Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study.

Autor: Daniels H; Population Data Science, Swansea University, Swansea, United Kingdom., Jones KH; Population Data Science, Swansea University, Swansea, United Kingdom., Heys S; Population Data Science, Swansea University, Swansea, United Kingdom., Ford DV; Population Data Science, Swansea University, Swansea, United Kingdom.
Jazyk: angličtina
Zdroj: Journal of medical Internet research [J Med Internet Res] 2021 Sep 24; Vol. 23 (9), pp. e15739. Date of Electronic Publication: 2021 Sep 24.
DOI: 10.2196/15739
Abstrakt: Background: Advancing the use of genomic data with routinely collected health data holds great promise for health care and research. Increasing the use of these data is a high priority to understand and address the causes of disease.
Objective: This study aims to provide an outline of the use of genomic data alongside routinely collected data in health research to date. As this field prepares to move forward, it is important to take stock of the current state of play in order to highlight new avenues for development, identify challenges, and ensure that adequate data governance models are in place for safe and socially acceptable progress.
Methods: We conducted a literature review to draw information from past studies that have used genomic and routinely collected data and conducted interviews with individuals who use these data for health research. We collected data on the following: the rationale of using genomic data in conjunction with routinely collected data, types of genomic and routinely collected data used, data sources, project approvals, governance and access models, and challenges encountered.
Results: The main purpose of using genomic and routinely collected data was to conduct genome-wide and phenome-wide association studies. Routine data sources included electronic health records, disease and death registries, health insurance systems, and deprivation indices. The types of genomic data included polygenic risk scores, single nucleotide polymorphisms, and measures of genetic activity, and biobanks generally provided these data. Although the literature search showed that biobanks released data to researchers, the case studies revealed a growing tendency for use within a data safe haven. Challenges of working with these data revolved around data collection, data storage, technical, and data privacy issues.
Conclusions: Using genomic and routinely collected data holds great promise for progressing health research. Several challenges are involved, particularly in terms of privacy. Overcoming these barriers will ensure that the use of these data to progress health research can be exploited to its full potential.
(©Helen Daniels, Kerina Helen Jones, Sharon Heys, David Vincent Ford. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 24.09.2021.)
Databáze: MEDLINE
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