Evidence map›Paper›PMID 35317023›Full record

ArticleAdvanced genetics (Hoboken, N.J.)2022

Community Consensus Guidelines to Support FAIR Data Standards in Clinical Research Studies in Primary Mitochondrial Disease.

Amel Karaa, Laura E MacMullen, John C Campbell, John Christodoulou, Bruce H Cohen, Thomas Klopstock, Yasutoshi Koga, Costanza Lamperti, Rob van Maanen, Robert McFarland and 6 more

Abstract read
In one paragraph

Article in Advanced genetics (Hoboken, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

16 authors.

Amel KaraaDepartment of Genetics, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Laura E MacMullenMitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
John C CampbellMinovia Therapeutics, Cambridge, MA 02138, USA.
John ChristodoulouMurdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Melbourne, Victoria 3052, Australia.
Bruce H CohenDepartment of Pediatrics and the Rebecca D. Considine Research Institute, Akron Children's Hospital, Akron, OH 44308, USA.
Thomas KlopstockFriedrich-Baur Institute, Department of Neurology, University Hospital, LMU, Munich 80336, Germany; German Center for Neurodegenerative Diseases (DZNE), Munich 80336, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich 80336, Germany; German Network for Mitochondrial Disorders (mitoNET), Munich 80336, Germany.
Yasutoshi KogaDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Kurume 830-0011, Japan.
Costanza LampertiUO Genetics and Neurogenetics, Fondazione IRCCS Instituto Neurologico C. Besta, Milan 20126, Italy.
Rob van MaanenKhondrion BV., Nijmegen 6525 EX, The Netherlands.
Robert McFarlandWCMR Newcastle University, Newcastle NE1 7RU, UK.
Sumit ParikhCleveland Clinic Foundation, Cleveland, OH 44195, USA.
Shamima RahmanUCL Great Ormond Street Institute of Child Health and Great Ormond, Street Hospital for Children NHS Foundation Trust, London WC1N 1EH, UK.
Fernando ScagliaDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, Hong Kong SAR NT, China.
Alexander V ShermanDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Philip YeskeUnited Mitochondrial Disease Foundation, Pittsburgh, PA 15239, USA.
Marni J FalkMitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Funding

The North American Mitochondrial Disease Consortium (NAMDC)U54NS078059 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI VAN HOVE, JOHAN L · 2011 to 2023
$17.5M
Primary Mitochondrial Disease Expert Curation PanelU24HD093483 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI FALK, MARNI J, GAI, XIAOWU · 2017 to 2023
$2.2M
NICHD NIH HHS U24 HD093483NINDS NIH HHS U54 NS078059
6 · The paper itself

Abstract

Primary mitochondrial diseases (PMD) are genetic disorders with extensive clinical and molecular heterogeneity where therapeutic development efforts have faced multiple challenges. Clinical trial design, outcome measure selection, lack of reliable biomarkers, and deficiencies in long-term natural history data sets remain substantial challenges in the increasingly active PMD therapeutic development space. Developing "FAIR" (findable, accessible, interoperable, reusable) data standards to make data sharable and building a more transparent community data sharing paradigm to access clinical research metadata are the first steps to address these challenges. This collaborative community effort describes the current landscape of PMD clinical research data resources available for sharing, obstacles, and opportunities, including ways to incentivize and encourage data sharing among diverse stakeholders. This work highlights the importance of, and challenges to, developing a unified system that enables clinical research structured data sharing and supports harmonized data deposition standards across clinical consortia and research groups. The goal of these efforts is to improve the efficiency and effectiveness of drug development and improve understanding of the natural history of PMD. This initiative aims to maximize the benefit for PMD patients, research, industry, and other stakeholders while acknowledging challenges related to differing needs and international policies on data privacy, security, management, and oversight.

Indexed as

clinical trialsdata sharingFAIR standardsprimary mitochondrial diseasetherapeutic developments

Identifiers

PMID35317023
PMCPMC8936395

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.