Abstract
Many current paediatric studies concern relationships between genes and environment and discuss aetiology, treatment and prevention of Mendelian and multifactorial diseases. Many of these studies depend on collection and long-term storage of data and biological material from affected children in biobanks. Stored material is a source of personal information of the donor and his family and could be used in an undesirable context, potentially leading to discrimination and interfering with a child’s right to an open future. Here, we address the normative framework regarding biobanking with residual tissue of children, protecting the privacy interests of young biobank donors (0–12 years). We analyse relevant legal documents concerning storage and use of children’s material for research purposes. We explore the views of 17 Dutch experts involved in paediatric biobank research and focus on informed consent for donation of leftover tissue as well as disclosure of individual research findings resulting from biobank research. The results of this analysis show that experts have no clear consensus about the appropriate rules for storage of and research with children’s material in biobanks. Development of a framework that provides a fair balance between fundamental paediatric research and privacy protection is necessary.
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Acknowledgements
This study was funded by the Netherlands Organisation for Health Research and Development (ZonMw). We thank the interviewees for offering us their insights and experiences.
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Kranendonk, E., Ploem, M. & Hennekam, R. Regulating biobanking with children’s tissue: a legal analysis and the experts’ view. Eur J Hum Genet 24, 30–36 (2016). https://doi.org/10.1038/ejhg.2015.59
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DOI: https://doi.org/10.1038/ejhg.2015.59
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