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A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome
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 a...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424983/ https://www.ncbi.nlm.nih.gov/pubmed/32787960 http://dx.doi.org/10.1186/s13023-020-01493-7 |
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author | Atalaia, Antonio Thompson, Rachel Corvo, Alberto Carmody, Leigh Piscia, Davide Matalonga, Leslie Macaya, Alfons Lochmuller, Angela Fontaine, Bertrand Zurek, Birte Hernandez-Ferrer, Carles Rheinard, Carola Gómez-Andrés, David Desaphy, Jean-François Schon, Katherine Lohmann, Katja Jennings, Matthew J. Synofzik, Matthis Riess, Olaf Yaou, Rabah Ben Evangelista, Teresinha Ratnaike, Thiloka Bros-Facer, Virginie Gumus, Gulcin Horvath, Rita Chinnery, Patrick Laurie, Steven Graessner, Holm Robinson, Peter Lochmuller, Hanns Beltran, Sergi Bonne, Gisèle |
author_facet | Atalaia, Antonio Thompson, Rachel Corvo, Alberto Carmody, Leigh Piscia, Davide Matalonga, Leslie Macaya, Alfons Lochmuller, Angela Fontaine, Bertrand Zurek, Birte Hernandez-Ferrer, Carles Rheinard, Carola Gómez-Andrés, David Desaphy, Jean-François Schon, Katherine Lohmann, Katja Jennings, Matthew J. Synofzik, Matthis Riess, Olaf Yaou, Rabah Ben Evangelista, Teresinha Ratnaike, Thiloka Bros-Facer, Virginie Gumus, Gulcin Horvath, Rita Chinnery, Patrick Laurie, Steven Graessner, Holm Robinson, Peter Lochmuller, Hanns Beltran, Sergi Bonne, Gisèle |
author_sort | Atalaia, Antonio |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7424983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74249832020-08-16 A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome Atalaia, Antonio Thompson, Rachel Corvo, Alberto Carmody, Leigh Piscia, Davide Matalonga, Leslie Macaya, Alfons Lochmuller, Angela Fontaine, Bertrand Zurek, Birte Hernandez-Ferrer, Carles Rheinard, Carola Gómez-Andrés, David Desaphy, Jean-François Schon, Katherine Lohmann, Katja Jennings, Matthew J. Synofzik, Matthis Riess, Olaf Yaou, Rabah Ben Evangelista, Teresinha Ratnaike, Thiloka Bros-Facer, Virginie Gumus, Gulcin Horvath, Rita Chinnery, Patrick Laurie, Steven Graessner, Holm Robinson, Peter Lochmuller, Hanns Beltran, Sergi Bonne, Gisèle Orphanet J Rare Dis Research 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. BioMed Central 2020-08-12 /pmc/articles/PMC7424983/ /pubmed/32787960 http://dx.doi.org/10.1186/s13023-020-01493-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Atalaia, Antonio Thompson, Rachel Corvo, Alberto Carmody, Leigh Piscia, Davide Matalonga, Leslie Macaya, Alfons Lochmuller, Angela Fontaine, Bertrand Zurek, Birte Hernandez-Ferrer, Carles Rheinard, Carola Gómez-Andrés, David Desaphy, Jean-François Schon, Katherine Lohmann, Katja Jennings, Matthew J. Synofzik, Matthis Riess, Olaf Yaou, Rabah Ben Evangelista, Teresinha Ratnaike, Thiloka Bros-Facer, Virginie Gumus, Gulcin Horvath, Rita Chinnery, Patrick Laurie, Steven Graessner, Holm Robinson, Peter Lochmuller, Hanns Beltran, Sergi Bonne, Gisèle A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title | A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title_full | A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title_fullStr | A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title_full_unstemmed | A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title_short | A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome |
title_sort | guide to writing systematic reviews of rare disease treatments to generate fair-compliant datasets: building a treatabolome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424983/ https://www.ncbi.nlm.nih.gov/pubmed/32787960 http://dx.doi.org/10.1186/s13023-020-01493-7 |
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