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Inflammatory Cytokines Associated With Perinatal Brain Injury

A Study to Determine If Inflammatory Cytokines Are Associated With Perinatal Brain Injury and Long Term Neurodevelopmental Handicap or Death

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01035697
Acronym
Cytokines
Enrollment
1067
Registered
2009-12-21
Start date
1999-07-31
Completion date
2004-05-31
Last updated
2019-03-22

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

Conditions

Cerebral Palsy, Infant, Low Birth Weight, Infant, Newborn, Infant, Premature, Infant, Small for Gestational Age

Keywords

NICHD Neonatal Research Network, Very Low Birth Weight (VLBW), Extremely Low Birth Weight (ELBW), Prematurity, Pro-inflammatory cytokines, Anti-inflammatory cytokines, Interleukin-1 (IL-1β), Interleukin-2 (IL-2), Interleukin-3 (IL-3), Interleukin-8 (IL-8), Interleukin-9 (IL-9), Tumor necrosis factor-α (TNF-α), Regulated upon Activation, Normal T-cell Expressed and Secreted (RANTES)

Brief summary

This observational study assessed whether measurements of certain pro-inflammatory and anti-inflammatory cytokines in the blood (either singly or in combination) at birth and/or up to day of life 21 can predict cerebral palsy at 18-22 months corrected age.

Detailed description

Inflammatory cytokines \[interleukin-1 (IL-1β), IL-8, IL-9, tumor necrosis factor-α (TNF-α), and RANTES\] but not anti-inflammatory cytokines released during the perinatal period have been associated with the development of periventricular leukomalacia (PVL) and cerebral palsy (CP) in near term and term infants. However, because blood samples were obtained on any day between day 1 and 18, these data cannot distinguish between prenatal and postnatal effects on neurological outcome. Furthermore, very low birth weight infants who are at the highest risk have not been studies. The goal of this study was to measure pro-inflammatory and anti-inflammatory cytokine levels at various times in the perinatal period (at birth up to day of life 21), since they may be elevated at different points in the disease process. Blood samples (whole blood spots, dried on filter paper) were obtained on day 1 within 4 hours after birth, and on days 3, 7, 14, and 21. Neurodevelopmental assessments were conducted at 18-22 months corrected age.

Interventions

None listed

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
National Center for Research Resources (NCRR)
CollaboratorNIH
NICHD Neonatal Research Network
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 72 Hours
Healthy volunteers
Yes

Inclusion criteria

* Infants 401-1,000 grams at birth

Exclusion criteria

* \>72 hours of age

Design outcomes

Primary

MeasureTime frame
Pro-cytokines increased and anti-inflammatory cytokines decreasedAt birth and/or up to Day 3±1

Secondary

MeasureTime frame
Type and severity of CP and other neurodevelopmental handicaps, the appearance of PVL, and neonatal mortality18-22 months corrected age
Abnormal pro-inflammatory and anti-inflammatory cytokines at birth are associated with prenatal insults (e.g., chorioamnionitis, occult intrauterine infection, early-onset neonatal sepsis, perinatal asphyxia, early death)At birth
Abnormal postnatal cytokine levels associated with postnatal insults (e.g., postnatal intraventricular hemorrhage, late-onset neonatal sepsis, bronchopulmonary dysplasia, chronic lung disease, and/or necrotizing enterocolitis)Up to Day of life 21
Pro-inflammatory cytokine elevations at the time of a workup for possible sepsis occur in infants with a positive bacterial blood culture and those with negative blood cultures who are treated with a full course of antibioticsUp to Day of life 21

Countries

United States

Outcome results

None listed

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