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Correlation Between CD64 and PCT Levels in Cerebrospinal Fluid and Degree of Hearing Impairment Sequelae in Neonates with Purulent Meningitis

Overview
Journal Exp Ther Med
Specialty Pathology
Date 2017 Dec 30
PMID 29285148
Citations 2
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Abstract

This study investigated the possible correlation between the degree of hearing impairment caused by neonatal purulent meningitis and the levels of CD64 and PCT in cerebrospinal fluid of patients, and assessed the prognostic value of such levels. We recorded data from 156 cases of neonatal purulent meningitis retrospectively. All the patients received brainstem response audiometry, and cerebrospinal fluid samples were collected within the first day after admission through lumbar puncture. Flow cytometry was used to detect CD64 levels and enzyme-linked fluorescent assay was used to detect PCT levels. The children with hearing impairment were followed up for 1 year and brainstem response audiometry was performed again in them. We found that 43.59% of the children showed different degrees of hearing impairment, and 55% of them did not fully recover. The levels of PCT and CD64 in cerebrospinal fluid of children with hearing impairment were significantly higher than those of children with normal hearing (P<0.01). The levels of PCT and CD64 in mild, moderate and severe hearing impaired children increased gradually with higher degrees of impairment, and the differences between groups were significant (P<0.01). During the follow-up, it was found that the levels of PCT and CD64 in children correlated well with the degree of hearing recovery, and the differences between groups were significant (P<0.01). In our study, approximately 1/4 children with purulent meningitis showed long-term hearing impairment. Based on our analyses, the levels of CD64 and PCT in cerebrospinal fluid can be used to predict the degree and long-term prognosis of hearing impairment caused by purulent meningitis in children.

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References
1.
Stevens J, Eames M, Kent A, Halket S, Holt D, Harvey D . Long term outcome of neonatal meningitis. Arch Dis Child Fetal Neonatal Ed. 2003; 88(3):F179-84. PMC: 1721546. DOI: 10.1136/fn.88.3.f179. View

2.
Bargui F, DAgostino I, Mariani-Kurkdjian P, Alberti C, Doit C, Bellier N . Factors influencing neurological outcome of children with bacterial meningitis at the emergency department. Eur J Pediatr. 2012; 171(9):1365-71. DOI: 10.1007/s00431-012-1733-5. View

3.
Simonin-Le Jeune K, Le Jeune A, Jouneau S, Belleguic C, Roux P, Jaguin M . Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increase. PLoS One. 2013; 8(9):e75667. PMC: 3787056. DOI: 10.1371/journal.pone.0075667. View

4.
Klinger G, Chin C, Beyene J, Perlman M . Predicting the outcome of neonatal bacterial meningitis. Pediatrics. 2000; 106(3):477-82. DOI: 10.1542/peds.106.3.477. View

5.
May M, Daley A, Donath S, Isaacs D . Early onset neonatal meningitis in Australia and New Zealand, 1992-2002. Arch Dis Child Fetal Neonatal Ed. 2005; 90(4):F324-7. PMC: 1721922. DOI: 10.1136/adc.2004.066134. View