Evidence map›Paper›PMID 37243885›Full record

ArticleCerebellum (London, England)2024

Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on Biomarkers.

Filippo M Santorelli, Hayley S McLoughlin, Justin M Wolter, Daniele Galatolo, Matthis Synofzik, David Mengel, Puneet Opal, AGI-WG2-Biomarkers Study Group

Abstract read
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Hereditary Ataxias in Argentina.Cerebellum (London, England) · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Filippo M SantorelliMolecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, Pisa, Italy. filippo3364@gmail.com.ORCID http://orcid.org/0000-0002-1359-9062
Hayley S McLoughlinDepartment of Neurology, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-4279-2758
Justin M WolterUNC Neuroscience Center, UNC School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, 27599, USA.ORCID http://orcid.org/0000-0002-3021-3993
Daniele GalatoloMolecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, Pisa, Italy.ORCID http://orcid.org/0000-0001-9402-2910
Matthis SynofzikDivision Translational Genomics of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-2280-7273
David MengelDivision Translational Genomics of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany. david.mengel@uni-tuebingen.de.ORCID http://orcid.org/0000-0002-4133-7182
Puneet OpalDepartment of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. p-opal@northwestern.edu.ORCID http://orcid.org/0000-0001-9110-2202
AGI-WG2-Biomarkers Study Group

Funding

Nonneuronal Mechanisms of Polyglutamine NeurodegenerationR01NS122751 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCLOUGHLIN, HAYLEY S · 2021 to 2025
$2.2M
Preclinical Development of Antisense Oligonucleotide Therapy for Spinocerebellar Ataxia Type 3U01NS106670 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCLOUGHLIN, HAYLEY SARAH, PAULSON, HENRY L · 2018 to 2021
$2.1M
Defining Biomarkers for Spinocerebellar Ataxia Type 3R21NS111154 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCLOUGHLIN, HAYLEY SARAH, OZ, GULIN · 2019 to 2019
$435k
Ministero della Salute RC5x100 and Rete RINNINDS NIH HHS R01 NS122751NINDS NIH HHS U01 NS106670
6 · The paper itself

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.

Indexed as

BiomarkersAnimalsAtaxiaBody FluidsDisease Models, AnimalHumansMiceSpecimen HandlingBiomarkersAtaxia Global InitiativeBiofluidsMarkersNeurodegenerativeProtocolsSamplesSCAStandards

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.