Chronic disease outcome metadata from German observational studies – public availability and FAIR principles

Metadata from epidemiological studies, including chronic disease outcome metadata (CDOM), are important to be findable to allow interpretability and reusability. We propose a comprehensive metadata schema and used it to assess public availability and findability of CDOM from German population-based...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Scientific data Ročník 10; číslo 1; s. 868 - 18
Hlavní autoři: Schwedhelm, Carolina, Nimptsch, Katharina, Ahrens, Wolfgang, Hasselhorn, Hans Martin, Jöckel, Karl-Heinz, Katzke, Verena, Kluttig, Alexander, Linkohr, Birgit, Mikolajczyk, Rafael, Nöthlings, Ute, Perrar, Ines, Peters, Annette, Schmidt, Carsten O., Schmidt, Börge, Schulze, Matthias B., Stang, Andreas, Zeeb, Hajo, Pischon, Tobias
Médium: Journal Article
Jazyk:angličtina
Vydáno: London Nature Publishing Group UK 05.12.2023
Nature Publishing Group
Nature Portfolio
Témata:
692/699/317
692/699/67
692/699/75
706/648/697
Chronic Disease
Chronic illnesses
Epidemiology
Humanities and Social Sciences
Humans
Metadata
multidisciplinary
Observational studies
Population studies
Science
Science (multidisciplinary)
ISSN:2052-4463, 2052-4463
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Metadata from epidemiological studies, including chronic disease outcome metadata (CDOM), are important to be findable to allow interpretability and reusability. We propose a comprehensive metadata schema and used it to assess public availability and findability of CDOM from German population-based observational studies participating in the consortium National Research Data Infrastructure for Personal Health Data (NFDI4Health). Additionally, principal investigators from the included studies completed a checklist evaluating consistency with FAIR principles (Findability, Accessibility, Interoperability, Reusability) within their studies. Overall, six of sixteen studies had complete publicly available CDOM. The most frequent CDOM source was scientific publications and the most frequently missing metadata were availability of codes of the International Classification of Diseases, Tenth Revision (ICD-10). Principal investigators’ main perceived barriers for consistency with FAIR principles were limited human and financial resources. Our results reveal that CDOM from German population-based studies have incomplete availability and limited findability. There is a need to make CDOM publicly available in searchable platforms or metadata catalogues to improve their FAIRness, which requires human and financial resources.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Undefined-1
ObjectType-Feature-3
content type line 23
ISSN:2052-4463
2052-4463
DOI:10.1038/s41597-023-02726-7