Evidence map›Paper›PMID 28303425›Full record

ArticleJournal of inherited metabolic disease2017

Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project.

Amel Karaa, Shamima Rahman, Anne Lombès, Patrick Yu-Wai-Man, Muniza K Sheikh, Sherita Alai-Hansen, Bruce H Cohen, David Dimmock, Lisa Emrick, Marni J Falk and 11 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of inherited metabolic disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. Review
  7. Moving towards clinical trials for mitochondrial diseases.Journal of inherited metabolic disease · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Article
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  13. Review
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 17 institutions in 4 countries.

Amel KaraaMassachusetts General Hospital, Boston, MA, USA.
Shamima RahmanUCL Great Ormond Street Institute of Child Health, London, UK.
Anne LombèsINSERM, Institut Cochin U1016, Paris, France.
Patrick Yu-Wai-ManWellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, UK.
Muniza K SheikhThe Emmes Corporation, Rockville, MD, USA.
Sherita Alai-HansenThe Emmes Corporation, Rockville, MD, USA.
Bruce H CohenAkron Children's Hospital, Akron, OH, USA.
David DimmockMedical College of Wisconsin, Milwaukee, WI, USA.
Lisa EmrickBaylor College of Medicine, Houston, TX, USA.
Marni J FalkChildren's Hospital of Philadelphia, Philadelphia, PA, USA.
Shana McCormackChildren's Hospital of Philadelphia, Philadelphia, PA, USA.
David MirskyChildren's Hospital Colorado, Aurora, CO, USA.
Tony MooreInstitute of Ophthalmology, University College London, London, UK.
Sumit ParikhCleveland Clinic, Cleveland, OH, USA.
John Shoffner, Atlanta, GA, USA.
Tanja TaivassaloMcGill University, Montreal, CA, USA.
Mark TarnopolskyMcMaster University, Hamilton, ON, Canada.
Ingrid TeinHospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Joanne C OdenkirchenNational Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Amy GoldsteinChildren's Hospital of Pittsburgh, 4401 Penn Avenue, Pittsburgh, PA, 15224, USA. dramygoldstein@gmail.com.ORCID 0000-0002-7675-3063
Mito Working Group Member Participants:
Children's Hospital of Philadelphia · USEmmes (United States) · USAID Atlanta · USAkron Children's Hospital · USBaylor College of Medicine · USChildren's Hospital Colorado · USChildren's Hospital of Pittsburgh · USCleveland Clinic · USGreat Ormond Street Hospital · GBInserm · FRMassachusetts General Hospital · USMcMaster University · CAMedical College of Wisconsin · USNational Institutes of Health · USUniversity of California, San Francisco · USUniversity of Toronto · CAWellcome Centre for Mitochondrial Research · GB

Funding

Career Development Program in Pediatric Diabetes Research (K12) at CHOPK12DK094723 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI WILLI, STEVEN M · 2011 to 2020
$3.6M
Medical Research Council G0701386Medical Research Council G1002570NIDA NIH HHS HHSN271201200034CNIDDK NIH HHS K12 DK094723
6 · The paper itself

Abstract

objectivesThe common data elements (CDE) project was developed by the National Institute of Neurological Disorders and Stroke (NINDS) to provide clinical researchers with tools to improve data quality and allow for harmonization of data collected in different research studies. CDEs have been created for several neurological diseases; the aim of this project was to develop CDEs specifically curated for mitochondrial disease (Mito) to enhance clinical research.

methodsNine working groups (WGs), composed of international mitochondrial disease experts, provided recommendations for Mito clinical research. They initially reviewed existing NINDS CDEs and instruments, and developed new data elements or instruments when needed. Recommendations were organized, internally reviewed by the Mito WGs, and posted online for external public comment for a period of eight weeks. The final version was again reviewed by all WGs and the NINDS CDE team prior to posting for public use.

resultsThe NINDS Mito CDEs and supporting documents are publicly available on the NINDS CDE website ( https://commondataelements.ninds.nih.gov/ ), organized into domain categories such as Participant/Subject Characteristics, Assessments, and Examinations.

conclusionWe developed a comprehensive set of CDE recommendations, data definitions, case report forms (CRFs), and guidelines for use in Mito clinical research. The widespread use of CDEs is intended to enhance Mito clinical research endeavors, including natural history studies, clinical trial design, and data sharing. Ongoing international collaboration will facilitate regular review, updates and online publication of Mito CDEs, and support improved consistency of data collection and reporting.

Indexed as

Biomedical ResearchCommon Data ElementsData CollectionHumansMitochondrial DiseasesNational Institute of Neurological Disorders and Stroke (U.S.)Nervous System DiseasesResearch DesignStrokeUnited States

Identifiers

PMID28303425
PMCPMC7783474
OpenAlexW2596391634

What OpenQuestion holds

Textmetadata
LicenceTDM
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.