# Brain metabolic changes associated with post-stroke pathological laughing and crying: an 18F-FDG-PET study in pontine stroke

**Authors:** Soojin Choi, Dae Hyun Kim, Won Jun Kang, Yong Wook Kim

PMC · DOI: 10.3389/fneur.2025.1641045 · Frontiers in Neurology · 2025-07-21

## TL;DR

This study uses PET imaging to find brain metabolic changes linked to uncontrollable laughing or crying after a stroke in the pons.

## Contribution

The study identifies specific brain regions with reduced metabolism associated with post-stroke pathological laughing and crying.

## Key findings

- PLC patients showed hypometabolism in the right superior frontal gyrus compared to non-PLC patients.
- Reduced metabolism in the right inferior and middle temporal gyri correlated with higher PLC severity scores.
- No brain regions showed positive correlations with PLC severity scores.

## Abstract

Pathological laughing and crying (PLC) is characterized by sudden, uncontrollable, and inappropriate episodes of laughter or crying. While previous studies have identified PLC-associated structural lesions, the underlying metabolic alterations in these patients remain unclear.

We aimed to investigate cerebral metabolic alterations in patients with PLC following pontine stroke using 18F-fluorodeoxyglucose-positron emission tomography imaging.

In this retrospective study, we included 49 patients with pontine stroke admitted to a tertiary inpatient rehabilitation hospital between January 2011 and December 2021. Patients were classified into PLC (n = 20) and non-PLC (n = 29) groups. 18F-fluorodeoxyglucose-positron emission tomography images obtained within 14 days of admission were analyzed using the SPM 12 software. Voxel-wise two-sample t-tests were performed to compare brain metabolism between the two groups (Pfamily-wise error-corrected < 0.05). Multiple regression analysis was conducted to identify brain regions significantly associated with PLC severity, adjusting for age and stroke lesion volume.

Compared with that of the non-PLC group, the PLC group exhibited significant hypometabolism in the right superior frontal gyrus (Pfamily-wise error-corrected < 0.05). Multiple regression analysis revealed that decreased metabolism in the right inferior and middle temporal gyri was significantly correlated with higher Pathological Laughter and Crying Scale scores, indicating greater PLC severity. No brain regions showed positive correlations with the Pathological Laughter and Crying Scale scores.

Our findings reveal that PLC following pontine stroke is associated with distinct patterns of hypometabolism, particularly in the right superior frontal gyrus and the right inferior and middle temporal gyri. These regions may contribute to the regulation of emotional expression and provide insights into the neural mechanisms underlying PLC.

## Linked entities

- **Chemicals:** 18F-fluorodeoxyglucose (PubChem CID 68614)
- **Diseases:** stroke (MONDO:0005098)

## Full-text entities

- **Genes:** HSPG2 (heparan sulfate proteoglycan 2) [NCBI Gene 3339] {aka HSPG, PLC, PRCAN, SJA, SJS, SJS1}
- **Diseases:** SAH (MESH:D013345), amyotrophic lateral sclerosis (MESH:D000690), Stroke (MESH:D020521), lesions (MESH:D009059), ischemic stroke (MESH:D002544), Parkinson's disease (MESH:D010300), neurological disorders (MESH:D009461), Depression (MESH:D003866), Crying (MESH:D003410), cerebral lesions (MESH:D002539), complex partial seizures (MESH:D012640), anxiety (MESH:D001007), demyelinating conditions (MESH:D003711), brain lesions (MESH:D001927), hemorrhagic strokes (MESH:D000083302), neurodegenerative disease (MESH:D019636), gray or white matter abnormalities (MESH:D055652), traumatic (MESH:D014947), post (MESH:D000094025), hemorrhagic (MESH:D006470), cerebellar disorders (MESH:D002526), diaschisis (MESH:D000087505), cognitive disorders (MESH:D003072), hypoxic brain injury (MESH:D002534), mood or anxiety disorders (MESH:D001008), pontine lesions (MESH:D020295), multiple sclerosis (MESH:D009103)
- **Chemicals:** 18F-FDG (MESH:D019788), glucose (MESH:D005947), serotonin (MESH:D012701)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12320536/full.md

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Source: https://tomesphere.com/paper/PMC12320536