Abstract
Neonatal Post-hemorrhagic hydrocephalus (PHH) develops partly due to an inflammatory process occurring after intraventricular hemorrhage whereas the majority of congenital hydrocephalus (CH) results from primary and secondary CNS malformations. We hypothesize that cerebrospinal fluid (CSF) content of inflammatory biomarkers is higher in neonatal PHH relative to CH. To test this hypothesis, we measured CSF concentrations of CCL-3, CXCL-12, CX3CL-1, IL-10 and P-selectin in both conditions.
Highlights
Neonatal Post-hemorrhagic hydrocephalus (PHH) develops partly due to an inflammatory process occurring after intraventricular hemorrhage whereas the majority of congenital hydrocephalus (CH) results from primary and secondary CNS malformations
Our findings suggest that PHH may be distinguished from CH based on its higher levels of CCL-3 and P-selectin
It appears that CH may not be distinguished from pre-term controls (PT) controls based on levels of inflammatory biomarkers
Summary
Neonatal Post-hemorrhagic hydrocephalus (PHH) develops partly due to an inflammatory process occurring after intraventricular hemorrhage whereas the majority of congenital hydrocephalus (CH) results from primary and secondary CNS malformations. We hypothesize that cerebrospinal fluid (CSF) content of inflammatory biomarkers is higher in neonatal PHH relative to CH. To test this hypothesis, we measured CSF concentrations of CCL-3, CXCL-12, CX3CL-1, IL-10 and P-selectin in both conditions
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