Setting a public health research agenda for Down syndrome: Summary of a meeting sponsored by the Centers for Disease Control and Prevention and the National Down Syndrome Society
- 11 November 2008
- journal article
- conference paper
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 146A (23) , 2998-3010
- https://doi.org/10.1002/ajmg.a.32581
Abstract
On November 8–9, 2007, a meeting entitled “Setting a Public Health Research Agenda for Down Syndrome” was held to review current knowledge, identify gaps, and develop priorities for future public health research related to Down syndrome. Participants included experts in clinical and molecular genetics, pediatrics, cardiology, psychiatry, psychology, neuroscience, epidemiology, and public health. Participants were asked to identify key public health research questions and discuss potential strategies that could be used to address those questions. The following were identified as priority areas for future public health research: identification of risk and preventive factors for physical health and cognitive outcomes, focusing on understanding the reasons for previously recognized disparities; improved understanding of comorbid conditions, including their prevalence, clinical variability, natural history, and optimal methods for their evaluation and treatment; better characterization of the natural history of cognition, language, and behavior; identification of mental health comorbidities and of risk and protective factors for their development; identification of strategies to improve enrollment in research studies; development of strategies for conveying up-to-date information to parents and health professionals; identification of interventions to improve cognition, language, mental health, and behavior; understanding the impact of educational and social services and supports; identification of improved methods for diagnosis of and interventions for Alzheimer disease; and understanding the effects of different types of health care on outcomes. Participants strongly supported the development of population-based resources for research studies and resources useful for longitudinal studies. This agenda will be used to guide future public health research on Down syndrome. Published 2008 Wiley-Liss, Inc.Keywords
This publication has 104 references indexed in Scilit:
- New Insights into Human Nondisjunction of Chromosome 21 in OocytesPLoS Genetics, 2008
- Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome ProjectGenetics in Medicine, 2008
- Stability and Change in Health, Functional Abilities, and Behavior Problems Among Adults With and Without Down SyndromeAmerican Journal on Mental Retardation, 2008
- Adult siblings of individuals with Down syndrome versus with autism: findings from a large-scale US surveyJournal of Intellectual Disability Research, 2007
- Epidemiology of Down syndromeMental Retardation and Developmental Disabilities Research Reviews, 2007
- Survival in infants with Down syndrome, Metropolitan Atlanta, 1979-1998The Journal of Pediatrics, 2006
- Stability and change in cognitive ability over the life span: a comparison of populations with and without Down's syndromeJournal of Intellectual Disability Research, 2005
- The routine and the traumatic in prenatal genetic diagnosis: does clinical information inform patient decision-making?Patient Education and Counseling, 2005
- Contrasting profiles of language development in children with williams and down syndromesDevelopmental Neuropsychology, 1997
- Psychosocial adaptation of fathers of children with autism, down syndrome, and normal developmentJournal of Autism and Developmental Disorders, 1992