The Collaborative Initiative on Fetal Alcohol Spectrum Disorders (CIFASD) is a multidisciplinary, international consortium of research projects and resource cores charged with improving prevention, diagnosis, and treatment of FASD. The Administrative Resource Core of the CIFASD (AdminC) has led this consortium since it was first established in 2003 and plays a critical leadership role in the coordination of research efforts and ensuring progress toward consortium goals. CIFASD addresses issues related to prenatal alcohol exposure across the lifespan, using a range of interrelated clinical and preclinical research approaches. This iteration of the consortium consists of multiple collaborative components including four resource U24 cores (AdminC, Dysmorphology, Informatics, and Outreach/Dissemination), nine U01 research projects (clinical, basic science, and/or translational) and two exploratory/developmental UH2 projects. One goal of the CIFASD is to improve identification of individuals who have been affected by prenatal alcohol exposure. This will be accomplished by assessing biomarkers, such as immune and miRNA profiles, and by using neuroimaging techniques that may be more sensitive to subtle pathology seen in individuals who do not meet the diagnostic criteria for FAS. In addition, CIFASD will develop novel tools, such as 3D facial and neurobehavioral screening, which can be assessed remotely and made more universally accessible through eHealth. The use of telemedicine will also provide access to more detailed dysmorphology evaluations. Another goal is to identify risk and resiliency factors, including genetic influences that will help with understanding the mechanisms of alcohol's damaging effects and also lead to more targeted interventions. A third goal is to better understand the effects of prenatal alcohol exposure on consequences across the lifespan, including adulthood. Finally, an intervention for improving outcomes will be modified to a mobile platform, so that it can reach larger populations of individuals with FASD and their families. Collectively, these projects have the potential for moving the FASD field forward, improving the prevention, diagnosis, and treatment of FASD and serving a wide audience with the technologies available in eHealth.
The Specific Aims of the AdminC are to: 1) Provide scientific and administrative direction, leadership and oversight to CIFASD; 2) Facilitate communication among the various projects and the dissemination of results; 3) Assist with data management strategies; 4) Provide annual evaluations of progress; and 5) Provide assistance to projects with implementing eHealth technology. The AdminC provides the foundation for the interactive and supportive framework of CIFASD by establishing regular communications with all members through monthly conference calls and biannual meetings; leading the Steering Committee in the establishment and implementation of CIFASD priorities and policies; supporting the Science Advisory Board with its evaluations of progress on each component as well as the overall mission of CIFASD; as well as serving as the liaison between the consortium's project scientists and its NIAAA advisors.

Public Health Relevance

The consequences resulting from prenatal alcohol exposure are wide-ranging and a major and costly public health problem. The goal of the CIFASD consortium is to enhance the identification and treatment of FASD utilizing a multidisciplinary approach consisting of both basic science and clinical research. The collaborations among research projects will allow CIFASD to improve the diagnosis and treatment of FASD, moving the field forward in ways that could not be easily achieved by individual projects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
5U24AA014811-16
Application #
9698228
Study Section
Special Emphasis Panel (ZAA1)
Program Officer
Wang, Joe
Project Start
2003-09-30
Project End
2022-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
16
Fiscal Year
2019
Total Cost
Indirect Cost
Name
San Diego State University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
073371346
City
San Diego
State
CA
Country
United States
Zip Code
92182
Doyle, Lauren R; Moore, Eileen M; Coles, Claire D et al. (2018) Executive Functioning Correlates With Communication Ability in Youth With Histories of Heavy Prenatal Alcohol Exposure. J Int Neuropsychol Soc 24:1026-1037
Donald, Kirsten A; Hoogenhout, Michelle; du Plooy, Christopher P et al. (2018) Drakenstein Child Health Study (DCHS): investigating determinants of early child development and cognition. BMJ Paediatr Open 2:e000282
Suttie, Michael; Wozniak, Jeffrey R; Parnell, Scott E et al. (2018) Combined Face-Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders. Alcohol Clin Exp Res 42:1769-1782
Gross, Lauren A; Moore, Eileen M; Wozniak, Jeffrey R et al. (2018) Neural correlates of verbal memory in youth with heavy prenatal alcohol exposure. Brain Imaging Behav 12:806-822
Charness, Michael E (2018) The adolescent brain cognitive development study external advisory board. Dev Cogn Neurosci 32:155-160
Hendrickson, Timothy J; Mueller, Bryon A; Sowell, Elizabeth R et al. (2018) Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. Dev Cogn Neurosci 30:123-133
Bodnar, Tamara S; Raineki, Charlis; Wertelecki, Wladimir et al. (2018) Altered maternal immune networks are associated with adverse child neurodevelopment: Impact of alcohol consumption during pregnancy. Brain Behav Immun 73:205-215
Dou, Xiaowei; Menkari, Carrie; Mitsuyama, Rei et al. (2018) L1 coupling to ankyrin and the spectrin-actin cytoskeleton modulates ethanol inhibition of L1 adhesion and ethanol teratogenesis. FASEB J 32:1364-1374
Suttie, Michael; Wetherill, Leah; Jacobson, Sandra W et al. (2017) Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure. Alcohol Clin Exp Res 41:1471-1483
Idrus, Nirelia M; Breit, Kristen R; Thomas, Jennifer D (2017) Dietary choline levels modify the effects of prenatal alcohol exposure in rats. Neurotoxicol Teratol 59:43-52

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