Abstract
The Ataxia Global Initiative (AGI) aims to serve as a platform to facilitate clinical trial readiness for the hereditary ataxias. Clinical trials for these diseases have been hampered by the lack of objective measures to study disease onset, progression, and treatment efficacy. While these issues are not unique to the genetic ataxias, the relative rarity of these diseases makes the need for such measures even more pressing to achieve statistical power in clinical trials. In this report, we have described the efforts of the AGI fluid biomarker working group (WG) in developing uniform protocols for biomarker sampling and storage, both for human and preclinical studies in mice. By reducing collection variability, we anticipate reduced noise in downstream biomarker analysis that will improve statistical power and minimize the necessary sample size. The emphasis has been on defining and standardizing the sampling and pre-analytical work-up of minimal set of biological samples, specifically blood plasma and serum, keeping in mind the need for harmonization of collection and storage that can be achieved with relatively limited cost and resources. An optional package is detailed for those centers that have the resources and commitment for additional biofluids/sample processing and storage. Finally, we have delineated similar standardized protocols for mice that will be important for preclinical studies in the field.
Original language | English (US) |
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Pages (from-to) | 881-886 |
Number of pages | 6 |
Journal | Cerebellum |
Volume | 23 |
Issue number | 3 |
DOIs | |
State | Published - Jun 2024 |
Funding
FMS, HSM, JMW, DG, MS, DM, and PO declare no competing interests. PO participates in a clinical trial funded by BioHaven Pharmaceuticals and consulted for Reata Pharmaceuticals and UCB Pharmaceuticals. HSM has previously received sponsored research support from Biogen, Lacerta, Roche, and uniQure, and consults for Lacerta Pharmaceuticals. F. M. S received funding from the Italian Ministry of Health (Ricerca Corrente and RC 5X1000; RF-2019–12370417, and Rete RIN in Rare Diseases), and by the EJP-RD network “PROSPAX: an integrated multimodal progression chart in spastic ataxias” grant (project 441409627 to F. M. S.). J. M. W, D. G., M. S., and D. M. were partially supported by grants from the Fondation de l’Ataxie Charlevoix-Saguenay ( www.arsacs.com ). H. S. M. is supported by a Seed Funding grant from the National Ataxia Foundation and NIH funding for her basic and translational science work on neurodegeneration: R21NS111154, R01 NS22751, and U01 NS106670. D. M. is supported by the Clinician Scientist Program of the Medical Faculty Tübingen (459–0-0) and the Elite Programme for Postdocs of the Baden-Württemberg Stiftung (1.16101.21).P. O. has participated in clinical trials funded by BioHaven Pharmaceuticals, the NIH (U01NS104326; READISCA), and the National Ataxia Foundation (CRC‐SCA natural history study). He also has received funding from the NIH for his basic science work on neurodegeneration: 1R01NS082351 and 1R01NS127204.
Keywords
- Ataxia Global Initiative
- Biofluids
- Markers
- Neurodegenerative
- Protocols
- SCA
- Samples
- Standards
ASJC Scopus subject areas
- Clinical Neurology
- Neurology