Current Status, Challenges, Policies, and Bioethics of Biobanks

Many biobanks were established as biorepositories for biomedical research, and a number of biobanks were founded in the 1990s. The main aim of the biobank is to store and to maintain biomaterials for studying chronic disease, identifying risk factors of specific diseases, and applying personalized drug therapies. This report provides a review of biobanks, including Korean biobanks and an analysis of sample volumes, regulations, policies, and ethical issues of the biobank. Until now, the top 6 countries according to the number of large-scale biobanks are the United Kingdom, United States, Sweden, France, the Netherlands, and Italy, and there is one major National Biobank of Korea (NBK) and 17 regional biobanks in Korea. Many countries have regulations and guidelines for the biobanks, and the importance of good management of biobanks is increasing. Meanwhile, according to a first survey of 456 biobank managers in the United States, biobankers are concerned with the underuse of the samples in their repositories, which need to be advertised for researchers. Korea Biobank Network (KBN) project phase II (2013-2015) was also planned for the promotion to use biospecimens in the KBN. The KBN is continuously introducing for researchers to use biospecimens in the biobank. An accreditation process can also be introduced for biobanks to harmonize collections and encourage use of biospecimens in the biobanks. KBN is preparing an on-line application system for the distribution of biospecimens and a biobank accreditation program and is trying to harmonize the biobanks.

[1]  Eleftheria Zeggini,et al.  The effect of next-generation sequencing technology on complex trait research , 2011, European journal of clinical investigation.

[2]  K. Voelkerding Next-Generation Sequencing : A New Revolution in Molecular Diagnostics ? , 2009 .

[3]  B. Elger,et al.  Consent and anonymization in research involving biobanks , 2006, EMBO reports.

[4]  T. Faunce Ethical Issues in Governing Biobanks: Global Perspectives , 2009 .

[5]  Geoff Watts,et al.  UK Biobank opens its data vaults to researchers , 2012, BMJ : British Medical Journal.

[6]  Melissa A. Austin,et al.  Genebanks: A Comparison of Eight Proposed International Genetic Databases , 2003, Public Health Genomics.

[7]  Edwin Cuppen,et al.  Disclosure of individual genetic data to research participants: the debate reconsidered. , 2011, Trends in genetics : TIG.

[8]  O. Park,et al.  Opening of the National Biobank of Korea as the Infrastructure of Future Biomedical Science in Korea , 2012, Osong public health and research perspectives.

[9]  K. Mossman The Wellcome Trust Case Control Consortium, U.K. , 2008 .

[10]  N. Hawkins,et al.  Ethical implications of the use of whole genome methods in medical research , 2009, European Journal of Human Genetics.

[11]  Susanne B Haga,et al.  Ethical, legal, and social implications of biobanks for genetics research. , 2008, Advances in genetics.

[12]  Otlowski Developing an appropriate consent model for biobanks: In defence of 'broad' consent' , 2008 .

[13]  R. Mohler TIME Magazine on “10 Ideas Changing the World Right Now” , 2009 .

[14]  G. Henderson,et al.  Characterizing biobank organizations in the U.S.: results from a national survey , 2013, Genome Medicine.

[15]  C. Rotimi,et al.  Tailoring the process of informed consent in genetic and genomic research , 2010, Genome Medicine.

[16]  A. McGuire,et al.  Research ethics and the challenge of whole-genome sequencing , 2008, Nature Reviews Genetics.

[17]  Simon C. Potter,et al.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.

[18]  S. Terry,et al.  What are the biggest challenges and opportunities for biorepositories in the next three to five years? , 2010, Biopreservation and biobanking.

[19]  Megan Scudellari,et al.  Biobank managers bemoan underuse of collected samples , 2013, Nature Medicine.

[20]  Werner Zolg,et al.  The Proteomic Search for Diagnostic Biomarkers , 2006, Molecular & Cellular Proteomics.

[21]  H. Greely The uneasy ethical and legal underpinnings of large-scale genomic biobanks. , 2007, Annual review of genomics and human genetics.

[22]  Bok-Ghee Han,et al.  A Strategic Plan for the Second Phase (2013–2015) of the Korea Biobank Project , 2013, Osong public health and research perspectives.

[23]  Emilie Devries-Seguin Biobanks in the Literature , 2008 .

[24]  F. Betsou,et al.  Standard Preanalytical Coding for Biospecimens: Defining the Sample PREanalytical Code , 2010, Cancer Epidemiology, Biomarkers & Prevention.

[25]  A. Mauron,et al.  Ethical Issues in Governing Biobanks: Global Perspectives , 2008 .

[26]  W. Kannel,et al.  The Framingham Study An Epidemiological Approach to Coronary Heart Disease , 1966, Circulation.

[27]  Jane Kaye,et al.  Principles and Practice in Biobank Governance , 2009 .

[28]  International Society for Biological and Environmental Repositories , 2005 .