genetic research pediatric nursing: the state of the science janet k. williams, phd, rn, faan mnrs...
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Genetic ResearchPediatric Nursing: The State of
the Science
Janet K. Williams, PhD, RN, FAAN
MNRS 2009
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Genetic Research: Pediatrics
• Genetic discoveries
• Research issues
• Research and children
• Knowledge gaps
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Genetic Discoveries
• Traditional categories– Chromosomal abnormalities– Monogenic- Mendelian disorders– Multifactorial/polygenic disorders– Mitochondrial disorders
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Genetic Discoveries
• Single gene– Mutations in one gene- ex. Cystic fibrosis
• >1600 known mutations• 5 mutation classes according to effect on CFTR
protein• Some mutations associated with clinical
manifestations, others less predictable
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Genetic Discoveries
• Disorders in genome architecture-Mutations associated with dysmorphic syndromes• Sporadic inheritance• ex-microdeletion syndromes- DiGoerge, syndrome,
Williams syndrome
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Genetic Discoveries
• Insights into taxonomy of human disease– Distinct forms of a condition- ex.diabetes
mellitus– Labeling account for mechanisms and
pathways of a disease rather than symptom description
– May resolve questions relating to variable symptoms, progression, response to therapy
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Genetic Discoveries
• Genome wide association studies– Scan genome [not just the coding regions] to
generate hypotheses about genome regions associated with specific phenotypes
– Allow study of pathways from gene expression to common diseases or traits
– Association accepted when• Large effect• Replicated• Made sense
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Genetic Discoveries
• GWAS- limitations• Small odds ratios• May need hundreds of associations needed to
account for heritability of a common disorder• Unknown environmental factors
• Current pediatric examples (PubMed)• GWAS and ADHD (ages 5-17, and parents)• GWAS and bone mineral density in childhood
(N=1518children in longitudinal child health study)
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Genetic Discoveries
• Areas of relevance to children’s health – in press issue Journal of Pediatric Psychology
• 6 papers- parent decision making with new genetic testing, health care delivery systems, research on behavioral phenotypes (eating disorders), parental attitudes about genetic testing of children
– In press issue Journal of Pediatric Nursing• 3 papers- acquisition of concept of genetics,
therapy response in cancer and mental illness
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Genetic Discoveries
• Areas of relevance to child health– In press issue Biological Research for Nursing
• Prior articles include clinical diagnoses for which children may be at risk based on family history- ex. cardiac arrythmias
– 2008 volume 17 special issue Psycho-oncology
• 14 papers-decision making, family communication, health behaviors
• Excellent future research discussion
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Genetic Discoveries
• Genetic ‘information’-clarify terminology– Can refer to a person’s DNA and the
instructions in that DNA– Can refer to what is communicated by health
professionals regarding one’s risk for disease or risk to have offspring with a disease
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Genetic Discovery Resources
• UI online courses– http://www.continuetolearn.uiowa.edu/ccp/de/regform.htm
• Postdoctoral fellowships– T32 funded- UI, U Pittsburgh, NIH
• NINR SGI– http://www.ninr.nih.gov/Training/TrainingOpportunitiesIntramural/
SummerGeneticsInstitute/
• NHGRI Summer Workshop in Genomics– http://www.genome.gov/10000217
• ISONG annual conference Oct 16-19– http://www.isong.org/
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Funding opportunities
• NINR
• NHGRI/ELSI
• ANF
• Sigma Theta Tau chapters
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Research issues
• Categories of nursing research in genetics and pediatrics– Studies are about children but children are not
the subjects– Children are members of families in studies– Children are subjects in studies
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Research issues
• Theoretical/conceptual frameworks– Clinical problem– Theoretical relevance
• Research purpose– Response to having specific genetic
characteristics, family issues• Ex. Communication of risk, clinical decision
making, quality of life, emotional status, health behaviors
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Research issues
• Human subjects concerns– Protection of children as a vulnerable
population– Sensitive topics– Parental permission, children assent
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Research issues
• Population definition– Genetic characteristics of population as
inclusion criteria• Genetic heterogeneity in diagnosis?
• Methods– Appropriate measures for age groups– Sample size with rare conditions
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About children
• Metcalfe, 2009– Role of genetics- population clients at end of life– Framework- professional practice quality evaluation– Purpose- nurse perceptions of importance and
confidence in caring for children with genetic conditions
– Sample- n=100 hospice nurses in UK– Methods- questionnaire with 4 scenarios– Findings-1 child/month, important, supporting child
and family is demanding, nurses need support
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Study of family issue
• Clarke, 2008– Role of genetics- population women with BRCA1/2
mutation– Framework-clinical disclosure– Purpose-communication of risk information to offspring– Sample- 24 women with BRCA1/2 mutation in a
therapy group, 71% with children ages 2-30,45% with prior cancer diagnosis
– Methods-grounded theory approach– Findings- predisclosure, disclosure, impact of
disclosure phases
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Study of family issue
• Norris, 2009– Role of genetics- population women with BRCA1/2
mutation– Framework- clinical response to risk– Purpose- family context of communication and
decision– Sample- 5 women with BRCA1/2 mutation, 3
husbands, 6 daughters, 3 sons (ages 15-25)– Methods- descriptive qualitative– Findings- disclosure varied, with some uncertain how
or when, children learn informally of risk
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Study of children
• Christian, 2006– Role of genetics- population children with CF– Framework-Self management-development– Purpose- intervention for day to day disease management– Sample-n=116 children ages 8-12 with mild CF– Methods- randomized. E=finding out about dx, explaining
CF related differences, teasing, keeping up with peers. Home visit and small group.
– Findings E > C scores on impact of illness, < lonely, >global self worth. Functional health and physiologic health n.s.
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Study of children
• Iles-2008– Role of genetics- population youth with CF– Framework- transition services and development – Purpose program evaluation in transitional clinic– Sample n=50,13-24 year old– Methods-interview, some completed a QOL measure– Findings- nurses were like family- hesitant to share
worries about future with nurses
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Study of family issue
• Gallo, 2008– Role of genetics-population children with single gene
disorders– Framework- clinical parental concerns– Purpose- parental concerns re privacy, disclosure,
employment, insurability– Sample- n=142 parents in 86 families, children with
scd, cf, pku, nf, hemoplilia, thalassemia, Marfan syndrome
– Methods- semi-structured interview, thematic analysis– Findings- less concern re privacy than other topics
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Study of children
• Giarelli, 2008– Role of genetics- population youth with MS, parents, hcp
– Framework-Transition to self management
– Purpose-identify basic psychologic issue in transition to self management
– Sample- n=37 children with MS ages 14-21, 16 young adults with MS ages 22-34, 39 parents (20 w MS), 16 hcp
– Methods-questionnaires and interviews
– Findings- becoming fit and fitting in- a survival goal. changes in knowledge, attitudes, behavior by all
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Study of children
• Sparbel, 2008– Role of genetics- population teens with
parent/grandparent with HD– Framework- development– Purpose-explore experiences of teens living in HD
families – Sample- n=32 teens ages 14-18– Methods-descriptive qualitative, focus groups– Findings- watching & waiting, alone in the midst of
others, family life is kind of hard, having to be like an adult
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Study of children
• Williams, in press– Role of genetics- population teens with
parent/grandparent with HD– Framework- Caregiving, development0– Purpose- examine caregiving by teens– Sample- n=24 teens ages 14-18– Methods-descriptive qualitative, focus groups– Findings- tasks and responsibilities, & subjective
burden similar to adult cg; cg in context of personal risk, & decisional responsibility unique to teens
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Summary
• Genetic/Genomic pediatric nursing research – Interdisciplinary body of knowledge– Interdisciplinary research teams– Clear definition of genetic aspects of population– Clinical vs. community populations– Multiple site data collection for diversity and sample size– Programs of research extending from descriptive to
experimental designs– Citations available upon request