# Effects of non-HDL-C and statin therapy on mortality in ARDS: a retrospective cohort study

**Authors:** Haiming Hu, Jin Wei, Lijuan Zhao, Yixing Zhu, Geer Zhou, Anqi Zhao, De Chang

PMC · DOI: 10.3389/fmed.2025.1594164 · Frontiers in Medicine · 2025-07-30

## TL;DR

This study finds that statin therapy reduces short-term mortality in ARDS patients, especially those with high non-HDL cholesterol.

## Contribution

The study identifies non-HDL-C as a potential marker for ARDS patients who may benefit most from statin therapy.

## Key findings

- Statin therapy significantly reduced short-term mortality in ARDS patients.
- The benefit of statins was more pronounced in patients with elevated non-HDL-C levels.
- Kaplan-Meier and Cox regression analyses confirmed the protective effect of statins.

## Abstract

Acute respiratory distress syndrome (ARDS) is a critical and potentially fatal condition marked by inflammation and coagulation disorders. Statins, a class of cholesterol-lowering medications, have been explored for potential anti-inflammatory properties, yet their exact role in ARDS remains unclear.

Patients diagnosed with ARDS were sourced from the MIMIC-IV database (version 3.0). To balance baseline characteristics, propensity score matching (PSM) was applied. Short-term mortality was evaluated using Kaplan–Meier survival analysis. Factors associated with short-term mortality were determined using both univariate and multivariate Cox regression analyses. The potential impact of unmeasured confounding was assessed using the E-value. Additionally, subgroup analyses were performed to investigate heterogeneity and evaluate the robustness of the findings.

The study included 10,368 ARDS patients, of whom 5,184 received statin therapy and 5,184 did not. Kaplan–Meier analysis revealed significantly lower short-term mortality in the statin-treated group. Both univariate (HR, 0.48; 95% CI, 0.41–0.58; p < 0.001) and multivariate (HR, 0.49; 95% CI, 0.41–0.58; p < 0.001) Cox regression analyses revealed that statin therapy significantly decreased short-term mortality. Subsequent subgroup analyses further indicated that the beneficial effect of statins was more evident in patients with elevated non-HDL-C levels.

Statin therapy appears to confer significant clinical benefits in ARDS patients, particularly in those with high non-HDL-C levels. These findings indicate that non-HDL-C might be a useful marker for identifying ARDS patients who may benefit most from statin therapy.

## Linked entities

- **Diseases:** acute respiratory distress syndrome (MONDO:0006502), ARDS (MONDO:0006502)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** tissue (MESH:D017695), acute respiratory failure (MESH:D012131), COVID-19 (MESH:D000086382), hepatic complications (MESH:D008107), acute lung injury (MESH:D055371), chronic renal insufficiency (MESH:D051436), diabetes (MESH:D003920), Tumors (MESH:D009369), hyper (MESH:D007589), renal disease (MESH:D007674), sepsis (MESH:D018805), inflammation (MESH:D007249), hypoxemia (MESH:D000860), uremia (MESH:D014511), death (MESH:D003643), cardiogenic pulmonary edema (MESH:D011654), stroke (MESH:D020521), lung cancer (MESH:D008175), myocardial infarction (MESH:D009203), asthma (MESH:D001249), liver failure (MESH:D017093), coagulation disorders (MESH:D001778), heart disease (MESH:D006331), clotting disorders (MESH:D020141), ARDS (MESH:D012128), liver cancer (MESH:D006528)
- **Chemicals:** atorvastatin (MESH:D000069059), TC (-), Aspirin (MESH:D001241), dexamethasone (MESH:D003907), creatinine (MESH:D003404), oxygen (MESH:D010100), lipid (MESH:D008055), cholesterol (MESH:D002784), simvastatin (MESH:D019821), methylprednisolone (MESH:D008775), rosuvastatin (MESH:D000068718), H2O (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12345366/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12345366/full.md

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Source: https://tomesphere.com/paper/PMC12345366