Although autism is among the most highly heritable of mental disorders, its pathogenesis is poorly understood and may include environmental co-factors. Furthermore, there are no biomarkers with which to screen for disease or identify those at risk for disease. The Autism Birth Cohort (ABC) is nested within the MoBa, a Norwegian prospective, unselected, population-based pregnancy cohort (N >107,000). ASD cases are prospectively ascertained through screening of the entire MoBa population with questionnaires at 36m, 5y, 7y, and 8y, and via referrals and a national patient registry. All diagnoses are validated, and biologic samples are collected serially through pregnancy and early childhood. Implementation of early screening and diagnostic assessments provides a rich view of longitudinal trajectory and nascent signs and symptoms, and creates new opportunities to define their pathogenesis. Biologic and clinical phenotypes of ASD determined here will enable current and future generations of investigators to pursue powerful genotypic and environmental factor association analyses. Although other prospective birth cohorts track selected high risk populations, at present, the ABC is the only large cohort wherein information and samples are collected from all children and both of their parents prior to, and independent of, diagnosis and severity of disease. Biologic samples are optimized for genetic, transcriptomic, proteomic, microbiologic and toxicologic analyses. Linkage to nationwide health registries enables extensive longitudinal follow-up of the cohort at low cost.
Aims i nclude: (1) Complete, enlarge, and characterize the ABC through continued ascertainment, diagnosis, and assessment of cases of ASD (N=550-750) and age-matched controls (N=550-750);(2) Investigate: a) potential causes of, and b) early markers for ASD, including targeted examination of pre- and perinatal candidate exposures (parental age;nutrition and xenobiotics;ultrasound and assisted reproductive technologies;infection and host immunity;immunizations and other iatrogenic factors;oxidative stress responses) and heritable susceptibilities, and prospective mining of the maternal and cord blood transcriptome and proteome for ASD biomarkers;(3) Investigate trajectories of ASD and associated features (diagnostic stability, symptoms/neuroregulatory features, head circumference/somatic growth, and biological indices). Our hypothesis is that systematic, prospective, serial analyses of ABC subjects that begin in prenatal life will reveal insights into early signs and symptoms, diagnostic stability and pathogenesis that would not be otherwise obtained.

Public Health Relevance

The reported prevalence of ASD has increased 5-1 Ox over the past 20y. Whether these disorders are truly more frequent now is controversial;nonetheless, the burden is profound in human and economic terms. Our project will exploit a large, prospective birth cohort with unique data, biologic samples and laboratory platforms to discover clues to pathogenesis, and biomarkers that will drive research and clinical management in new directions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01NS047537-08
Application #
8640909
Study Section
Special Emphasis Panel (ZNS1-SRB-G (46))
Program Officer
Moy, Claudia S
Project Start
2003-09-30
Project End
2014-02-28
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
8
Fiscal Year
2013
Total Cost
$6,537,537
Indirect Cost
$1,470,952
Name
Columbia University (N.Y.)
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Bjelland, Elisabeth Krefting; Owe, Katrine Mari; Pingel, Ronnie et al. (2016) Pelvic pain after childbirth: a longitudinal population study. Pain 157:710-6
Zambrana, Imac M; Vollrath, Margarete E; Sengpiel, Verena et al. (2016) Preterm delivery and risk for early language delays: a sibling-control cohort study. Int J Epidemiol 45:151-9
Hermansen, Tone Kristine; Røysamb, Espen; Augusti, Else-Marie et al. (2016) Behavior and inhibitory control in children with prenatal exposure to antidepressants and medically untreated depression. Psychopharmacology (Berl) 233:1523-35
Panasevich, Sviatlana; HÃ¥berg, Siri Eldevik; Aamodt, Geir et al. (2016) Association between pregnancy exposure to air pollution and birth weight in selected areas of Norway. Arch Public Health 74:26
Wood, Mollie E; Lapane, Kate; Frazier, Jean A et al. (2016) Prenatal Triptan Exposure and Internalising and Externalising Behaviour Problems in 3-Year-Old Children: Results from the Norwegian Mother and Child Cohort Study. Paediatr Perinat Epidemiol 30:190-200
Magnus, Maria C; Karlstad, Øystein; Midtun, Øivind et al. (2016) Maternal plasma total neopterin and kynurenine/tryptophan levels during pregnancy in relation to asthma development in the offspring. J Allergy Clin Immunol 138:1319-1325.e4
Bøe, Tormod; Hysing, Mari; Zachrisson, Henrik Daae (2016) Low Family Income and Behavior Problems in Norwegian Preschoolers: Is Child Emotionality a Marker for Sensitivity of Influence? J Dev Behav Pediatr 37:213-22
Vollrath, Margarete Erika; Sengpiel, Verena; Landolt, Markus A et al. (2016) Is maternal trait anxiety a risk factor for late preterm and early term deliveries? BMC Pregnancy Childbirth 16:286
Rotroff, Daniel M; Joubert, Bonnie R; Marvel, Skylar W et al. (2016) Maternal smoking impacts key biological pathways in newborns through epigenetic modification in Utero. BMC Genomics 17:976
Heitmann, K; Havnen, G C; Holst, L et al. (2016) Pregnancy outcomes after prenatal exposure to echinacea: the Norwegian Mother and Child Cohort Study. Eur J Clin Pharmacol 72:623-30

Showing the most recent 10 out of 301 publications