Astrocytic Markers and the Pre-ataxic Period of SCA3/MJD - BIGPRO Study Astrocytes

• Conditions: Machado-Joseph Disease; Spinocerebellar Ataxia Type 3; SCA3; MJD
• Interventions: Diagnostic Test: Molecular Diagnosis; Diagnostic Test: Clinical Scales - Baseline; Diagnostic Test: Blood Draw - Baseline; Diagnostic Test: Quality of Life Assessment - Baseline; Diagnostic Test: Clinical Scales - Follow-up 12 months; Diagnostic Test: Quality of Life Assessment - Follow-up 12 months; Diagnostic Test: Blood Draw - Follow-up 12 months; Diagnostic Test: Clinical Scales - Follow-up 24 months; Diagnostic Test: Blood Draw - Follow-up 24 months; Diagnostic Test: Quality of Life Assessment - Follow-up 24 months

• Registration Number: NCT04419974
• Lead Sponsor: Hospital de Clinicas de Porto Alegre

Brief Summary

The study will consist of a prospective observation of subjects in a natural history design. The investigators will monitor changes of clinical scales, quality of life, messenger ribonucleic acid (mRNA) of candidate genes (CCL11, TNFSF14, FCGR3B, CLC, and SLA) (and their peptide products, when possible), and eotaxin and S100B serum levels, in order to determine which of them is (are) the most sensitive. Participants will be stratified in three groups: ataxic carriers, pre-ataxic carriers and non-carriers (controls).

Detailed Description

Spinocerebellar ataxia type 3, or Machado-Joseph disease (SCA3/MJD), is an autosomal dominant neurodegenerative disorder caused by a CAG expansion at ATXN3. The gene product is a 42kDa protein called ataxin-3, widely expressed in neurons and peripheral tissues. Physiological roles of ataxin-3 include, at least, ubiquitination and regulation of misfolded proteins, cytoskeletal organization and focal adhesions development, and transcriptional regulation, most often as a transcriptional corepressor. One purpose of the present study is to detect a possible association between altered transcription patterns of candidate genes and disease progression. On the other hand, previous evidences suggest that the disease process linked to polyQ aggregation in neuronal cell ("cell-autonomous process") might be worsened by what happens outside the neuronal cell ("non-cell-autonomous process"). Initial evidences lead to the role of astrocytes. This is a major depart from the traditional understanding of polyglutamine diseases, and comprises the main focus of the present study.

The main hypothesis of this study is that the SCA3/MJD clinical features may be in part associated to astrocytic processes. In order to test it, peripheral level of LIGHT protein (encoded by TNFSF14) and eotaxin (encoded by CCL11) - both expressed in astrocytes -, and of S100B (a myelin damage marker), will be measured. The investigators speculate if they can be biomarkers of disease progression and of pathological process, even before symptoms onset. In case this is positive, their responsiveness to change will be tested to check if it is better than those of clinical scales.

The second aim is to test if disease progression can be associated with changes in the transcriptional pattern of candidate genes FCGR3B, CLC and SLA.

"BIGPRO study - Astrocytes" intends to identify variations in these candidates and validate them as SCA3/MJD biomarkers. The study will consist of a prospective observation of subjects in a natural history design. Changes in clinical scales, quality of life, messenger ribonucleic acid (mRNA) of candidate genes (CCL11, TNFSF14, FCGR3B, CLC, and SLA) (and their peptide products, when possible), and eotaxin and S100B serum levels will be monitored in order to determine which of them is (are) the most sensitive. Participants will be stratified in three groups: ataxic carriers, pre-ataxic carriers and non-carriers (controls). For each asymptomatic carrier, the time until start of disease will be estimated according to the individual CAG expanded sequence (CAGexp) and subject's age. Clinical scales Scale for the Assessment and Rating of Ataxia (SARA), Neurological Examination Scale for SCA (NESSCA), International Co-operative Rating Scale (ICARS), Inventory of Non-ataxia Symptoms (INAS), SCA Functional Index (SCAFI), Composite Cerebellar Functional Severity Score (CCFS) and Quality of Life measurements (EQ-5D and SF-36), will be applied at baseline, at 12 months and at 24 months, in all subjects (all three groups). Eotaxin, TNFSF14, S100B and mRNAs, will be measured in the same moments. Progression rates of all these variables will be estimated through mixed-models, including, as covariates, age, group and their interactions.

Study Timeline

• Study Start: 2017-03-18
• Study First Submitted: 2020-04-07
• Status Verified: 2020-06
• Study First Submitted QC: 2020-06-03
• Last Update Submitted: 2020-06-03
• Study First Posted: 2020-06-09
• Last Update Posted: 2020-06-09
• Primary Completion: 2020-12
• Study Completion: 2021-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 95

Inclusion Criteria

• Individuals with molecular diagnosis of SCA3/MJD
• Individuals at 50% risk of inheriting SCA3/MJD mutation without any clinical manifestation

Exclusion Criteria

• Refusal to sign informed consent
• Other diagnosed neurological conditions;
• Diabetes Mellitus;
• Chronic allergy (asthma, eczema, urticaria)
• Eosinophilia on baseline

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Ataxic carriers	Clinical Scales - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Quality of Life Assessment - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Pre-ataxic carriers	Molecular Diagnosis	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Blood Draw - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Related controls	Molecular Diagnosis	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Ataxic carriers	Blood Draw - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Quality of Life Assessment - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Clinical Scales - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Quality of Life Assessment - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Blood Draw - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Blood Draw - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Ataxic carriers	Clinical Scales - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of 3 points or more.
Pre-ataxic carriers	Clinical Scales - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Quality of Life Assessment - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Related controls	Blood Draw - Follow-up 24 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Quality of Life Assessment - Follow-up 24 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Pre-ataxic carriers	Blood Draw - Baseline	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Clinical Scales - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Blood Draw - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Quality of Life Assessment - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Related controls	Clinical Scales - Baseline	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Blood Draw - Baseline	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Clinical Scales - Follow-up 24 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Pre-ataxic carriers	Quality of Life Assessment - Follow-up 12 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Pre-ataxic carriers	Clinical Scales - Follow-up 24 months	Subjects with a CAG repeat expansion on ATXN3 and Scale for Assessment and Rating of Ataxia (SARA) of less than 3 points.
Related controls	Quality of Life Assessment - Baseline	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Blood Draw - Follow-up 12 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Quality of Life Assessment - Follow-up 12 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.
Related controls	Clinical Scales - Follow-up 12 months	Subjects without a CAG repeat expansion on ATXN3, but with a first degree relative affected by the disease.

Primary Outcome Measures

Name	Time	Method
Change in serum concentrations of Eotaxin	24 months	pg/ml
Change in serum concentrations of S100B	24 months	μg/l
Change in expression of TNFSF14	24 months	Fold change (FC)
Change in expression of CCL11	24 months	Fold change (FC)
Change in SF-36 (Short-form 36)	24 months	Quality of life scale evaluating 8 domains through 36 questions. Domain scores decrease with worsening in quality of life.
Change in EQ-5D-3L (EuroQoL 5 Domains evaluated in 3 levels)	24 months	Quality of life scale evaluating 5 domains and a visual analog scale. Domain scores increase with worsening in quality of life. In the visual analog scale, worse scores mean decrease in quality of life.

Secondary Outcome Measures

Name	Time	Method
Change in expression of CLC	24 months	Fold change (FC)
Change in expression of SLA	24 months	Fold change (FC)
Change in expression of FCGR3B	24 months	Fold change (FC)

Trial Locations

Locations (1)

Hospital de Clinicas de Porto Alegre; 🇧🇷 Porto Alegre, Rio Grande Do Sul, Brazil