The declining cost of DNA sequencing has been accompanied by a proliferation of companies selling ‘direct-to-consumer genetic testing’ (DTC-GT) services. Many of these are marketed online as tools for enabling citizens to make more informed decisions about their health, wellness and lifestyle. We assessed the ‘information for consumers’ provided by these companies at the prepurchase stage, which could influence initial decisions to part with money, data or tissue samples. A scoping exercise revealed 65 DTC-GT companies advertising their services online to consumers in the United Kingdom, of which 15 met our inclusion criteria. We benchmarked their consumer information against the good practice principles developed by the UK Human Genetics Commission (HGC). No provider complied with all the HGC principles and overall levels of compliance varied considerably. Although consent for testing was discussed by all but one company, information about data reuse for research or other purposes was often sparse and consent options limited or unclear. Most did not provide supplementary support services to help users better understand or cope with the implications of test results. We provide recommendations for updating the preconsumer transparency aspects of the HGC guidelines to ensure their fitness-for-purpose in this rapidly changing market. We also recommend improving coordination between relevant governance bodies to ensure minimum standards of transparency, quality and accountability. Although DTC-GT has many potential benefits, close partnership between consumers, industry and government, along with interdisciplinary science input, are essential to ensure that these innovations are used ethically and responsibly.
New DNA sequencing technology has spawned a growing market in genetic testing services sold directly to members of the public,1, 2 rather than being ordered by a clinician for medical reasons.3 These direct-to-consumer genetic tests (DTC-GT) are being marketed online, promising purchasers insights about their ancestral past and present states, for example, being overweight, future risks ranging from premature balding to cancer, or even their own or their child’s potential for intellectual or sporting achievement.4, 5 Health-, wellness- and lifestyle-related services represent an important subsector of this market. Although most are not strictly ‘medical’, many vendors of such services claim that these can empower consumers to make better health decisions by highlighting aspects of their genetic make-up that could affect their clinical risks or mediate the influence of lifestyle factors, medicines, nutritional choices or fitness regimes.6
Although an exciting idea, DTC-GT comes with many uncertainties and challenges and given the psychosocial and privacy implications of genetic test results, it can represent a source of personal and societal risk. There is still limited evidence of the clinical utility of some of these tests, despite other types of personal and social value that purchasers may derive from them.3 Importantly, the extent to which consumers understand what they are buying, how they understand the results, what behaviours these trigger and what will happen with their genetic information after the transaction, is still lacking.7, 8 Despite this uncertainty, governance of this rapidly diversifying sector has been hobbled by the multiplicity of bodies potentially involved in their oversight or regulation (Figure 1). For example, concerns about such products and services can span in vitro medical device safety, consumer rights, fair advertising and data protection.9, 10, 11, 12 To compound this, services sold online in one country may be underpinned by operations located in other regions with different regulatory jurisdictions, making it difficult for consumers to easily judge their rights for protection and recourse. Mindful of liability risks, many DTC-GT companies are marketing their services as ‘information products’ rather than medical products, with the intent of them being ‘for educational purposes only’ and stipulate that the test results are not for diagnostic use. In the United Kingdom, the DTC-GT industry is minimally regulated. Owing to this lightweight governance, health-care practitioners and professional bodies, such as the Association for Molecular Pathology,13 the European Society for Human Genetics14 and the American College of Medical Genetics and Genomics,15 have called for further guidelines and standards and have released their own (sometimes conflicting) guidance. In addition, consumer rights groups such as GeneWatch UK are becoming more vocal.16
Concerns have also been raised about the scientific integrity and clinical utility of some DTC-GT services, particularly those based on genome-wide association studies, which tend to have low discriminatory and predictive validity.17 The transparency of providers’ activities has also been called into question relating to quality criteria and quality assurance.18 Although some guidelines cover scientific considerations, for example, how to communicate the strength of evidence underpinning various genetic predictions,19 consistent global industry standards for transparency in the DTC-GT sector do not currently exist.11 Importantly, aside from scientific and clinical considerations, the ethical principles such as transparency, accountability and accessibility and choices and the quality of companies' supporting information for customers is largely unchecked; a situation which has drawn attention from policymakers20 and the biomedical industry itself.21
In the United Kingdom, companies are permitted to provide DTC-GT services to members of the public.22 Mindful of this, the UK government established a working group as part of the Human Genetics Commission (HGC), to advise on ethical practices within the industry. This included multidisciplinary stakeholders such as medical doctors, scientists, lawyers, professional organisations, government and a company that was offering DTC-GT (deCODE Genetics).23, 24 The HGC’s ‘Common Framework of Principles for DTC-GT’ were released in 2010 and remain the only multi-stakeholder-developed consensus guidelines focussed on best practice in DTC-GT in the UK. Significantly, the HGC’s framework included specific recommendations relating to prepurchase ‘information for consumers’ which are particularly useful for benchmarking the transparency of DTC-GT companies, as is the focus of this study. Although other relevant guidelines have since been released by specialist medical groups and professional organisations such as the European Society of Human Genetics, they do not cover issues of transparency or prepurchase information in depth. For the purposes of our analysis, we therefore selected the key HGC principles relating to ‘information for consumers’ and sought to identify to what extent these recommended practices have been adopted by the sector, thereby assessing the responsiveness of the industry in adopting best practice standards.25
We searched for companies actively advertising to UK consumers for health-, lifestyle- and wellness-related DTC-GT through Google UK searches, using the keywords ‘genetic testing’, ‘health’, ‘wellness’ and ‘lifestyle’. For the purposes of the study, we defined active advertising in terms of companies’ appearance in the first five pages of an online search on google.co.uk or appearing via ‘google ads’. We acknowledge the variability in search engine results and so, during the search process, we also identified a commercial website where DTC-GT companies pay to advertise and list their services to UK consumers,26 which we used to verify and supplement our findings. Of the companies identified by these searches, we selected only those offering DNA testing for health, lifestyle and wellness and excluded companies offering neonatal services or only performing ancestry or paternity testing or not actively trading; for example, a telomere testing service that was described as ‘coming soon’. Additionally, by default, we excluded private medical services where tests are recommended by a clinician, focussing our attention only on those services that consumers can order directly online. The search took place between 15 January and 30 June 2016.
To assess the transparency of information available to consumers at the prepurchase stage, we extracted key documents from companies’ websites for review. The target documents included terms of service (ToS), privacy statements, frequently asked questions and informed consent documents, where available online. One company also had a ‘Code of Practice’ statement, which we included. We worked on the principle that all the necessary key information should be presented openly to potential purchasers in these documents, without them having to search each website extensively for fragments of information or wait until after ordering the service.
We created an initial checklist of assessment questions consisting of 16 key criteria derived from the section of the HGC guidelines concerning ‘Information for prospective consumers’. A pilot review assessed the applicability of the checklist to current DTC-GT provider practices.27 During this process, an additional 12 questions were added to the checklist, in most cases consisting of more detailed subquestions associated with a broader item from the original HGC recommendations (see Supplementary Table S1 for details).
In the second phase, we moved to a full assessment, involving three evaluators: an expert in biomarkers and quality assessment (JH), a specialist in health information governance and data protection (RG), and two solicitors specialising in ethical practice (Daniel Donaldson and Sean Folan, providing a single rating sheet). A training process for assessors took place to ensure common interpretation of the language and concepts used in the criteria and resolve ambiguities in advance of the task. The detailed assessment exercise took place between February and June 2016. For each criterion, the available information was classified as ‘Addressed’, ‘Not Addressed’ or ‘Not Applicable’. Inconsistencies were resolved through discussion and, where necessary, arbitrated by a fourth independent evaluator (CP).
Sixty-five companies were identified from the broad search. These companies offered a range of services within the broad categories of ancestry, paternity testing, neonatal testing, beauty (skincare) and ageing (telomere testing), as well as health, wellness and lifestyle. Out of these, we selected those offering DNA testing in health, lifestyle and wellness (N=15), as per our inclusion criteria, meaning that 50 were eliminated from our review. The 15 remaining companies encompassed services prioritising physical fitness-, nutrition- and health-related wellness, lifestyle and phenotypic traits, in addition to those concerned with disease susceptibility, drug sensitivity, disease prevention and disease risk assessment (Table 1).
The 15 DTC-GT providers selected offered a diversity of services within the test categories presented in Supplementary Information as defined in the HGC guidelines, ranging from presymptomatic tests, carrier testing, testing for disease susceptibility traits, pharmacogenetics, nutrigenetics and lifestyle/behavioural traits. Some providers focussed on one or two types of service, whereas others cover several of these categories. For example, only 3/15 services included carrier testing while 13/15 companies offered testing for nutrigenetic and lifestyle/behavioural traits’ testing (Table 1).
Only 10/15 eligible companies were registered in the United Kingdom. Others were registered elsewhere but were nevertheless attempting to engage with UK consumers. In some cases, it was difficult to identify the origins of the company based on the information provided on their consumer-facing website, for example, language such as ‘principal place of business’ was used ambiguously.
Not all companies provided similar documentation such as ToS and privacy statements, frequently asked questions or informed consent templates. In some cases, these were referred to using different words or combined within the same document. For example, some companies embedded informed consent statements within their ToS or privacy statements, while others supplied separate detailed informed consent forms. Additionally, one company had a ‘Code of Practice’ statement and one had a separate ‘Family Considerations’ document as well as a separate ‘Biobank’ consent form.
All reviewers remarked on both the variability of the reviewed documents’ format and content. Reviewers noted that, in some cases, the term ‘genetic data’ was not defined, there was little or no information about genetics or risks specific to genetics. Also, that the scope of testing performed was not always adequately explained and no assurances were given that further testing would not take place for purposes beyond those for which the test was purchased.
Overall compliance with HGC principles
As illustrated in Figure 2, none of the DTC-GT companies reviewed complied with every HGC recommendation. There did not appear to be any clear differences in the providers’ tendency to comply with the HGC criteria depending on whether the type of service emphasised health-related traits (eg, carrier status, drug sensitivity, inherited conditions) or lifestyle and wellness factors (eg, diet-, weight loss-, nutrition- and fitness-related traits), and for this reason, we have not presented a separate analysis.
Some criteria were widely met by the companies in the sample and others hardly at all. Table 2 summarises the most and least frequently adhered-with principles (the full list of criteria used are provided in Supplementary Information). An important differentiating factor between DTC-GT providers was the extent to which they were explicit about the ways in which they protected users’ information, their intended future uses of customers’ data and the options available for differential consent of withdrawal. These considerations are the focus of the section below.
Consent for genetic testing
A key ethical principle specified by HGC is that patients should be required to give informed consent for genetic tests to be undertaken. Most companies (14/15) followed at least one of the following three themes. These themes were identified in the reviewer’s discussion: Theme A: the company explicitly stated in their ToS or privacy statement that informed consent was required before testing. In all, 7/15 stated that customers would be asked to sign a separate informed consent document (eg, after receiving the kit) if they wished to proceed with the test. Only one provided the informed consent document on their webpage, while one provided their informed consent document upon request (by email). Theme B: the company mentioned consent within their ToS or privacy statements, indicating that if the consumer agreed with these then they would be assumed to have given informed consent for testing (5/15). This did not require ticking a separate box. For example, ‘You acknowledge that by agreeing to the terms of this privacy statement when purchasing services on this site, you are giving us your explicit consent to process this sensitive personal data related to you.’ Or ‘By proceeding with any test you are formally providing your informed consent to undergo a specific test’.
Theme C: the company included statements to say, ‘we shall not process any data without your consent’ but did not specify what the consent process involved (2/15).
One company (1/15) neither mentioned the requirement for informed consent nor provided an informed consent form in the prepurchase documentation we reviewed. Therefore, the rigour and transparency of the consent processes provided by companies were highly variable.
Consent for reuse of genetic data
Only four companies explicitly discussed the reuse of customers’ genetic data for research using specific and defined terminology, but they did so with varying levels of transparency. One company explicitly defined ‘aggregate data’ as different from ‘individual level’ genetic data and stated that it automatically shared ‘aggregate’ genetic data for research if the service was purchased but required a separate informed consent for the use of ‘individual level’ genetic data in research. Another three companies stated that ‘anonymised’ genetic data would be shared for research without defining what ‘anonymised’ meant. Of these three, only one explicitly sought separate informed consent to share this data for research through an opt-in mechanism (as recommended by the HGC), while the other two automatically shared deidentified genetic data in research if the service was purchased. A fifth company simply claimed ownership of customers’ data but gave no specific information about how this might be used. Some companies made no specific reference to secondary uses of the genetic data, making it impossible to judge their policies or practise in this regard. The variability in approach between companies was marked, those providing detailed information boosted confidence in their service offering and companies offering no information appeared weak in comparison.
Withdrawal of consent/cancellation of service
Only one company was explicit about the consequences of withdrawing from the testing service, including what would happen to customers’ genetic data upon account closure. This company’s information clearly differentiated withdrawal from the testing service and withdrawal of consent for future uses of data in research, thereby allowing consumers to retain the testing service account even if they decided to withdraw from research. The remaining companies were much less clear on this point; some discussed the possibility of closing your account if you no longer wanted to use the service but were not clear on what would happen to the genetic data. Several (6/15) companies mentioned the right to cancel the purchase and offered a cooling off period but did not discuss what would happen to any genetic data that may have been generated prior to cancellation. The distinction between the right to cancel a service (cooling off period) and the right to withdraw after participating in testing should be made clearer and both options should be available to the consumer.
Client confidentiality and data protection
Although many providers (9/15) referred to data protection law(s) applying to their service, only one company explicitly stated that it was registered with the UK Information Commissioner’s Office as a data controller. Many gave general statements such as ‘we shall not use or process your data without your consent’. Furthermore, as some companies spanned operations in several jurisdictions, a variety of laws governing uses of customers’ tissue samples and genetic data were mentioned, with potential to confuse consumers as to their rights and confidentiality.
Test accuracy and scope
In the United Kingdom, and approximately 60 other countries, ISO15189 is the current standard for accreditation of laboratories that perform medical genetic tests, and ISO15189 states laboratories should participate in regular External Quality Assessment (EQA) to ensure the accuracy of their test results. However, for companies offering DCT-GT for ‘information and educational purposes only’ there is no requirement for ISO15189 accreditation (and thus participation in EQA), although this does not prevent them from voluntarily conforming with ISO standards and participating in EQA. A second quality indicator is the CE-mark, a well-known symbol designed to enable consumers to verify the quality and safety of products in the European Union (EU). The CE-mark is required for diagnostic kits under the soon to be updated, EU Directive on in-vitro diagnostic medical devices. In the United Kingdom, the CE-mark is given by the Medicines and Healthcare Products Regulatory Agency (MHRA), the body responsible for ensuring that medical diagnostic tests reach these standards in the United Kingdom. Some DTC-GT services do fall under the remit of the CE-mark, even if the DTC-GT service provided is informational rather than medical diagnostic testing. However, MHRA only reviews services related to testing for disease and disease risk, thus genetic testing for nutrition, lifestyle and behavioural traits—representing a large section of the current market—is not covered under this remit. Moreover, the assessment required for the CE-mark only covers the testing kit/eg, the sample collection kit and not other aspects of the service, such as the quality of consumer information, transparency or data protection which will also remain unclear under the new EU in-vitro Diagnostic Regulation.
We analysed companies’ consumer prepurchase information relating to these three points (ISO accreditation, participation in EQA and CE-marking). Relatively few companies mentioned accreditation of the laboratories used or indicated why this might be relevant. Two companies referred to ISO17025, a standard for accrediting laboratories’, which is not widely recognised as the standard for medical testing in the United Kingdom or EU; and one referenced Clinical Pathology Accreditation, which has been phased out since 2009. One referred to AABB accreditation (standards of transfusion medicine and cellular therapies to optimise patient and donor care and safety) which appeared irrelevant to the DTC-GT service, and one referred to the Care Quality Commission without specifying how this applied to their service. Only one company mentioned ISO15189 accreditation of the laboratory used, which appeared to be specific to the BRCA1/BRCA2 testing service. This provider also mentioned participation in a recent, relevant, EQA scheme. One company referred to CLIA, the US standard for clinical laboratory testing; however, CLIA does not require the same level of depth as ISO15189, the latter requiring more depth on quality management, the establishment of continual quality improvement and true audit-based monitoring. No other companies mentioned participation in EQA schemes.
Although the MHRA recommends that consumers search for the CE-mark associated with DTG-GT kits when purchasing products,28 none of the companies mentioned CE-marking in their prepurchase information. This is not to say that some companies did not have CE-marking, but rather that this information was not made clear within their prepurchase information, despite its possible influence on consumers’ decisions.
Although some companies referred to laboratory accreditation, as described above, all companies included disclaimers in their consumer information, stating that they offered no guarantee of the quality of their laboratory results. Most also stated that the tests were not for diagnostic use and were for information and educational purposes only. The lack of information of these quality indicators or mention of accreditation that seemed irrelevant could lead the educated reader to a sense of distrust in the quality services offered. Greater efforts must be made to address these quality concerns in this field.
Pretest and posttest genetic counselling and expert advice
The HGC recommends that genetic counselling should accompany any genetic tests ‘in the context of inherited or heritable disorders’. Three out of the 15 services we reviewed included tests relating to carrier status of heritable disorders but only two offered posttest genetic counselling. In addition to inherited disorders, test results for health, lifestyle and wellness factors can also be confusing for purchasers or may suggest lifestyle changes for which expert advice in the form of a face to face or telephone consultation with an expert may be beneficial. We extended this principle of a consultation to encompass all types of test and expert council (nutrition, fitness, drug sensitivity etc), most companies (9/15) did not specify that customers would have an opportunity to speak to a counsellor or trained expert as part of their standard service. Four companies offered an optional pretest consultation and six a posttest consultation. Posttest consultation was offered as an optional service to purchase in half of these cases. Even those services that performed best in the overall assessment of best practice fell short on this criterion, and overall, there was no obvious trend for more counselling to be offered by companies meeting more HGC criteria. An open discussion needs to be had with the industry about minimum standards of diligence in conveying information back to consumers that also extends beyond hereditary disease situations.
Formal complaints process
Across all the companies reviewed, there was a consistent lack of information for consumers regarding a formal complaints process. Only 3/15 companies provided some information about a complaints process and one of those stated that ‘all decisions of the management are final’. There was a lack of reference to any external body to which complaints could be made if the consumer was not satisfied, most likely because there is no overarching body currently in place that could fulfil this role.
The HGC published its principles and recommendations in 2010, with a view to guiding companies active in or entering the DTC-GT space. This remains the only available set of guidelines that has been developed by representatives of major stakeholders, including industry members and regulatory bodies. Although other guidelines exist, these typically represent the viewpoints of single organisations, such as those representing health-care professionals.
The company that contributed to the HGC committee is no longer a provider of DTC-GT and none of the companies reviewed in this study participated in writing the HGC principles, indeed most did not exist at that time. This illustrates the growing disconnect between the sector offering services and the existing guidance, which is not fully addressed by newer academic guidelines developed by individual stakeholder groups.13, 14, 15
Our analysis shows that none of the vendors actively targeting UK consumers comply fully with the HGC principles and the industry has not so far embraced the self-regulatory approach that was envisaged at the time these were developed. Adherence with individual HGC criteria is typically inadequate and varies widely. The information provided to prospective purchasers is, in many cases, lacking in detail or unclearly worded, and the stated ToS can be ambiguous. Even those companies that performed best overall in our assessment fell short on the provision of counselling or expert advice as part of their service or even as an add-on. One company stated its own best practice criteria (‘Code of Practice’) on its website, without any reference to these being grounded in any external guidance,29 suggesting that while the sector is beginning to recognise the need for ethical and quality standards there is still an absence of consensus on a single set of accepted criteria. We also identified aspects of the existing HGC guidance that require updating or extension to meet the needs of this rapidly evolving market. These include increased emphasis on the transparency of vendors’ ToS and privacy statements concerning their products and services and future uses of customers’ data, a clearer distinction between cancelling a service and withdrawing permission for data re-use, and the need for formal complaints procedures and explicit consent processes. Companies need to better address the language used to describe genetic data; indeed 7/15 companies did not even specify ‘genetic’ or ‘DNA’ when referring to data in their ToS and privacy statements but simply talked about ‘your personal data’. Greater specification of the accuracy and reliability of tests used, and their ability to be used in medical decision making, alongside references to appropriate and current quality standards, such as laboratory accreditation, participation in proficiency testing and CE-marking (where applicable), are also needed to help consumers make informed purchasing decisions. A lack of counselling or an opportunity to discuss test results with an expert also represents an important weakness in this sector, given the expertise required to properly interpret test results and the fact that some results may lead to anxiety for consumers. Although a few companies offer a personalised consultation as part of their service, some either sell it as an extra service or make recommendations on how to obtain it, but many simply do not mention this as an option in their consumer-facing documents. These deficits in information and counselling may help to explain the results of recent research, indicating that DTG-GT can leave consumers more confused about their health, rather than more enabled to manage it effectively.30
Although we made efforts to identify all companies selling DTC-GT services to UK consumers in the areas of ‘health, wellness and lifestyle’, this review must be regarded as a snapshot of a rapidly evolving market that deserves ongoing monitoring and governance. At this time, no single government body or professional association fulfils this oversight role in the United Kingdom or globally.
Our analysis focussed only on the online documentation offered by vendors to potential customers at the prepurchase stage, which may influence their decisions to part with money, tissue samples or personal data (Figure 2). We looked specifically at the documents relating to fair marketing such as quality of service, data protection, consumer safety, transparency and accountability. We acknowledge that vendors may provide additional information elsewhere, such as on separate protected websites available postpurchase or in paper documents provided alongside test kits; however, our perspective was that key information should be available ‘front-of-house’ in an accessible and central form, even if repeated elsewhere, in order to support informed choice at the point of sale. Arguably, the transparency and usefulness of this information may also indicate companies’ broader philosophies, experience and management practices, although we leave this for others to unpack through a more in-depth analysis of purchased products and services.
Our emphasis on the HGC guidelines was driven by our focus, for the purposes of this study, on UK consumers and the UK market, given the time elapsed since the HGC was disbanded and our awareness of the complex and somewhat disjointed state of UK regulation, which spans multiple bodies and relies heavily on industry self-governance (Figure 3). This fragmentation has also been described in a recent systematic review of European guidelines, recommendations and position statements.12 Our assessment was based on a simple, actionable, yes/no checklist. We did not specifically examine the fitness-for-purpose of contract language relevant to the HGC principles and this would merit further study. Our interdisciplinary team nevertheless included experts in genetics, laboratory testing standards, eHealth, consumer rights law, information governance and bioethics. As our review included companies offering a range of health-related, wellness, fitness, testing services, we were able to compare across sectors of the market; however, no major differences in HGC compliance between these types of company were discernible from our analysis, although we acknowledge the relatively small study size.
Our results are consistent with a recent review of the United States’ DTC-GT market, which also revealed inconsistent provision of information regarding security protocols and tissue retention, along with significant gaps around transparency, readability and informed consent processes for the reuse of data and tissue samples in research, despite most companies posting privacy statements.31 In addition to DTC-GT companies transacting solely with consumers, those involving physicians can also exhibit poor practices. For example, in our study the DTC-GT company that performed worst on the HGC-derived transparency criterion had medical doctors both on the management board and in providing posttesting counselling as part of the service, while in the US study two out of the three companies failing to seek consent for research uses of customers’ data or samples also explicitly required physicians to be involved in ordering the service.31
Conclusions and recommendations
Companies selling genetic tests directly to the public are proliferating in both number and diversity and are becoming increasingly popular with consumers seeking to understand or optimise their current and future health and wellbeing. Given the psychosocial and privacy implications of genetic test results, and their potential use by insurers, they also represent a source of personal and societal risk. Alongside the decreasing costs of genome sequencing, the value of the DTC-GT sector has been projected to reach a $340 million by 2022,32, 33 which may tempt some businesses to be less stringent with their offerings to reach lucrative markets of both direct citizen consumers and indirect consumers, such as commercial data brokers. However, companies which fail to innovate ethically and responsibly not only damage public trust but are also at at greater commercial risk.34 For this reason, standards for quality, transparency and accountability will prove increasingly essential, both for consumer protection and for the sustainability of this business sector.
Our study reveals that over the past 6 years since the HGC principles were released in the United Kingdom, self-regulation of DTC-GT in the United Kingdom has not led to consistent quality and transparency for consumers, with uptake of the HGC principles being inadequate and patchy. This leads us to question the efficacy of the current self-regulatory approach, which also reflects the absence of an integrated oversight body for DTC-GT in the United Kingdom, where relevant responsibilities are currently distributed across multiple agencies.
Although the HGC guidelines remain valuable for informing best practice, they require updating to account for industry trends, including not only the proliferation of DTC-GT companies but also the diversification of their products and services, as well as emerging business practices such as the harvesting of customers’ data for further research or resale, which threaten to compromise privacy and personal control. Given that DTC-GT are typically sold online, single-nation approaches are unlikely to be sufficient and global governance mechanisms with proactive oversight and regulatory alignment are needed to protect consumers, maintain public trust and drive quality standards in the industry. This is a challenging prospect and our study demonstrates the difficulty of achieving this in one country alone. In this respect, it has been observed that numerous European policy reports on DTC-GT have been written but few have been implemented.12
We recommend new efforts to agree minimum standards of transparency and quality, with appropriate mechanisms of review and certification of DTC-GT providers to increase the accountability of companies active in the DTC-GT market. Providing an independent trusted quality mark would benefit both consumers and health-care professionals dealing with questions from patients who have purchased or are thinking of purchasing DTC-GT services.35
The results of our study have shone a light on inadequacy of the prepurchase information currently being provided to UK consumers by DC-GT companies and its inconsistencies with the principles for good practice laid out by the HGC. Our suggestions for improving transparency and consumer support, decreasing risk and improving governance add to others in the literature and are compatible with several ongoing developments, such as the EuroGenTest tool, which has been designed to aid professionals and consumers through choices about purchasing DTC-GT.36 Although there is clearly a need to improve the transparency, quality and accountability of DTC-GT companies operating in the United Kingdom, in this global service market, laboratories and business operations may be distributed across jurisdictions and greater international collaboration is also needed to agree consistent and actionable standards and mechanisms of governance.
Although DTC-GT offers opportunities for consumers to better understand and manage their personal health and wellness, industry self-regulation has failed to ensure compliance with best practice and the transparency of the information available to guide consumers’ purchasing decisions falls short on many criteria. Improving transparency, quality and accountability in this fast-evolving sector is essential to protect consumers and ensure responsible innovation and business practices. Achieving this will require partnership between citizens, industry and government, alongside interdisciplinary science input. As a first measure, we suggest revisiting and updating the 2010 HGC guidelines in the United Kingdom to take account of innovations and changes in this market and to create a specific set of criteria on transparency of prepurchase information. We also recommend greater dialogue between the various stakeholders, including companies, as well as increased coordination between regulatory bodies concerned with consumer genetic testing, such as regulators of medical devices, consumer safety, data protection and fair marketing, to address their gaps and misalignments (Figure 3). In this global market, new initiatives to seek wider agreements on international standards for quality, transparency and certification are also called for.
Su P : Direct-to-consumer genetic testing: a comprehensive view. YALE J Biol Med 2013; 86: 359–365.
Gollust SE, Wilfond BS, Hull SC : Direct-to-consumer sales of genetic services on the Internet. Genet Med 2003; 5: 332–337.
Turrini M, Prainsack B : Beyond clinical utility: the multiple values of DTC genetics. Appl Transl Genomics 2016; 8: 4–8.
Covolo L, Rubinelli S, Ceretti E, Gelatti U : Internet-based direct-to-consumer genetic testing: a systematic review. J Med Internet Res 2015; 17: e279.
Phillips AM : ‘Only a click away—DTC genetics for ancestry, health, love…and more: a view of the business and regulatory landscape’. Appl Transl Genomics 2016; 8: 16–22.
Harvey A : Genetic risks and healthy choices: creating citizen-consumers of genetic services through empowerment and facilitation. Sociol Health Illness 2010; 32: 365–381.
Kaufman DJ, Bollinger JM, Dvoskin RL, Scott JA : Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing. J Genet Counsel 2012; 21: 413–422.
McGrath SP, Coleman J, Najjar L, Fruhling A, Bastola DR : Comprehension and data-sharing behavior of direct-to-consumer genetic test customers. Public Health Genomics 2016; 19: 116–124.
Padilla A, Border P : Consumer genetic testing. Houses of Parliament. Parliamentary Offices of Science and Technology. POST note, Vol 407, 2012.
Brice P : The shifting sands of direct-to-consumer genetic test regulation. http://www.phgfoundation.org/blog/16573. Accessed September 2016.
Wright CF, Hall A, Zimmern RL : Regulating direct-to-consumer genetic tests: what is all the fuss about? Genet Med 2011; 13: 295–300.
Rafiq M, Ianuale C, Ricciardi W, Boccia S : Direct-to-consumer genetic testing: a systematic review of European Guidelines, Recommendations, and Position Statements. Genet Testing Mol Biomarkers 2015; 19: 535–547.
Association for Molecular Pathology Position Statement: direct access genetic testing (direct to consumer genetic testing) - February 2015. https://www.amp.org/publications_resources/position_statements_letters/documents/AMPpositionstatementDTCtesting-FINAL_002.pdf Accessed September 2016.
European Society of Human Genetics: Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes. Eur J Hum Genet 2010; 18: 1271–1273.
ACMG Board of Directors: Direct-to-consumer genetic testing: a revised position statement of the American College of Medical Genetics and Genomics. Genet Med 2015; 18: 207–208.
http://www.genewatch.org. Accessed September 2016.
Kraft P, Hunter DJ : Genetic risk prediction—are we there yet? N Engl J Med 2009; 360: 1701–1703.
European Academies Science Advisory Council 2012. Direct-to-consumer genetic testing for health-related purposes in the European Union. Available at: http://www.easac.eu/fileadmin/Reports/EASAC_Genetic_Testing_Web_complete.pdf. Accessed September 2016.
Little J, Higgins JP, Ioannidis JP et al: STrengthening the REporting of Genetic Association studies (STREGA)—an extension of the STROBE statement. Eur J Clin Invest 2009; 39: 247–266.
Personal genetic profiling services lack evidence for claims. Press release: http://nuffieldbioethics.org/news/2010/personal-genetic-profiling-services-lack-evidence-for-claims/. Accessed September 2016.
Cussins J : Direct-to-consumer genetic tests should come with a health warning. Pharm J 2015; 294: 7845.
Borry P, van Hellemondt RE, Sprumont D et al: Legislation on direct-to-consumer genetic testing in seven European countries. Eur J Hum Genet 2012; 20: 715–721.
Human Genetics Commission A Common Framework of Principles for Direct-to-Consumer Genetic Testing Services. HGC; London. 2010, pp 1–15.
Grimaldi KA, Look MP, Scioli GA, Clavero JC, Marinos S, Tagaris T : Personal genetics: regulatory framework in Europe from a service provider's perspective. Eur J Hum Genet 2011; 19: 382–388.
Medical profiling and online medicine: the ethics of 'personalised healthcare' in a consumer age. http://nuffieldbioethics.org/project/personalised-healthcare-0/. Accessed September 2016.
DNA testing choices: www.dnatestingchoices.co.uk. Accessed September 2016.
Hall J, Pagliari C, Amato J : Transparency in the Marketing of Direct-to-Consumer Genetic Tests in the UK: Scoping Review and Consultation. European Society of Human Genetics Conference; May 2016; Barcelona, Spain.
https://www.theguardian.com/technology/2014/dec/02/google-genetic-testing-23andme-uk-launch. Accessed September 2016.
www.dnafit.com. Accessed September 2016.
Carere DA, Kraft P, Kaphingst KA, Roberts JS, Green RC : Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing. Genet Med 2016; 18: 65–72.
Laestadius LI, Rich JR, Auer PL : All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms. Genet Med 2016, e-pub ahead of print doi:10.1038/gim.2016.136.
Bryant T : Global study on direct-to-consumer genetic testing market size, share and demand outlook 2016 to 2022 – credence research’. Salisonline 2016, http://www.salisonline.org/health/global-study-on-direct-to-consumer-genetic-testing-market-size-share-and-demand-outlook-2016-to-2022-credence-research/. (accessed 2 November 2016).
Madhav A : Global direct-to-consumer genetic testing market to reach worth USD 340 mn by 2022: rising awareness about genetic diseases to drive the market growth – credence research. http://www.mobilecomputingtoday.co.uk/3358/global-direct-consumer-genetic-testing-market-reach-worth-usd-340-2022-rising-awareness-genetic-diseases-drive-market-growth-credence-research/ N.p., 2016. Web. 2 Nov. 2016. (accessed 2 November 2016).
van der Wouden CH, Carere DA, Maitland-van der Zee AH, Ruffin MT 4th, Roberts JS, Green RC : Consumer perceptions of interactions with primary care providers after direct-to-consumer personal genomic testing. Ann Intern Med 2016; 164: 513–522.
Jackson L, Goldsmith L, Skirton H : Guidance for patients considering direct-to-consumer genetic testing and health professionals involved in their care: development of a practical decision tool. Fam Pract 2014; 31: 341–348.
None of the authors received direct funding for this project. We thank Legal Spark, 22 Montrose Street, Glasgow G1 1RE which provided Daniel Donaldson, LLB and Sean Folan’s expertise pro bono for help with the review and for helpful discussions on the assessment criteria. And many thanks to Stuart Scott, Clinical Scientist at UKNEQAS for helpful discussions and input. External help with diagrams was supported by Vivactiv Ltd. CP is a grant holder on the ESRC-funded Administrative Data Research Centre for Scotland, Grant Number ES/L007487/1.
The study was conceived and designed by JAH, in collaboration with CP. JAH and JA undertook the pilot review to inform the criteria. JAH, RG, Daniel Donaldson and Sean Folan (acknowledged) conducted the full independent assessments. JAH and CP drafted the manuscript, with input from RG, which was reviewed and approved by all authors.
The authors declare no conflict of interest.
Supplementary Information accompanies this paper on European Journal of Human Genetics website
About this article
Cite this article
Hall, J., Gertz, R., Amato, J. et al. Transparency of genetic testing services for ‘health, wellness and lifestyle’: analysis of online prepurchase information for UK consumers. Eur J Hum Genet 25, 908–917 (2017). https://doi.org/10.1038/ejhg.2017.75
Genome sequencing in healthcare: understanding the UK general public’s views and implications for clinical practice
European Journal of Human Genetics (2020)
Frontiers in Genetics (2020)
Science and Engineering Ethics (2020)
European Journal of Public Health (2020)
SSRN Electronic Journal (2019)