# The effect of bright light therapy on glycemic control and cortisol rhythmicity in depression: a randomized controlled trial

**Authors:** Jie Fang, Xinyu Li, Shukun Zhu, Qinghong Hu, Ting Wang, Jiakuai Yu, Ximing Qin, Daomin Zhu

PMC · DOI: 10.3389/fpsyt.2026.1743465 · Frontiers in Psychiatry · 2026-02-11

## TL;DR

Bright light therapy may improve blood sugar control and cortisol patterns in depressed patients, offering a non-drug treatment option.

## Contribution

This study demonstrates that bright light therapy can improve glycemic control and cortisol rhythmicity in depression.

## Key findings

- Bright light therapy reduced fasting blood glucose and cortisol mesor compared to dim light.
- Changes in blood glucose were positively linked to changes in cortisol mesor within the bright light therapy group.

## Abstract

Depressed patients with comorbid metabolic disorders have poorer quality of life and prognosis. Pharmacological interventions carries risks of liver and kidney toxicity, which highlights the need for safer non-pharmacological alternatives. Experimental data suggest that light exposure modulates cortisol secretion, thereby influencing metabolic outcomes in depression. We hypothesized that bright light therapy may ameliorate metabolic disturbances by modulating cortisol secretion.

In this randomized controlled trial, hospitalized patients with depression were assigned to receive either bright light therapy (BLT) or dim-light control condition. The pre−specified primary endpoint was the change in fasting blood glucose (FBG) and cortisol rhythm indices from baseline to post−treatment. Secondary endpoints included changes in other glycolipid parameters, and scores on the Hamilton Depression (HAMD) and Anxiety (HAMA) scales. Treatment effects were evaluated using linear mixed−effects models with baseline adjustment.

After the 2−week intervention, the BLT group showed a significant reduction in fasting blood glucose (95% CI: 0.280 to 0.600; p < 0.001) and cortisol mesor (95% CI: −2.677 to −0.064; p = 0.040) compared to the control group. Within the BLT group, the change in FBG was positively associated with the change in cortisol mesor after adjusting for covariates (β = 0.053, 95% CI: 0.016 to 0.122, p = 0.036).

The findings of this study support a potential mechanism whereby BLT modulates cortisol rhythmicity, which in turn may contribute to improved glycemic control, pointing to its potential therapeutic benefit for addressing metabolic disturbances in depression.

https://www.chictr.org.cn/bin/project/edit?pid=260569, identifier ChiCTR2500097364.

## Linked entities

- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** dizziness (MESH:D004244), XL (MESH:D000080345), BLT (MESH:D005921), epilepsy (MESH:D004827), glycemic abnormalities (MESH:D000014), organic brain injury (MESH:D001930), intellectual disability (MESH:D008607), hypertension (MESH:D006973), narrow-angle glaucoma (MESH:D015812), cataracts (MESH:D002386), type 2 diabetes (MESH:D003924), thyroid disorders (MESH:D013959), Depressed (MESH:D003866), liver and kidney toxicity (MESH:D056486), glaucoma (MESH:D005901), manic (MESH:D001714), dementia (MESH:D003704), retinal lesions (MESH:D012164), cardiac diseases (MESH:D006331), psychiatric (MESH:D001523), diabetes (MESH:D003920), macular degeneration (MESH:D008268), Anxiety (MESH:D001007), Headache (MESH:D006261), Metabolic disturbances (MESH:D024821), Sleep Disorders (MESH:D012893), HPA axis dysfunction (MESH:D007027), blurred vision (MESH:D014786), major depression (MESH:D003865), metabolic dysregulation (MESH:D021081), metabolic disorders (MESH:D008659), hypercortisolism (MESH:D003480), blindness (MESH:D001766), mood disorders (MESH:D019964), obesity (MESH:D009765), neurological diseases (MESH:D020271)
- **Chemicals:** sertraline (MESH:D020280), FBG (-), TG (MESH:D013866), alcohol (MESH:D000438), serotonin (MESH:D012701), Glucose (MESH:D005947), fluoxetine (MESH:D005473), steroid hormone (MESH:D013256), prednisone (MESH:D011241), lipid (MESH:D008055), Cortisol (MESH:D006854), citalopram (MESH:D015283), triglyceride (MESH:D014280), TC (MESH:D013667), glycolipid (MESH:D006017), norepinephrine (MESH:D009638), cholesterol (MESH:D002784), blood glucose (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932458/full.md

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Source: https://tomesphere.com/paper/PMC12932458