# Associations of serum lipid traits with DLBCL: a prospective cohort study from the UK Biobank

**Authors:** QingQing Luo, ShanShan Cai, LinHui Hu, Ya Wang, Li Yu

PMC · DOI: 10.3389/fnut.2026.1707450 · Frontiers in Nutrition · 2026-02-10

## TL;DR

Lower levels of certain blood lipids are linked to a higher risk of developing a common type of lymphoma, suggesting potential early warning signs.

## Contribution

This study identifies specific serum lipid traits as early indicators of diffuse large B-cell lymphoma risk in a large prospective cohort.

## Key findings

- Lower ApoA, HDL, and TC levels are significantly associated with increased DLBCL risk.
- Lipid levels decline in the years before diagnosis, with steeper drops in the last 5 years.
- Non-linear associations were found for ApoA and HDL, but not for TC.

## Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma (NHL), accounting for approximately 30% of all NHL cases. While serum lipids have been associated with various cancers, their relationship with the risk of DLBCL remains largely unexplored.

This prospective cohort study included 339,172 participants from the UK Biobank. Baseline serum levels of apolipoproteins A and B (ApoA/B), high-and low-density lipoprotein cholesterol (HDL/LDL), total cholesterol (TC), and triglycerides (TG) were measured. The associations between lipid profiles and DLBCL risk were assessed using Cox proportional hazards models, and restricted cubic spline (RCS) analysis. Subgroup analyses and temporal lipid trajectories were also performed.

Over a median follow-up of 13.8 years, 1,207 participants developed DLBCL. Lower levels of ApoA, HDL, and TC were significantly associated with increased DLBCL risk. RCS analysis revealed non-linear associations for ApoA and HDL, and a linear association for TC (P for non-linearity: 0.048, 0.017, and 0.139, respectively). Subgroup analysis indicated a significant interaction with age. Temporal trajectory analysis showed a gradual decline in ApoA and HDL levels during the 10 years prior to diagnosis, with a steeper drop in the last 5 years.

Reduced levels of ApoA, HDL, and TC are linked to a higher risk of DLBCL. Notably, lipid changes precede clinical diagnosis by several years, suggesting their potential as early indicators for DLBCL risk stratification and preventive strategies.

## Linked entities

- **Proteins:** APOA1 (apolipoprotein A1), APOB (apolipoprotein B)
- **Chemicals:** HDL (PubChem CID 6323542)
- **Diseases:** DLBCL (MONDO:0018905), non-Hodgkin lymphoma (MONDO:0018908)

## Full-text entities

- **Genes:** ABCG1 (ATP binding cassette subfamily G member 1) [NCBI Gene 9619] {aka ABC8, WHITE1}, PON1 (paraoxonase 1) [NCBI Gene 5444] {aka ESA, MVCD5, PON}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, ABCA1 (ATP binding cassette subfamily A member 1) [NCBI Gene 19] {aka ABC-1, ABC1, CERP, HDLCQTL13, HDLDT1, HPALP1}
- **Diseases:** NHL (MESH:D008228), TC (MESH:C535937), tumorigenesis (MESH:D063646), B-cell lymphoma (MESH:D016393), Digestive and Kidney Diseases (MESH:D007674), lymphoma (MESH:D008223), TG (MESH:C566031), hematologic malignancy (MESH:D019337), lipid (MESH:D011017), DLBCL (MESH:D016403), lung, prostate, liver, and colorectal cancers (MESH:D015179), hypertension (MESH:D006973), death (MESH:D003643), inflammation (MESH:D007249), insulin resistance (MESH:D007333), Diabetes (MESH:D003920), cancers (MESH:D009369)
- **Chemicals:** lipid (MESH:D008055), reactive oxygen species (MESH:D017382), Cholesterol (MESH:D002784), alcohol (MESH:D000438), TC (-), TG (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12929521/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929521/full.md

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Source: https://tomesphere.com/paper/PMC12929521