# Liquid chromatography-tandem mass spectrometry technology revealed differences in serum metabolites between rheumatoid arthritis patients in different seasons

**Authors:** Jipeng Peng, Yunyun Song, Xuemei Yuan, Feng Luo, Can Liu, Changming Chen, Qiuyi Wang, Wukai Ma, Xueming Yao

PMC · DOI: 10.3389/fimmu.2026.1758782 · Frontiers in Immunology · 2026-02-10

## TL;DR

This study used mass spectrometry to find seasonal changes in blood metabolites of rheumatoid arthritis patients, suggesting seasonal factors influence disease metabolism.

## Contribution

The study identifies season-specific metabolite variations in rheumatoid arthritis patients using LC-MS/MS, revealing potential biomarkers for seasonal disease monitoring.

## Key findings

- Seasonal differences in serum metabolites were observed, with significant variations in 'Lipids and Lipid-Like Molecules' and 'Organic acids and derivatives'.
- 62 common differentially expressed metabolites were identified across seasons, with distinct metabolites in each comparison group.
- Key metabolites like Behenic acid and Phosphatidylinositol-3,4,5-trisphosphate were linked to Carbohydrate and Lipid metabolism pathways.

## Abstract

Using liquid chromatography-tandem mass spectrometry (LC-MS/MS) technology, we investigated differences in serum metabolites among rheumatoid arthritis (RA) patients in different seasons.

Serum samples were collected from 60 patients meeting the diagnostic criteria for RA and divided into four groups based on different seasons. Metabolites in the serum samples were analyzed using a liquid chromatography-mass spectrometry (LC-MS) system comprising the Waters ACQUITY UPLC I-Class plus/Thermo QE plus ultra-high-performance liquid chromatography and high-resolution mass spectrometry instruments. Principal component analysis (PCA), partial least squares discriminant analysis (PLS-DA), and orthogonal partial least squares discriminant analysis (OPLS-DA) to identify seasonally differential metabolites and investigate their metabolic pathways and enrichment patterns.

A total of 3,787 metabolites were detected in serum, with the majority of differentially expressed metabolites classified as “Lipids and Lipid-Like Molecules.” Metabolites in the serum of RA patients across the four seasons exhibited varying degrees of differences. The significantly different metabolites identified between groups were 223 (C1_vs_C2), 977 (C1_vs _C3), and 778 (C1_vs_C4), with 62 common different metabolites among them. These differential metabolites were primarily found in the “Lipids and Lipid-Like Molecules” and “Organic acids and derivatives” categories. We also identified key differentially expressed metabolites. C1_vs_C2 includes Behenic acid (d3), Stizolamine, and Cyanidin 7-arabinoside; C1_vs_C3 includes Phosphatidylinositol-3,4,5-trisphosphate, N-Docosahexaenoyl Threonine, and Alginic acid; C1_vs_C4 includes 9,10-DiHOME, Perfluorotridecanoic acid, and 3,4-Dehydro-gamma,chi-carotene. KEGG metabolic pathway enrichment analysis showed that the differential metabolites were enriched in metabolic pathways such as Carbohydrate metabolism and Lipid metabolism.

This study elucidates the regulatory role of seasonal factors in serum metabolic profiles of RA patients. The identified seasonally variable metabolites may provide potential reference points for seasonal monitoring of RA and optimization of personalized treatment regimens, opening new metabolomics perspectives for disease diagnosis and management.

## Linked entities

- **Chemicals:** Behenic acid (d3) (PubChem CID 44256493), Stizolamine (PubChem CID 21780519), Cyanidin 7-arabinoside (PubChem CID 131752265), Phosphatidylinositol-3,4,5-trisphosphate (PubChem CID 643963), N-Docosahexaenoyl Threonine (PubChem CID 156963081), 9,10-DiHOME (PubChem CID 9966640), Perfluorotridecanoic acid (PubChem CID 3018355), 3,4-Dehydro-gamma,chi-carotene (PubChem CID 23426022)
- **Diseases:** rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351] {aka COX, COX8, COX8-2, COX8L, MC4DN15, VIII}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, LOX (lysyl oxidase) [NCBI Gene 4015] {aka AAT10}, Ahr (aryl-hydrocarbon receptor) [NCBI Gene 11622] {aka Ah, Ahh, Ahre, In, bHLHe76}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, PLA2G1B (phospholipase A2 group IB) [NCBI Gene 5319] {aka PLA2, PLA2A, PPLA2}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}
- **Diseases:** type 2 diabetes (MESH:D003924), pulmonary interstitial lesions (MESH:D017563), tenderness (MESH:D063806), hypersensitivity (MESH:D004342), immune dysregulation (OMIM:614878), arthritis (MESH:D001168), RA (MESH:D001172), stiffness (MESH:C566112), lipid metabolism disorders (MESH:D052439), joint deformity (MESH:D016916), gastrointestinal disorders (MESH:D005767), loss of function (MESH:D006315), immune dysfunction (MESH:D007154), colitis (MESH:D003092), peptic ulcers (MESH:D010437), joint pain (MESH:D018771), bone erosion (MESH:D014077), joint swelling (MESH:D007592), insulin resistance (MESH:D007333), autoimmune disease (MESH:D001327), gastric tumors (MESH:D013274), vitamin D deficiency (MESH:D014808), metabolic abnormalities (MESH:D008659), fever (MESH:D005334), Inflammatory (MESH:D007249), morning stiffness (MESH:D048968), metabolic syndrome (MESH:D024821), pain (MESH:D010146), dyslipidemia (MESH:D050171), alcohol abuse (MESH:D000437), gout (MESH:D006073), gastroenteritis (MESH:D005759), mental disorders (MESH:D001523), diabetic (MESH:D003920), swelling (MESH:D004487), neuroinflammation (MESH:D000090862)
- **Chemicals:** Behenic acid (MESH:C007547), steroids (MESH:D013256), palmitic acid (MESH:D019308), DHA (MESH:D004281), LPS (MESH:D008070), Lipid (MESH:D008055), alcohols (MESH:D000438), Organoheterocyclic Compounds (MESH:D006571), Anthocyanins (MESH:D000872), glucose (MESH:D005947), threonine (MESH:D013912), ice (MESH:D007053), short-chain fatty acids (MESH:D005232), C1 (MESH:C400149), Alginic acid (MESH:D000077322), Carboxylic Acids and Derivatives (-), melatonin (MESH:D008550), sphingomyelin (MESH:D013109), bile acids (MESH:D001647), LTB4 (MESH:D007975), SR9243 (MESH:C000602007), leukotrienes (MESH:D015289), d3 (MESH:D002762), Amino Acids (MESH:D000596), PS (MESH:D010718), leflunomide (MESH:D000077339), PC (MESH:D010713), Phosphatidylinositol-3,4,5-trisphosphate (MESH:C060974), FA (MESH:D005227), Carbohydrate (MESH:D002241), water (MESH:D014867), phospholipid (MESH:D010743), Carotenoids (MESH:D002338), methotrexate (MESH:D008727), free fatty acids (MESH:D005230), AA (MESH:D016718), stearic acid (MESH:C031183), PGE2 (MESH:D015232), N-Arachidonoyl Dopamine (MESH:C474941), cholesterol (MESH:D002784), blood sugar (MESH:D001786), methanol (MESH:D000432), PGJ2 (MESH:C037112), Vitamin D (MESH:D014807), PA (MESH:D011478), formic acid (MESH:C030544), Glycerophospholipids (MESH:D020404), Perfluorotridecanoic acid (MESH:C000720141), TC (MESH:D013667), polysaccharide (MESH:D011134), lipoic acid (MESH:D008063), UA (MESH:D014527), cortisol (MESH:D006854), prostaglandin (MESH:D011453), C4 (MESH:C058899), triglycerides (MESH:D014280), acetonitrile (MESH:C032159), pentose phosphate (MESH:D010428)
- **Species:** Phaeophyceae (brown algae, class) [taxon 2870], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

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## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929458/full.md

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Source: https://tomesphere.com/paper/PMC12929458