Literature DB >> 19006076

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.

Sonja A Rasmussen1, Nedra Whitehead, Sarah A Collier, Jaime L Frías.   

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.

Entities:  

Mesh:

Year:  2008        PMID: 19006076     DOI: 10.1002/ajmg.a.32581

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  19 in total

1.  Down syndrome: national conference on patient registries, research databases, and biobanks.

Authors:  Mary Lou Oster-Granite; Melissa A Parisi; Leonard Abbeduto; Dorit S Berlin; Cathy Bodine; Dana Bynum; George Capone; Elaine Collier; Dan Hall; Lisa Kaeser; Petra Kaufmann; Jeffrey Krischer; Michelle Livingston; Linda L McCabe; Jill Pace; Karl Pfenninger; Sonja A Rasmussen; Roger H Reeves; Yaffa Rubinstein; Stephanie Sherman; Sharon F Terry; Michelle Sie Whitten; Stephen Williams; Edward R B McCabe; Yvonne T Maddox
Journal:  Mol Genet Metab       Date:  2011-07-13       Impact factor: 4.797

2.  Modeling travel impedance to medical care for children with birth defects using Geographic Information Systems.

Authors:  Eric M Delmelle; Cynthia H Cassell; Coline Dony; Elizabeth Radcliff; Jean Paul Tanner; Csaba Siffel; Russell S Kirby
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2013-09-02

3.  Functional genomic analysis of amniotic fluid cell-free mRNA suggests that oxidative stress is significant in Down syndrome fetuses.

Authors:  Donna K Slonim; Keiko Koide; Kirby L Johnson; Umadevi Tantravahi; Janet M Cowan; Zina Jarrah; Diana W Bianchi
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

4.  Specialized Pediatric Growth Charts For Electronic Health Record Systems: the example of Down syndrome.

Authors:  S Trent Rosenbloom; Tracy L McGregor; Qingxia Chen; Angel Qi An; Stephanie Hsu; William D Dupont
Journal:  AMIA Annu Symp Proc       Date:  2010-11-13

5.  Patterns of change in nonverbal cognition in adolescents with Down syndrome.

Authors:  Marie Moore Channell; Angela John Thurman; Sara Teresa Kover; Leonard Abbeduto
Journal:  Res Dev Disabil       Date:  2014-08-09

6.  Factors associated with the timeliness of postnatal surgical repair of spina bifida.

Authors:  Elizabeth Radcliff; Cynthia H Cassell; Sarah B Laditka; Judy K Thibadeau; Jane Correia; Scott D Grosse; Russell S Kirby
Journal:  Childs Nerv Syst       Date:  2016-05-14       Impact factor: 1.475

7.  Women's knowledge, attitudes, and beliefs about Down syndrome: a qualitative research study.

Authors:  Denise M Levis; Shelly Harris; Nedra Whitehead; Rebecca Moultrie; Kara Duwe; Sonja A Rasmussen
Journal:  Am J Med Genet A       Date:  2012-04-27       Impact factor: 2.802

8.  Hospitalizations among people with Down syndrome: a nationwide population-based study in Denmark.

Authors:  Jin Liang Zhu; Henrik Hasle; Adolfo Correa; Diana Schendel; J M Friedman; Jørn Olsen; Sonja A Rasmussen
Journal:  Am J Med Genet A       Date:  2013-02-12       Impact factor: 2.802

9.  Racial/ethnic differences in hospital use and cost among a statewide population of children with Down syndrome.

Authors:  Taletha Mae Derrington; Milton Kotelchuck; Katrina Plummer; Howard Cabral; Angela E Lin; Candice Belanoff; Mikyong Shin; Adolfo Correa; Scott D Grosse
Journal:  Res Dev Disabil       Date:  2013-07-26

10.  Growth Charts for Children With Down Syndrome in the United States.

Authors:  Babette S Zemel; Mary Pipan; Virginia A Stallings; Waynitra Hall; Kim Schadt; David S Freedman; Phoebe Thorpe
Journal:  Pediatrics       Date:  2015-11       Impact factor: 7.124

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