLD and ALF (BMI < 25 kg/m

conclusionsNeutrophil-associated inflammatory markers are independently associated with MASLD and ALF. Specifically, the ln-transformed NHR and SII show promise as diagnostic markers for MASLD and ALF, respectively. Moreover, elevated ln-transformed NPR is independently associated with an increased risk of all-cause mortality in individuals with MASLD, highlighting the potential clinical relevance of these inflammatory markers in the context of steatotic liver disease.

Indexed as

Fatty LiverNeutrophilsAdultAgedBiomarkersCohort StudiesFemaleHumansInflammationLiver CirrhosisMaleMiddle AgedNutrition SurveysRisk FactorsUnited StatesYoung AdultBiomarkersAdvanced liver fibrosisInflammatory markersMetabolic dysfunction-associated steatotic liver diseaseNeutrophilPopulation-based study

Identifiers

PMID40281626
PMCPMC12032722

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.