Evidence map›Paper›PMID 40641363›Full record

ArticleThe clinical respiratory journal2025

Causal Associations Between Cystatin and Lung Cancer: A Two-Sample Mendelian Randomization Study.

Chunling Zhang, Riya Wu, Hang Liu, Shihuan Yu

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Article in The clinical respiratory journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chunling ZhangDepartment of Pulmonary Disease, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Riya WuDepartment of Pulmonary Disease, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Hang LiuDepartment of Pulmonary Disease, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Shihuan YuDepartment of Pulmonary Disease, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.ORCID https://orcid.org/0009-0001-3779-9042

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe cystatin family is particularly relevant in lung cancer research due to its links to inflammation, protease balance, and tumor progression. Although population-based studies have documented associations between cystatin and lung cancer, causal relationships remain undetermined.

methodsBased on genomic statistics of seven different cystatins and three subtypes of lung cancer, we conducted a two-sample Mendelian randomization (MR) study. The inverse-variance weighted (IVW) method was the main approach for causality estimation. The weighted median, simple mode, weighted mode, and MR-Egger regression methods were further employed to validate the main findings. In the sensitivity analysis, horizontal pleiotropy was assessed by MR-Egger regression and Cochran's Q test. MR-PRESSO and Radial MR methods were used to identify heterogeneity and remove outliers.

resultsGenetically predicted Cystatin 8 was causally associated with squamous cell lung carcinoma (OR = 1.062, 95% CI: 1.004-1.124, p = 0.035). No causal relationships were found for genetically predicted cystatin 8, -B, -D, -F, or -M with squamous cell lung carcinoma, lung adenocarcinoma, and NSCLC. However, outliers were identified between Cystatin D, -M, and -F using MR-PRESSO and Radial MR. After the removal of outliers, the association between Cystatin D and lung adenocarcinoma turned significant (OR = 1.178, 95% CI: 1.023-1.358, p = 0.023). Sensitivity analyses confirmed the robustness of main results after outliers removal.

conclusionGenetically predicted Cystatin 8 was causally associated with squamous cell lung carcinoma. Future population-based studies are required to substantiate these results.

Indexed as

Carcinoma, Squamous CellCystatinsLung NeoplasmsMendelian Randomization AnalysisGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single NucleotideCystatinscausal correlationcystatinlung adenocarcinomaMendelian randomizationnon‐small cell lung cancersquamous cell lung carcinoma

Identifiers

PMID40641363
PMCPMC12246730

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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 OpenQuestion graph.