Down syndrome early childhood omics, deep phenotyping, and epidemiology in texas: decode IT cohort

Active Cooperative Agreement Awarded Last action

Award ID
U01HD116485
Recipient
Awarding agency
Obligated
$4,006,991

Award facts

Assistance listing
93.310 Trans-NIH Research Support
Completion date 45% complete
Funding agency
Office of the Director National Institutes of Health, Department of Health and Human Services
Place of performance
Atlanta, GA 30322, USA

Award details come from USAspending.gov.

Description

Abstract
/summary down syndrome (DS) is one of the most common genetic syndromes, with a birth prevalence of 1 in 700 that has been increasing in recent years. Children with DS encounter many adverse health outcomes including 1) structural birth defects - which are associated with significant morbidity and mortality; 2) abnormal hematopoiesis - which infers a 20-fold increased risk of acute leukemia; and 3) neurodevelopmental disorders - which significantly impact functional independence and quality of life. However, there are important gaps in our understanding: 1) inter-individual variability exists among children with DS in relation to these phenotypes that cannot be fully explained; 2) the natural history of these phenotypes among children with DS has not been comprehensively evaluated, limiting health supervision guidelines and targets for intervention; and 3) children with DS, particularly those from underrepresented minorities, have often been excluded from participation in research that could improve their outcomes. In this application, we seek to address these gaps in knowledge. Specifically, in response to RFA-OD-24-003 (down syndrome cohort research sites for the include project), we propose to leverage the texas birth defects registry (tbdr) - one of the world's largest and most diverse population-based active birth defects surveillance systems - to develop the down syndrome early childhood omics, deep phenotyping, and epidemiology in texas: decode IT cohort. As part of decode IT, we will recruit an ethnically and geographically diverse birth cohort of children with DS with the objectives of 1) conducting deep phenotyping and 2) collecting biospecimens for omics assessments. Our research team is uniquely poised to develop this population-based cohort of children with DS. We bring expertise in DS research and recruitment (lupo and rasmussen), DS-related birth defects (agopian), DS-associated hematopoiesis (rabin), and neurodevelopment in children with DS (jacola). Furthermore, we have an extensive record of collaborations. Therefore, we propose the following aims: 1) recruit children with DS to the decode IT cohort; 2) conduct deep phenotyping on children with DS enrolled in decode IT - with a particular emphasis on structural birth defects, hematopoietic development, and neurodevelopment; 3) prospectively collect biospecimens on children with DS enrolled in decode IT for biomarker and omics studies. Impact: through decode IT we will establish a large population-based cohort (n=1,000 children with DS) that will provide the necessary foundation for propelling our understanding, prediction, and prevention of associated adverse health outcomes in children with DS.

Transactions

Action Obligated Date
Amendment $2,011,187
Amendment $0
Amendment $0
Amendment $1,661,792
Amendment -$1,878,147
Amendment $1,661,792
Amendment -$1,878,147
Amendment $1,661,792
Amendment -$1,878,147
Original award $2,644,869

Subawards

Subrecipient Amount Awarded
The Regents Of The University Of California. San Francisco DECODE IT Cohort $28,359
Baylor College Of Medicine $487,467
The Johns Hopkins University $80,678
University Of Texas Health Science Center At Houston $253,661
Baylor College Of Medicine $484,540
ST. Jude Children's Research Hospital Graduate School Of Biomedical Sciences, LLC $491,406
The Johns Hopkins University $80,678
The Regents Of The University Of California. San Francisco $28,359
University Of Texas Health Science Center At Houston Agreement: $133,346 Dr. Agopian (M-PI) will work closely with Drs. Lupo, Rabin and Jacola to contribute his birth defects phenotyping expertise to the team… $133,346
ST Jude Children's Research Hospital Inc. Agreement: $280,517 Dr. Jacola will lead the study team responsible for the cognitive and neurodevelopmental phenotyping for children with Down syndrome… $280,517
The Johns Hopkins University Agreement: $80,678 Dr. Rasmussen will work with contact PI Dr. Lupo to provide overall program administrative and financial management for the DECODE IT… $80,978
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Quick answers

Who received award U01HD116485?

U01HD116485 was awarded to Emory University by National Institute of Child Health and Human Development (National Institutes of Health) on September 17, 2024.

How much is award U01HD116485 worth?

$4,006,991 has been obligated on U01HD116485.

Which agency awarded U01HD116485?

National Institute of Child Health and Human Development (National Institutes of Health) awarded U01HD116485, with funding from Office of the Director (National Institutes of Health).

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