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

Journal of Inherited Metabolic Disease - Tập 40 - Trang 403-414 - 2017
Amel Karaa1, Shamima Rahman2, Anne Lombès3, Patrick Yu-Wai-Man4,5,6, Muniza K. Sheikh7, Sherita Alai-Hansen7, Bruce H. Cohen8, David Dimmock9, Lisa Emrick10, Marni J. Falk11,12, Shana McCormack11,12, David Mirsky13, Tony Moore14,15,16, Sumit Parikh17, John Shoffner18, Tanja Taivassalo19, Mark Tarnopolsky20, Ingrid Tein21, Joanne C. Odenkirchen22, Amy Goldstein23
1Massachusetts General Hospital, Boston, USA
2UCL Great Ormond Street Institute of Child Health, London, UK
3INSERM, Institut Cochin U1016, Paris, France
4Wellcome Trust Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne, UK
5NIHR Biomedical Research Centre at Moorfields Eye Hospital, London, UK
6UCL, Institute of Ophthalmology, London, UK
7The Emmes Corporation, Rockville, USA
8Akron Children’s Hospital, Akron, USA
9Medical College of Wisconsin, Milwaukee USA
10Baylor College of Medicine, Houston, USA
11Children’s Hospital of Philadelphia, Philadelphia, USA
12University of Pennsylvania Perelman School of Medicine, Philadelphia, USA
13Children's Hospital Colorado, Aurora, USA
14Institute of Ophthalmology, University College London, London, UK
15Moorfields Eye Hospital, London, UK
16Department of Ophthalmology, University of California, San Francisco, USA
17Cleveland Clinic, Cleveland, USA
18Atlanta, USA
19McGill University, Montreal, USA
20McMaster University, Hamilton, Canada
21Hospital for Sick Children, University of Toronto, Toronto, Canada
22National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, USA
23Children’s Hospital of Pittsburgh, Pittsburgh, USA

Tóm tắt

The 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. Nine 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. The 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. We 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.

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