Evidence map›Paper›PMID 42484951›Full record

ArticleCerebellum (London, England)2026

Comprehensive Characterization of Clinical Phenotypes and CTG Repeat-Associated Manifestations in Spinocerebellar Ataxia Type 8.

Deli Yang, Chao Tang, Yu Zhan, Lang Yang, Xiaoyang Lei, Xiaoxue Peng, Dian He

Abstract read
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In one paragraph

Article in Cerebellum (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Deli YangDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China.
Chao TangDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China.
Yu ZhanDepartment of Neurology, Zhejiang Provincial People's Hospital Bijie Hospital, Bijie, China.
Lang YangDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China.
Xiaoyang LeiDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China.
Xiaoxue PengDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China.
Dian HeDepartment of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, 550000, Guizhou Province, China. hedian@gmc.edu.cn.

Funding

Guizhou Provincial Science and Technology Support Program Project 2025-117the Guizhou Provincial Clinical Medical Research Center Construction Project - Neurological Disease Research LCZX[2025]003
6 · The paper itself

Abstract

Spinocerebellar ataxia type 8 (SCA8) is traditionally characterized as a cerebellar syndrome, yet emerging evidence suggests significant phenotypic heterogeneity. The complex non-linear relationship between genetic burden and clinical severity remains understudied. We analyzed 172 SCA8 patients using advanced data mining techniques. Complete clinical demographic data were available for the cohort, with precise genetic repeat numbers available for 171 individuals. K-means clustering identified patient subtypes, while Gaussian Graphical Models (GGM) visualized symptom topology. We developed exploratory machine learning models (Decision Tree/Random Forest) and employed Generalized Additive Models (GAM) to characterize non-linear genotype-phenotype dynamics. Clustering identified three distinct phenotypes: Severe Multi-system (12%), Mild/Atypical (38%), and Classical Cerebellar (50%). Network analysis revealed ataxia as a central hub, while ocular motor disorders acted as bridges between symptom clusters. A machine learning-derived decision tree stratified patients with promising exploratory performance (AUC: 0.82-0.89) using only three clinical checkpoints (pyramidal signs, speech disorders, and hyperreflexia), showing predictive patterns distinct from genetic repeat length. Additionally, GAM analysis identified a potential non-linear inflection point at ~ 100 CTG repeats. This hypothesis-generating observation provides a preliminary mathematical context for the paradoxical "low-repeat/high-severity" phenotype in the Severe cluster. SCA8 is a multi-dimensional spectrum disorder rather than a uniform cerebellar disease. Our exploratory diagnostic modeling provides a computational framework for understanding symptom predictors, while non-linear modeling provides novel insights into pathogenic heterogeneity, offering an exploratory foundation for future personalized management and clinical trial design.

Indexed as

Spinocerebellar AtaxiasTrinucleotide Repeat ExpansionAdultClustering AlgorithmsFemaleGenetic Association StudiesHumansMachine LearningMaleMiddle AgedPhenotypeSpinocerebellar DegenerationsClinical phenotypic heterogeneityCluster analysisCTG repeat expansionGenotype-phenotype correlationSpinocerebellar ataxia type 8

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.