# Systemic immuno-metabolic inflammatory indices (neutrophil-to-HDL cholesterol ratio and systemic inflammation response index) are strongly associated with metabolic dysfunction-associated steatotic liver disease: a propensity score-matched study

**Authors:** Huimin Liang, Boqiao Wang, Deyuan Zhang, Zhongzhong Zhang, Xu Chen, Yijia Xu, Chengwei Zhang, Jinyang Li, Jie Yang, Pengjiao Xi, Jianwei Zhang, Yan Zhang, Haize Ge

PMC · DOI: 10.3389/fimmu.2026.1768302 · Frontiers in Immunology · 2026-03-09

## TL;DR

This study shows that two blood-based immune-metabolic markers, NHR and SIRI, are strongly linked to metabolic liver disease and can improve early detection when combined with ALT.

## Contribution

The study introduces a combined model of NHR, SIRI, and ALT as a novel diagnostic tool for MASLD with high accuracy and clinical accessibility.

## Key findings

- NHR and SIRI are independently associated with MASLD after propensity score matching.
- The combined model of NHR, SIRI, and ALT achieved an AUC of 0.865, significantly outperforming ALT alone.
- The model showed good calibration and stability with minimal overfitting after internal validation.

## Abstract

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is increasingly recognized as a systemic immuno-metabolic disorder characterized by chronic low-grade inflammation and dysregulated innate immune activation. Circulating immune-related indices derived from routine blood tests may reflect early immuno-metabolic imbalance and provide accessible markers for identifying disease-associated immune dysregulation.

To investigate the associations of two systemic immuno-metabolic inflammatory indices, namely the neutrophil-to-high-density lipoprotein cholesterol ratio (NHR) and the systemic inflammation response index (SIRI) with MASLD, and to evaluate their combined discriminative performance.

In this retrospective case–control study, adult participants attending a tertiary hospital between November 2023 and October 2024 were enrolled. After strict eligibility screening, propensity score matching (1:1) was applied to balance demographic characteristics and comorbidities, yielding 522 matched individuals (261 with MASLD and 261 without MASLD). Multivariable conditional logistic regression was used to assess associations between immuno-metabolic inflammatory indices and MASLD. Discriminatory performance was assessed using receiver operating characteristic (ROC) curves. The DeLong test, Net Reclassification Improvement (NRI), and Integrated Discrimination Improvement (IDI) were used to evaluate discriminative ability. Model calibration was evaluated using the Hosmer-Lemeshow test, Brier score, and calibration curves. Internal validation was performed using 2,000 bootstrap resamples.

After propensity score matching, both NHR and SIRI were independently associated with MASLD in multivariable analysis. The combined model integrating NHR, SIRI, and alanine aminotransferase (ALT) demonstrated optimal discriminative performance (AUC = 0.865, sensitivity = 72.41%, specificity = 84.30%), significantly outperforming the ALT-only model (DeLong test, Z = -8.3083, P < 0.001). The total Net Reclassification Improvement (NRI) was 0.345 (95% CI: 0.245–0.438), and the total Integrated Discrimination Improvement (IDI) was 0.348 (95% CI: 0.282–0.424, P < 0.001). The Hosmer-Lemeshow test (χ² = 11.043, df = 8, P = 0.199) and Brier score (0.151, 95% CI: 0.134–0.168) confirmed good model calibration, and the calibration curve showed excellent agreement between predicted probabilities and actual incidence. Internal validation through 2,000 bootstrap resamples resulted in a corrected AUC of 0.866 (95% CI: 0.836–0.897), with an average optimism of -0.001, indicating good model stability and minimal risk of overfitting.

Systemic immuno-metabolic inflammatory indices reflecting innate immune activation and lipid-related anti-inflammatory dysfunction (NHR and SIRI) are closely associated with MASLD. The combined assessment of NHR, SIRI, and ALT provides a robust, clinically accessible approach with significant incremental value for identifying immuno-metabolic risk in MASLD, highlighting the central role of systemic immune dysregulation in metabolic liver disease.

Diagnostic contribution of NHR, SIRI, and ALT to MASLD identification. This schematic summarizes the diagnostic roles of the neutrophil-to-HDL-cholesterol ratio (NHR), the Systemic Inflammation Response Index (SIRI), and alanine aminotransferase (ALT) in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD). NHR demonstrated the strongest discriminative capacity among single biomarkers, whereas SIRI showed favorable sensitivity. Integrating these indices into a combined model further improved diagnostic accuracy, yielding an AUC of 0.865 and supporting their application in early screening and risk stratification.Diagram outlining NAFLD immune-inflammatory profiling with a liver illustration. Neutrophil-to-HDL-cholesterol ratio (NHR), Systemic Inflammation Response Index (SIRI), and ALT are presented as markers. It highlights NHR as a strong discriminator and SIRI as a sensitive marker, showing a combined model improving accuracy (AUC 0.865), with emphasis on systemic immune dysregulation and immunometabolic risk identification.

Diagnostic contribution of NHR, SIRI, and ALT to MASLD identification. This schematic summarizes the diagnostic roles of the neutrophil-to-HDL-cholesterol ratio (NHR), the Systemic Inflammation Response Index (SIRI), and alanine aminotransferase (ALT) in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD). NHR demonstrated the strongest discriminative capacity among single biomarkers, whereas SIRI showed favorable sensitivity. Integrating these indices into a combined model further improved diagnostic accuracy, yielding an AUC of 0.865 and supporting their application in early screening and risk stratification.

## Linked entities

- **Diseases:** Metabolic Dysfunction-Associated Steatotic Liver Disease (MONDO:0013209), MASLD (MONDO:0013209)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** immune (MESH:D007154), immuno-metabolic disorder (MESH:D000163), immune dysregulation (OMIM:614878), MASLD (MESH:D008107), inflammation (MESH:D007249)
- **Chemicals:** cholesterol (MESH:D002784), lipid (MESH:D008055)

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006849/full.md

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Source: https://tomesphere.com/paper/PMC13006849