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Stroke. 2001;32:1242-1249

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(Stroke. 2001;32:1242.)
© 2001 American Heart Association, Inc.

Original Contributions

Ethical and Methodological Issues in Pedigree Stroke Research

Bradford Burke Worrall, MD; Donna T. Chen, MD, MPH James F. Meschia, MD

From the Departments of Neurology and Health Evaluation Sciences (B.B.W.) and Southeastern Rural Mental Health Research Center and Institute of Law, Psychiatry, and Public Policy (D.T.C.), University of Virginia, Charlottesville; and Department of Neurology, Mayo Clinic Jacksonville (Fla) (J.F.M.). Drs Worrall and Chen contributed equally to the preparation of this article.

Correspondence to Bradford Burke Worrall, MD, University of Virginia Health Systems No. 800394, Charlottesville, VA 22908. E-mail DoChen{at}cc.nih.gov


*    Abstract
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 *Abstract
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 down arrowPedigree Research and Bioethics
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Background—Stroke is a complex genetic disorder with a variable phenotype. Investigations of heritable factors in complex genetic disorders use pedigree and genetic techniques, which pose different ethical and methodological challenges than those routinely encountered in therapeutic research. Building consensus on acceptable research practices in this field is vital to the success of multicentered collaborations.

Summary of Review—We review important ethical and methodological concerns related to the collection, storage, and release of pedigree research information. The human studies aspects of pedigree research are complicated methodologically because individuals can be active or passive participants and pedigrees can be proband derived, partially validated, or fully validated. Current research ethics frameworks do not work well outside of a dyadic researcher-subject relationship. Privacy and confidentiality for family members must be considered in pedigree research. Investigators should anticipate potential conflicts of interest among family members when designing a pedigree research protocol.

Conclusions—We propose a "proband-initiated contact" methodology in which the proband or the proband’s designate allows identification of potential families without breaching the privacy of individuals in the family. In situations in which family history data are collected without direct contact between researchers and individuals in the proband’s family, an Institutional Review Board may waive consent by family members after appropriate review of the protocol and application of rules for granting waivers of consent. Certificates of Confidentiality should be considered.


Key Words: ethics, medical • family • patient selection • pedigree • stroke


*    Introduction
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 *Introduction
down arrowPedigree Research in...
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Stroke can be viewed as a complex genetic disorder with variable expression and intermediate phenotypes such as carotid atherosclerosis. Technological advances and the human genome sequence have improved our ability to dissect out inherited components of complex disorders through 2 complementary strategies: pedigree and genetic research. These forms of research raise specific ethical and methodological issues not typically encountered in acute therapeutic trials or secondary prevention studies. Pedigree research relies on accurate ascertainment of family history. In its most rudimentary form, this approach is similar to that used in routine clinical care. Genetic research looks for mutations or polymorphisms of genes associated with a disease or an intermediate phenotype. Pedigree information remains crucial to the process of elucidating the genetics of multifactorial diseases.1 Genetic research can incorporate pedigree studies, as in linkage analyses,2 or be independent from family historical data, as in case-control association studies.3

Issues of privacy, consent, and confidentiality surround DNA samples in genetic research,4 5 and concerns about consent for future uses of banked DNA have sparked unresolved national and international debate.6 7 8 Pedigree research presents equally challenging dilemmas that merit consideration.9 We present some of the major issues encountered in planning and executing pedigree studies of stroke and suggest practical ways to address some of them. We suggest neither that these are the only relevant ethical issues nor that the approaches discussed are the only viable solutions. Our purpose is to contribute to an informed debate. Because adequately powered pedigree and genetic studies typically require collaboration of many investigators at multiple sites, it is important to build consensus on acceptable research practices in this field.


*    Pedigree Research in Cerebrovascular Disease
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The exact role of heritable factors in cerebrovascular disease remains poorly characterized. Large population-based studies have not consistently identified family history as an independent risk factor for cerebrovascular disease,10 11 12 as they have for coronary disease. This may in part be due to diagnostic limitations inherent in relying solely on clinical and historical information in the era before routine use of CT. Nonetheless, stroke has been recognized as a common feature of single-gene disorders such as sickle cell disease13 and homocysteinuria.14 Recent pedigree-driven research has characterized single-gene stroke disorders, including cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).2 15 Established cerebrovascular risk factors such as hypertension16 and diabetes17 exhibit strong familial clustering.

Attempts to investigate heritable risk for stroke have followed many strategies. Lack of accurate and verifiable information on the occurrence and subtype of stroke has limited traditional population-based and cross-sectional epidemiological studies. Large-scale data banks with comprehensive clinical information, including family history, may serve as a starting point to investigate the genetics of cerebrovascular disease. Future studies should emphasize careful characterization of phenotype.


*    Pedigree Research Paradigms
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Pedigree research utilizes both single-family and multifamily pedigrees. Different issues attend these 2 strategies, although both raise concerns about privacy and confidentiality. In general, identities of participants in research are protected by techniques such as substituting coded information for personal identifiers or removing personal identifiers altogether, thereby rendering the data anonymous.18 Single-family pedigrees are usually documented exhaustively and contain multigenerational data. The completeness of family data makes ensuring anonymity more difficult, especially in small, defined communities or for rare diseases. A family tree may be uniquely identifiable by the nature of its branches. Strategies to protect family identity have included omission of sex information in unaffected family members or collapsing children into a single icon on published pedigree diagrams.18 Multifamily research uses portions of families such as twin, sibling, or parent-child pairs. The time these data remain linked to personal identifiers may be shorter than in studies using complete pedigrees. Greater assurances of privacy can be made when each pedigree is concealed within the collection of research units.


*    Pedigree Research and Bioethics
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Research ethics gives considerable weight to voluntary informed consent to protect individuals from risk.19 20 21 Ethical principles outlined in the Belmont Report22 and their applications inform federal regulations governing human subjects research in the United States.23 24 Traditional interpretations of these principles and regulations offer guidance most explicitly in the realm of clinical trials, in which a dyadic researcher-participant relationship exists. Outside of that relationship, these interpretations sometimes fail to offer adequate guidance for investigators using other research paradigms such as health services,25 epidemiological,26 and pedigree research.

Collecting family history is an integral part of routine clinical care used in medical decision making and risk stratification for many diseases. Family history remains the most appropriate and efficient means of screening for and stratifying genetic risk for common, multigenic conditions such as stroke and is also an efficient and cost-effective way to screen for single-gene disorders. The advent of presymptomatic and carrier status testing for single-gene disorders has engendered debate about the rights of family members.27 Genetic counseling often includes family members, and discussion has ensued regarding release of information to family members at risk for genetic disease.28

Genetic exceptionalism, the belief that genetic information is unique among medical information and requires special additional safeguards, continues to influence policy and practice29 and could potentially impede collection of complete family history data. Nevertheless, some public health authorities have called for a shift in policies regarding genetic information and advocated for routine pedigree collection for all patients.30 Since the vast majority of diseases are likely caused by an interaction between genetic and environmental factors, the distinction between "genetic" and "nongenetic" diseases is increasingly blurred and could potentially justify this shift.31 However, there are precedents of discrimination based solely on family history,32 and many still legitimately fear discrimination for having a disease perceived to run in families.33

Pedigree methodologies have been essential in identifying and characterizing a multitude of heritable diseases, but concerns about privacy in the era of genomics have brought new scrutiny to the use of family history data. For example, prompted by a complaint from a father of participants in a twin registry, the Office of Protection From Research Risk (OPRR) (now known as the Office of Human Research Protections) temporarily suspended all federal research funds at Virginia Commonwealth University (VCU).34 The father objected to the gathering of information regarding his medical history without his consent during the process of gathering his daughter’s family medical history. The decision of OPRR to intervene was reportedly due in large part to the failure of the local Institutional Review Board (IRB) to document that they had sufficiently considered potential risks to family members, including breach of privacy and unauthorized release of information.

Responding to the VCU situation, the American Society of Human Genetics (ASHG) offered a framework for IRB review of pedigree research,35 and the OPRR issued a statement admonishing all researchers and IRBs to consider risk to family members in their ethical assessment of research protocols.36 Questions have arisen regarding to what extent researchers should consider risks to family members even when their medical histories are collected only from probands.35


*    Pedigree Recruitment
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Identification of Probands and Pedigrees
Potential probands referred for participation will typically have the following basic characteristics: a personal and family history of stroke and an ability to provide informed consent directly or through a surrogate. Screening for familial clustering of stroke is performed after the proband has agreed to participate. Approximately 1 in 10 patients who present with ischemic stroke reports having a living sibling with a history of stroke37 ; therefore, a multifamily paradigm focusing on siblings offers an efficient methodology for pedigree stroke research. Surviving parents or children with premature disease can potentially provide information for linkage analysis in associated genetic studies.

Identification of families with clustering of any disease depends on the ability of probands to recognize and report the occurrence of disease among family members. Lack of knowledge, misinformation, or poor recollection may complicate pedigree research. Stroke makes pedigree research even more problematic because the disease can compromise attention, arousal, and communication. There is a strong scientific justification for contacting family members to verify proband reported histories.

Identification of disease clustering requires accurate pedigree characterization. When designing a protocol, researchers must decide whether data will be collected solely from the proband or if family history information will be validated through contacting family members. The decision of whether or not to validate data should be based on scientific, ethical, and logistical considerations and will have implications for the role of family members in the study.

Pedigree research participation can be classified as active or passive, and pedigrees can be categorized on the basis of degree of validation (TableDown). In studies in which the proband provides all information, family members are not contacted and can be considered passive participants. In this framework, the proband is the only person given the opportunity to provide informed consent. This would constitute a proband-derived pedigree. By contrast, probands and family members can all act as active participants, with each providing his/her own medical information and giving informed consent for participation, thereby creating a fully validated pedigree. When using this active participant framework, researchers attempt to contact all family members eligible for the protocol. In so doing, a picture of mixed participation will often occur, creating a partially validated pedigree. Some family members will be contacted successfully, and others will not. Of those contacted, some will give consent and join as active participants, some may opt for passive participation, and some will explicitly object to inclusion of their information. Investigators have at times chosen to put information about nondissenting members into the pedigree and left dissenting members in as "no information."38 Family members who are not successfully contacted could be considered passive participants. Family members who decline participation present a challenge since omitting family history information on these "nonparticipants" may render information from other consenting family members unusable. From an epidemiological point of view, there may be utility in including interested members and nonidentifiable basic demographic data of dissenting members to determine whether there are systematic differences between consenting, nondissenting, and dissenting "groups."


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  		Table 1. Levels of Pedigree Participation and Pedigree Information

Consent for Probands and Other Active Participants
All potential active participants need to be approached for informed consent.20 22 23 24 Concerns about diminished capacity to provide informed consent for research apply to persons with stroke.39 Pedigree research has some advantages over therapeutic research in its ability to address these concerns. Pedigree research is "noninterventional" and potentially as low risk as other observational studies. Researchers seeking informed consent from a patient of questionable capacity can formally assess capacity; wait for the return of capacity since family history data may not be time sensitive; or seek out guardians or surrogates. Statutes regarding surrogate consent for research differ by state, and interpretation of these statues differs by institution. The Patient Self-Determination Act encourages the completion of advance directives and designation of surrogate decision makers in the clinical arena.40 The precise role that advance directives and surrogate decision makers will play in the realm of research is still to be determined.41

Passive Participants
The recent VCU case raises the question of whether collecting family history information from research subjects ought to require explicit consent from each family member even when it is not necessary to contact them for scientific purposes. The ASHG expressed concern that requiring written informed consent from every member of a study pedigree could have a detrimental effect on pedigree research.28 42 Contacting all members of a pedigree could represent a broad-scale intrusion into their lives.

Some have suggested that family member "participation" could be evaluated by an IRB for consideration of waived consent.35 This mechanism, described in Title 45 of Code of Federal Regulations part 46 (45 CFR 46),23 has strict requirements and is currently applicable only to research subjects. It is unclear whether waived consent would be an appropriate paradigm for considering hearsay information about family members. However, if investigators consider these family members to be research participants, the option to waive consent is potentially available to them and their IRB. Whether or not passive participants are classified as research subjects, pedigree investigators designing research protocols need to consider the possibility that family members may incur bystander risks and implement mechanisms to minimize those risks.

Nonparticipants
Bioethical principles relating to privacy and autonomy of one family member can conflict with principles related to autonomy and justice for another. Similar questions about individual responsibility in a larger societal context are debated in other ethical traditions.43 44 45 46 Bioethicists are exploring relationships between group and individual rights and responsibilities in several contexts.47 48 49 Families may be considered unique communities with instances of higher mutual obligations. If so, family members may have some obligation to one another with regard to participation in pedigree research. However, there are no obligations to donate blood, bone marrow, or organs even among family members, and there is no duty to participate in research.

In multifamily studies, one dissenting member may preclude others from participating (eg, one twin can keep the other from being an eligible study subject). Some authors propose a concept of multiple ownership of family history, which still leaves open the question of prevailing rights.28 In the clinical context, patients have the right to discuss their family history with their physician. Although family history information that has not been verified is considered hearsay,28 it remains useful for medical decision making and risk stratification. Medical family histories have been treated as part of an individual’s medical record, and privacy protections traditionally have not extended beyond routine safeguards. In research that is not focused on heritability, family historical information is often collected in an anonymous and dichotomous fashion (eg, family history of stroke is recorded as positive or negative). Pedigree research requires that medical data be linked to specific familial relationships. Including only those members of a pedigree who provide written informed consent could introduce scientific bias. If unverified family history data belong to the proband and other active participants, then we suggest that family history data may be used in research even over the objections of nonproband family members provided that the data are collected without personal identifiers and that identity cannot be inferred secondary to family relationships.

Proband-Initiated Contact Methodology
When designing pedigree research protocols using active participation, investigators must decide how to contact family members. Can a researcher approach family members on the basis of information collected from the proband (so-called cold contacting)? Does the answer to this question depend on the stigma or potential stigma associated with the disease under study? Stroke is a relatively nonstigmatized illness, but potential genetic risk may be stigmatizing. Discussion of ethical considerations surrounding subject recruitment in other research disciplines, such as epidemiological and social science research, may offer some guidance.26 50 51 Concepts such as "guardian consent" for groups or communities may have relevance to pedigree research.52 Similar to some cluster research scenarios in which a "guardian" for the group gives consent for the other members to be approached to participate, the proband may be able to give consent for researchers to approach family members. Each family member then gives or denies consent for his/her own active participation. In cluster research, guardian consent is used to avoid having one individual’s decision to decline participation impinge on the involvement of others in the group.52

If probands or other nonresearchers make the initial contact, family members can elect to be contacted by the investigator without the investigator needing to know any personal details a priori. In this proband-initiated contact methodology, potential families could be identified and contacted without the investigator breaching the privacy of individuals in the family (FigureDown). Investigators can contact family members directly once a relationship has been established. This methodology undoubtedly adds complexity to pedigree research. Nevertheless, the proband-initiated contact method seeks to balance ethical and scientific considerations and can be subjected to empirical study for appropriateness and effectiveness in various research contexts.



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  		Figure 1.

Potentially coercive forces acting on family members change depending on who makes contact. If family members feel that their participation in research may affect the delivery of care to the proband, they may feel undue pressure to enroll in the study. Proband-initiated contact could be more or less coercive than investigator-initiated contact depending on the family. However, proband-initiated contact better simulates regular family decision-making dynamics.


*    Storage and Release of Information
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Data Security
Investigators must consider how data will be stored and accessed for analyses. Generally, efforts to limit access to data still linked to potential identifiers improve both the security of the data set and allow for more objective assessment of the data. Reviewing source documents, data entry, and closeout of the data set may necessitate verification of information with the use of individual identifiers. Database management, storage, and statistical analyses usually can be performed with the use of coded information or information that has been rendered anonymous. Database safeguarding systems should help to prevent both intentional and accidental breeches of security. Advances in information technology offer new procedures that can improve the security in storage and management of research data.53 Encryption and nonidentifiable codes facilitate protection of information.54 The potential risk for and possible consequences of deducible identity and breeches of security ought to be reviewed with potential subjects during the informed consent process.

Publication and Other Intentional Release of Information
Researchers have a duty to subjects to make important findings publicly known but not at the expense of protection of privacy. Journals vary in the handling of single-family pedigrees,55 and the acceptability of alteration of information to preserve anonymity is still debated.56 57 Two guidelines for publication of pedigrees both call for informed consent by the patient for publication of identifying information.56 57 These recommendations do not clarify what information is "identifying," nor do they specify whether all family members in a pedigree constitute "patients." Publishing potentially identifying information without consent may constitute forcing an investigator-subject relationship on family members without consent.58 The risk of accidental discovery of published personal clinical information without proper counseling needs to be considered.59

When any release of clinical data is planned, potential legal and fiduciary obligations to the proband and family members, who have or have not consented, merit consideration during the planning phase.

Release of data to future researchers for exploratory analyses and systematic overviews is increasingly common. Although all future analyses cannot be anticipated, the potential for them should be discussed, and options for informed consent should be planned.

Proband Access to Information
During the informed consent process for many types of clinical research, participants are routinely offered access to relevant individual data and the results of the research on study completion. In pedigree research this practice may not be appropriate since the clinical implications of the results may not be known with certainty. Adequate comprehension of the implications of pedigree and genetic information may be difficult to achieve outside of formal genetic counseling. During the design phase of a study, decisions should be made and procedures specified for relaying or withholding information about risk for the disease under investigation and for other inherited diseases identified during the course of research or subsequent analyses. Decisions about who on the research team bears the responsibility of relaying information and to whom the information should be conveyed ought to be made before subject recruitment.

Family Access to Information
In the clinical setting, release of information to at-risk family members outside of a patient-physician relationship can be appropriate and, at times, is imperative.28 In the research setting, the degree of risk is likely less certain, and therefore arguments in favor of releasing information to family members may not carry the same weight. Additionally, persons who decline to contribute to the pedigree may have diminished rights to request access to information collected even though it may affect their understanding of genetic risk.

Decisions about disclosure to other family members can be discussed with active participants in pedigree research at the time of initial consent. In fully validated pedigrees, family members can discuss issues about disclosure within the family and agree on how to handle disclosure. In research using proband-derived pedigrees, direct disclosure by the researchers to other family members is less likely to be an issue but could be decided on by the proband. Partially validated pedigrees have unique problems since concealment of identity within the family may not be possible. Information on children in a pedigree may allow accurate inference about the risk status of their parents analogous to asymptomatic genetic testing in autosomal dominant diseases in clinical practice. Conflict may occur, such as when one member of a family asks to see pedigree information and another family member gives information with the stipulation that no one in the family finds out about it.

Third Party Access to Information
Society is currently conflicted about its preferences over privacy and confidentiality; the Office of Management and Budget recently proposed increased public access to data collected as part of federally funded medical research,60 while privacy concerns have dominated discussions of the Health Insurance Portability and Accountability Act.61 Although family history data are not equivalent to genetic information, third party access to family history data could affect an individual’s access to affordable healthcare.32 When pedigree data are linked to genetic data, third parties may attempt to get access to the information to look at other areas of the genome for disease genes. Release of research data to such third parties without consent by research participants is a significant violation of confidentiality. However, many research participants do not realize that some healthcare coverage agreements have clauses that include, or could be construed to include, consent for the agency to collect information from researchers. Some investigators are informing potential research participants of this possibility.

Third parties may attempt to compel disclosure if information is stored in any identifiable way. In the United States, Certificates of Confidentiality may offer some legal protection for researchers from compelled disclosure.62 They have typically been used in mental health and substance abuse research63 and may have applications in pedigree and genetic research.64 However, these certificates offer no protection in the aforementioned situation in which a researcher is presented a signed consent for release of information. The only protection when this type of release is truly undesired—on the part of the researcher or on the part of the participant, even if signed consent was obtained—may be maintaining the data without any personal identifiers rendering them completely anonymous. One of the authors (J.F.M.) obtained a Certificate of Confidentiality from the National Institute of Mental Health for the Siblings With Ischemic Stroke Study, a multicentered trial investigating genetic causes of ischemic stroke.65 Obtaining Certificates of Confidentiality may become increasingly important as pedigree, genetic, and genomic research continues to progress at a rapid rate.

Individual and the Greater Community Issues
Recently, DeCode, a commercial venture in Iceland, obtained a license for a national database linking medical records to genetic material, renewing concerns about community versus individual rights in the era of genetic research.66 This is notable because the company sought and obtained authorization to create this database using the ideas of "community consent" and "presumed consent" for individuals with an anonymous option to "opt out" for those who wish to decline participation.67 This has led to extensive public68 and professional debates,67 69 particularly on the potential linking of medical records to DNA data that may not be sufficiently secure.70 However, since use of the database for genotypic exploration requires explicit individual consent, those in charge of the database believe that the potential for unchecked exploration of genetic foundations for diseases will be low.67 Public opinion strongly favors the database,68 although approximately one tenth of the Icelandic population has declined to participate.69 Some have raised the concern that in such a small country as few as 3 pieces of basic information may allow identification of individuals despite efforts to de-identify the data.71

Concerns about use of data and cultural implications of data are receiving renewed attention in communities such as Native American tribes. Disclosure of population-based data could adversely affect group privacy.48 The rights and responsibilities of groups may also depend on their degree of identification as a community.47 72 These unresolved issues are being actively discussed in the public health arena, and how they are resolved will likely affect pedigree and genetic research in discrete populations. The issues around privacy and disclosure are on the forefront of national debate not only because of advances in genetics but also because of the increased potential for and recent steep rise in rapid information sharing in this electronic information age.


*    Conclusions
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 up arrowAbstract
 up arrowIntroduction
 up arrowPedigree Research in...
 up arrowPedigree Research Paradigms
 up arrowPedigree Research and Bioethics
 up arrowPedigree Recruitment
 up arrowStorage and Release of...
 *Conclusions
down arrowReferences
 
Pedigree research can establish the heritability of disease whether by itself or in conjunction with genetic techniques such as linkage analyses. Pedigree research begins with interviewing a proband. Family members can then participate either actively or passively. There is greater confidence in assigning phenotype in active participants. Stroke patients may have diminished capacity to consent or an impaired ability to provide accurate information about family members. When the data set is adequately secured, it may be appropriate for governing IRBs to grant a waiver of consent for passive participant family members if they are considered research subjects. Certificates of Confidentiality may offer additional protections to active participants in pedigree research. We have proposed a proband-initiated contact method as an ethical means of recruiting family members to be active participants. This method avoids cold contacting of potential study subjects and protects the privacy of all family members. Addressing ethical issues in pedigree research is complicated methodologically because the unit of study is a group and because individuals can participate at multiple levels, creating potential for conflict between individual and group rights and responsibilities. Pedigree and genetic research can benefit from further advances in applicable research ethics that are carefully considered, internally consistent, clearly articulated, and well accepted.


*    Acknowledgments
 
This project was supported in part by a clinical research training fellowship grant from the American Academy of Neurology (to Dr Worrall); by the National Institute of Mental Health of the National Institutes of Health (grant No. P50 MH49173) (for Dr Chen); and by the National Institute of Neurological Disorders and Stroke of the National institutes of Health (grant No. NS39987) (to Dr Meschia). The authors wish to thank Carol Freund, PhD; Karen C. Johnston, MD, MSc; Franklin Miller, PhD; Donald Rosenstein, MD; and Benjamin Wilfond, MD, for their critical review and advice during the preparation of this manuscript.


*    Footnotes
 
Reprint requests to Donna T. Chen, MD, MPH, Department of Clinical Bioethics, Warren G. Magnuson Clinical Center, National Institutes of Health, 10 Center Dr, Bldg 10, Room 1C-118, Bethesda, MD 20892.

The opinions expressed are those of the authors and do not necessarily reflect the opinions or policies of the National Institutes of Health or the Department of Health and Human Services.

Received November 1, 2000; revision received February 28, 2001; accepted March 7, 2001.


*    References
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 up arrowIntroduction
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 *References
 

  1. Scheuner MT, Wang SJ, Raffel LJ, Larabell SK, Rotter JI. Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood. Am J Med Genet. 1997;71:315–324.[Medline] [Order article via Infotrieve]
  2. Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, Bach MA, Bousser MG. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet. 1993;3:256–259.[Medline] [Order article via Infotrieve]
  3. Elbaz A, Poirier O, Moulin T, Chedru F, Cambien F, Amarenco P, for the GENIC Investigators. Association between the Glu298Asp polymorphism in the endothelial constitutive nitric oxide synthase gene and brain infarction. Stroke. 2000;31:1634–1639.[Abstract/Free Full Text]
  4. Report of a WHO Meeting on Ethical Issues in Medical Genetics. Proposed international guidelines on ethical issues in medical genetics and genetic services. December 15–16, 1997; Geneva, Switzerland. Available at: http://www.who.int/ncd/hgn/hgnethic.htm. Accessed September 1, 2000.
  5. The American Society of Human Genetics. ASHG report: statement on informed consent for genetic research. Am J Hum Genet. 1996;59:471–474.[Medline] [Order article via Infotrieve]
  6. Elias S, Annas GJ. Generic consent for genetic screening. N Engl J Med. 1994;330:1611–1613.[Free Full Text]
  7. Biesecker LG, Wilfond BS, Wells RJ. Generic consent for genetic screening. N Engl J Med. 1994;331:1024; comment 1025.[Free Full Text]
  8. HUGO Ethic Committee. Statement on DNA sampling: control and access. 1998; London, UK. Available at: http://www.gene.ucl.ac.uk/hugo/sampling.html. Accessed September 1, 2000.
  9. Frankel MS, Teich AH. Ethical and Legal Issues in Pedigree Research. Washington, DC: American Association for the Advancement of Science; 1993.
  10. Kiely DK, Wolf PA, Cupples LA, Beiser AS, Myers RH. Familial aggregation of stroke: the Framingham Study. Stroke. 1993;24:1366–1371.[Abstract/Free Full Text]
  11. Earley CJ, Kittner SJ, Feeser BR, Gardner J, Epstein A, Wozniak MA, Wityk R, Stern BJ, Price TR, Macko RF, Johnson C, Sloan MA, Buchholz D. Stroke in children and sickle-cell disease: Baltimore-Washington Cooperative Young Stroke Study. Neurology. 1998;51:169–176.[Abstract/Free Full Text]
  12. Liao D, Myers R, Hunt S, Sharhar E, Paton C, Burke G, Province M, Heiss G. Familial history of stroke and stroke risk: the Family Heart Study. Stroke. 1997;28:1908–1912.[Abstract/Free Full Text]
  13. Powars DR, Wilson B, Imbus C. The natural history of stroke in sickle cell disease. Am J Med. 1978;65:461–471.[Medline] [Order article via Infotrieve]
  14. Mudd SH, Skovby F, Levy HL. The natural history of homocystinuria due to cystathionine beta-synthase deficiency. Am J Hum Genet. 1985;37:1–31.[Medline] [Order article via Infotrieve]
  15. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia. Ann N Y Acad Sci. 1997;826:213–217.[Abstract/Free Full Text]
  16. Lascaux-Lefebvre V, Ruidavets J, Arveiler D, Amouyel P, Haas B, Cottel D, Bingham A, Ducimetiere P, Ferrieres J. Influence of parental history of hypertension on blood pressure. J Hum Hypertens. 1999;13:631–636.[Medline] [Order article via Infotrieve]
  17. Allen C, Palta M, D’Alessio DJ. Risk of diabetes in siblings and other relatives of IDDM subjects. Diabetes. 1991;40:831–836.[Abstract]
  18. Byers PH, Ashkenas J. Pedigrees—publish? Or perish the thought? Am J Hum Genet. 1998;63:678–681.[Medline] [Order article via Infotrieve]
  19. Beauchamp TL, Childress JF, eds. Principles of Biomedical Ethics. 4th ed. London, UK: Oxford University Press; 1994.
  20. World Medical Association Declaration of Helsinki. Recommendations guiding physicians in biomedical research involving human subjects. JAMA. 1997;277:925–926.[Medline] [Order article via Infotrieve]
  21. The Nuremberg Code. JAMA. 1997;276:1691.
  22. The National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. The Belmont Report: ethical principles and guidelines for the protection of human subjects of research. April 18, 1979; Bethesda, Md. Available at: http://helix.nih.gov:8001/ohsr/mpa/belmont.phtml. Accessed September 1, 2000.
  23. Department of Health and Human Services/National Institutes of Health/Office for Protection from Research Risks. Code of Federal Regulations: Title 45 Public Welfare Part 46: protection of human subjects. Revised June 18, 1991; Bethesda, Md. Available at: http://ohrp.osophs.dhhs.gov/humansubjects/guidance/45cfr46.htm. Accessed September 1, 2000.
  24. 21 CFR 50 (last revised July 23, 1997) and 21 CFR 56 (last revised October 2, 1996). Available at: http://www.fda.gov/opacom/morechoices/fed996.html. Accessed September 1, 2000.
  25. Institute of Medicine. Protecting Data Privacy in Health Services Research. Washington, DC: National Academy Press; 2000.
  26. Coughlin SS, Beauchamp TL. Ethics, scientific validity, and the design of epidemiologic studies. Epidemiology. 1992;3:343–347.[Medline] [Order article via Infotrieve]
  27. Wilfond BS, Fost N. The cystic fibrosis gene: medical and social implications for heterozygote detection. JAMA. 1990;263:2777–2783.
  28. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure. ASHG statement: professional disclosure of familial genetic information. Am J Hum Genet. 1998;62:474–483.[Medline] [Order article via Infotrieve]
  29. Annas GJ, Glantz LH, Roche PA. Drafting the genetic privacy act: science policy and practical considerations. J Law Med Ethics. 1995;23:360–366.[Medline] [Order article via Infotrieve]
  30. Hayflick SJ, Eiff MP. Role of primary care providers in the delivery of genetics services. Community Genet. 1998;1:18–22.[Medline] [Order article via Infotrieve]
  31. Khoury MJ. Relationship between medical genetics and public health: changing the paradigm of disease prevention and the definition of a genetic disease. Am J Med Genet. 1997;71:289–291.[Medline] [Order article via Infotrieve]
  32. Johnston R, Seitz K. Policy choices available in genetic counseling for people at-risk for Huntington’s disease. Psychiatr Q. 1981;53:194–200.[Medline] [Order article via Infotrieve]
  33. Slaughter LM. Genetic information must remain private to prevent discrimination, spur research. Genet Testing. 1998;2:17–20.[Medline] [Order article via Infotrieve]
  34. Mathews J. Father’s complaint shut down research; U.S. agencies act on privacy. Washington Post. January 12, 2000:B07.
  35. The American Society of Human Genetics. Should family members about whom you collect only medical history information for your research be considered "human subjects"? March 28, 2000; Bethesda, Md. Available at: http://www.faseb.org/genetics/ashg/policy/pol-38.htm. Accessed September 1, 2000.
  36. Wadman M. US geneticists encouraged to play by the book. Nature. 2000;404:530.
  37. Meschia JF, Brown RD, Brott TG, Hardy J, Rubino FA, Atkinson EJ, O’Brien PC, Hall L. Planning a sibling pair genetics study in ischemic stroke. Neurology. 2000;54(suppl 3);A300. Abstract.
  38. Schrock CR. Permission and confidentiality in publishing pedigrees. JAMA. 1998;280:1826–1827.[Free Full Text]
  39. Report and Recommendations of the National Bioethics Advisory Commission. Research involving persons with mental disorders that may affect decisionmaking capacity. Vol I. December 1998; Rockville, Md. Available at: http://bioethics.gov/capacity/TOC.htm Accessed September 1, 2000.
  40. The Patient Self-Determination Act 42 U.S.C. §§ 1395cc(f)(1), 1396a(w)(1). Federal Register. 1995;60:33262–33294. Available at: http://hippo.findlaw.com/hippoadv.html# Anchor64566. Accessed September 1, 2000.
  41. Sunderland T, Dukoff R. Surrogate decision making and advance directives with cognitively impaired research subjects. In: Pincus HA, Lieberman JA, Ferris S, eds. Ethics in Psychiatric Research: A Resource Manual for Human Subjects Protection. Washington, DC: American Psychiatric Association; 1999:107–127.
  42. Wadman M. Geneticists oppose consent ruling. Nature. 2000;404:114–115.
  43. Levi BH. Four approaches to doing ethics. J Med Philos. 1996;21:7–39.[Medline] [Order article via Infotrieve]
  44. Fisher CB. A relational perspective on ethics-in-science decisionmaking for research with vulnerable populations. IRB: Rev Human Subj Res. 1997;19:1–4.
  45. Tong R. An introduction to feminist approaches to bioethics: unity in diversity. J Clin Ethics. 1996;7:13–19.[Medline] [Order article via Infotrieve]
  46. Rubinstein HG. If I am only for myself, what am I? A communitarian look at the privacy stalemate. Am J Law Med. 1999;25:203–231.[Medline] [Order article via Infotrieve]
  47. Sommerville A, English V. Genetic privacy: orthodoxy or oxymoron? J Med Ethics. 1999;25:144–150.[Abstract]
  48. Weijer C, Goldsand G, Emanuel EJ. Protecting communities in research: current guidelines and limits of extrapolation. Nat Genet. 1999;23:275–280.[Medline] [Order article via Infotrieve]
  49. Foster MW, Sharp RR, Freeman WL, Chino M, Bernsten D, Carter TH. The role of community review in evaluating the risks of human genetic variation research. Am J Hum Genet. 1999;64:1719–1727.[Medline] [Order article via Infotrieve]
  50. van Meter KM. Methodological and design issues: techniques for assessing the representatives of snowball samples. NIDA Res Monogr. 1990;98:31–43.[Medline] [Order article via Infotrieve]
  51. Beauchamp TL, Faden RR, Wallace RJ, Walters LR, eds. Ethical Issues in Social Science Research. Baltimore, Md: Johns Hopkins University Press; 1982:436.
  52. Edwards SJ, Braunholtz DA, Lilford RJ, Stevens AJ. Ethical issues in the design and conduct of cluster randomised controlled trials. BMJ. 1999;318:1407–1409.[Free Full Text]
  53. Hodge JG Jr, Gostin LO, Jacobson PD. Legal issues concerning electronic health information: privacy, quality, and liability. JAMA. 1999;282:1466–14671.[Abstract/Free Full Text]
  54. Gaudet D, Arsenault S, Belanger C, Hudson T, Perron P, Bernard M, Hamet P. Procedure to protect confidentiality of familial data in community genetics and genomic research. Clin Genet. 1999;55:259–264.[Medline] [Order article via Infotrieve]
  55. Bennett RL, Steinhaus KA, Uhrich SB, O’Sullivan CK, Resta RG, Lochner-Doyle D, Markel DS, Vincent V, Hamanishi J. Recommendations for standardized human pedigree nomenclature: Pedigree Standardization Task Force of the National Society of Genetic Counselors. Am J Hum Genet. 1995;56:745–752.[Medline] [Order article via Infotrieve]
  56. Protecting human research subjects: institutional review board guidebook. Washington, DC: Office for Human Research Protection; 1993:5.42–5.56. Available at: http://ohrp.osophs.dhhs.gov/irb/irb_guidebook.htm. Accessed September 1, 2000.
  57. International Committee of Medical Journal Editors. Protection of patients’ rights to privacy. BMJ. 1995;311:1272.[Free Full Text]
  58. Botkin JR, McMahon WM, Smith KR, Nash JE. Permission and confidentiality in publishing pedigrees. JAMA. 1998;280:1826–1827.
  59. Fontanarosa PB, Glass RM. Informed consent for publication. JAMA. 1997;278:682–683.[Medline] [Order article via Infotrieve]
  60. Office of Management and Budget. Uniform administrative requirements for grants and agreements with institutions of higher education, hospitals, and other non-profit organizations. OMB circular A-110. Federal Register. 1999;64:54926–54930. Available at: http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?dbname=1999_register&docid=99–26264-filed.pdf. Accessed September 1, 2000.
  61. Recommendations of the Secretary of Health and Human Services, pursuant to section 264 of the Health Insurance Portability and Accountability Act of 1996. Confidentiality of individually identifiable health information. September 11, 1997. Available at: http://www.epic.org/privacy/medical/hhs_recommendations_1997.html. Accessed September 1, 2000.
  62. Section 303(a) of the Public Health Service Act [42 U.S.C. 242a(a)]. Available at: http://www.hrsa.dhhs.gov/quality/certconf.htm. Accessed September 1, 2000.
  63. Shore D, Steinberg JA. Administrative issues and informed consent. In: Pincus HA, Lieberman JA, Ferris S, eds. Ethics in Psychiatric Research: A Resource Manual for Human Subjects Protection. Washington, DC: American Psychiatric Association; 1999:241.
  64. Earley CL, Strong LC. Certificates of confidentiality: a valuable tool for protecting genetic data. Am J Hum Genet. 1995;57:727–731.[Medline] [Order article via Infotrieve]
  65. Siblings With Ischemic Stroke Study (SWISS). Major on-going stroke trials. Stroke. 2000;31:1478.
  66. McInnis MG. The assent of a nation: genethics and Iceland. Clin Genet. 1999;55:234–239.[Medline] [Order article via Infotrieve]
  67. Gulcher JR, Stefansson K. The Icelandic Healthcare Database and informed consent. N Engl J Med. 2000;342:1827–1830.[Free Full Text]
  68. Gulcher J, Stefansson K. An Icelandic saga on a centralized healthcare database and democratic decision making. Nat Biotechnol. 1999;17:620.[Medline] [Order article via Infotrieve]
  69. Jonatansson H. Iceland’s Health Sector Database: a significant head start in the search for the biological grail or an irreversible error? Am J Law Med. 2000;26:31–67.[Medline] [Order article via Infotrieve]
  70. Annas GJ. Rules for research on human genetic variation: lessons from Iceland. N Engl J Med. 2000;342:1830–1833.[Free Full Text]
  71. Palsson B, Thorgeirsson S. Genetic databases: decoding developments in Iceland. Nat Biotechnol. 1999;17:407.[Medline] [Order article via Infotrieve]
  72. Weijer C, Emanuel EJ. Ethics: protecting communities in biomedical research. Science. 2000;289:1142–1144. [Free Full Text]



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