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Original Articles

Role of cerebrospinal fluid tau protein levels as a biomarker of brain injury in pediatric status epilepticus

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Pages 782-790 | Received 02 Jun 2021, Accepted 25 Aug 2021, Published online: 15 Sep 2021
 

Abstract

Background

Various biomarkers have been studied for predicting etiology and outcome in status epilepticus (SE); cerebrospinal fluid (CSF) total tau (t-tau) protein levels is foremost among them. Only handful of studies are available regarding role of t-tau in childhood SE.

Methodology

This prospective study was conducted in a tertiary care center of Northern India in children 6 months −12 years of age. The Cases were patients with convulsive status epilepticus (CSE) whereas Controls were patients without SE and normal CSF. The t-tau levels were done in CSF of both the groups. The outcome was assessed by GOS-E Peds score.

Results

A total of 50 (62% males) cases and 15 (67% males) controls were enrolled in the study. SE was generalized in 78% cases whereas 14% had refractory SE. Most common etiology of CSE was acute symptomatic (52%), followed by prolonged febrile seizure (24%), remote symptomatic group (14%), unknown etiology (8%) and progressive disorder (2%). Case fatality rate was 10%. Poor outcome was seen in 30% cases. Median (IQR) CSF t-tau levels was significantly lower 2.6 × 103 (0.5–9.4 × 103) pg/ml in cases vs 10.6 × 103 (6.0–14.2 × 103) pg/ml in controls (p = 0.004). There was no significant correlation seen between type, duration, etiology and response to antiepileptic drugs of SE with CSF t-tau levels. Also, no significant correlation of poor sensorium, outcome of SE and critical care needs with CSF t-tau levels was noted.

Conclusion

CSF t-tau is not a useful diagnostic or prognostic biomarker in pediatric SE.

Author contributions

Shivanjali Sood, Chandrika Azad, Jasbinder Kaur, and Pankaj Kumar: conceptualization, data collection, literature search, and manuscript writing. Vishal Guglani and Seema Singla: conceptualization, literature search, and manuscript writing.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Figure 1. Flow chart of cases and controls.

Figure 1. Flow chart of cases and controls.

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