- Research article
- Open Access
A scoping review of genetics and genomics research ethics policies and guidelines for Africa
BMC Medical Ethics volume 22, Article number: 39 (2021)
Genetics and genomics research (GGR) is increasingly being conducted around the world; yet, researchers and research oversight entities in many countries have struggled with ethical challenges. A range of ethics and regulatory issues need to be addressed through comprehensive policy frameworks that integrate with local environments. While important efforts have been made to enhance understanding and awareness of ethical dimensions of GGR in Africa, including through the H3Africa initiative, there remains a need for in-depth policy review, at a country-level, to inform and stimulate local policy development and revision on the continent.
To identify and characterize existing ethics-related guidelines and laws applicable to GGR across much of Africa, we conducted a scoping review of English language policy documents identified through databases, repositories, and web searches. Thirty-six documents were included and coded using a framework that contained a range of themes across five analytical categories: (1) respect, (2) beneficence, (3) justice, (4) independent oversight, and (5) bans and prohibitions. Data analysis software (NVivo 12) was used to organize, code, and tabulate information according to document characteristics and topics. Illustrative examples of policy requirements were selected for inclusion.
Documents that met inclusion criteria spanned 20 years; published between 1996 and 2018, with the majority (58%) published after 2009. About two-thirds were denoted as “guidelines,” and slightly more than half were non-exclusive to GGR. Very few (six) country-level documents identified were specific to GGR. Requirements related to the principle of “respect” appeared most often across all documents, relative to other principles and processes. The most commonly stated ban was on reproductive cloning. Other prohibitions applied to germline editing, undue inducements in research, sample use for commercial purposes, employee mandatory DNA testing, fetal sex selection, stem cell use, eugenics, and research without public health benefits.
Enforceable policies that are indispensable to the ethical conduct and review of GGR are either deficient or missing in many African countries. Existing international, GGR-specific ethics guidelines can be used to inform GGR policy development at a country-level, in conjunction with insight from country specific ethics committees and other local stakeholders.
Due to scientific advancements and the decreased cost of genomic sequencing technologies, genetics and genomics research (GGR) has increased in high-income countries [1, 2]. However, the growth and development of GGR is currently raising critical ethical concerns. For example, until recently, researchers within many less-resourced countries, including several across sub-Saharan Africa, who did not have access to up-to-date facilities, technologies, or training and who faced significant financial barriers, had to rely on genetic analyses being conducted outside of the countries of specimen origin. For many, this contributed to “a sense of mistrust and exploitation,” particularly among African researchers and research participants . Even more so, foreign research teams would come to the continent, conduct research, and leave without much benefit to local populations . At the same time, in a phenomenon that is described as “brain drain,” some accomplished African researchers—due to the challenging research environment—have left the continent in order to participate more fully in advancing the science of GGR . In order to ensure equitable development of GGR and increase African populations’ chances for access to the preventive, diagnostic and therapeutic benefits, there is a need to identify and address these ethical challenges. Other common ethical challenges in GGR in Africa and elsewhere include issues related to informed consent [3,4,5,6,7], privacy and confidentiality (e.g., re-identifiability and data breaches) [3, 4, 7, 8], community engagement [7, 9, 10], data sharing [6, 8, 11, 12], and return of research results and incidental findings [6, 13,14,15].
A critical ingredient necessary to achieving the goal of meaningful representation and engagement of African researchers and populations in the global enterprise of GGR is the development of robust ethical, legal and policy frameworks . The Human Heredity and Health in Africa (H3Africa) initiative was launched in 2010 in collaboration with the U.S. National Institutes of Health (NIH), the U.K. Wellcome Trust and the African Society for Human Genetics after a March 2009 meeting in Cameroon in order to begin studying genetic diversity in Africa. Part of H3Africa’s mission is to identify the scientific, ethical, and practical questions that accompany GGR in Africa . Since 2010, H3Africa has published a white paper and other guidance documents to provide robust recommendations, and a comprehensive framework for ethical GGR in the African setting . However, the guidance documents are generic and may not readily integrate with unique country level considerations. H3Africa has also sought to recognize the importance of generating local policies for GGR that are specific and responsive to different country contexts and, to the extent possible, reflective of the considerations and guidance provided by the H3Africa framework. However, at a country-level, according to a 2017 review, regulatory documents across much of Africa are “either absent, outdated, conservative or difficult to navigate” . Where GGR policies and regulations do exist, it is currently unclear to what extent they reflect the recommendations and guidance that has been carefully articulated by the H3Africa Working Group on Ethics and other international organizations.
As part of a larger project to empirically establish guidelines for GGR in Uganda, we conducted a scoping review of the literature to evaluate existing guidelines, policies and laws related to the ethics and oversight of GGR, with a particular emphasis on documents developed by and for Africa. Our primary goal was to characterize the nature of existing governance documents that address the ethical oversight of GGR in Africa, and identify areas where those documents converge or diverge, as well as major gaps in policy frameworks.
This review sought to understand the nature of existing guidelines that are meant to inform the ethical oversight of GGR in Africa. We conducted our assessment by way of document collection, review, and synthesis, using a scoping review methodology. Scoping reviews are useful for assessing a research or policy area and identifying gaps . The scoping review method that we utilized was proposed by Arksey and O’Malley (2005) which includes the following seven processes: (1) identify a research question, (2) identify relevant documents, (3) select documents, (4) chart data, (5) collate, (6) summarize and report results, and (7) consult with relevant stakeholders [17, 18].
Data sources and search strategy
We conducted the search from October to December 2019. Documents were identified by reviewing existing databases and repositories—the U.S Office for Human Research Protections (OHRP) International Compilation of Human Research Standards, and policy documents published by H3Africa—as well as from a 2017 paper published by de Vries et al. that identified several GGR policy documents [6, 12, 19]. Several national documents, as well as documents authored by international organizations (“international documents”), were identified through these searches. For completeness, for each of the 54 African countries we also conducted a Google search for the following search strings: genetic AND guidelines AND [country name], genomic AND guidelines AND [country name], genetic AND guidance AND [country name], genomic AND guidance AND [country name], genetic AND policy AND [country name], genomic AND policy AND [country name], genetic AND law AND [country name], genomic AND law AND [country name], genetic AND code AND [country name], genomic AND code AND [country name], genetic AND act AND [country name], genomic AND act AND [country name]. In addition, we ran a search for websites of Ministries of Health in Africa and searched specifically for GGR policies on those government websites.
Documents were eligible for inclusion if they constituted guidance, policy, or law addressing ethical aspects of GGR. Documents applicable to at least one country in Africa, or to Africa in general, were included. We excluded documents that were not written in English, or that only discussed biobanking of genetic information. We did not apply any date restrictions to the search.
We used Microsoft Excel to track documents and their basic characteristics. One hundred and fifty-five documents were initially identified as potentially eligible. Following de-duplication, 99 were excluded, leaving 56 for further screening. These documents, which appeared to be relevant based on their titles, were then reviewed to determine whether they met eligibility criteria. They were first screened for key words to identify whether they discussed genetics or genomics research in Africa or an African country. Next, they were screened to determine if they addressed ethics issues (as opposed to providing operational or technical guidance). This process resulted in exclusion of 18 additional documents, leaving 38 that were read again carefully, in full, to verify eligibility. This final review resulted in exclusion of two more documents for not meeting criteria, leaving 36 documents for data extraction and analysis (Fig. 1).
Data abstraction, coding and analysis
Following collection of documents, we used a tracking spreadsheet to organize them into two major categories: documents that were GGR specific, and documents that were GGR non-specific. Within these two categories we further organized the documents by year of publication, level of organization, publishing institution, country, and level of authority. To support analysis of content within the documents, a codebook was created by all authors drawing heavily from the H3Africa Ethics and Governance Framework for Best Practice in Genomic Research and Biobanking in Africa . We organized data according to codes (categories) and sub codes (topics). The codes covered five broad categories, three of which addressed core research ethics principles  including: (1) respect (topics: consent; sensitive to and respectful of African values, cultures, norms, or leadership; transparency; community engagement; and respect or dignity for participants), (2) beneficence (topics: potential harms or avoidance of harms; feedback of genetic results; benefits of research; capacity building; and responsiveness), and (3) justice (topics: managing data and samples; nondiscrimination; fairness and fair international collaboration).The fourth category, independent oversight, addressed institutional processes or systems that can support adherence to ethical principles (topics: ethics review; governance frameworks; and role of government). The last category, bans and prohibitions, was used to identify impermissible types of GGR. During the process of reviewing documents, the topics were iteratively revised for clarity and some new ones were added.
All documents that met the inclusion criteria were imported into NVivo 12  and coded using the defined coding framework by one member of the research team (BC) whose coding was reviewed by two other members (JA, JMB) to ensure appropriate and consistent application of codes. Any coding discrepancies were discussed and resolved through consensus among the three members of the coding team. Frequencies, percentages and data visualizations were generated using NVivo 12 and Microsoft Excel.
Results are presented in three parts. First, we present an overview of the main characteristics of the guidance documents. Second, we highlight the distribution of categories and issues across the documents. Lastly, we present key findings from each of the five categories from our coding framework.
Characteristics of documents reviewed
Thirty-six documents were included in our analysis. Their basic characteristics are detailed in this section and summarized in Table 1. Documents that met inclusion criteria spanned 20 years and were published between 1996 and 2018, with the majority (58%) published after 2009. Five documents were published in 2017, the most of any year, all of which were published by H3Africa. The 36 English language documents represented 14 of the 54 countries in Africa. Only four countries (Gambia, Malawi, Tanzania, and South Africa) published documents that exclusively addressed GGR [22,23,24,25,26,27]. The type of publishing organization varied. A majority (22) of the documents were published by a national institution such as a Ministry of Health, rather than by an international organization such as the World Health Organization (WHO).
The documents spanned different levels of authority, ranging from more enforceable (e.g., laws or acts) to less enforceable (e.g., guidelines or policies, and statements or declarations). Laws and acts also tended to be broader in scope (6 out of the 7 laws/acts were broader documents). A majority (64%) of documents were denoted as “guidelines,” and slightly more than half (56%) were non-exclusive to GGR. For example, in the National Research Ethics Review Guideline, published in Ethiopia, GGR is embedded in the text that covers broader research ethics issues, whereas Policy Requirements, Procedures, and Guidelines for Conduct and Review of Genetic Research in Malawi is solely dedicated to GGR in Malawi [23, 28]. One document, Human Genetics and Genomics in South Africa: Ethical, Legal, and Social Implications Consensus Study was categorized as a guideline despite being labeled a “consensus study” as it provides ethical guidance for the South African government for GGR [29, 30].
Distribution of categories and topics across documents
As shown in Table 2, requirements related to the principle of respect appeared most often across all documents, relative to other principles and processes that we coded. Thirty of the 36 documents referred to an application of respect, with the most common being consent which was referred to in 27 (75%) of documents. Within the category of consent, 8 documents discussed the content of the informed consent form, 7 documents discussed issues related to consent procedures, 6 documents discussed broad consent and the permissibility of broad consent, and 5 documents discussed withdrawal of consent. The second most common representation of respect across documents was reflected in provisions that emphasized the need for GGR to be sensitive to and respectful of African values, cultures, norms or leadership—noted across 19 documents. Additionally, of the documents that discussed respect, 15 discussed the importance of transparency, and 11 discussed sharing or disseminating study information, 9 discussed community engagement, and 7 discussed respect for participant rights and dignity.
The second most frequently coded principle across documents was beneficence, being represented in 26 (72%) of the 36 documents. Of the documents that mentioned beneficence, 24 discussed potential harms or avoidance of harms, and of these, a majority (20 documents) focused on issues of privacy, confidentiality or security involving genetic and genomic information. Several documents also mentioned feedback of genetic results; discussed in nearly half (17) of the documents. Only about one third (12) of documents explicitly provided guidance or articulated requirements related to realizing the benefits of GGR (e.g., sharing benefits with local communities). Finally, 11 documents discussed the need for GGR capacity building. Capacity building refers to the strengthening and supporting of research infrastructure for GGR and biobanking in Africa, including career support . Other less frequently noted issues included special protections for vulnerable populations, raised in three documents.
We identified instances of the principle of justice across 22 (61%) of the documents. Issues discussed most frequently involved rights and interests related to data and samples (20 documents) and included content addressing the sharing of data and samples (16 documents), data rights (8 documents), data use agreements (8 documents), and material and sample rights (8 documents). The export of samples, and intellectual property rights were discussed in 6 and 5 documents respectively. Issues related to nondiscrimination were discussed across 13 documents. While 6 documents mentioned the need to ensure fair distribution of benefits and burdens of research and only 1 document mentioned the need to ensure research is relevant to local populations.
The fourth category in our coding framework is independent oversight, which was identified in 24 (67%) documents. Ethics review—one approach to operationalizing independent oversight—was referred to most often within this category: in 23 documents. Additionally, components of ethics review were broken down into the function or role of the ethics review (6 documents), ethics review procedures (3 documents), and the content of the ethics review (1 document). Lastly, how organizations should be governed, and the role of government were noted in 7 and 4 documents respectively.
Finally, bans or prohibitions (declarations of impermissible activities or types of GGR) were identified in 12 (33%) documents. The most common ban was on research that included reproductive cloning, which was prohibited in nearly half of the documents that mentioned a ban or prohibition (5 documents).
Additional characteristics of provisions according to identified categories
The ethics principle of respect was the most commonly identified category across guidance documents. Respect was discussed in the context of the following applications: consent; sensitivity to and respect for African values, cultures, norms, and leadership; transparency; community engagement; and respect or dignity for participants. In what follows, we describe how each of these appeared in the sampled documents.
Consent considerations appeared in various ways across the documents, including in defining elements that must be included in an informed consent form, describing required consent procedures, and characterizing the permissibility or features of broad consent.
Documents articulated required elements of informed consent in order to emphasize the importance of obtaining valid and comprehensive informed consent when conducting research with biological samples. However, only two documents (one from South Africa and one from H3Africa) noted that consent forms should include the possibility of incidental findings and should identify whether the research participant wants to receive those findings [27, 31].
The documents referenced consent procedures in different ways. Some documents emphasized that informed consent is not a single event (e.g., “The informed consent process for genomic studies starts prior to research, is on-going during the research and continues even after the research is over”) . Other documents placed emphasis on this and the importance of verifying that consent procedures are indeed facilitating participant understanding (e.g., “Depending on the target population, H3Africa researchers may be required in some studies to demonstrate a participant’s understanding of research study elements during the consent process. This is particularly relevant to studies targeting populations who may be perceived as vulnerable to exploitation, like those with cognitive impairments.”) .
Broad consent—including its permissibility and constitutive elements—was noted in very few (6) documents. Three of the six documents mentioning broad consent were H3Africa documents [13, 14, 32] while the other three were documents from 2013 or later from Nigeria and South Africa. For example, The Policy Statement on Storage of Human Samples in Biobanks and Biorepositories in Nigeria stated that it “[supports] ‘broad consent’ at this time but not ‘blanket consent’ or ‘gifting’” . However, the Zambian National Health Research Act remained silent on broad consent but does prohibit withdrawal of samples from individuals for any “unspecified future health research activity or unspecified storage.” .
Withdrawal of consent was specifically mentioned in a total of five documents—four international documents: H3Africa Framework for African Genomics and Biobanking, H3Africa Guideline for Informed Consent (Third Edition), Human Gene Organization (HUGO) Statement on DNA Sampling Control and World Medical Association (WMA) Declaration of Taipei on Ethical Considerations Regarding Health Databases and Biobanks [11, 13, 32, 35] and one national document: Human Genetics and Genomics in South Africa: Ethical, Legal, and Social Implications . The documents indicate that researchers should make it possible for participants to withdraw consent, but also state that withdrawal of consent is not possible in circumstances where samples have been permanently de-identified or if data have already been published [13, 32].
Of the eight documents that do not mention consent, two were international documents (one of which was a decision support tool for feedback of individual genetic results), and six were national documents (two of which were national laws).
Sensitive to and respectful of african values, cultures, norms or leadership
Some applications of respect that appeared in the documents were coded as “sensitive to and respectful of African values, cultures, norms or leadership.” This code spans many topics, and thus appeared in various forms. Almost all of the international documents (11 of 14) recommended being sensitive to and respectful of African values, cultures, norms, or leadership. However, only 8 of the 22 national documents were found to address this requirement explicitly. Additionally, this requirement was generally noted when discussing consent or feedback of results to participants, where emphasis was placed on acknowledging communitarian norms common in parts of Africa. When international documents discussed this issue, it was represented in very similar language across documents (e.g., communication between researchers and participants, and between researchers and communities should be “sensitive to their social and cultural context”) . National documents also tended to operationalize this concept in terms of cultural and epistemic sensitivity—for example, the National Guidelines for Research Involving Humans as Research Participants published by the Uganda National Council for Science and Technology (UNCST), notes that “indigenous knowledge of the community should be recognized” . They also identified specific local groups that should be involved in GGR, such as the Ministry of Health, and local collaborators and institutions .
Provisions related to transparency were identified across 15 documents. Often this appeared as an emphasis on the importance of complete disclosure of relevant information during consent and feedback of genetic results, including clear articulation of available options. For example, Guidelines of the National DNA Bank, published by the Federal Ministry of Health in Gambia, explains that “researchers should state in their proposals which results, if any, they will make available to research subjects. The research subjects have a right to know, but can decide that they do not want to know,” . Indeed, 11 of the 15 documents discuss sharing or disseminating study information in an appropriate manner.
Community engagement and its applications were mentioned mostly in international documents and in only three national documents—those from South Africa, Tanzania, and Malawi. For instance, the Human DNA Regulation Act (2009) from Tanzania states that Technical Committees consisting of individuals from public and private sectors (e.g., representatives from the National Institute for Medical Research, a biotechnology department from an in-country University, the Department of Social Welfare, etc.) should reach out to members of communities with “relevant expertise” when necessary in order to make decisions about the ethics of GGR in Tanzania , while the Policy Requirements, Procedures and Guidelines for the Conduct and Review of Human Genetic Research in Malawi emphasizes the need for “stakeholder consultations” that “fits [Malawi’s] own context” .
In contrast to national documents, international documents were found to explicitly use the term “community engagement” in their guidelines [9, 13, 14, 32, 38, 39]. Indeed, H3Africa has developed a document that exclusively provides recommendations for community engagement in GGR and defines it as “a process of informing, consulting and actively involving relevant communities that have a legitimate interest in the research process,” . Other H3Africa documents offer bulleted recommendations of how to engage the community in GGR and the importance of doing so.
Participant rights and dignity
Lastly, an issue that was emphasized the least under the category of respect was respect for participant rights and dignity. This issue was referenced in a more abstract way (e.g., by stating rights claims of the participants). Documents tended to emphasize participants and citizens’ rights at large. For example, one document noted that “everyone has a right to respect for their dignity and for their rights regardless of their genetic characteristics” .
We identified standards and requirements related to the principle of beneficence within 26 documents (72%). Beneficence was discussed in the context of the following issues: potential harms or avoidance of harms, feedback of genetic results, benefits of research, capacity building and responsiveness.
Potential harms or avoidance of harms
Potential harms or avoidance of harms associated with GGR was the most noted issue under the category of beneficence, appearing across 67% of all documents. The issue arose most in documents that were classified as international, in guidelines, and in documents that were limited to GGR. Some documents emphasized stigma, while others emphasized collateral or secondary harms that accrued outside the individual research participant, such as familial, communal, or ethnic harms (e.g., harm to one’s ethnic group). Twelve documents were coded as not directly addressing harms or harm avoidance, with only one of those 12 being an international document—a decision support tool for feedback of individual genetic results . The other 11 documents that do not mention this issue include both national guidelines/policies and laws/acts.
The most common representations of potential harms from GGR related to informational harms and therefore documents emphasized the importance of privacy, confidentiality, and data and sample security. Similar language was used across documents to signal this. For example, a Gambian guidelines states that “the protection of confidentiality has the highest priority,” , and a South African guideline states that “confidentiality of all medical information is essential, and this is particularly the case with genetic registers…,” . The importance of de-identifying samples is emphasized to protect privacy, but few documents note the possibility of re-identification, which can diminish protections. The Policy Statement on Storage of Human Samples in Biobanks and Biorepositories, the National Health Research Ethics Committee of Nigeria notes this possibility by not only outlining how there could be a privacy breach, but also differentiating between anonymized and de-identified data (e.g., “De-identified data is not necessarily anonymized data because the personally identifying information may be able to be re-associated with the data at a later time. Anonymized data is a particularized subset of de-identified data” .
Feedback of genetic results
The next issue in terms of frequency of appearance under the category of beneficence was feedback of genetic results. A majority of documents (9 documents) that discussed feedback of genetic results were published by national institutions. The way in which feedback of genetic results was discussed in the documents varied. For example, some documents mentioned whether or not information should be shared with family members (7 documents), while others required that information be shared in a culturally sensitive way and that communities should be engaged accordingly. However, one GGR policy states that individual results should not be given back to study participants . Lastly, little guidance was provided with respect to handling incidental findings or using genetic counselors when returning results.
Benefits of research
Half of the documents that mention the benefits of GGR were national documents. Those documents emphasized benefits of research for the country and the benefits of research (e.g., positive public health outcomes, or individual health benefits) for research participants and their communities. Additionally, two of the international documents articulated the benefits of GGR for the world at large [13, 36].
Capacity building was discussed in both international and national documents almost equally; however, no documents provided a formal definition of capacity building (sometimes referred to as capacity development). One document articulated the targets for capacity building (i.e., “It is of key importance that genomic research and biobanking conducted in Africa lead to substantive building of research capacity, including both human resources and research infrastructure” . When capacity building was necessary and who was responsible for capacity building was also rarely mentioned. Capacity building was discussed similarly across the documents, using similar language that emphasized the importance for capacity building and that researchers in Africa, or within a specific country, should be trained to conduct GGR in their country.
Overall, justice considerations were infrequently identified across the documents. However, issues that intersected with the principle of justice were identified in the context of guidance and policies related to the management of data and samples. Topics that were coded within this included patents and intellectual property, and sample re-use. Issues of nondiscrimination, fairness, fair international collaboration were less commonly mentioned, though they did appear relatively frequently in H3Africa and HUGO documents.
Managing data and samples
We categorized data and sample management as an application of the principle of justice due to the connection between good governance of data and samples and principles of fairness in access. Within this issue, many topics are drawn out that discuss the components of data and sample management such as sharing, which was referred to the most, following rights, agreements, and storage. Documents that refer to the sharing of data and samples tended to be concerned with the historical exploitation of African researchers, intellectual property, data, and the African population in general throughout the GGR process. Furthermore, documents that referred to the management of data and samples were overwhelmingly guidelines or policies and published by national entities. Another trend that we noted was that over time, there was an increase in the discussion of data and sample management and its various components. The issue is mostly referred to in documents published from 2009 to 2018. Lastly, the documents that mention this issue tended to be solely concerned with data, biobanking, or samples, and mentioned one of these terms in the title, rather than documents that were concerned with ethical health research in general.
Nondiscrimination was mentioned in 7 guideline documents and 5 statements or declarations. Furthermore, documents that were limited to ethical discussion of GGR referred to nondiscrimination more than documents that were broader in scope. When documents did refer to discrimination, they tend to also use the term stigma, and the potential harms associated with GGR resulting in discrimination. For example, some international documents specifically noted the importance of offering protections in research and recommended providing counseling to research participants due to the potential stigma and discrimination that could emerge from GGR among individuals from Africa [9, 32, 35, 39].
The fourth category applied in the identified documents is independent oversight. Independent oversight includes institutional processes or systems that facilitate adherence to research ethics principles. This includes ethics review of protocols, deployment of governance frameworks, and articulating the role of government in oversight.
Ethics review was often noted in international documents and was frequently discussed as an important safeguard when samples are being collected from individuals for research. Two H3Africa documents suggested that ethics committees in various African countries may be inadequately equipped to review GGR, and experts may need to be consulted by ethics committees to support review processes [13, 14]. This was connected back to the need for capacity strengthening, but in this case with a focus on the training needs of research ethics committees . Additionally, five documents, including three national documents, indicated that there must be ethics review and approval in order to conduct secondary analyses of samples [13, 27, 28, 32, 37].
Governance framework and role of government
The issue of governance is mostly noted in international documents and is often referred to in the context of management of samples. For example, documents use language such as “an appropriate governance framework for genomics resources should outline the policies (data and sample sharing…) regulatory matters, as well as entities… that deal with applications to access and use genomic resources,” . With respect to the role of government, some documents addressed the role of government in regulatory processes involving GGR, including defining the jurisdiction of national ethics committees and other legal regulatory bodies [25,26,27].
Bans and prohibitions
The most commonly stated ban was one on reproductive cloning [5, 23, 27, 34, 40]. Others bans or prohibitions applied to germline editing [23, 41], undue inducements in research [25, 36], sample use for commercial purposes [23, 25], employee mandatory DNA testing , fetal sex selection , stem cell use [26, 27, 40], eugenic purposes , and research without public health benefits . One such example from the literature includes Nigeria’s Good Clinical Practice Regulations where the National Agency for Food and Drug Administration and Control states that “No gene therapy trials shall be carried out which result in modifications to the participant's germ line genetic identity,” . Additionally, Malawi’s Policy Requirements, Procedures and Guidelines for the Conduct and Review of Human Genetic Research, declares that “where there is no therapy, and prevention strategies are unknown or unproven, genetic testing is unethical and is herein prohibited as such research cannot offer a therapeutic and/or public health value,” . No other document mentioned a prohibition of genetic testing in its entirely, absent benefit to participants.
Genetics and genomics research have the potential to make advances against a wide range of communicable and noncommunicable diseases affecting populations within low-resourced countries, including across Sub-Saharan Africa. Successful realization of these benefits partly depends on identification and establishment of local (country) ethics norms and processes. By its nature, especially given the amount and type of information that can be revealed about research participants (as individuals, families, communities or races) GGR raises significant and unique ethical concerns. Consequently, in order to effectively address these and related concerns, formal guidelines and regulations are needed to provide clarity for researchers and research oversight entities, as well as increase public trust and confidence in GGR are needed.
The majority of documents identified by this scoping review constituted guidelines or policies published by national entities that referenced special provisions for GGR in the context of a broader set of requirements related to the appropriate conduct of research. Very few (six) country-level documents identified were specific to GGR. International documents were found to be more likely to address GGR exclusively; however, the majority of international documents were developed by one organization—the H3Africa Consortium. Although an important contribution, international guidance documents do not lend themselves readily to local enforcement at a country level. Clearly, a tension exists between development of uniform multi-national standards and guidelines for the ethical conduct of GGR, and development of local policies that align with existing systems of governance and oversight, as well as local norms and values. A 2013 study concerned with GGR in Nigeria noted one of the greatest difficulties in GGR regulation as: “harmonizing the different laws and customs that apply to genomic research in different jurisdictions… [and] [meeting] the needs of Nigerian communities and research participants” . Policy reviews, such as the present, can be helpful in guiding deliberation regarding localization of provisions within international frameworks and identifying variations across jurisdictions that might suit a country’s needs. There is also value, as discussed further below, in identifying gaps in policy.
Different types of governance documents applicable to GGR in Africa serve different functions. Whether a document is a framework, guideline, statement, or law reflects not only the level of enforceability, but also often the degree to which there is consensus (professionally or socio-culturally) regarding the ethical implications of advances in the field of genetics and genomics. A framework or guideline, for example, can be more readily established and modified than a law, and can therefore remain more closely connected to scientific developments and capabilities. Scientific innovation moves at a pace that often cannot be matched by the law. Statements, which are typically international, can drive broader change in policy or practice, or preserve and advance global interests. Laws can play an important role in setting the outer boundaries of acceptable or unacceptable research, reducing societal uncertainty, and governing uses of genetic information that present significant risk to individuals or groups, especially uses that are inconsistent with basic rights. The law must do so in a manner that is fair and clear, taking into account the balance of various stakeholder interests to promote public benefit and reduce harm. While ethics and law overlap, and the law may generally support or be supported by ethics norms, it also operates within procedural and jurisdictional limits.
While recently published policy frameworks, such as that from South Africa , are noteworthy for their comprehensive coverage of the topic, a gap exists with respect to publication of country-level GGR-specific policies and laws across a majority of the African countries in our review. Others have noted that national policies are important to the management of genetic/genomic data and samples . Due to historical and ongoing concerns about exploitation through research in Africa, especially with respect to data and sample management and the increased ease in the ability to share data and samples, the gap is particularly noteworthy . Further, those involved in developing or updating GGR policies should consider harmonization with other existing or emerging frameworks for governance of biobanks and oversight of emerging data science capabilities, including the use of artificial intelligence and machine learning in “big data” research. Data science and biobanking have far wider application, raise additional ethics and regulatory issues, and deserve focused scholarly and policy attention; but as “facilitators” of GGR, it would be short-sighted not to consider opportunities for mutual and integrated strengthening of ethics and regulatory frameworks across these areas. Such opportunities are likely to increase in the coming years, especially given recent investments by the U.S. National Institutes of Health in the Harnessing Data Science for Health Discovery and Innovation in Africa (DS-I Africa) program . Here we emphasize that although policy documents are imperative to supporting ethical conduct of GGR in Africa, this is only one piece of the puzzle: securing local sources of funding for GGR, providing ethics committees with necessary resources, and advancing ethics training for researchers and others is also critical. However, due to the gaps and lack of specificity in national guidance documents, ethics committees in many countries may feel ill prepared and indeed may disparately and inconsistently formulate determinations regarding management of data and samples . The limited coverage of capacity building across documents is especially noteworthy, given aforementioned concerns about “brain drain” on the continent.
Furthermore, our review found that H3Africa documents tended to include more emerging themes—such as broad consent, data sharing, community engagement, respect for African leadership, and governance of biobanks—compared to other documents. Documents that represented national perspectives did not always address these elements. This is not particularly surprising given that most H3Africa documents emerged within five years prior to this review, that the organization had access to a wealth of expertise in ethics and governance of GGR, and that it facilitated interaction of leaders from multiple African countries to work together to create state of the art guidelines and frameworks . H3Africa has had a tremendous impact on the development of ethics guidance across a range of domains, within the consortium. Indeed, its focus on fostering African (professional) leadership in the area of GGR is particularly noteworthy and lessons can be drawn from experiences with this model to potentially foster greater integration of similar principles in national policies. At the community level, practices and procedures such as those described within emerging models for community engagement and oversight in research can serve to help integrate community values in GGR in way that enhances its relevance and ethical quality [29, 30]. Policy development and revision can proceed at a local level with these frameworks in mind. A challenge for the future will be to do this, while maintaining some degree of communication and coordination to advance discussions of the ethical, legal and societal implications of GGR across geopolitical boundaries on the continent, given that the H3Africa network is only funded through 2021 . Other organizations, such as the African Academy of Sciences, could be resourced to continue to advance this goal.
A limitation of this scoping review is that within our search we only considered documents available in English. We recognize that there may have been documents that met the rest of our inclusion criteria, but written in other languages. Additionally, we acknowledge that our focus was on documents that explicitly addressed GGR, which means that we did not address the content of other broader policies or guidelines that could have applied to GGR, simply by virtue of it being a form of research. We also note that our search strategy, which included identifying documents from existing compilations and internet searches using key words, could have missed documents due to limitations of the databases searched, the key words used, or the fact that the search did not include collection of “offline” documents. Furthermore, because we didn’t include scholarly literature in our scoping review, we may have missed explications of guidance documents that may have expressed how these guidance documents have been implemented, studied or interpreted. Finally, there is one document related to data sharing and data accessibility published by H3Africa that was not included because it was published after our search was completed . Nonetheless, we believe it important to periodically evaluate the characteristics of existing formal governance documents, such as those reviewed in this study (as they exist “on their face”) to identify areas where those documents intersect, as well as major gaps in coverage.
Our review found that local, enforceable policies which are indispensable for the increase of ethical GGR are either deficient or missing in many African countries. We suggest that existing international, GGR-specific, ethics guidelines be used to inform country-level GGR policy development, in conjunction with insight from country specific ethics committees and other local stakeholders. H3Africa’s comprehensive ethical framework can be used as a baseline for each African country. Each country can adopt relevant components of this framework and contextualize them within their local policy environments combined with relevant evidence generated using inclusive participatory approaches in order to create country-specific, enforceable frameworks. This process will ultimately promote the conduct of ethical GGR and will contribute to maximizing benefits for African researchers and populations.
Availability of data and materials
Data sources are available on request to the corresponding author. The coding framework applied in this study is provided with the manuscript.
Genetics and Genomics Research
National Institutes of Health
Human Gene Organization
Human Heredity and Health in Africa
Office for Human Research Protections
Uganda National Council for Science and Technology
World Health Organization
World Medical Association
Akintola SO, Callier SL, Ogundiran TO. Personalizing medicine in nigeria by tailoring the research profess: points to consider for genomic research. Curr Pharmacogenomics Pers Med. 2013;11(4):267–73. https://doi.org/10.2174/18756921113119990010.
Tiffin N. Unique considerations for advancing genomic medicine in African populations. Pers Med. 2014;11(2):187–96. https://doi.org/10.2217/pme.13.105.
Chanda-Kapta P, Kapata N, Moraes N, Chongwe G, Munthali J. Genomic research in Zambia: confronting the ethics, policy and regulatory frontiers in the 21st Century. Health Res Policy Syst. 2015;13(60):1–7. https://doi.org/10.1186/s12961-015-0053-4.
Yakubu A, Tindana P, Matimba A, et al. Model framework for governance of genomic research and biobanking in Africa ? A content description [version 2; peer review: 3 approved]. AAS Open Research. 2018;1(13). doi:https://doi.org/10.12688/aasopenres.12844.2
UNESCO. Universal Declaration on the Human Genome and Human Rights. Published online 1997.
de Vries J, Munung SN, Matimba A, et al. Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries. BMC Med Ethics. 2017;18(1):8. https://doi.org/10.1186/s12910-016-0165-6.
Staunton C, Moodley K. Challenges in biobank governance in Sub-Saharan Africa. BMC Med Ethics. 2013;14(1):35. https://doi.org/10.1186/1472-6939-14-35.
H3Africa Consortium. H3Africa Consortium Data Sharing, Access and Release Policy. Published online April 2020.
H3Africa Community Engagement Working Group for the Human Heredity and Health (H3Africa) Consortium. H3Africa Guidelines for Community Engagement (Version Two). Published online September 2017.
Barugahare J, Kutyabami P. Nature and history of the CIOMS International Ethical Guidelines and implications for local implementation: a perspective from East Africa. Dev World Bioeth. 2020;20(4):175–83. https://doi.org/10.1111/dewb.12249.
World Medical Association. World Medical Association Declaration of Taipei on Ethical Considerations Regarding Health Databases and Biobanks. Published online 2016.
H3Africa Consortium. High-Level Principles on Ethics, Governance and Resource Sharing. H3Africa. Accessed September 24, 2020. https://h3africa.org/index.php/about/ethics-and-governance/
H3Africa Working Group on Ethics. Ethics and Governance Framework for Best Practice in Genomic Research and Biobanking in Africa. Published online 2017.
H3Africa Working Group on Ethics. H3Africa Guideline for the Return of Individual Genetic Research Findings. Published online 2017.
Wonkam A, de Vries J. Returning incidental findings in African genomics research. Nat Genet. 2020;52(1):17–20. https://doi.org/10.1038/s41588-019-0542-4.
H3Africa Working Group on Ethics. Harnessing Genomic Technologies Toward Improving Health in Africa: Opportunities and Challenges. Recommendations for the H3Africa Initiative to the Wellcome Trust and the National Institutes of Health. Published online January 2011.
Levac D, Colquhoun H, O’Brien KK. Scoping studies: advancing the methodology. Implement Sci. 2010;5(69):1–9.
Arksey H, O’Malley L. Scoping studies: towards a methodological framework. Null. 2005;8(1):19–32. doi:https://doi.org/10.1080/1364557032000119616
Office for Human Research Protections. International Compilation of Human Research Standards 2019 Edition. Published 2019. Accessed 24 Sept 2020. https://www.hhs.gov/ohrp/sites/default/files/2019-International-Compilation-of-Human-Research-Standards.pdf
Beauchamp TL, Childress JF. Principles of Biomedical Ethics. 8th ed. Oxford University Press; 2019.
QSR International Pty Ltd. NVivo (12).; 2019. https://www.qsrinternational.com/nvivo-qualitative-data-analysis-software/home
Federal Ministry of Health. Guidelines of the National DNA bank, The Gambia. Published online September 2001.
National Health Sciences Research Committee. Policy Requirements, Procedures and Guidelines for the Conduct and Review of Human Genetic Research in Malawi. Published online September 2012.
The National Research Council of Malawi. Procedures and Guidelines for Access and Collection of Genetic Resources in Malawi. Published online 2002.
Parliament of the United Republic of Tanzania. The Human DNA Regulation Act.; 2009.
The Medical Research Council of South Africa. Guidelines on Ethics for Medical Research: Reproductive Biology and Genetic Research. Published online 2002.
Department of Science and Technology. Human Genetics and Genomics in South Africa: Ethical, Legal, and Social Implications Consensus Study.; 2018.
Federal Democratic Republic of Ethiopia Ministry of Science and Technology. National Research Ethics Review Guideline. Published online September 2014.
Schroeder D, Chatfield K, Singh M, Chennells R, Herissone-Kelly P. The San Code of Research Ethics. In: Schroeder D, Chatfield K, Singh M, Chennells R, Herissone-Kelly P, eds. Equitable Research Partnerships: A Global Code of Conduct to Counter Ethics Dumping. SpringerBriefs in Research and Innovation Governance. Springer International Publishing; 2019:73–87. doi:https://doi.org/10.1007/978-3-030-15745-6_7
Beaton A, Hudson M, Milne M, et al. Engaging Māori in biobanking and genomic research: a model for biobanks to guide culturally informed governance, operational, and community engagement activities. Genet Med. 2017;19(3):345–51. https://doi.org/10.1038/gim.2016.111.
H3Africa Consortium. Decision Tree for Feedback of Individual Genetic Results. Published online 2017.
H3Africa Consortium. H3Africa Guideline for Informed Consent Third Edition. Published online 2017.
National Health Research Ethics Committee of Nigeria. Policy Statement on Storage of Human Samples in Biobanks and Biorepositories in Nigeria. Published online 2013.
Parliament of Zambia. The National Health Research Act.; 2013.
HUGO Ethics Committee. HUGO Ethics Committee: Statement on DNA Sampling: Control and Access. Published online February 1998.
HUGO Council. Statement on the Principled Conduct of Genetics Research. Published online March 21, 1996.
Uganda National Council for Science and Technology (UNCST). National Guidelines for Research Involving Humans as Research Participants. Published online July 2014.
HUGO Ethics Committee. HUGO Ethics Committee: Statement on Gene Therapy Research. Published online April 2001.
HUGO Ethics Committee. HUGO Ethics Committee: Statement on Human Genomic Databases. Published online December 2002.
International Society for Stem Cell Research. Guidelines for the Conduct of Human Embryonic Stem Cell Research. Published online December 21, 2006.
National Agency for Food and Drug Administration and Control. Good Clinical Practice Regulations Nigeria. Published online 2009.
Barchi F, Little MT. National ethics guidance in Sub-Saharan Africa on the collection and use of human biological specimens: a systematic review. BMC Med Ethics. 2016;17(64):1–25. https://doi.org/10.1186/s12910-016-0146-9.
Harnessing Data Science for Health Discovery and Innovation in Africa. NIH Office of Strategic Coordination- The Common Fund. Published October 23, 2019. Accessed 22 March 2021. https://commonfund.nih.gov/africadata
H3Africa. Funding. H3Africa.org. Accessed 19 Jan 2021. https://h3africa.org/index.php/resource/funding/
We would like to acknowledge Angie Boyce for her contribution to data collection at an early stage of this project, and Bakari Sibert for his support with initial development of the coding framework.
Research reported in this publication was supported by the National Human Genome Research Institute of the National Institutes of Health under Award Number U01HG009822. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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Ali, J., Cohn, B., Mwaka, E. et al. A scoping review of genetics and genomics research ethics policies and guidelines for Africa. BMC Med Ethics 22, 39 (2021). https://doi.org/10.1186/s12910-021-00611-9
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