Promoting diversity and inclusion in neuroscience and neuroethics.
Promoting diversity and inclusion in neuroscience and neuroethics.
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DOI:
10.1016/j.ebiom.2021.103359
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发表时间:
2021-05
期刊:
影响因子:
11.1
通讯作者:
Matshabane OP
中科院分区:
文献类型:
--
作者:
Matshabane OP
Neuroscience is moving at breakneck speed towards understanding how the nervous system and the human brain function in order to develop novel treatments for neurological, neurodevelopmental and psychiatric disorders. Pursuing responsible neuroscience research requires a range of potential ethical, legal, and social implications (ELSI) to be addressed. Neuroethics seeks to address these ethical considerations. Like other biological sciences, neuroscience and neuroethics struggle with diversity yet there are compelling reasons to foster diversity in these disciplines. I argue that these fields need to commit to the inclusion of diverse individuals for at least two reasons. First, as a matter of social justice, individuals who have been systemically oppressed and marginalised could (and should) benefit from contextually relevant research which includes their priorities and views. Second, for the advancement of science, it is increasingly clear that diverse groups yield the most innovative and impactful scientific solutions. The underrepresentation of some groups among researchers and patient cohorts forces us to reflect on who will likely benefit from the neuroscience and to consider whether there are potential gaps¿ including possibly overlooked bias¿ in the research agendas, questions, methodologies, and resultant neurotechnologies. For example, increasingly the neuroethics agenda seems to focus on neurotechnological advancements, commercialisation of devices and brain data privacy. Dominating questions relate to the use of expensive novel technologies, such as deep brain stimulation, responsive neurostimulation, neuro-wearables, as well as brain-computer interfaces. While investigating ethical implications of these topics is certainly important, the results may not be immediately relevant to people from marginalised communities¿ particularly those from low-income and middle-income countries (LMICs) in Africa and other continents¿ given that they are almost exclusively available to select individuals in high income countries (HICs). Ironically, the majority of people with disabilityadjusted life years (DALYs) related to neurological, psychiatric, and substance-use disorders live in LMICs [2],[3].Furthermore, in LMICs, there are other priorities for neuroscience research, like identifying cost-effective innovative therapies for the highly prevalent neuroinfectious diseases of the central nervous system¿ such as meningitis and encephalitis [1]. Additionally, stroke¿ which is the second largest cause of death in the world and has more than 80% of its burden accounted for by people in LMICs¿ is also a neurological illness of priority. In Sub-Saharan Africa (SSA) for instance, stroke incidence rates are increasing, with more younger people being affected as compared to people from European descent and occurrences leading to worse outcomes [3]. With the exception of the African Neurobiobank for Precision Stroke Medicine: ELSI Project (part of the Human Heredity and Health [H3Africa] consortia)[3], and the Africa Ethics Working Group (part of the Global Initiative in Neuropsychiatric Ethics [NeuroGene])¿ ethical implications of neuroscience research on the African continent have hardly been investigated. Including researchers and research participants from Africa and other LMICs in the conceptualisation and design of international neuroscience and neuroethics research would be one way of fostering opportunities to critically re-consider ethical questions and priorities.
DOI:
10.1016/s1474-4422(18)30403-4
发表时间:
2019-01
期刊:
The Lancet. Neurology
影响因子:
--
作者:
GBD 2016 Dementia Collaborators
通讯作者:
GBD 2016 Dementia Collaborators
影响因子:
168.9
作者:
通讯作者:
--
影响因子:
5.4
作者:
Akinyemi RO;Jenkins C;Nichols M;Singh A;Wahab K;Akpalu A;Sarfo FS;Owolabi LF;Obiako R;Akinyemi J;Ojebuyi B;Adigun M;Musbahu R;Bello A;Titiloye M;Calys-Tagoe B;Ogunronbi M;Uvere E;Laryea R;Fakunle A;Adeleye O;Olorunsogbon O;Ojo A;Adesina D;Mensah N;Oguike W;Coleman N;Mande A;Uthman M;Kalaria RN;Jegede A;Owolabi M;Ovbiagele B;Arulogun O
通讯作者:
Arulogun O