# Hypothalamic Atrophy and Textural Changes in Polyglutamine Ataxias

**Authors:** Livia Rodrigues, Thiago J. R. Rezende, Alberto R. M. Martinez, Breno Massuyama, Jose Luiz Pedroso, Orlando G. P. Barsottini, Juan Eugenio Iglesias, Simone Appenzeller, Letícia Rittner, Marcondes C. França

PMC · DOI: 10.1007/s12311-026-01978-4 · Cerebellum (London, England) · 2026-03-23

## TL;DR

This study finds that the hypothalamus shrinks and changes texture in certain types of spinocerebellar ataxia, suggesting early disease involvement.

## Contribution

The study expands on prior findings by showing hypothalamic atrophy and textural changes in multiple polyglutamine ataxia subtypes.

## Key findings

- Significant hypothalamic atrophy was found in SCA1, SCA3, and SCA6 compared to controls.
- Texture analysis showed widespread changes in SCA1, SCA3, and SCA6 across all hypothalamic subregions.
- Atrophy and texture changes correlated with disease duration and severity in SCA1 and SCA3.

## Abstract

Background. Spinocerebellar ataxia (SCA) presents a complex genetic landscape, with over 40 subtypes. These autosomal dominant disorders manifest late onset and severe disability, primarily impacting the cerebellum but also involving other nervous system structures. While a single study has linked hypothalamic atrophy to SCA3, further research is needed to confirm and/or expand this association. This study aimed to investigate hypothalamic involvement in PolyQ SCAs, focusing on SCA 1, 2, 3, and 6. Methods. We studied 135 adult patients with genetically confirmed SCA (SCA1, SCA2, SCA3, and SCA6) and 117 healthy controls. Hypothalamic subregions were segmented using H-SynEx, and both volumetric and texture features were extracted from MR images. Group differences were assessed with the Mann–Whitney U test, and associations with disease duration and severity (measured by SARA) were examined using Spearman’s rank correlation. Results. Significant atrophy of hypothalamic subregions was observed in SCA1, SCA3, and SCA6 when compared with controls, with the anterior subregion being affected in all cases. Texture analysis revealed widespread alterations in SCA1, SCA3, and SCA6 across all subregions. In SCA1 and SCA3, both volumetric and texture measures correlated with disease duration and SARA scores. These findings suggest that hypothalamic involvement in SCAs is complex and may occur before overt clinical manifestations. Key words: Ataxia, Polyglutamine disease, Hypothalamus, MRI, Volumetry

## Linked entities

- **Diseases:** Spinocerebellar ataxia (MONDO:0000437), SCA1 (MONDO:0008119), SCA2 (MONDO:0008458), SCA3 (MONDO:0007182), SCA6 (MONDO:0008457)

## Full-text entities

- **Genes:** ATXN3 (ataxin 3) [NCBI Gene 4287] {aka AT3, ATX3, JOS, MJD, MJD1, SCA3}, KCNC3 (potassium voltage-gated channel subfamily C member 3) [NCBI Gene 3748] {aka KSHIIID, KV3.3, SCA13}, ATXN1 (ataxin 1) [NCBI Gene 6310] {aka ATX1, D6S504E, SCA1}, ATXN2 (ataxin 2) [NCBI Gene 6311] {aka ATX2, SCA2, TNRC13}, Atxn3 (ataxin 3) [NCBI Gene 110616] {aka 2210008M02Rik, ATX3, MJD1, Mjd, Sca3, ataxin-3}, CACNA1A (calcium voltage-gated channel subunit alpha1 A) [NCBI Gene 773] {aka APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2}, Atxn1 (ataxin 1) [NCBI Gene 20238] {aka 2900016G23Rik, Atx1, Gm10786, Sca1}
- **Diseases:** neurological disorders (MESH:D009461), anterior hypothalamic damage (MESH:D007027), cerebellar ataxia (MESH:D002524), neuronal death (MESH:D009410), amyotrophic lateral sclerosis (MESH:D000690), dysphagia (MESH:D003680), Polyglutamine disease (MESH:D030342), Ataxia (MESH:D001259), SCA (MESH:D020754), extra-cerebellar damage (MESH:D002526), disorders (MESH:D009358), thyroid or adrenal disorders (MESH:D013959), sensory loss (MESH:C580162), diabetes insipidus (MESH:D003919), wasting syndrome (MESH:D019282), gliosis (MESH:D005911), SCA 1, 2 and 3 (MESH:D017827), frontotemporal dementia (MESH:D057180), psychiatric (MESH:D001523), sleep and/or autonomic disorders (MESH:D012893), cord (MESH:D013118), dysautonomia (MESH:D054969), hypogonadism (MESH:D007006), autosomal dominant degenerative disorder (MESH:D019636), neuroendocrine disorders (MESH:D018358), dysfunction (MESH:D006331), PolyQ diseases (MESH:D004194), atrophy (MESH:D001284), dystonia (MESH:D004421)
- **Chemicals:** PolyQ (MESH:C097188), H (MESH:D006859), Polyglutamine Ataxias (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13006454/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13006454/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006454/full.md

---
Source: https://tomesphere.com/paper/PMC13006454