Evidence map›Paper›PMID 42836120›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2026

Inflammation-Mediated Causal Effects of MRI-Defined Body-Composition Obesity Axes on Chronic Obstructive Pulmonary Disease, Asthma, and Allergic Rhinitis: A Mendelian Randomization Study.

Bo Zeng, Chaoqun Zhou, Li Li, Yongbo Zhu

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In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Bo Zeng *Department of Otolaryngology-Head and Neck Surgery, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, People's Republic of China.
Chaoqun Zhou *Department of Oncology, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, People's Republic of China.
Li LiDepartment of Spine Surgery, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, People's Republic of China.ORCID 0009-0007-4917-4641
Yongbo ZhuDepartment of Otolaryngology-Head and Neck Surgery, The First Affiliated Hospital of Yangtze University, Jingzhou, Hubei, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Obesity is heterogeneous; conventional anthropometric measures combine fat distribution, ectopic fat deposition, and muscle volume, limiting refined causal inference for chronic airway diseases. We used four magnetic resonance imaging (MRI)-defined obesity axes to assess their causal effects on chronic obstructive pulmonary disease (COPD), asthma, and allergic rhinitis (AR), and to evaluate mediation by circulating inflammatory proteins. Methods: Genetic instruments were selected for four MRI-defined obesity axes. Two-sample Mendelian randomization (MR) used inverse-variance weighting as the primary method, with complementary sensitivity analyses and false discovery rate correction. Non-overlapping FinnGen outcome data were used for discovery, with replication in the Global Biobank Meta-analysis Initiative for COPD and asthma and the Million Veteran Program for AR, followed by meta-analysis. Two-step MR assessed inflammatory protein mediation. Results: Genetically predicted general obesity axis was associated with increased risks of COPD (OR = 1.125, 95% CI: 1.012-1.250), asthma (OR = 1.533, 95% CI: 1.426-1.647), and AR (OR = 1.624, 95% CI: 1.328-1.987). The lower-body fat axis was associated with higher risks of COPD (OR = 1.192, 95% CI: 1.088-1.306) and asthma (OR = 1.135, 95% CI: 1.052-1.224). No causal evidence was observed for the other obesity axes. Replication and meta-analysis largely supported these findings, except for general obesity and AR, which showed borderline pooled evidence ( Conclusion: MRI-defined obesity axes provided genetic evidence supporting potential causal associations with airway diseases through inflammatory mediation pathways.

Indexed as

AdiposityAsthmaInflammationInflammation MediatorsMagnetic Resonance ImagingObesityPulmonary Disease, Chronic ObstructiveRhinitis, AllergicFemaleGenetic Predisposition to DiseaseHumansMaleMendelian Randomization AnalysisMiddle AgedPhenotypePolymorphism, Single NucleotideInflammation Mediatorsallergic rhinitisasthmachronic obstructive pulmonary diseaseMendelian randomizationobesity axes

Identifiers

PMID42836120
PMCPMC13637657

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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.