The UK Health Data Research Alliance presents five recommendations for improving data collection for inclusive health research.
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Change history
28 February 2025
A Correction to this paper has been published: https://doi.org/10.1038/s41591-025-03612-y
References
Public Health England. https://go.nature.com/4hHs4Dy (August, 2020).
Pineda-Moncusí, M. et al. Sci. Data 11, 221 (2024).
Office for National Statistics. https://go.nature.com/415ePY1 (accessed 16 July 2024).
Scobie, S., Spencer, J. & Raleigh, V. Nuffield Trust https://go.nature.com/40KkocN (June, 2021).
Health Data Research UK. https://go.nature.com/4hNmIqf (accessed 16 July 2024).
Quattroni, P. et al. Zenodo https://doi.org/10.5281/zenodo.13890530 (2024).
UK Health Data Research Alliance. Zenodo https://doi.org/10.5281/zenodo.8138229 (2023).
Government Analysis Function. https://go.nature.com/40LN6u3 (accessed 16 July 2024).
Office for National Statistics. https://go.nature.com/3Erxgxb (accessed 16 July 2024).
Harron, K. L. et al. Int. J. Epidemiol. 46, 1699–1710 (2017).
Office for National Statistics. https://go.nature.com/3ErxqVj (accessed 16 July 2024).
Office for National Statistics. https://go.nature.com/3EnkAXU (31 July 2024).
Routen, A. Nat. Med. 28, 16–18 (2022).
Akbari, A. BMJ Open 14, e077675 (2024).
Office of the United Nations High Commissioner for Human Rights. https://go.nature.com/4hKXqJt (accessed 16 July 2024).
Acknowledgements
This Comment presents key insights from the Alliance Special Interest Group on Ethnicity Coding Standards. We are very grateful for the contribution of all group participants, covering a broad range of stakeholder views, including patient and public representatives, the National Health Service and other data providers, academia, researchers, and system-level stakeholders. K.K. is supported by the National Institute for Health Research (NIHR) Applied Research Collaboration East Midlands, the NIHR Leicester Biomedical Research Centre, and the British Heart Foundation Centre of Excellence.
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K.K. is the director of the Centre for Ethnic Health Research, University of Leicester, and chaired the Office for National Statistics Ethnicity Working Group. All other authors declare no competing interests.
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Quattroni, P., Routen, A., Alderman, J. et al. Five ways to enhance the diversity and quality of health data. Nat Med 31, 1747–1750 (2025). https://doi.org/10.1038/s41591-025-03545-6
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DOI: https://doi.org/10.1038/s41591-025-03545-6
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