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Serum S100 protein could predict altered consciousness in glyphosate or glufosinate poisoning patients

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Abstract
BACKGROUND: Central nervous system (CNS) complications such as seizures and reduced consciousness are important in glufosinate and may occur in severe glyphosate poisoning. The aim of this study was to assess the possible role of serum S100B protein as a biochemical marker of CNS complications associated with glyphosate or glufosinate poisoning. METHODS: The study enrolled 40 patients (23 glyphosate poisoning and 17 glufosinate poisoning). Altered consciousness and seizure were observed during hospitalization. S100B level was measured with fully automated modular analytic E170 system using electrochemoluminometric immunoassay. RESULTS: Among 40 patients, neurologic features were observed in 12 patients with a median time to onset of 21.5 (IQR 8.25-24.75) h. Serum S100B concentrations measured on admission were higher in the group with neurologic features than in the group without neurologic features [0.148 μg/L (IQR 0.128-0.248) vs. 0.072 μg/L (IQR 0.047-0.084), p < .001]. Univariate analysis of measured patient raw parameters using a ROC curve showed that S100B was a significant predictor of neurologic features in glyphosate and glufosinate poisoning. The area under the ROC curve was 0.894 (95% confidential interval 0.791-0.998). When S100B was set at 0.0965, its sensitivity and specificity for predicting neurologic features in glyphosate and glufosinate poisoning were 92% and 82%, respectively. CONCLUSIONS: In our pilot study, S100B was a significant predictor of neurologic complications in patients with glyphosate and glufosinate poisoning. Large prospective cohorts are needed to confirm this finding.
All Author(s)
J. W. Lee ; Y. J. Choi ; S. Park ; H. W. Gil ; H. Y. Song ; S. Y. Hong
Issued Date
2017
Type
Article
Keyword
S100 proteinpoisoningconsciousness disorders
Publisher
American Academy of Clinical Toxicology
European Association of Poisons Centres and Clinical Toxicologists
ISSN
1556-3650
Citation Title
Clinical Toxicology
Citation Volume
55
Citation Number
5
Citation Start Page
357
Citation End Page
359
Language(ISO)
eng
DOI
10.1080/15563650.2017.1286013
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/1847
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