Evidence map›Paper›PMID 39371127›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Establishing a Core Outcome Set for Creatine Transporter Deficiency and Guanidinoacetate Methyltransferase Deficiency.

Zahra Nasseri Moghaddam, Emily K Reinhardt, Audrey Thurm, Beth K Potter, Maureen Smith, Celeste Graham, Beth H Tiller, Steven A Baker, Deborah A Bilder, Regina Bogar and 20 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Zahra Nasseri MoghaddamDepartment Pediatrics, University of British Columbia, Vancouver, BC, Canada.ORCID 0009-0007-4968-9573
Emily K ReinhardtBoard of Directors & Staff, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0009-0009-1771-8768
Audrey ThurmNational Institute of Mental Health, NIH, Bethesda, MD, USA.ORCID 0000-0002-0489-9485
Beth K PotterSchool of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.ORCID 0000-0001-8374-6542
Maureen SmithPatient Partner, University of Ottawa, Ottawa, ON, Canada.ORCID 0000-0002-2885-7028
Celeste GrahamBoard of Directors & Staff, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Beth H TillerPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Steven A BakerDepartment of Transfusion Medicine, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0002-8421-7519
Deborah A BilderHuntsman Mental Health Institute, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0003-2202-5746
Regina BogarPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Jacobus BritzPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Rachel CaffertyPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Daniel P CollerBoard of Directors & Staff, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Ton J DeGrauwScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Vicky HallPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Gerald S LipshutzDavid Geffen School of Medicine at the University of California-Los Angeles, Los Angeles, CA, USA.ORCID 0000-0001-7876-6776
Nicola LongoScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0002-3677-1216
Saadet Mercimek-AndrewsScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0001-8396-6764
Judith S MillerCenter for Autism Research, Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID 0000-0002-0796-0923
Marzia PasqualiScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0003-4217-4546
Gajja S SalomonsScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0003-2509-3648
Andreas SchulzeScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0001-8491-1095
Celine P WheatonPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Kayla F WilliamsPatient/Family Partner, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Sarah P YoungScientific Medical Advisory Board, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0000-0002-7671-016X
Jasmine LiDepartment Pediatrics, University of British Columbia, Vancouver, BC, Canada.
Sofia BalogBoard of Directors & Staff, Association for Creatine Deficiencies, Carlsbad, CA, USA.
Theresa SeluckyFine Point Consulting, Los Angeles, CA, USA.
Sylvia Stockler-IpsirogluDepartment Pediatrics, University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-6542-423X
Heidi WallisBoard of Directors & Staff, Association for Creatine Deficiencies, Carlsbad, CA, USA.ORCID 0009-0007-6304-0578

Funding

Neurodevelopmental and Behavioral Phenotyping ZICMH002961 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI THURM, AUDREY · 2017 to 2025
$12.6M
Intramural NIH HHS ZIC MH002961
6 · The paper itself

Abstract

Creatine transporter (CTD) and guanidinoacetate methyltransferase (GAMT) deficiencies are rare inborn errors of creatine metabolism, resulting in cerebral creatine deficiency. Patients commonly exhibit intellectual and developmental disabilities, often accompanied by behavior problems, delayed speech, seizures, and motor impairments. There is currently no efficacious treatment for CTD, while the current management for GAMT requires lifelong treatment with a protein restricted diet and intake of high amounts of oral supplements. Efforts to develop effective, sustainable treatments for these disorders are limited by the lack of clinical and patient-derived meaningful outcomes. A core outcome set (COS) can facilitate consensus about outcomes for inclusion in studies. Unfortunately, patient and caregiver perspectives have historically been overlooked in the COS development process, thus limiting their input into the outcome selection. We partnered with caregivers and health professionals to establish the first COS for CTD and GAMT. The COS developed includes seven outcomes ("Adaptive Functioning", "Cognitive Functioning", "Emotional Dysregulation", "MRS Brain Creatine", "Seizure/Convulsions", "Expressive Communication", and "Fine Motor Functions") for both CTD and GAMT, and an additional outcome for GAMT ("Serum/Plasma Guanidinoacetate") that are important to stakeholders and consequently should be considered for measurement in every clinical trial. Caregivers were valued partners throughout the COS development process, which increased community engagement and facilitated caregiver empowerment. We expect this COS will ensure a patient-centered approach for accelerating drug development for CTD and GAMT, make clinical trial results comparable, minimize bias in clinical trial outcome selection, and promote efficient use of resources.

Indexed as

Core outcome set (COS)Creatine transporter deficiencyGuanidinoacetate methyltransferase deficiencyPatient-centered researchPatient-informed drug developmentRare disease

Identifiers

PMID39371127
PMCPMC11451665

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LicenceCC BY-NC-ND
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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.