Over the past 30 years, variants in the genes SNCA, PRKN, LRRK2, GBA1, and others, have been recognized as important to the etiology of Parkinson disease (PD)1. In approximately 10% or more of patients with PD in North America, testing will uncover a major pathogenic variant (manuscript in preparation; LC et al). When inherited, the disease can be autosomal dominant, often with age-related reduced penetrance and, predominantly, later onset, or it can be autosomal recessive, caused by gene variants that are mostly fully penetrant leading to early or young onset1. In addition to variants in the major genes listed above, at least 90 PD risk loci have been discovered by genome-wide association studies (GWAS) that contribute to heritability2.

In the United States (U.S.), genetic testing for PD is widely available through commercial companies, including direct-to-consumer (DTC) testing, and may be offered at no cost through research studies and biopharma-sponsored testing programs3. Research studies like PD GENEration, Parkinson’s Progression Markers Initiative, and others are actively enrolling individuals with PD, with the goal to expand genetic testing, making it more accessible, including outside the U.S4. Increasingly neurologists and other health care providers (HCPs) may face questions about PD genetics, genetic test results, and risks. Independently, patients with a family history of PD or individuals, just curious about their risks for adult-onset conditions, may also seek this information.

Genetic communication about PD may be perceived as challenging due to its complex inheritance, yet HCPs can gain confidence in this area by learning basic PD genetics concepts and how to access resources to aid them in risk assessment and counseling, including resources for finding genetic professionals. We provide recommendations for PD genetic risk communication based on our experience of providing genetic counseling to over 10,000 individuals, both affected and unaffected, as part of several large national PD studies (NCT04477785, NCT04994015). Highlighted as well, is the importance of being aware of genetic advances, working collaboratively with HCPs with genetics expertise, and when relevant, referring directly to genetic counselors who are familiar with PD. This is due to the complexities of risk assessment, nuances of risk communication, genetic testing considerations, and ethical issues related to this disorder as outlined in this article. Although this article is targeted primarily to neurologists, especially those working with patients with movement disorders, some of the high-level points and takeaways may be of use to general practitioners. Advanced topics, illustrative cases, and risk calculations may be especially beneficial to PD specialists working in the field.

PD genetic risk communication put into action

Setting the stage

Genetic risk communication for PD, as part of formal genetic counseling, can occur in different settings, for various indications—clinical or research, and for predictive, diagnostic, or prenatal reasons. Regardless of the setting, genetic counselors are trained to adhere to the following best practices for risk communication5,6.

  • Use of plain language

  • Provide only important key elements (less is more)

  • Keep the discussion interactive

  • Avoid framing biases (giving both the positive and negative views)

  • Avoid qualifiers such a low, slight, or high risk

  • Use absolute rather than relative risks

  • Draw attention to the fact that a risk may change over time

  • Compare risks to disease prevalence or other baseline comparators

  • Consider the use of visual aids especially for those with low numerical literacy

Genetic counselors may see individuals with PD concerns in genetics, prenatal, or neurology clinics, and through PD research initiatives. Due to their expertise, they may also see asymptomatic individuals seeking predictive genetic testing. In contrast, physicians will see mostly symptomatic patients with manifest disease, in a neurology setting, where testing fits into the diagnostic category. Increasingly, they may see individuals with prodromal disease who do not yet meet clinical criteria for a diagnosis. This may be especially true as biomarkers are developed and enter the clinical arena. A distinct and separate group—at-risk, asymptomatic individuals—may be interested in baseline evaluations or simply consultations and may be armed with genetic test results they have procured through DTC testing or through relatives in their family who did genetic testing.

For individuals with PD, the genetics discussion in the neurology setting will center on implications to their care, but may quickly turn to their family members, as has been our experience, as well as that of others7. Although risk discussions in neurology are common, genetic risk discussions uniquely shift the unit of care from the patient to the family, often requiring a different approach. This may be especially true when encountering individuals from other cultures where there is a strong emphasis on the family unit8. One of the more common questions we are asked by research participants receiving PD genetic testing is what the risk of their children (or other relatives) is for developing the disorder. In the following sections we provide guidance on addressing this and similar questions including those related to causation.

Risk assessment comes first

Before a provider can provide accurate genetic risk communication, a genetic risk assessment needs to happen. Reviewing a patient’s medical and family histories is the first assessment step before embarking on genetic and risk discussions. A family history that is targeted for neurological conditions that includes two to three generations can be an important risk assessment tool. Ancestry can be another relevant inquiry in PD, since PD variants can vary across populations affecting risk1,4. For instance, obtaining family history intake that includes Lewy body dementia may indicate the potential for GBA1 variants, especially in a family that is Ashkenazi Jewish1,4. In addition, it can be helpful to inquire if a patient or someone in the family has had genetic testing and if results are known. It is not uncommon for GBA1 testing to have been done in a prenatal setting in other relatives as part of carrier testing for Gaucher disease, and positive Gaucher results may not be understood to be connected to the risk of developing PD9. To aid in family history intake, short, targeted family history intake questionnaire forms have been developed by researchers for various PD projects and can be HCP- or patient-facing10.

A key concept to consider while performing risk assessment is whether the PD is of early or late onset. Given that there are different genetic etiologies and inheritance patterns for early (<50 years) and late-onset PD (≥50 years), age of onset (ideally confirmed diagnosis) should be ascertained. When disease onset is of young onset (30s or younger), this can be due to major genetic factors that are fully penetrant by early or mid-adulthood and, typically, inheritance is autosomal recessive. This contrasts with late-onset disease, which most often is due to a complicated interplay between multiple genes, some rare but mostly common and of variable effect size, as well as environmental factors; thus, it follows a multifactorial pattern of inheritance with higher cumulative risk as age progresses. Those who fall between age ranges can represent either category but often have an earlier manifestation of a late-onset form of PD, sometimes observed with GBA1 or LRRK2 forms of PD7,11.

Targeted genetics education without testing

Following risk assessment, targeted education about PD genetics can be provided based on patient background and needs. The following can be briefly explained without knowledge of patient genetic status:

  • Basic genetics concepts

  • Inheritance patterns

  • Options for genetic testing

  • Potential value of testing

Specific talking points can be used, depending on the situation (Table 1), as well as visual aids explaining multifactorial inheritance (Fig. 1) and other forms of inheritance, when relevant. Estimates for relative risk for PD based on degree of relationship to the affected (including up to third degree) are available, ascertained from North American data12. In general, the lifetime risk for PD to a first-degree relative of someone with late-onset PD is doubled (Table 2). Lastly, interest, understanding, and perceptions of this information by the patient can be explored.

Table 1 Talking points to share with patients with late-onset Parkinson’s disease (PD).
Fig. 1: The jar and shapes can help demonstrate the multifactorial model of inheritance to patients.
figure 1

Sample statement: Environmental factors (blue triangles) increase over time and can reach a disease threshold (top of jar). Genetic vulnerability (yellow beads), with which we are born, contributes to the jar, but is mostly static. Lifestyle habits such as moderate aerobic exercise may add “protective rims” to make the jar taller, raising the disease threshold.

Table 2 Quick view for risk counseling.

Genetic testing considerations

PD genetic testing, if pursued or already performed, can inform and fine-tune the risk assessment and education discussed above. Testing, whether narrow or broad, will vary in the usefulness of information provided. The most encountered test will be the gene panel that may include a handful to many genes and variants, more or less established as linked to PD3. Many panels, though not all, will include variants associated with both early and late-onset forms of PD. Ideally, for PD, the testing will include deletion and duplication analysis in addition to the latest sequencing technology. Importantly, full sequencing of the GBA1 gene should be performed, especially in those who are of Ashkenazi Jewish ancestry3,4. The most popular DTC tests available in the U.S. for PD tend to be targeted to two major variants, one in GBA1 the other in LRRK2 ( Research testing options can greatly differ, depending on the goals of the study4. Genetic testing programs will vary in the release of variants of uncertain significance (VUS), which can complicate risk counseling, causing confusion to both patient and provider. Comprehensive and newer genetic tests, including polygenic risk scores for PD that combine minor gene variant effects, will likely make their way increasingly into the clinical arena, adding to testing options and information available for counseling13. In addition to the scope and techniques of genetic testing, the ethnicity or ancestry of the individual being tested will determine how informative results are3,4.

A best practice for genetic testing that directly impacts risk counseling includes first testing the person with the disorder in the family. This allows for clarity in the meaning of results for the patient and other unaffected relatives who may desire testing. When testing is needed from an affected person in the family not especially interested, pressure on decision-making and ethical dilemmas can occur, which will be discussed later in another section. Fully informed consent for genetic testing involves pre-test education and discussion of risks, benefits, and limitations. It is a process and not just a signature on a consent form. There can be challenges and specific considerations for obtaining informed consent when there is cognitive impairment—not uncommon in PD, health literacy limitations, spoken-language differences, psychological stress, and other factors5. A full discussion of considerations for genetic testing for PD as relates to risk assessment and communication are outside the scope of this paper, but multiple publications are available to which the reader can refer4,7,14.

Education and risk communication following genetic testing

With genetic data provided from testing, risk estimates considered prior to testing can be revised and recalculated. With the addition of genetic testing, risk counseling becomes more precise and nuanced (Table 2). A corollary is that genetic test results can be personalized and refined with gathered histories on the patient. When estimating genetic risks using test results, it can be helpful to place them within the context of an individual’s age (risk increases over time for PD), ancestry (e.g., European vs Asian, Ashkenazi Jewish), and family history (both maternal and paternal)7.

Residual PD risk due to negative genetic test results

In both sporadic and familial forms of PD, in most populations, genetic results for major variants are usually negative11. Risk communication is still important for negative results since misperceptions may occur15. One commonly held misperception of patients is that a negative result on genetic testing means that there is not a genetic contribution or, even, that they do not have PD. Patients may infer that their children will not be at risk to develop disease. This will require clarification, with the reminder that typically PD is caused by multiple factors, including minor or unknown genetic ones not currently tested. An estimation of residual risk to relatives and asymptomatic patients following negative genetic testing can be provided based on available clinical and family histories and the scope of testing performed (refer to Table 2/Case 1 in Supplement). A reminder to the patient regarding how a PD diagnosis is made can also be helpful.

Negative genetic test results when the testing is narrow in scope or lacking can falsely reassure families. Another important caveat to communicate is that genetic data for PD have been collected mostly on European populations16. The result is that PD genetic test results and lab interpretations that appear “normal” may not be as informative for those from non-European populations.

Monogenic gene variants and PD risk

PD genetic test results, when positive, will commonly involve the major genes LRRK2, GBA1, and PRKN11. For these three genes and the other established PD genes, principles of monogenic inheritance will apply (Table 3) with some exceptions such as reduced penetrance and variable expressivity. Being familiar with these concepts (Table 4) and the various types of inheritance and associated risks—autosomal dominant, autosomal recessive, multifactorial and, less so, X-linked—will be important for risk assessment and communication. When a gene variant does not follow a classic Mendelian pattern of inheritance, featuring reduced penetrance, risk estimates for a condition are most often probabilities. Typically, population or empirical data are the beginning point to consider for an a priori genetic risk. For neurodegenerative disorders like PD, these are typically observed data in a population across an interval of time, and often will be expressed as a cumulative risk of disease to a specific age17.

Table 3 Established monogenic PD genes (ordered alphabetically and by inheritance)a.
Table 4 Important genetic terms for PD risk communication.

Another consideration is that variants in the same gene may have a different penetrance1. The use of up-to-date, accurate population data for a specific gene variant is vital for calculating risk estimates. When using penetrance data, note that data ascertainment, sample sizes, and population biases may erode quality of the data17. Another limitation of the data is that it is not entirely clear how various demographic features modulate PD genetic risks such as ancestral background or gender. Another limitation is that some penetrance data, especially for GBA1, are based on case-control studies providing only odds ratios (ORs). If used, ORs and relative risks (RR) should be converted to absolute risk estimates for the patient18.

Family histories are invaluable in that they may provide additional clues as to how variants have been expressed in a particular family, add insight into the potential for other shared factors, providing personalized risks. As of yet, risk calculators for neurodegenerative disorders such as PD are not widely available for clinical use to combine all the different factors, genetic and non genetic, that contribute to an individual person’s overall risk for disease18. Various algorithms such as PREDICT-PD and prodromal criteria have been developed19,20, focusing on early clinical features of PD, which may inform counseling as the tools become more refined and are able to incorporate more genetic data including data from non-European populations.

Complexities related to types of positive genetic test results

PD genetic test results can be complicated, depending on the type of result. For instance, there has been the observation that carriers of autosomal recessive variants may have a slightly increased risk for later-onset PD; however, research continues in this area and conclusions are mixed21,22. In the meantime, it can be conveyed that there is not a definite answer regarding risk to those carrying an autosomal recessive PD gene variant, but, if confirmed, is likely of low magnitude and of later onset.

Generally, when two pathogenic PD variants are identified, this is consistent with autosomal recessive inheritance. However, another complexity, similar to that of other autosomal recessive genetic disorders, is whether the variants are on the same (cis) or different (trans) chromosomes, since this is not typically revealed by genetic testing. Determining the phase, cis or trans, is important since a cis phase would mean that both variants are on the same chromosome and inherited from one parent, versus trans where each chromosome in the pair would have a variant, with one variant copy inherited from each parent. If phase of the variants cannot be readily determined by clinical information, this would be important to clarify with additional testing of parents/other affected family members since it will impact the recurrence risks provided.

Another complex type of PD result is copy number variants such as rare gene duplications and triplications of the SNCA gene and deletions and duplications commonly observed for the PRKN gene. Providers may be less familiar with these types of gene variants; however, these unique variants follow the same Mendelian rules for monogenic disease1.

Finally, the vast number of pathogenic gene variants (400+), and the potential for recombinant alleles, reported for the GBA1 gene pose their own challenges to risk communication, requiring special attention. Some of these rarer variants have limited empirical data from which to base risk estimates7. For most GBA1 variants, there is the association with Gaucher disease, an autosomal recessive lysosomal disorder that can manifest in childhood or be present unknowingly in mildly expressing adults and be amenable to treatment9. For a few GBA1 variants, some quite commonly carried, such as the E326K variant, this is not the case: Gaucher disease is not caused by carrying biallelic GBA1 variants, even though the variant is thought to be associated with PD23. This additional aspect of the GBA1 gene, namely its association with Gaucher disease, impact on reproductive risk, and potential medical action, requires added time to discuss and creates complexity to risk communication9.

Risk communication resources for the clinician

PD variant penetrance data and interpretation for monogenic PD genes

In Table 2, we provide a quick view of general risk statements for the most encountered situations in various PD settings. In addition, other useful resources for PD risk estimates can be found at GeneReviews, an online database that provides up-to-date summaries for specific PD genes, as well an overview. In addition to these resources, HCPs can now access estimates of PD genetic risk, based on current and reviewed published data, in one location, the Disease Penetrance Table (, developed by PD genetic counselors at Indiana University14. In this penetrance table, the data for each variant type are paired with general statements that can be used in PD risk communication. This information can be used for counseling individuals at risk and shared with affected patients who have questions about risks to offspring, siblings, parents, and other close relatives. It can be discussed with the patient the importance of sharing genetic risk information with key relatives. A family sharing handout that is patient–facing is available for downloading from this website.

It was mentioned, earlier, that visual aids can be instructive when communicating genetic risk. When considering the use of visual aids to enhance risk counseling, it is suggested the number and type of visual aids used should be carefully considered. For example, it is observed that icon arrays can be helpful in displaying absolute risks. Various online sites offer free access to templates to create risk communication graphics. A combined table of resources for PD risk assessment and communication, especially as relates to positive gene test results, are provided for the clinician for easy access (Table 5).

Table 5 Parkinson’s disease (PD) genetic risk communication resources for the clinician.

Specific cases, presented below, are provided for the clinician that further illustrate risk assessment and risk communication for various scenarios in the genetic counseling session:

The genetics referral

When dealing with complex genetic issues of the affected patient, asymptomatic patients, relatives at risk, prenatal issues, or complicated genetics test results, a referral to a genetics expert is warranted. This is also the case if the risk discussion is beyond the comfort level of the HCP. It is important to have established professional relationships with genetic counselors on site or locally, so that when these indications do arise, a genetics referral can be easily made (Table 5). Genetic counselor specialties that will likely be most useful to PD patients and their families are as follows: neurology, adult genetics, general genetics, and prenatal centers for individuals planning families. Alternatively, providers can make use of remote genetic counseling services that are expanding nationwide and globally, offer services regardless of residence, and potentially affordable.

Ethical considerations of genetic testing and risk communication

There are several different ethical issues that can arise with neurogenetic conditions involving testing, risk assessment and communication5,6. It should be stressed that the core ethical considerations (e.g., autonomy, beneficence) in genetic counseling are generally approached from predominantly Western cultural values and that other cultures may have different views, especially as it relates to the patient26. Ethical issues can arise when there are conflicting views between the patient and at-risk relatives (e.g., children, siblings) about genetic testing and with patients and providers when requesting genetic testing that is contrary to guidelines/standards of care (e.g., requests to test minors or a pregnancy when it will not impact reproductive decisions). Clinicians can find guidance on these issues looking to literature developed for predictive genetic testing for Huntington disease27, in existence since the 1980s, and adapted for other hereditary neurological conditions. This guidance emphasizes that it should be the patient’s decision to be tested and there should not be coercion. This means that the patient’s decision about testing needs to be respected and the patient should not be pressured to be tested or not tested.

There can be conflict and potentially ethical issues when a patient’s desire to test or not test is contrary to the desires of other at-risk family members. It can be challenging to determine whose rights take precedence when weighing a patient’s right to know or not know28. For at-risk family members, their ability to be tested may depend on knowing whether an affected family member has an identifiable pathogenic variant. DNA banking is an option that respects an individual’s right not to know, yet, at the same time, allows an individual’s DNA to be preserved for future testing.

Although it is recommended that neurologists refer for predictive testing, it can be helpful to be aware of published guidelines including those for Huntington disease genetic testing27, and statements from professional organizations, including the American Academy of Pediatrics and the American College of Medical Genetics25, the American Society of Human Genetics29 and the National Society of Genetic Counselors, who have agreed that predictive genetic testing for adult-onset conditions should not be done on minors. With adult-onset neurological conditions, there is no clinical indication to test children since results would not impact their medical care in childhood. Minors are also not tested to preserve their autonomy and right to an open future. Furthermore, testing a pregnancy for an adult-onset condition should not be done if the results will not impact reproductive decisions since continuance of a positive pregnancy would be akin to testing a minor30. As expected, there has not been a strong interest in prenatal or preconception testing for PD documented. Thus, providers should avoid making assumptions about a patient’s interest in pursuing prenatal or preconception testing for PD, and this should be explored on a case-by-case basis with appropriate referrals to genetics professionals if considering this testing.

Patients with PD often express concerns about insurance coverage and the potential of genetic discrimination. The Genetic Information Nondiscrimination Act (GINA) is an important U.S. law passed in 2008 that provides protection from health insurance and employment discrimination related to genetic test results and family history. However, there are some significant limitations in protections; genetic test results may affect obtaining life, disability, and long-term care insurance. There are online resources available for talking about the risk of genetic discrimination, key points to convey, and information that that can be downloaded and provided to patients (Table 5). Although these are important considerations for asymptomatic individuals, it can be explained that they are less relevant for those who are already diagnosed with the condition.

While, ultimately, genetic test results are the patient’s private and confidential information, the fact that results could impact the risk provided to other family members and potentially have implications for their care needs to be conveyed. This is especially true for GBA1 variants and autosomal recessive PD variants, such as PRKN, that are potentially medically actionable given the reproductive implications and, in the case of GBA1, the association with Gaucher disease. In the event that a patient refuses to disclose to family members their diagnosis of PD and genetic test results (if tested), the healthcare provider does not have a duty to warn at-risk family members but does have a duty to inform the patient about potential risks to their relatives31.

Another ethical consideration is whether there is a duty to recontact when new genetic tests become available, impacting risk assessment and counseling. Advances will continue to be made in understanding the genetics of conditions like PD and genetic test results that may be uncertain for now. Especially for patients with VUS or negative genetic test results, it will be important to emphasize the importance of recontacting their genetics clinic and/or healthcare provider to obtain updates or determine whether newer or additional genetic testing should be considered. The American College of Medical Genetics and Genomics issued a statement that the duty to recontact to learn about genetic advances needs to be a shared responsibility and is not solely the responsibility of the healthcare provider32. If new genetic information is obtained by the individual or their family, it would be important to emphasize the sharing of such information so that updates of prior risk estimates can be provided.

A last important point, considering the principles of equity and justice, is that, historically, mostly European populations have been included in genetic and genomic databases. Lack of inclusion of other ancestral groups has limited our knowledge about the genetic contribution to PD in those underrepresented. Thus, genetic test results and interpretations may have reduced accuracy and utility across certain populations33. This should be acknowledged by clinicians as risk assessment, communication, and counseling on PD genetics are provided and testing becomes more widespread for PD. Hopefully, the work performed by GP2 and others will begin to address these gaps in PD genetic data, allowing for genetic information to be useful and relevant for underserved and underrepresented populations.

In conclusion we have established that genetic risk communication is different than other types of risk communication in the neurology setting, and this applies to PD. Genetic data are not confined to the individual patient but ripple out to others in the family. Questions can arise surrounding the risk of occurrence and recurrence of PD in individuals and families. Emotionally charged questions such as “Do I need to worry about my children getting this?” deserve good risk communication and triage, regardless of whether a person has received genetic testing.

We have illustrated how PD genetic test results can be complex, featuring both autosomal recessive and autosomal dominant gene variants, including many that act within a multifactorial/complex mode of inheritance. Additional complexities are the need to consider copy number variants and recombinant alleles, reduced penetrance, and the association of GBA1 variants with Gaucher disease. We recommend that HCPs first assess their comfort level with PD genetics and risk communication. In addition, they will need to assess the needs and background of the patient as it relates to risk information. If providing their own risk counseling, providers can adapt best practices as outlined in this article, using resources developed by experts in the field. We recommend adapting risk estimates to medical and family histories, demographics, and other risk assessments, for a personalized touch. It is important for HCPs to acknowledge the gap in genetic data and interpretation for non-European populations. Finally, neurologists will benefit from collaborating with HCPs trained in PD genetics, as well as genetic counselors, as they navigate discussions surrounding PD genetics and risk.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.