Therapeutic efficacy of quercetin in experimental pulmonary fibrosis: A meta‑analysis

Pulmonary fibrosis (PF) is a fatal chronic disease characterized by progressive interstitial scarring, alveolar destruction and a persistent decline in lung function. The present study evaluated the therapeutic effects of quercetin, a natural flavonoid with potent antioxidant and anti-inflammatory properties, in animal models of PF (PROSPERO registration no. INPLASY202530122). A comprehensive literature search was performed across PubMed, Web of Science, Embase, Cochrane Library and Ovid from inception to January 2025, identifying 25 eligible preclinical studies. Data were extracted and analyzed for outcomes in three main categories: Fibrotic changes, inflammatory responses and oxidative stress parameters. Random-effects meta-analysis was employed, followed by meta-regression analysis to examine study heterogeneity. The analysis indicated that quercetin administration was associated with improvements in fibrotic indicators, showing reduced collagen deposition and improved histopathological scores. Anti-inflammatory effects were observed through modulation of cytokine levels and inflammatory cell infiltration. Additionally, quercetin demonstrated effects on oxidative stress markers, showing enhanced antioxidant capacity and reduced oxidative damage. Meta-regression analysis identified a number of moderating factors, including dosage, treatment duration, animal model selection and induction method, which contributed to heterogeneity across studies. The findings suggest that quercetin may provide beneficial effects in experimental PF models through multiple pathways. However, notable heterogeneity was observed among included studies, indicating the need for cautious interpretation of results. Further investigation with standardized protocols is recommended to validate these preliminary findings.

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Publication Details

Journal
Experimental and Therapeutic Medicine
Published
2025-12-22
DOI
https://doi.org/10.3892/etm.2025.13054
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00

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article

Therapeutic efficacy of quercetin in experimental pulmonary fibrosis: A meta‑analysis

Lanhua Cai, Long Chen, Chunmei Lin
Experimental and Therapeutic Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Therapeutic efficacy of quercetin in experimental pulmonary fibrosis: A meta‑analysis

Lanhua Cai, Long Chen, Chunmei Lin
article en

Abstract

Pulmonary fibrosis (PF) is a fatal chronic disease characterized by progressive interstitial scarring, alveolar destruction and a persistent decline in lung function. The present study evaluated the therapeutic effects of quercetin, a natural flavonoid with potent antioxidant and anti-inflammatory properties, in animal models of PF (PROSPERO registration no. INPLASY202530122). A comprehensive literature search was performed across PubMed, Web of Science, Embase, Cochrane Library and Ovid from inception to January 2025, identifying 25 eligible preclinical studies. Data were extracted and analyzed for outcomes in three main categories: Fibrotic changes, inflammatory responses and oxidative stress parameters. Random-effects meta-analysis was employed, followed by meta-regression analysis to examine study heterogeneity. The analysis indicated that quercetin administration was associated with improvements in fibrotic indicators, showing reduced collagen deposition and improved histopathological scores. Anti-inflammatory effects were observed through modulation of cytokine levels and inflammatory cell infiltration. Additionally, quercetin demonstrated effects on oxidative stress markers, showing enhanced antioxidant capacity and reduced oxidative damage. Meta-regression analysis identified a number of moderating factors, including dosage, treatment duration, animal model selection and induction method, which contributed to heterogeneity across studies. The findings suggest that quercetin may provide beneficial effects in experimental PF models through multiple pathways. However, notable heterogeneity was observed among included studies, indicating the need for cautious interpretation of results. Further investigation with standardized protocols is recommended to validate these preliminary findings.

Experimental and Therapeutic MedicineVol. 31(2)
Jinan University (CN), Guangdong Provincial Hospital of Traditional Chinese Medicine (CN), Gaozhou People's Hospital (CN)
Guangzhou Municipal Science and Technology Project
Good health and well-being
Openalex Percentile: Top 29%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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