# Association between chronic stress-related amygdala metabolic activity and distant metastasis in colorectal cancer

**Authors:** Hyun Joo Kim, Sejin Ha, Chanmin Joung, Sungeun Kim, Kisoo Pahk

PMC · DOI: 10.3389/fendo.2026.1747732 · 2026-02-03

## TL;DR

High amygdala metabolic activity in brain scans is linked to distant metastasis in colorectal cancer, suggesting chronic stress may influence cancer spread.

## Contribution

Amygdala metabolic activity is proposed as a novel imaging biomarker for predicting distant metastasis in colorectal cancer.

## Key findings

- Elevated amygdala metabolic activity was significantly associated with distant metastasis in CRC patients.
- An AmygA cutoff of 1.159 predicted metastasis with 71.4% sensitivity and 89.1% specificity.
- Elevated AmygA remained an independent predictor of distant metastasis in multivariable analysis.

## Abstract

Chronic stress has been implicated in cancer progression through neuroendocrine and inflammatory pathways, but its role in colorectal cancer (CRC) remains uncertain. The amygdala, a key stress-responsive brain structure, demonstrates measurable metabolic activity on 18F-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) and may serve as a surrogate imaging biomarker of chronic stress. This study aimed to investigate whether elevated amygdala metabolic activity (AmygA) is associated with distant metastasis in patients with CRC.

This study included patients with newly diagnosed CRC who underwent pre-treatment ¹8F-FDG PET/CT and curative-intent surgery between January 2019 and December 2023. AmygA was defined as the ratio of maximum standardized uptake value (SUVmax) of the amygdala to the mean standardized uptake value (SUVmean) of the ipsilateral temporal lobe. Receiver-operating characteristic curve analysis determined the optimal AmygA threshold for predicting distant metastasis, and multivariable logistic regression identified independent predictors.

Seventy-six patients were analyzed, of whom 21 (27.6%) had distant metastasis. AmygA was significantly higher in patients with distant metastasis than in those without (1.17 ± 0.06 vs. 1.08 ± 0.06; p < 0.001). The optimal AmygA cutoff value for predicting distant metastasis was 1.159, yielding 71.4% sensitivity and 89.1% specificity (area under the curve = 0.844; p < 0.001). Univariable analysis identified advanced T stage, lymph node metastasis, elevated AmygA, increased spleen SUVmax, and higher serum tumor marker levels as significant variables. In prespecified parsimonious multivariable logistic regression models with bootstrap internal validation, elevated AmygA (> 1.159) remained independently associated with distant metastasis.

Elevated amygdala metabolic activity on pre-treatment ¹8F-FDG PET/CT, a surrogate marker of chronic stress, was independently associated with distant metastasis in CRC. AmygA might serve as a novel imaging biomarker for risk stratification and offer insight into stress-related neural mechanisms underlying metastatic progression.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CXCR2 (C-X-C motif chemokine receptor 2) [NCBI Gene 3579] {aka CD182, CDw128b, CMKAR2, IL8R2, IL8RA, IL8RB}, CXCL1 (C-X-C motif chemokine ligand 1) [NCBI Gene 2919] {aka FSP, GRO1, GROa, MGSA, MGSA-a, NAP-3}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}
- **Diseases:** osteoporosis (MESH:D010024), infection (MESH:D007239), T (MESH:D001260), endometrial cancer (MESH:D016889), tumorigenic (MESH:D002471), hypertension (MESH:D006973), mood or psychotic disorders (MESH:D000341), CRC (MESH:D015179), distant metastasis (MESH:D009362), autoimmune or chronic inflammatory diseases (MESH:D019693), dementia (MESH:D003704), lymph node (MESH:D000072717), stomach, lung, breast, endometrium, head and neck, and skin cancers (MESH:D001943), lymph node metastasis (MESH:D008207), head and neck and endometrial cancers (MESH:D006258), metastatic disease (MESH:D000092182), DM (MESH:D009223), psychiatric (MESH:D001523), Cancer (MESH:D009369), diabetes mellitus (MESH:D003920), dyslipidemia (MESH:D050171), inflammation (MESH:D007249), node (MESH:D012804), neurologic disorders (MESH:D009461), cachexia (MESH:D002100), stroke (MESH:D020521)
- **Chemicals:** 18F-FDG (MESH:D019788), catecholamines (MESH:D002395), CA 19 (-), Alcohol (MESH:D000438), steroids (MESH:D013256), blood glucose (MESH:D001786), norepinephrine (MESH:D009638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909207/full.md

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Source: https://tomesphere.com/paper/PMC12909207