Understanding of the consequences to children of learning genetic risk information is based primarily on data extrapolated from adults. No studies have been done that assess the relationship between knowledge of genetic risk and a child's self-concept. We also have yet to learn how children cope with genetic information and how their coping strategies are affected by their parents' approach to coping. The purpose of this study is to describe the relationship among adolescent girl's self-concept, coping, and adjustment associated with knowledge of genetic risk of an X-linked disorder, fragile X. We will also describe strategies mothers use to help their daughters cope with this information. Using a multigroup cohort design, we will study 60 girls (15- 18 yrs) and their mothers from families with fragile X. We will enroll mother/daughter dyads with 3 categories of knowledge about the girl's genetic risk: 1) carrier, 2) noncarrier, and 3) at-risk to be a carrier. Each mother/daughter dyed will complete a number of quantitative and qualitative measures.
Our specific aims are to: 1) Describe self-concept, coping, and adjustment in adolescent girls with knowledge of their genetic risk (carrier, noncarrier, and at-risk) for an X-linked disorder. 2) To describe a) how mothers have chosen to discuss genetic risk information with their daughters, b) parental """"""""coaching"""""""" of coping behaviors, and c) their perceptions of how their daughters are managing this information. 3) Describe adolescent girls' knowledge of fragile X and how it is inherited; how they learned their carrier, noncarrier, or at-risk status; their own definitions of the words carrier, noncarrier, and at-risk; and how they think knowledge of genetic risk influences family and peer relationships. 4) To establish baseline measurements on a cohort of adolescent girls with these 3 categories of knowledge of genetic risk so that we can follow the developing self-concept in future longitudinal studies considering developmental tasks, coping behaviors, adjustment, and parental role experimentation. We hypothesize that: a. Carrier and at-risk adolescent girls will be more similar than noncarriers in self-concept, coping, and adjustment, b. Carrier and at-risk adolescent girls who place a high value on a future parental role will have a lower self-concept than those that do not.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Research Grants (R03)
Project #
1R03HD044647-01A1
Application #
6812271
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Kau, Alice S
Project Start
2004-08-05
Project End
2006-07-31
Budget Start
2004-08-05
Budget End
2005-07-31
Support Year
1
Fiscal Year
2004
Total Cost
$77,000
Indirect Cost
Name
Duke University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
McConkie-Rosell, Allyn; Heise, Elizabeth Melvin; Spiridigliozzi, Gail A (2012) Influence of genetic risk information on parental role identity in adolescent girls and young women from families with fragile X syndrome. J Genet Couns 21:59-71
McConkie-Rosell, Allyn; Del Giorno, Jacqueline; Heise, Elizabeth Melvin (2011) Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective. J Genet Couns 20:58-69
Wehbe, Ramsey M; Spiridigliozzi, Gail A; Heise, Elizabeth M et al. (2009) When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families. Am J Med Genet A 149A:1190-9
McConkie-Rosell, Allyn; Heise, Elizabeth Melvin; Spiridigliozzi, Gail A (2009) Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome. J Genet Couns 18:313-25
McConkie-Rosell, Allyn; Spiridigliozzi, Gail A; Melvin, Elizabeth et al. (2008) Living with genetic risk: effect on adolescent self-concept. Am J Med Genet C Semin Med Genet 148C:56-69