# Impact of a Longer-Term Physical Activity Intervention on Inflammatory and Oxidative Stress Biomarkers in Older People with Metabolic Syndrome

**Authors:** Maria Magdalena Quetglas-Llabrés, Margalida Monserrat-Mesquida, Silvia García, Marina Ródenas-Munar, David Mateos, Lucía Ugarriza, Cristina Gómez, Antoni Sureda, Cristina Bouzas, Josep A. Tur

PMC · DOI: 10.3390/antiox15020151 · Antioxidants · 2026-01-23

## TL;DR

Long-term physical activity in older adults with metabolic syndrome reduces oxidative stress and inflammation, improving overall metabolic health.

## Contribution

Demonstrates the long-term benefits of sustained physical activity on redox balance and inflammation in individuals with metabolic syndrome.

## Key findings

- Increased physical activity reduced reactive oxygen species and malondialdehyde levels over five years.
- Participants showed improved antioxidant enzyme activity and reduced myeloperoxidase with increased activity.
- Physical activity was linked to better metabolic markers like reduced BMI and improved insulin sensitivity.

## Abstract

Metabolic syndrome (MetS) is characterised by cardiometabolic risk factors and is closely associated with increased oxidative stress and chronic low-grade inflammation. MetS is largely driven by adverse lifestyle behaviours, particularly physical inactivity, and regular physical activity is recognised as a central strategy for its prevention and management. This study aimed to assess the long-term impact of a five-year follow-up period of physical activity on oxidative stress, inflammatory biomarkers, and cardiometabolic health in adults with MetS. Forty participants diagnosed with MetS (50% men, aged 55–75 years) were selected and stratified into two groups: those who increased their physical activity and those who reduced it during the intervention. Physical activity was assessed using metabolic equivalent task minutes per week (MET·min/week), and evaluations were performed at baseline, 3 years, and 5 years. Participants who increased physical activity showed a progressive reduction in reactive oxygen species (ROS) produced by peripheral blood mononuclear cells (PBMCs), together with a decrease in plasma malondialdehyde (MDA). Antioxidant enzyme activities, including catalase and superoxide dismutase, exhibited a favourable long-term profile, with recovery or maintenance of higher activity levels by the end of follow-up, reflecting enhanced endogenous antioxidant defence. Inflammatory status improved and was characterised by a reduction in myeloperoxidase (MPO) activity and a sustained increase in plasma interleukin-15 (IL-15). These participants also showed reductions in body weight, body mass index (BMI), waist circumference, fasting glucose, and glycosylated haemoglobin A1c (HbA1c), consistent with improved insulin sensitivity and metabolic control. Participants who reduced physical activity tended to show unfavourable trajectories in several biomarkers. Increasing physical activity over time is associated with substantial improvements in redox balance, inflammatory status, and cardiometabolic health in adults with MetS. These findings reinforce the central role of physical activity as a fundamental therapeutic component within lifestyle interventions aimed at mitigating metabolic dysfunction and preventing MetS progression.

## Linked entities

- **Proteins:** Cat (Catalase), IL15 (interleukin 15)
- **Chemicals:** malondialdehyde (PubChem CID 10964)
- **Diseases:** metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, MPO (myeloperoxidase) [NCBI Gene 4353], CAT (catalase) [NCBI Gene 847], INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** insulin resistance (MESH:D007333), weight (MESH:D015431), CVD (MESH:D002318), hypertension (MESH:D006973), hypertriglyceridemia (MESH:D015228), abdominal obesity (MESH:D056128), abdominal adiposity (MESH:D000007), adiposity (MESH:D018205), T2DM (MESH:D003924), Diabetes (MESH:D003920), cancer (MESH:D009369), mitochondrial dysfunction (MESH:D028361), mitochondrial overload (MESH:D019190), MetS (MESH:D024821), injury to (MESH:D014947), Inflammatory (MESH:D007249), metabolic dysregulation (MESH:D021081), impaired metabolic flexibility (MESH:D008659), overweight (MESH:D050177), falls (MESH:C537863), obese (MESH:D009765), fatty liver (MESH:D005234)
- **Chemicals:** carbohydrates (MESH:D002241), MDA (MESH:D008315), fatty acid (MESH:D005227), haem (MESH:D006418), guaiacol (MESH:D006139), H2O2 (MESH:D006861), LDL-C (-), superoxide (MESH:D013481), ROS (MESH:D017382), glucose (MESH:D005947), LPS (MESH:D008070), Lipid (MESH:D008055), polyphenols (MESH:D059808), ATP (MESH:D000255), tetraguaiacol (MESH:C430963), acetonitrile (MESH:C032159), triglyceride (MESH:D014280), hypochlorous acid (MESH:D006997), EDTA (MESH:D004492), sugars (MESH:D000073893), Ficoll (MESH:D005362), N-methyl-2-phenylindole (MESH:C520322), methanol (MESH:D000432), cholesterol (MESH:D002784), HCl (MESH:D006851), 2',7'-dichlorofluorescein diacetate (MESH:C029569)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938367/full.md

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Source: https://tomesphere.com/paper/PMC12938367