# Association Between Unsaturated Fatty Acid Levels and Chronic Obstructive Pulmonary Disease: A Bidirectional Mendelian Randomization Study

**Authors:** Shuai Jiang, Lili Lu, Xiaojun Wang, Xunxia Zhu, Xiaoyu Chen, Hung‐Chen Chang, Xuchao Gu, Fuzhi Yang, Xuanqi Liu, Xuelin Zhang, Xiaoyong Shen

PMC · DOI: 10.1111/crj.70179 · The Clinical Respiratory Journal · 2026-03-07

## TL;DR

This study finds a bidirectional link between unsaturated fatty acids and COPD, suggesting dietary changes could help prevent the disease.

## Contribution

The study provides novel evidence of a causal relationship between specific unsaturated fatty acids and COPD using bidirectional Mendelian randomization.

## Key findings

- Higher levels of DHA, LA, omega-3, omega-6, and PUFAs are associated with reduced COPD risk.
- Genetic liability to COPD is linked to increased levels of monounsaturated fatty acids.
- The causal relationship is supported with minimal horizontal pleiotropy affecting results.

## Abstract

Observational studies have revealed that the levels of unsaturated fatty acids (UFAs) may influence the development, progression, and management of chronic obstructive pulmonary disease (COPD). To investigate the association between UFAs and COPD, we performed a bidirectional Mendelian randomization (MR) study.

We extracted summary genome‐wide association statistics (GWAS) for UFAs (N = 115 082) among population from UK Biobank study by measuring circulating lipoprotein lipid concentrations. The genetic instrument for COPD was derived from the FinnGen, which included 338 303 COPD controls and 20 066 cases of the disease. Measured at the genome‐wide significance level, independent genetic variations associated with each characteristic were considered instrumental factors. Two‐sample MR analysis was mainly conducted utilizing the inverse‐variance‐weighted (IVW) approach, complemented by the weighted median method and the MR‐Egger regression.

IVW MR analysis significantly demonstrated that the level of docosahexaenoic acid (DHA) (OR 0.812, 95% CI 0.719–0.918, p < 0.001), linoleic acid (LA) (OR 0.850, 95% CI 0.781–0.926, p < 0.001), the levels of omega‐3 fatty acids (OR 0.884, 95% CI 0.781–0.99, p = 0.049), omega‐6 fatty acids (OR 0.878, 95% CI 0.812–0.950, p = 0.001), and polyunsaturated fatty acids (PUFAs) (OR 0.901, 95% CI 0.827–0.982, p = 0.018) all linked to a higher risk of COPD. Moreover, in reverse direction MR analysis, genetic liability to COPD showed associations with higher levels of monounsaturated fatty acids (MUFAs) (OR 1.040, 95% CI 1.010–1.071, p = 0.008). Horizontal pleiotropy is not likely to materially skew the causative estimates from sensitivity analysis.

Our research added credence to the current evidence that suggests a bidirectional causal link between UFAs and COPD. It is imperative to comprehend this connection in order to effectively prevent and manage COPD.

Our MR analysis demonstrated that kinds of unsaturated fatty acids (UFAs) could be causal protective factors of chronic obstructive pulmonary disease (COPD). It reminded people to modify dietary nutrition, especially increasing the intake of UFAs to prevent COPD.

## Linked entities

- **Chemicals:** docosahexaenoic acid (PubChem CID 445580), linoleic acid (PubChem CID 5280450), omega-3 fatty acids (PubChem CID 56842239)
- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, SCD (stearoyl-CoA desaturase) [NCBI Gene 6319] {aka FADS5, MSTP008, SCD1, SCDOS, hSCD1}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351] {aka COX, COX8, COX8-2, COX8L, MC4DN15, VIII}, MMRN1 (multimerin 1) [NCBI Gene 22915] {aka ECM, EMILIN4, GPIa*, MMRN}, LOX (lysyl oxidase) [NCBI Gene 4015] {aka AAT10}, LTA (lymphotoxin alpha) [NCBI Gene 4049] {aka LT, TNFB, TNFSF1, TNLG1E}, PPIG (peptidylprolyl isomerase G) [NCBI Gene 9360] {aka CARS-Cyp, CYP, SCAF10, SRCyp}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}
- **Diseases:** death (MESH:D003643), insulin resistance (MESH:D007333), cardiovascular disease (MESH:D002318), diabetic nephropathy (MESH:D003928), respiratory diseases (MESH:D012140), mitochondrial (MESH:D028361), inflammation (MESH:D007249), respiratory infections (MESH:D012141), COPD susceptibility gene, family with sequence similarity 13 member A (MESH:D001321), deterioration of lung function (MESH:D055371), asthma (MESH:D001249), emphysema (MESH:D004646), lung disease (MESH:D008171), dysbiosis (MESH:D064806), chronic bronchitis (MESH:D029481), COPD (MESH:D029424), fatty liver (MESH:D005234), obesity (MESH:D009765)
- **Chemicals:** LTB4 (MESH:D007975), PUFAs (MESH:D005231), eicosanoid (MESH:D015777), PM2.5 (-), FA (MESH:D005227), MUFA (MESH:D005229), lipid (MESH:D008055), DHA (MESH:D004281), nitrogen oxides (MESH:D009589), ATP (MESH:D000255), oxylipin (MESH:D054883), glucose (MESH:D005947), ROS (MESH:D017382), short-chain FAs (MESH:D005232), LA (MESH:D019787), triglyceride (MESH:D014280), carbon (MESH:D002244), Omega-3 FAs (MESH:D015525), PGE2 (MESH:D015232), Omega-6 FAs (MESH:D043371)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

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## Figures

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## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967058/full.md

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Source: https://tomesphere.com/paper/PMC12967058