High plasma glutamate concentrations are associated with infarct growth in acute ischemic stroke

Excitotoxic and inflammatory mechanisms have been demonstrated as mediating early neurologic deterioration (END) in patients with cerebral infarction. Here we investigate whether molecular markers associated with END are related to the volume and outcome of the diffusion weighted image (DWI) lesion...

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Veröffentlicht in:Neurology 2008-12, Vol.71 (23), p.1862-1868
Hauptverfasser: CARSTELLANOS, M, SOBRINO, T, PEDRAZA, S, MOLDES, O, PUMAR, J. M, SILVA, Y, SERENA, J, GARCIA-GIL, M, CASTILLO, J, DAVALOS, A
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container_end_page 1868
container_issue 23
container_start_page 1862
container_title Neurology
container_volume 71
creator CARSTELLANOS, M
SOBRINO, T
PEDRAZA, S
MOLDES, O
PUMAR, J. M
SILVA, Y
SERENA, J
GARCIA-GIL, M
CASTILLO, J
DAVALOS, A
description Excitotoxic and inflammatory mechanisms have been demonstrated as mediating early neurologic deterioration (END) in patients with cerebral infarction. Here we investigate whether molecular markers associated with END are related to the volume and outcome of the diffusion weighted image (DWI) lesion in acute ischemic stroke. MRI was performed on admission and at 72 hours in 197 patients with acute hemispheric infarction of
doi_str_mv 10.1212/01.wnl.0000326064.42186.7e
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Glutamate, l-arginine, interleukin-6 (IL-6), and tumor necrosis factor-alpha levels were analyzed in blood samples obtained on admission. DWI lesion growth was found in 144 (73%) patients (median increase 38 [6.5, 83.4] cm(3)) and END occurred in 58 (29.4%) patients. Baseline glutamate (r = 0.71), l-arginine (r = -0.35), and IL-6 levels (r = 0.50) showed a high and significant correlation with the DWI lesion enlargement (all p &lt; 0.001). After adjustment for potential confounders, glutamate levels were the only molecular marker associated with DWI lesion enlargement at 72 hours (beta = 0.21; SD = 0.07; p = 0.004). Molecular markers of early neurologic deterioration may play a role as mediators of lesion growth in cerebral ischemia. 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NIH Stroke Scale was scored at the same intervals. END was defined as an increase &gt;/=4 points within the 3 days. Glutamate, l-arginine, interleukin-6 (IL-6), and tumor necrosis factor-alpha levels were analyzed in blood samples obtained on admission. DWI lesion growth was found in 144 (73%) patients (median increase 38 [6.5, 83.4] cm(3)) and END occurred in 58 (29.4%) patients. Baseline glutamate (r = 0.71), l-arginine (r = -0.35), and IL-6 levels (r = 0.50) showed a high and significant correlation with the DWI lesion enlargement (all p &lt; 0.001). After adjustment for potential confounders, glutamate levels were the only molecular marker associated with DWI lesion enlargement at 72 hours (beta = 0.21; SD = 0.07; p = 0.004). Molecular markers of early neurologic deterioration may play a role as mediators of lesion growth in cerebral ischemia. 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M</creatorcontrib><creatorcontrib>SILVA, Y</creatorcontrib><creatorcontrib>SERENA, J</creatorcontrib><creatorcontrib>GARCIA-GIL, M</creatorcontrib><creatorcontrib>CASTILLO, J</creatorcontrib><creatorcontrib>DAVALOS, A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CARSTELLANOS, M</au><au>SOBRINO, T</au><au>PEDRAZA, S</au><au>MOLDES, O</au><au>PUMAR, J. M</au><au>SILVA, Y</au><au>SERENA, J</au><au>GARCIA-GIL, M</au><au>CASTILLO, J</au><au>DAVALOS, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High plasma glutamate concentrations are associated with infarct growth in acute ischemic stroke</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2008-12-02</date><risdate>2008</risdate><volume>71</volume><issue>23</issue><spage>1862</spage><epage>1868</epage><pages>1862-1868</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><coden>NEURAI</coden><abstract>Excitotoxic and inflammatory mechanisms have been demonstrated as mediating early neurologic deterioration (END) in patients with cerebral infarction. Here we investigate whether molecular markers associated with END are related to the volume and outcome of the diffusion weighted image (DWI) lesion in acute ischemic stroke. MRI was performed on admission and at 72 hours in 197 patients with acute hemispheric infarction of &lt;12 hours' duration. DWI lesion enlargement was calculated as the absolute difference between volumes on admission and day 3 of evolution. NIH Stroke Scale was scored at the same intervals. END was defined as an increase &gt;/=4 points within the 3 days. Glutamate, l-arginine, interleukin-6 (IL-6), and tumor necrosis factor-alpha levels were analyzed in blood samples obtained on admission. DWI lesion growth was found in 144 (73%) patients (median increase 38 [6.5, 83.4] cm(3)) and END occurred in 58 (29.4%) patients. Baseline glutamate (r = 0.71), l-arginine (r = -0.35), and IL-6 levels (r = 0.50) showed a high and significant correlation with the DWI lesion enlargement (all p &lt; 0.001). After adjustment for potential confounders, glutamate levels were the only molecular marker associated with DWI lesion enlargement at 72 hours (beta = 0.21; SD = 0.07; p = 0.004). Molecular markers of early neurologic deterioration may play a role as mediators of lesion growth in cerebral ischemia. Plasma glutamate concentration is the most powerful and independent predictor biomarker of lesion enlargement in the acute phase of ischemic stroke, and so may well be useful as a signature of tissue at risk of infarction.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>18971451</pmid><doi>10.1212/01.wnl.0000326064.42186.7e</doi><tpages>7</tpages></addata></record>
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subjects Arginine - blood
Biological and medical sciences
Cerebral Infarction - blood
Cerebral Infarction - etiology
Chi-Square Distribution
Chromatography, High Pressure Liquid - methods
Diffusion Magnetic Resonance Imaging
Female
Glutamic Acid - blood
Humans
Image Processing, Computer-Assisted
Interleukin-6 - blood
Linear Models
Male
Medical sciences
Neurology
Retrospective Studies
Stroke - complications
Time Factors
Tumor Necrosis Factor-alpha - blood
Vascular diseases and vascular malformations of the nervous system
title High plasma glutamate concentrations are associated with infarct growth in acute ischemic stroke
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