# Disrupted brain topological network and its association with clinical features in posterior cortical atrophy

**Authors:** Min Chu, Qianqian He, Min Cui, Hong Ye, Caishui Yang, Liyong Wu

PMC · DOI: 10.1093/braincomms/fcag014 · Brain Communications · 2026-01-20

## TL;DR

This study finds that brain network changes in posterior cortical atrophy are linked to cognitive decline and specific symptoms like visual and spatial difficulties.

## Contribution

The study identifies specific brain network alterations in PCA and their associations with clinical symptoms.

## Key findings

- Global and nodal structural network metrics are altered in PCA patients.
- Network changes in parietal, occipital, and frontal regions correlate with cognitive and perceptual symptoms.
- Frontal nodes contribute to left-right disorientation and color agnosia in PCA.

## Abstract

The characteristics of structural brain topological network alterations and their correlation with clinical features in posterior cortical atrophy (PCA) remain elusive. This study aims to explore the structural topological network alterations and their correlation with clinical features in PCA. Thirty-four patients with PCA and 34 healthy controls were enrolled in this cross-sectional study and underwent diffusion tensor imaging, structural MRI and neuropsychological assessment. The graph theory method was applied to capture the individual structural properties of the network. Partial correlation analysis was conducted to investigate the clinical relevance of the network properties. The global metrics of the structural and topological network are altered in the PCA group. The nodal metrics were changed in the occipital, parietal, temporal and frontal lobes. Global network metrics are associated with cognition and disease severity. For the node associated with apraxia, finger agnosia, left-right disorientation and agnosia for colour, face and object, we observed a similar but not identical nodal distribution, which was mainly distributed in the parietal cortex. Notably, we observed frontal nodes, including the orbital gyrus, contribute to the left-right disorientation and colour agnosia, and the rectus contributes to the object agnosia. This study helps us understand the underlying mechanism of the symptom network in PCA and provides a promising biomarker for PCA.

Chu et al. demonstrated altered global and nodal structural network metrics in patients with posterior cortical atrophy. These network changes, distributed across parietal, occipital, temporal, and frontal lobes, were associated with cognition, disease severity, and specific visuospatial and perceptual symptoms.

Graphical AbstractFor image description, please refer to the figure legend and surrounding text.

## Linked entities

- **Diseases:** posterior cortical atrophy (MONDO:0018899)

## Full-text entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** prosopagnosia (MESH:D020238), hemi-neglect (MESH:C565524), oculomotor apraxia (MESH:C537423), disorientation (MESH:D003221), apraxia (MESH:D001072), white matter degeneration (MESH:D056784), Lewy body (MESH:D020961), atrophic (MESH:D020966), PCA (MESH:D001284), malignancies (MESH:D009369), AD (MESH:D000544), substance abuse (MESH:D019966), psychiatric disorders (MESH:D001523), atrophy of white matter (MESH:D000090122), vision-related cognitive deficits (MESH:D014786), alexia (MESH:D004410), cognitive impairment (MESH:D003072), Dementia (MESH:D003704), amyloid (MESH:C000718787), Gerstmann syndrome (MESH:D005862), executive dysfunction (MESH:D006331), Colour agnosia (MESH:D000377), depression (MESH:D003866), degeneration of (MESH:D009410), cerebrovascular disease (MESH:D002561), nodal (MESH:D013611), infections (MESH:D007239), brain regions (MESH:D001927), Optic ataxia (MESH:D001259), epilepsy (MESH:D004827)
- **Chemicals:** 18F-AV45 (MESH:C545186), FA (MESH:D005492), 18F-FDG (MESH:D019788), ORBmid (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12971006/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12971006/full.md

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Source: https://tomesphere.com/paper/PMC12971006