# The relationship between oxidative balance score, depression, and survival among adult cancer survivors in the United States

**Authors:** Qu Zhang, Yemei Wu, Qianyu Fan, Wenxi Zhou, Min Liu

PMC · DOI: 10.3389/fnut.2025.1622588 · Frontiers in Nutrition · 2025-07-16

## TL;DR

This study explores how oxidative balance and depression affect cancer survival in U.S. survivors, finding that higher oxidative balance is linked to better outcomes.

## Contribution

The novel contribution is identifying that high oxidative balance may protect cancer survivors, with depression paradoxically linked to lower mortality in this subgroup.

## Key findings

- Higher oxidative balance score (OBS) is associated with reduced cancer mortality in cancer survivors.
- Depression alone does not correlate with mortality, but in high-OBS individuals, depression is linked to lower cancer mortality.
- Oxidative balance may have a protective effect, suggesting interactions between nutrition and psychological factors in cancer survival.

## Abstract

Depression and oxidative balance score (OBS) are linked to disease risk, yet their combined effects on cancer survival remain unclear. This study assessed OBS, depression, and mortality in cancer survivors.

Utilizing a prospective, population-based cohort design, this analysis enrolled 1,455 adult cancer survivors (age ≥20 years) through the National Health and Nutrition Examination Survey (NHANES) from 1999 to 2018. The OBS was related to diet and exercise, and depression was self-reported. Depressive symptomatology was measured using the established Patient Health Questionnaire-9 (PHQ-9) self-report questionnaire. Depression was defined as a total PHQ-9 score > 4, indicating the presence of depressive symptoms. A score ≤ 4 was considered to indicate no depression. Mortality outcomes (all-cause, cancer-specific, non-cancer) were tracked via the National Death Index through 2019. Cox models adjusted for demographics, socioeconomic status, and comorbidities.

Over 80–90 months, 329 deaths occurred (102 cancer-related). Higher OBS predicted reduced mortality (per-unit HR = 0.94, 95% CI: 0.90–0.98). In OBS tertiles, Tertile 3 vs. Tertile 1 showed HR = 0.30 (95% CI: 0.14–0.63) for cancer mortality. Depression alone had no mortality association (HR = 1.24, 95% CI: 0.49–3.18). However, within the highest OBS tertile, depressed patients exhibited lower cancer mortality (HR = 0.18, 95% CI: 0.05–0.71) versus non-depressed counterparts.

Elevated OBS is protective in cancer survivors. Depression may paradoxically reduce mortality risk in high-OBS subgroups, suggesting nutrition-psychology interactions.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## 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}
- **Diseases:** hyperlipidemia (MESH:D006949), cardiovascular disease (MESH:D002318), Depressive (MESH:D003866), metastasis (MESH:D009362), concentration impairment (MESH:C567712), melanoma (MESH:D008545), Death (MESH:D003643), Cancer (MESH:D009369), inflammation (MESH:D007249), breast (MESH:D061325), prostate cancer (MESH:D011471), cardiometabolic diseases (MESH:D024821), anhedonia (MESH:D059445), psychological disorders (MESH:D000067073), fatigue (MESH:D005221), psychomotor alterations (MESH:D011596), cervical cancer (MESH:D002583), psychiatric (MESH:D001523), sleep dysfunction (MESH:D012893), suicidal ideation (MESH:D001072), OBS (MESH:D028361), breast cancer (MESH:D001943), (HPA) axis dysfunction (MESH:D007027), prostate (MESH:D011472), chronic diseases (MESH:D002908), diabetes (MESH:D003920)
- **Chemicals:** beta-carotene (MESH:D019207), selenium (MESH:D012643), Cortisol (MESH:D006854), lipid (MESH:D008055), ROS (MESH:D017382), carotenoids (MESH:D002338), Caffeine (MESH:D002110), alcohol (MESH:D000438), copper (MESH:D003300), Vitamin C (MESH:D001205), magnesium (MESH:D008274), vitamin E (MESH:D014810), serotonin (MESH:D012701), hydroxyl radicals (MESH:D017665), zinc (MESH:D015032), vitamins C and E (-), heme iron (MESH:D006418), flavonoids (MESH:D005419), calcium (MESH:D002118), cotinine (MESH:D003367), iron (MESH:D007501)
- **Species:** Spinacia oleracea (spinach, species) [taxon 3562], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307194/full.md

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Source: https://tomesphere.com/paper/PMC12307194