Elevated glutamate and lactate predict brain death after severe head trauma
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/173045 |
Resumo: | Objective: Clinical neurological assessment is challenging for severe traumatic brain injury (TBI) patients in the acute setting. Waves of neurochemical abnormalities that follow TBI may serve as fluid biomarkers of neurological status. We assessed the cerebrospinal fluid (CSF) levels of glutamate, lactate, BDNF, and GDNF, to identify potential prognostic biomarkers of neurological outcome. Methods: This cross-sectional study was carried out in a total of 20 consecutive patients (mean [SD] age, 29 [13] years; M/F, 9:1) with severe TBI Glasgow Coma Scale ≤ 8 and abnormal computed tomography scan on admission. Patients were submitted to ventricular drainage and had CSF collected between 2 and 4 h after hospital admission. Patients were then stratified according to two clinical outcomes: deterioration to brain death (nonsurvival, n = 6) or survival (survival, n = 14), within 3 days after hospital admission. CSF levels of brain-derived substances were compared between nonsurvival and survival groups. Clinical and neurological parameters were also assessed. Results: Glutamate and lactate are significantly increased in nonsurvival relative to survival patients. We tested the accuracy of both biomarkers to discriminate patient outcome. Setting a cutoff of >57.75, glutamate provides 80.0% of sensitivity and 84.62% of specificity (AUC: 0.8214, 95% CL: 54.55–98.08%; and a cutoff of >4.65, lactate has 100% of sensitivity and 85.71% of specificity (AUC: 0.8810, 95% CL: 54.55–98.08%). BDNF and GDNF did not discriminate poor outcome. Interpretation: This early study suggests that glutamate and lactate concentrations at hospital admission accurately predict death within 3 days after severe TBI. |
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Stefani, Marco AntonioModkovski, RafaelHansel, GiseleZimmer, Eduardo RigonCarvalho, Afonso Kopczynski deMüller, Alexandre PastorisStrogulski, Nathan RyzewskiRodolphi, Marcelo SalimenCarteri, Randhall Bruce KreismannSchmidt, André PratoOses, Jean PierreSmith, Douglas H.Portela, Luis Valmor Cruz2018-02-28T02:28:08Z20172328-9503http://hdl.handle.net/10183/173045001055927Objective: Clinical neurological assessment is challenging for severe traumatic brain injury (TBI) patients in the acute setting. Waves of neurochemical abnormalities that follow TBI may serve as fluid biomarkers of neurological status. We assessed the cerebrospinal fluid (CSF) levels of glutamate, lactate, BDNF, and GDNF, to identify potential prognostic biomarkers of neurological outcome. Methods: This cross-sectional study was carried out in a total of 20 consecutive patients (mean [SD] age, 29 [13] years; M/F, 9:1) with severe TBI Glasgow Coma Scale ≤ 8 and abnormal computed tomography scan on admission. Patients were submitted to ventricular drainage and had CSF collected between 2 and 4 h after hospital admission. Patients were then stratified according to two clinical outcomes: deterioration to brain death (nonsurvival, n = 6) or survival (survival, n = 14), within 3 days after hospital admission. CSF levels of brain-derived substances were compared between nonsurvival and survival groups. Clinical and neurological parameters were also assessed. Results: Glutamate and lactate are significantly increased in nonsurvival relative to survival patients. We tested the accuracy of both biomarkers to discriminate patient outcome. Setting a cutoff of >57.75, glutamate provides 80.0% of sensitivity and 84.62% of specificity (AUC: 0.8214, 95% CL: 54.55–98.08%; and a cutoff of >4.65, lactate has 100% of sensitivity and 85.71% of specificity (AUC: 0.8810, 95% CL: 54.55–98.08%). BDNF and GDNF did not discriminate poor outcome. Interpretation: This early study suggests that glutamate and lactate concentrations at hospital admission accurately predict death within 3 days after severe TBI.application/pdfengAnnals of clinical and translational neurology. Hoboken, NJ. Vol. 4, no. 6 (Jun. 2017), p. 392-402Lesões encefálicas traumáticasLíquido cefalorraquidianoBiomarcadoresElevated glutamate and lactate predict brain death after severe head traumaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001055927.pdf001055927.pdfTexto completo (inglês)application/pdf574286http://www.lume.ufrgs.br/bitstream/10183/173045/1/001055927.pdfaf61656d438b9da9e65299a7b31621e4MD51TEXT001055927.pdf.txt001055927.pdf.txtExtracted Texttext/plain44675http://www.lume.ufrgs.br/bitstream/10183/173045/2/001055927.pdf.txt9e849baa114034752e7d97efdb241d38MD52THUMBNAIL001055927.pdf.jpg001055927.pdf.jpgGenerated Thumbnailimage/jpeg2005http://www.lume.ufrgs.br/bitstream/10183/173045/3/001055927.pdf.jpgfc6abcf3daad579f6254673d21ef1033MD5310183/1730452018-10-29 09:12:57.659oai:www.lume.ufrgs.br:10183/173045Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2018-10-29T12:12:57Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Elevated glutamate and lactate predict brain death after severe head trauma |
title |
Elevated glutamate and lactate predict brain death after severe head trauma |
spellingShingle |
Elevated glutamate and lactate predict brain death after severe head trauma Stefani, Marco Antonio Lesões encefálicas traumáticas Líquido cefalorraquidiano Biomarcadores |
title_short |
Elevated glutamate and lactate predict brain death after severe head trauma |
title_full |
Elevated glutamate and lactate predict brain death after severe head trauma |
title_fullStr |
Elevated glutamate and lactate predict brain death after severe head trauma |
title_full_unstemmed |
Elevated glutamate and lactate predict brain death after severe head trauma |
title_sort |
Elevated glutamate and lactate predict brain death after severe head trauma |
author |
Stefani, Marco Antonio |
author_facet |
Stefani, Marco Antonio Modkovski, Rafael Hansel, Gisele Zimmer, Eduardo Rigon Carvalho, Afonso Kopczynski de Müller, Alexandre Pastoris Strogulski, Nathan Ryzewski Rodolphi, Marcelo Salimen Carteri, Randhall Bruce Kreismann Schmidt, André Prato Oses, Jean Pierre Smith, Douglas H. Portela, Luis Valmor Cruz |
author_role |
author |
author2 |
Modkovski, Rafael Hansel, Gisele Zimmer, Eduardo Rigon Carvalho, Afonso Kopczynski de Müller, Alexandre Pastoris Strogulski, Nathan Ryzewski Rodolphi, Marcelo Salimen Carteri, Randhall Bruce Kreismann Schmidt, André Prato Oses, Jean Pierre Smith, Douglas H. Portela, Luis Valmor Cruz |
author2_role |
author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Stefani, Marco Antonio Modkovski, Rafael Hansel, Gisele Zimmer, Eduardo Rigon Carvalho, Afonso Kopczynski de Müller, Alexandre Pastoris Strogulski, Nathan Ryzewski Rodolphi, Marcelo Salimen Carteri, Randhall Bruce Kreismann Schmidt, André Prato Oses, Jean Pierre Smith, Douglas H. Portela, Luis Valmor Cruz |
dc.subject.por.fl_str_mv |
Lesões encefálicas traumáticas Líquido cefalorraquidiano Biomarcadores |
topic |
Lesões encefálicas traumáticas Líquido cefalorraquidiano Biomarcadores |
description |
Objective: Clinical neurological assessment is challenging for severe traumatic brain injury (TBI) patients in the acute setting. Waves of neurochemical abnormalities that follow TBI may serve as fluid biomarkers of neurological status. We assessed the cerebrospinal fluid (CSF) levels of glutamate, lactate, BDNF, and GDNF, to identify potential prognostic biomarkers of neurological outcome. Methods: This cross-sectional study was carried out in a total of 20 consecutive patients (mean [SD] age, 29 [13] years; M/F, 9:1) with severe TBI Glasgow Coma Scale ≤ 8 and abnormal computed tomography scan on admission. Patients were submitted to ventricular drainage and had CSF collected between 2 and 4 h after hospital admission. Patients were then stratified according to two clinical outcomes: deterioration to brain death (nonsurvival, n = 6) or survival (survival, n = 14), within 3 days after hospital admission. CSF levels of brain-derived substances were compared between nonsurvival and survival groups. Clinical and neurological parameters were also assessed. Results: Glutamate and lactate are significantly increased in nonsurvival relative to survival patients. We tested the accuracy of both biomarkers to discriminate patient outcome. Setting a cutoff of >57.75, glutamate provides 80.0% of sensitivity and 84.62% of specificity (AUC: 0.8214, 95% CL: 54.55–98.08%; and a cutoff of >4.65, lactate has 100% of sensitivity and 85.71% of specificity (AUC: 0.8810, 95% CL: 54.55–98.08%). BDNF and GDNF did not discriminate poor outcome. Interpretation: This early study suggests that glutamate and lactate concentrations at hospital admission accurately predict death within 3 days after severe TBI. |
publishDate |
2017 |
dc.date.issued.fl_str_mv |
2017 |
dc.date.accessioned.fl_str_mv |
2018-02-28T02:28:08Z |
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Estrangeiro info:eu-repo/semantics/article |
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2328-9503 |
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001055927 |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Annals of clinical and translational neurology. Hoboken, NJ. Vol. 4, no. 6 (Jun. 2017), p. 392-402 |
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