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A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome

dc.contributor.authorAtalaia, Antonio
dc.contributor.authorThompson, Rachel
dc.contributor.authorCorvo, Alberto
dc.contributor.authorCarmody, Leigh
dc.contributor.authorPiscia, Davide
dc.contributor.authorMatalonga, Leslie
dc.contributor.authorMacaya, Alfons
dc.contributor.authorLochmuller, Angela
dc.contributor.authorFontaine, Bertrand
dc.contributor.authorZurek, Birte
dc.contributor.authorHernandez-Ferrer, Carles
dc.contributor.authorRheinard, Carola
dc.contributor.authorGómez-Andrés, David
dc.contributor.authorDesaphy, Jean-François
dc.contributor.authorSchon, Katherine
dc.contributor.authorLohmann, Katja
dc.contributor.authorJennings, Matthew J
dc.contributor.authorSynofzik, Matthis
dc.contributor.authorRiess, Olaf
dc.contributor.authorYaou, Rabah B
dc.contributor.authorEvangelista, Teresinha
dc.contributor.authorRatnaike, Thiloka
dc.contributor.authorBros-Facer, Virginie
dc.contributor.authorGumus, Gulcin
dc.contributor.authorHorvath, Rita
dc.contributor.authorChinnery, Patrick
dc.contributor.authorLaurie, Steven
dc.contributor.authorGraessner, Holm
dc.contributor.authorRobinson, Peter
dc.contributor.authorLochmuller, Hanns
dc.contributor.authorBeltran, Sergi
dc.contributor.authorBonne, Gisèle
dc.date.accessioned2020-08-18T03:47:47Z
dc.date.available2020-08-18T03:47:47Z
dc.date.issued2020-08-12
dc.date.updated2020-08-18T03:47:47Z
dc.description.abstractAbstract Background Rare diseases are individually rare but globally affect around 6% of the population, and in over 70% of cases are genetically determined. Their rarity translates into a delayed diagnosis, with 25% of patients waiting 5 to 30 years for one. It is essential to raise awareness of patients and clinicians of existing gene and variant-specific therapeutics at the time of diagnosis to avoid that treatment delays add up to the diagnostic odyssey of rare diseases’ patients and their families. Aims This paper aims to provide guidance and give detailed instructions on how to write homogeneous systematic reviews of rare diseases’ treatments in a manner that allows the capture of the results in a computer-accessible form. The published results need to comply with the FAIR guiding principles for scientific data management and stewardship to facilitate the extraction of datasets that are easily transposable into machine-actionable information. The ultimate purpose is the creation of a database of rare disease treatments (“Treatabolome”) at gene and variant levels as part of the H2020 research project Solve-RD. Results Each systematic review follows a written protocol to address one or more rare diseases in which the authors are experts. The bibliographic search strategy requires detailed documentation to allow its replication. Data capture forms should be built to facilitate the filling of a data capture spreadsheet and to record the application of the inclusion and exclusion criteria to each search result. A PRISMA flowchart is required to provide an overview of the processes of search and selection of papers. A separate table condenses the data collected during the Systematic Review, appraised according to their level of evidence. Conclusions This paper provides a template that includes the instructions for writing FAIR-compliant systematic reviews of rare diseases’ treatments that enables the assembly of a Treatabolome database that complement existing diagnostic and management support tools with treatment awareness data.
dc.identifier.citationOrphanet Journal of Rare Diseases. 2020 Aug 12;15(1):206
dc.identifier.urihttps://doi.org/10.1186/s13023-020-01493-7
dc.identifier.urihttps://doi.org/10.20381/ruor-25076
dc.identifier.urihttp://hdl.handle.net/10393/40850
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.titleA guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome
dc.typeJournal Article

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