Skip to content

Developmental Impact of NICU Exposures (DINE)

Developmental Impact of Neonatal Intensive Care Unit (NICU) Exposures: Environmental Influences on Child Health Outcomes (ECHO)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03061890
Acronym
DINE
Enrollment
600
Registered
2017-02-23
Start date
2017-04-01
Completion date
2023-08-31
Last updated
2023-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prematurity

Keywords

children's environmental health, prematurity, preterm birth, phthalates, NICU, stress, lung health, neurodevelopment, growth

Brief summary

The DINE study will test the hypothesis that potentially avoidable NICU-based exposures contribute to the neuro-cognitive and somatic impairments prevalent among NICU graduates. This hypothesis is drawn from the documented impact of phthalate exposure on early development in term-born children, and the acknowledged presence of these toxic chemicals in the NICU. Third trimester in utero exposure to phthalates have been linked to poorer childhood performance in cognition, motor function, attention, hyperactivity and social behavior. Phthalate exposure is also associated with altered onset of puberty and asthma. The multi-site cohort and approach will clarify the role of NICU-based phthalate exposure on high-prevalence clinical outcomes.

Detailed description

Background: Each year in the United States, over 300,000 preterm infants are admitted to neonatal intensive care units (NICUs) where they are exposed to a chemical-intensive hospital environment during a developmentally vulnerable period. Many life-saving and supportive respiratory, nutritional, hematologic and pharmaceutical therapies in the NICU expose preterm infants to potentially harmful chemicals during a life stage analogous to the third trimester of gestation. The NIH-funded DINE study capitalizes on the infrastructure, biorepositories, and extensive clinical databases of four existing preterm cohorts to explore the hypothesis that early life exposure to phthalates adversely impacts neurodevelopment, lung function, growth, adiposity, and pubertal development in childhood. The scientific premise of the DINE study is that early life exposure to phthalates, a class of chemical plasticizers ubiquitous in the NICU, has long-lasting harmful effects on child health and development, and that these harmful effects are magnified in children born preterm. This premise is based on strong evidence of multisystem adverse health effects in term-born children who are exposed to phthalates in utero during the third trimester of pregnancy or in early infancy. In preterm infants, however, rigorously obtained data on the health effects of phthalates are scant. Dermal, inhalational and intravenous exposures to phthalates are widespread in some NICUs, where preterm infants are cared for during the sensitive third trimester developmental window. Moreover, premature infants experience a high prevalence of the adverse health effects that are associated with early life exposures to phthalates in term-born children, including altered neurodevelopment, poor pulmonary function, and maladapted growth. A rigorous, well-designed, sufficiently powered study of NICU-based phthalate exposures and long-term health outcomes of preterm infants has the potential to change care practices, promote regulatory policy changes and lead to mitigation of phthalate exposures in the NICU. Significance: The proposed research is expected to identify modifiable sources of developmental risk for NICU patients that can inform and improve hospital care and long-term outcome. Moreover, our findings could lead to relatively inexpensive NICU interventions, such as use of non-phthalate containing medical materials, dosing guidelines for elemental metals and guidance for parents and staff on infant stress-reduction, and policy changes (e.g. regulation of the phthalates used in medical devices or changes to the trace metal content of parenteral nutrition) with significant positive potential impacts on life-long morbidities common among NICU graduates. Information gleaned from studying our highly-exposed, highly-vulnerable population may elucidate health impacts of early life exposures that translate to risk reduction in the general population.

Interventions

None listed

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
Albert Einstein College of Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 12 Years

Inclusion criteria

* Children who were study participants in one of the four extant preterm cohorts (PROP, TOLSURF, NICU-HEALTH, and PENUT) that comprise the combined DINE cohort and who were followed to study endpoint at one of the clinical sites in DINE. * Newly recruited preterm infants admitted to the NICU at the Icahn School of Medicine at Mount Sinai * Newly recruited preterm and term infants who participated in the PRISM study at University of Rochester * Parents agreed to be re-contacted or local Institutional Review Board (IRB) grants permission to recontact families to obtain consent to participate in DINE.

Exclusion criteria

* Family requested that they not be contacted after their child completed the parent study * Family is unlikely to be available for long-term follow-up

Design outcomes

Primary

MeasureTime frameDescription
Association between NICU environmental exposures and lung health and asthma measured by Brief Respiratory QuestionnaireOne time between the ages of 3 to 4Brief Respiratory Questionnaire to determine association between exposure and lung health
Associations between NICU environmental exposures and lung health and asthma measured by the PROMIS® (Patient-Reported Outcomes Measurement Information System) Parent Proxy Asthma Impact item bankOne time between the ages of 5 to 6PROMIS® (Patient-Reported Outcomes Measurement Information System) Parent Proxy Asthma Impact item bank to determine association between exposure and asthma
Associations between NICU environmental exposures and lung health and asthma measured by PhenX (consensus measures for Phenotypes and eXposures) Toolkit measures of spirometry and bronchodilator responsivenessTwice between the ages of 8 to 12PhenX (consensus measures for Phenotypes and eXposures) Toolkit measures of spirometry and bronchodilator responsiveness to determine association between exposure and asthma
Associations between NICU environmental exposures and lung health and asthma measured by the PROMIS Pediatric Asthma Impact item bank.Twice between the ages of 8 to 12PROMIS Pediatric Asthma Impact item bank to determine the association between exposures and asthma
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Early Childhood Cognition BatteryTwice within 24 months between the ages of 3 to 5NIH Toolbox Early Childhood Cognition Battery to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Cognition BatteryTwice within 24 months between the ages of 7 to 9NIH Toolbox Cognition Battery to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Early Childhood Motor BatteryTwice within 24 months between the ages of 4 to 6NIH Toolbox Early Childhood Motor Battery to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Motor BatteryTwice between the ages of 8 to 12NIH Toolbox Motor Battery to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by Child Behavior Checklist (CBCL)One time between the ages of 3 to 4Child Behavior Checklist (CBCL) to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Cognitive Item bankThree times between the ages of 5 to 12PROMIS Cognitive Item bank to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Pediatric Mobility Item bankThree times between the ages of 5 to 12PROMIS Pediatric Mobility Item bank to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Pediatric Upper Extremity Item bankThree times between the ages of 5 to 12PROMIS Pediatric Upper Extremity Item to determine the associations between exposures and neurocognitive behavioral development
Associations between NICU environmental exposures and growth and obesity as measured by height, weight, head circumference, mid-upper arm circumference and bioimpedenceAnnually, up to 12 yearsMeasurement of height, weight, head circumference, mid-upper arm circumference and bioimpedence scale to determine associations between exposures and heathy growth and obesity
Associations between NICU environmental exposures and growth and obesity as measured by parent report height and weightAnnually, up to 12 yearsParent reported height and weight to determine associations between exposures and healthy growth and obesity
Associations between NICU environmental exposures and pubertal development measured by PhenX Assessment of Pubertal DevelopmentAnnually, up to 12 yearsPhenX Assessment of Pubertal Development to determine associations between exposures and pubertal development

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026