Journal
CLINICAL INFECTIOUS DISEASES
Volume 70, Issue 6, Pages 1161-1168Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciz325
Keywords
cerebrospinal fluid; tau; cerebral malaria; neurologic; cognitive; impairment
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Funding
- National Institute of Neurological Disorders and Stroke
- Fogarty International Center [R01NS055349, D43 NS078280]
- Indiana Alzheimer Disease Center [P30 AG010133]
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Background. Elevated concentrations of cerebrospinal fluid (CSF) tau, a marker of axonal injury, have been associated with coma in severe malaria (cerebral malaria [CM]). However, it is unknown whether axonal injury is related to long-term neurologic deficits and cognitive impairment in children with CM. Methods. Admission CSF tau concentrations were measured in 145 Ugandan children with CM and compared to clinical and laboratory factors and acute and chronic neurologic and cognitive outcomes. Results. Elevated CSF tau concentrations were associated with younger age, increased disease severity (lower glucose and hemoglobin concentrations, malaria retinopathy, acute kidney injury, and prolonged coma duration, all P < .05), and an increased CSF:plasma albumin ratio, a marker of blood-brain barrier breakdown (P < .001). Admission CSF tau concentrations were associated with the presence of neurologic deficits at hospital discharge, and at 6, 12, and 24 months postdischarge (all P <= .02). After adjustment for potential confounding factors, elevated log(10)-transformed CSF tau concentrations correlated with worse cognitive outcome z scores over 2-year follow-up for associative memory (beta coefficient, -0.31 [95% confidence interval [CI], -.53 to -.10]) in children <5 years of age, and for overall cognition (-0.69 [95% CI, -1.19 to -.21]), attention (-0.78 [95% CI, -1.34 to -.23]), and working memory (-1.0 [95% CI, -1.68 to -.31]) in children >= 5 years of age (all P < .006). Conclusions. Acute axonal injury in children with CM is associated with long-term neurologic deficits and cognitive impairment. CSF tau concentrations at the time of the CM episode may identify children at high risk of long-term neurocognitive impairment.
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