Over the past year, the Genetics Services Research Unit has completed several investigations in genetic counseling related research: One study of Bipolar disorder, an etiologically complex condition caused by genetic and environmental factors that affects 1-2% of the population aimed to understand the role of coping among adults adapting to bipolar disorder and the risk for a mood disorder in ones children. Methods: Adults were recruited from support/advocacy organizations to complete a web-based survey. Eligible participants reported having bipolar disorder and an unaffected child less than 31 years of age. Survey scales measured: illness perceptions, optimism, coping, adaptation, perception of childrens risk, and coping with risk to children. Our results found that participants were less well adapted to their condition than other populations of adults living with chronic conditions. Risks to ones children were associated with confidence in ones diagnosis (R=0.167, p=0.014), endorsing a genetic etiology (R=0-344, p<0.001), and having more affected individuals in the family (R=0.138, p=0.049). Multiple linear regression of parent adaptation included coping and optimism, and explained 55.9% of the variance (F=73.17, p<0.001). Multiple linear regression of parental coping included confidence in ones diagnosis and coping with bipolar disorder, and explained 10% of the variance (F=9.27, p<0.001). Effective coping strategies (active, social) may lead to greater adaptation to bipolar disorder and contribute to coping with risk to ones children. Confidence in ones own diagnosis affects parental perception of risk to ones children and to coping with perceived risk. Practice Implications: Clinical interventions aimed at increasing active and social coping with bipolar disorder are expected to lead to greater adaptation and more effective coping with perceived risks to ones children. Another study of parents with children with undiagnosed conditions explored the role of uncertainty. Uncertainty is a pervasive characteristic of illness. Yet little is known about the individual or situational factors that contribute to perceptions of uncertainty. This study aimed to examine the factors that contribute to perceived uncertainty among parents of a child with an undiagnosed condition. In this study, two hundred sixty six parents of a child, or children, affected by an undiagnosed medical condition for at least two years completed an electronically administered survey assessing theoretical predictors of perceived uncertainty. Multivariate linear regression analyses were used to identify the relationship of key variables to perceived uncertainty. Parents perceived control and optimism were negatively associated with uncertainty (B = -1.642, p <0.001, B = -0.300, p ≤0.01). Subjective disease severity was positively associated with perceived uncertainty (B = 1.388, p ≤0.001). Perceived control was negatively associated with two domains of uncertainty (ambiguity, p<0.001;lack of clarity, p<0.001). Our findings suggest that when parents experience greater uncertainty they feel less in control, which may lead to less effective coping and poorer adaptation. Areas where parents perceive greatest uncertainty may serve as targets for interventions to enhance perceptions of control over their childs condition. One study capitalized on the availability of new genetic technology. This study recruited 270 healthy insured adults age 25-40 from a parent research project, the Multiplex Initiative, which was conducted within a large health care system in Detroit MI, USA. All participants were offered a multiplex genetic test that assessed risk for eight conditions: type 2 diabetes, osteoporosis, hypertension, coronary heart disease, hypercholesterolemia, skin cancer, lung cancer and colorectal cancer. Data were collected from a baseline survey, a web-based decisional survey, and at the time of testing.
We aim ed to understand relationships between predictor variables and the decision to undergo testing using a conceptual model that originated from an amalgamation of the Theory of Planned Behavior and Protection Motivation Theory. Structural equation modeling identified response efficacy as a predictor (β=0.23, p<0.001) of attitudes toward multiplex genetic testing, which in turn predicted (β=0.46, p<0.001) intentions towards undergoing testing. Intentions to undergo testing were a strong predictor of testing behavior (β=0.97, p<0.001), with 17.67 fold higher uptake among those with intent to undergo testing than for those without. Overall, the tested model explained 56% of the variance in intentions and 95% of the variation in uptake. These findings support the use of variables from the Theory of Planned Behavior in modeling decision-making about a genetic test for multiple health conditions.

Project Start
Project End
Budget Start
Budget End
Support Year
8
Fiscal Year
2011
Total Cost
$831,290
Indirect Cost
Name
National Human Genome Research Institute
Department
Type
DUNS #
City
State
Country
Zip Code
Kaphingst, Kimberly A; Ivanovich, Jennifer; Lyons, Sarah et al. (2018) Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors. Transl Behav Med 8:71-79
Peay, Holly L; Biesecker, Barbara B; Wilfond, Benjamin S et al. (2018) Barriers and facilitators to clinical trial participation among parents of children with pediatric neuromuscular disorders. Clin Trials 15:139-148
Biesecker, Barbara B (2018) Genetic counselors as social and behavioral scientists in the era of precision medicine. Am J Med Genet C Semin Med Genet 178:10-14
Best, Megan; Newson, Ainsley J; Meiser, Bettina et al. (2018) The PiGeOn project: protocol for a longitudinal study examining psychosocial, behavioural and ethical issues and outcomes in cancer tumour genomic profiling. BMC Cancer 18:389
Edwards, Teresa P; Yopp, Justin M; Park, Eliza M et al. (2018) Widowed parenting self-efficacy scale: A new measure. Death Stud 42:247-253
Best, Megan; Newson, Ainsley J; Meiser, Bettina et al. (2018) The PiGeOn project: protocol of a longitudinal study examining psychosocial and ethical issues and outcomes in germline genomic sequencing for cancer. BMC Cancer 18:454
Shapira, Rachel; Turbitt, Erin; Erby, Lori H et al. (2018) Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery. Fam Cancer 17:485-493
Haakonsen Smith, Christy; Turbitt, Erin; Muschelli, John et al. (2018) Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention. J Genet Couns 27:252-262
Amendola, Laura M; Berg, Jonathan S; Horowitz, Carol R et al. (2018) The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. Am J Hum Genet 103:319-327
Lewis, Katie L; Umstead, Kendall L; Johnston, Jennifer J et al. (2018) Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial. Am J Hum Genet 102:540-546

Showing the most recent 10 out of 58 publications