Vaz Manjulika, Warrier Prasanna, Wai-Loon Ho Calvin, Bull Susan
Health and Humanities, St John's Research Institute, St John's Medical College, Bangalore, Karnataka, 560 034, India.
Department of Law and Centre for Medical Ethics and Law, The University of Hong Kong, Hong Kong SAR, China.
Wellcome Open Res. 2023 Mar 6;7:78. doi: 10.12688/wellcomeopenres.17628.2. eCollection 2022.
The promise of biobanking and genetic research (BGR) in the context of translational research towards improving public health and personalised medicine has been recognised in India. Worldwide experience has shown that incorporating stakeholders' expectations and values into the governance of BGR is essential to address ethical aspects of BGR. This paper draws on engagement with various stakeholders in the South Indian city of Bengaluru to understand how incorporating people's values and beliefs can inform policy making decisions and strengthen BGR governance within India. We adopted a qualitative research approach and conducted six focus group discussions with civil society members and seven in-depth interviews with key informants in BGR, identified through a targeted web search and snowballing methods, until data saturation was reached. Data were thematically analysed to identify emergent patterns. Specific themes relating to the ethics and governance of BGR emerged. Fears and uncertainty about future sample and data use, possibilities of discrimination and exploitation in the use of findings and the lack of comprehensive data protection policies in India along with expectations of enhanced contributor agency, control in future use of samples and data, benefit sharing, enhanced utility of samples, sustained BGR and public good, reflected tensions between different stakeholders' values and beliefs. Fair governance processes through an independent governance committee for biobanks and a system of ongoing engagement with stakeholders emerged as best practice towards building trust and respecting diversity of views and values. Ensuring public trust in BGR requires listening to stakeholders' voices, being open to counter narratives, and a commitment to long term engagement embedded in principles of participatory democracy. This is central to a 'people-centred governance framework' involving a negotiated middle ground and an equilibrium of governance which promotes social justice by being inclusive, transparent, equitable, and trustworthy.
在印度,生物样本库与基因研究(BGR)在朝着改善公众健康和个性化医疗的转化研究背景下所具有的前景已得到认可。全球经验表明,将利益相关者的期望和价值观纳入BGR的治理对于解决BGR的伦理问题至关重要。本文借鉴了与印度南部城市班加罗尔的各类利益相关者的互动,以了解如何将人们的价值观和信仰纳入考量能够为政策制定决策提供信息,并加强印度国内的BGR治理。我们采用了定性研究方法,与民间社会成员进行了六次焦点小组讨论,并通过有针对性的网络搜索和滚雪球法确定了BGR的关键信息提供者,对他们进行了七次深入访谈,直至达到数据饱和。对数据进行了主题分析以识别新出现的模式。出现了与BGR的伦理和治理相关的特定主题。对未来样本和数据使用的恐惧与不确定性、研究结果使用中存在歧视和剥削的可能性、印度缺乏全面的数据保护政策,以及对增强贡献者的自主权、对样本和数据未来使用的控制权、利益分享、样本效用的提高、持续的BGR和公共利益的期望,反映了不同利益相关者的价值观和信仰之间的紧张关系。通过设立独立的生物样本库治理委员会以及与利益相关者持续互动的系统来进行公平治理,成为建立信任以及尊重观点和价值观多样性的最佳实践。确保公众对BGR的信任需要倾听利益相关者的声音,接受不同的观点,并致力于基于参与式民主原则的长期互动。这对于一个“以人为本的治理框架”至关重要,该框架涉及协商达成的中间立场和治理的平衡,通过包容、透明、公平和可信赖来促进社会正义。