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ETHICS OF HUMAN GENETIC STUDIES IN SUB-SAHARAN AFRICA: THE CASE OF CAMEROON THROUGH A BIBLIOMETRIC ANALYSIS

机译:撒哈拉以南非洲人类遗传研究的伦理:通过学习分析喀麦隆的情况

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摘要

Many ethical concerns surrounding human genetics studies remain unresolved. We report here the situation in Cameroon. Objectives: To describe the profile of human genetic studies that used Cameroonian DNA samples, with specific focus on i) the research centres that were involved, ii) authorship, iii) population studied, iv) research topics and v) ethics disclosure, with the aim of raising ethical issues that emerged from these studies. Method: Bibliometric Studies; we conducted a PubMed-based systematic review of all the studies on human genetics that used Cameroonian DNA samples from 1989 to 2009. Results and Discussion: Fifty articles were identified, involving predominantly research centres from Europe (64%) and America (32%). Only 7 (14%) Cameroonian institutions and 14 (28%) Cameroonian authors were associated with these publications. At least 52% of publications were devoted to population genetics variation/migration patterns) amongst 30 Cameroonian ethnic groups. Very few studies concerned public health related genetic issues and only 5 (10%) references were found for hemoglobinopathies like sickle cell anaemia. Almost all DNA samples are ‘banked’ outside of the African continent. Capacity building, rights to the genetic information and benefits to the individuals, communities and populations who contribute to these studies are addressed. Conclusions: 1) Our data suggests the need for a wider debate towards building capacity and addressing ethical issues related to human genomic research in sub-Saharan Africa and specifically in Cameroon; 2) National ethical guidelines and regulations concerning the collection, use and storage of human DNA are urgently needed in Cameroon.
机译:围绕人类遗传学研究的许多道德担忧仍未解决。我们在这里报告喀麦隆的情况。目标:描述使用喀麦隆DNA样本的人类遗传研究的概况,特别关注i)所涉及的研究中心,ii)作者,III)学习,IV的研究主题和v)伦理披露,其中提高这些研究中出现的道德问题的目的。方法:派对学研究;我们对从1989年至2009年的喀麦隆DNA样本进行了基于喀麦隆DNA样本的所有研究的系统审查。结果和讨论:确定了五十条文章,主要涉及来自欧洲(64%)和美国的研究中心(32%) 。只有7个(14%)的喀麦隆机构和14名(28%)喀麦隆作者与这些出版物有关。至少52%的出版物致力于30个喀麦隆族群中的群体遗传变异/迁移模式。很少有关患有镰状细胞贫血等血红蛋白的相关遗传问题和仅5(10%)的参考文献。几乎所有DNA样本都是非洲大陆以外的“银行”。解决能力建设,遗传信息的权利和对这些研究有助于这些研究的个人,社区和人口的利益。结论:1)我们的数据表明需要更广泛的争论建设能力,并解决与撒哈拉以南非洲的人类基因组研究有关的道德问题,特别是在喀麦隆; 2)在喀麦隆迫切需要有关收集,使用和储存人体DNA的国家道德准则和法规。

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