# Effects of atorvastatin on inflammatory markers, lipid profile, liver enzymes, and pulmonary function in patients with lung diseases: a systematic review and meta-analysis of randomized controlled trials

**Authors:** Samane Baseri, Morteza Izadi, Mina Alimohammadi, Seyedeh Mahdieh Khoshnazar, Reza Nikdel, Kiavash Hushmandi

PMC · DOI: 10.1186/s40001-025-03782-y · 2026-01-19

## TL;DR

This study reviews how atorvastatin affects inflammation, cholesterol, and lung function in patients with lung diseases, finding some benefits but also potential evening airflow issues.

## Contribution

The study provides a meta-analysis of atorvastatin's effects on multiple biomarkers and pulmonary function in diverse lung diseases.

## Key findings

- Atorvastatin significantly reduced TNF-α and LDL cholesterol in lung disease patients.
- It improved 6MWD and FEF25-75 in COPD subgroups but worsened evening peak expiratory flow.
- No significant effects were observed for CRP, IL-6, triglycerides, HDL, FEV1, FVC, or oxygen saturation.

## Abstract

Pulmonary diseases are important causes of morbidity globally. Atorvastatin's pleiotropic effects, which include anti-inflammatory and lipid-lowering properties, may be beneficial for individuals with respiratory diseases. This meta-analysis evaluated the atorvastatin's effect on inflammatory biomarkers, lipid profile, liver enzymes, and pulmonary function in lung disease patients.

We systematically searched PubMed/MEDLINE, Scopus, Web of Science, Embase, CENTRAL, and Google Scholar for English-language RCTs until March 2025. The study evaluated inflammatory markers (CRP, IL-6, TNF-α), lipid profile (LDL, HDL, TC, TG), liver enzymes (ALT, AST), pulmonary function tests, and physical performance. Pooled weighted mean differences (WMDs) with 95% confidence intervals were calculated using random-effects models. Subgroup, heterogeneity, and publication bias analyses were conducted.

Seventeen RCTs (22 datasets; n = 1,344) on asthma, COPD, COVID-19, pulmonary hypertension, and associated disorders were analyzed. Atorvastatin substantially decreased TNF-α (WMD: − 0.20 pg/mL; 95% CI − 0.28 to − 0.11), LDL cholesterol (WMD: − 21.48 mg/dL; 95% CI − 30.82 to − 12.14), and TC (WMD: − 15.24 mg/dL; 95% CI − 28.28 to − 2.20), while improving 6MWD (WMD: 0.71; 95% CI 0.24 to 1.17) and FEF25-75 in COPD subgroups. Evening peak expiratory flow (PEF) was considerably lower (WMD: − 8.72; 95% CI − 14.96 to − 2.47), indicating worsening in airway airflow throughout the evening. There were no significant overall effects for CRP, IL-6, triglycerides, HDL, FEV1, FVC, or oxygen saturation.

Atorvastatin demonstrates anti-inflammatory and lipid-lowering efficacy in pulmonary disease patients, with mild functional respiratory benefits and modest improvements in physical performance. Additional large-scale studies are needed to validate clinical benefits and effective treatment methods.

The online version contains supplementary material available at 10.1186/s40001-025-03782-y.

## Linked entities

- **Proteins:** CRP (C-reactive protein), IL6 (interleukin 6), TNF (tumor necrosis factor), GPT (glutamic--pyruvic transaminase), GOT1 (glutamic-oxaloacetic transaminase 1), LDL (LDL cholesterol), HSD11B1 (hydroxysteroid 11-beta dehydrogenase 1), CD55 (CD55 molecule (Cromer blood group)), TG (thyroglobulin)
- **Chemicals:** atorvastatin (PubChem CID 60823)
- **Diseases:** asthma (MONDO:0004979), COPD (MONDO:0005002), pulmonary hypertension (MONDO:0005149), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, EGR1 (early growth response 1) [NCBI Gene 1958] {aka AT225, G0S30, KROX-24, NGFI-A, TIS8, ZIF-268}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** fatigue (MESH:D005221), lung cancer (MESH:D008175), infectious conditions (MESH:D003141), respiratory disorders (MESH:D012131), cancer (MESH:D009369), chronic bronchitis (MESH:D029481), heartburn (MESH:D006356), Asthma (MESH:D001249), TB (MESH:D014376), conditions (MESH:D020763), Pulmonary tuberculosis (MESH:D014397), infection (MESH:D007239), rhabdomyolysis (MESH:D012206), ILDs (MESH:D017563), myositis (MESH:D009220), liver impairment (MESH:D017093), respiratory symptoms (MESH:D012818), obstructive sleep apnea syndrome (MESH:D020181), lung injury (MESH:D055370), ARDS (MESH:D012128), obstructive disease (MESH:D001157), fever (MESH:D005334), infectious lung diseases (MESH:D008171), community-acquired pneumonia (MESH:D003147), pneumonia (MESH:D011014), airway inflammation (MESH:D007249), NAFLD (MESH:D065626), chronic (MESH:D002908), pulmonary hypertension (MESH:D006976), COVID-19 (MESH:D000086382), cardiovascular disease (MESH:D002318), cough (MESH:D003371), liver disease (MESH:D008107), liver damage (MESH:D056486), asthmatic (MESH:D013224), mucous-obstructive respiratory diseases (MESH:D012140), COPD (MESH:D029424), PEF (MESH:C564040)
- **Chemicals:** Atorvastatin (MESH:D000069059), lopinavir (MESH:D061466), Hothersall (-), nitric oxide (MESH:D009569), coenzyme Q10 (MESH:C024989), lipid (MESH:D008055), leukotrienes (MESH:D015289), ritonavir (MESH:D019438), cholesterol (MESH:D002784), ezetimibe (MESH:D000069438), pitavastatin (MESH:C108475), salbutamol (MESH:D000420), fluvastatin (MESH:D000077340), triglycerides (MESH:D014280), rosuvastatin (MESH:D000068718), pravastatin (MESH:D017035), TC (MESH:D013667), Simvastatin (MESH:D019821), aspirin (MESH:D001241), TG (MESH:D013866), mevalonate (MESH:D008798), O2 (MESH:D010100), asbestos (MESH:D001194), bilirubin (MESH:D001663)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12825185/full.md

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Source: https://tomesphere.com/paper/PMC12825185