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Association between apolipoprotein E genotype and outcome of traumatic brain injury
The prognosis of traumatic brain injury is quite variable and not fully explained by the known factors. This study is to examine if the polymorphism of apolipoprotein E (apoE) influences the outcome of traumatic brain injury. Over a period of twelve months, we prospectively studied 100 patients who...
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Published in: | Acta neurochirurgica 2003-08, Vol.145 (8), p.649-654 |
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creator | Chiang, M-F Chang, J-G Hu, C-J |
description | The prognosis of traumatic brain injury is quite variable and not fully explained by the known factors. This study is to examine if the polymorphism of apolipoprotein E (apoE) influences the outcome of traumatic brain injury.
Over a period of twelve months, we prospectively studied 100 patients who sustained traumatic brain injuries and were admitted to our neurosurgical unit.
Nineteen patients were apoE4+ and 81 patients were apoE4-. There was no significant difference between apoE4+ and apoE4- groups in the cause of injury (p=0.288), type of brain injury (p=0.983) and choice of treatment (p=0.88). The proportion of patients with a lower GCS ( |
doi_str_mv | 10.1007/s00701-003-0069-3 |
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Over a period of twelve months, we prospectively studied 100 patients who sustained traumatic brain injuries and were admitted to our neurosurgical unit.
Nineteen patients were apoE4+ and 81 patients were apoE4-. There was no significant difference between apoE4+ and apoE4- groups in the cause of injury (p=0.288), type of brain injury (p=0.983) and choice of treatment (p=0.88). The proportion of patients with a lower GCS (<13), indicating a poor prognosis, was higher in the apoE4+ group (73.7%) than that in apoE4- group (61.7%), although the difference was not significant (p=0.654). Six patients (7.4%) in the apoE4- group and 5(26.3%) in the apoE4+ group had been drinking alcohol at the time of injury (p=0.018). The mean duration of hospital stay for apoE4+ patients was significantly longer than for apoE4- patients (p<0.001). Six months after injury, 10 of 19 patients (52.6%) with apoE4 had an unfavorable outcome (dead, vegetative state, or severe disability) compared with 20 of the 81 (24.1%) patients without apoE4 (p=0.017). The apoE4+ patients had a significantly longer hospital stay and unfavorable outcomes after brain injury.
This study discloses a significant genetic association between the apoE genotypes and outcomes of traumatic brain injury. Patients with apoE4 allele are more likely to have an unfavorable clinical outcome after brain injury.</description><identifier>ISSN: 0001-6268</identifier><identifier>EISSN: 0942-0940</identifier><identifier>DOI: 10.1007/s00701-003-0069-3</identifier><identifier>PMID: 14520543</identifier><language>eng</language><publisher>Austria: Springer Nature B.V</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Apolipoproteins ; Apolipoproteins E - genetics ; Brain damage ; Brain Injuries - genetics ; Brain Injuries - therapy ; Female ; Genotype ; Glasgow Coma Scale ; Humans ; Male ; Middle Aged ; People with disabilities ; Polymorphism, Genetic - genetics ; Predictive Value of Tests ; Prognosis ; Prospective Studies</subject><ispartof>Acta neurochirurgica, 2003-08, Vol.145 (8), p.649-654</ispartof><rights>Springer-Verlag/Wien 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-f51e18335bbd882aab7795271edc4c7ce5c40dc11da72bcef225ed0dfc359a3f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14520543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiang, M-F</creatorcontrib><creatorcontrib>Chang, J-G</creatorcontrib><creatorcontrib>Hu, C-J</creatorcontrib><title>Association between apolipoprotein E genotype and outcome of traumatic brain injury</title><title>Acta neurochirurgica</title><addtitle>Acta Neurochir (Wien)</addtitle><description>The prognosis of traumatic brain injury is quite variable and not fully explained by the known factors. This study is to examine if the polymorphism of apolipoprotein E (apoE) influences the outcome of traumatic brain injury.
Over a period of twelve months, we prospectively studied 100 patients who sustained traumatic brain injuries and were admitted to our neurosurgical unit.
Nineteen patients were apoE4+ and 81 patients were apoE4-. There was no significant difference between apoE4+ and apoE4- groups in the cause of injury (p=0.288), type of brain injury (p=0.983) and choice of treatment (p=0.88). The proportion of patients with a lower GCS (<13), indicating a poor prognosis, was higher in the apoE4+ group (73.7%) than that in apoE4- group (61.7%), although the difference was not significant (p=0.654). Six patients (7.4%) in the apoE4- group and 5(26.3%) in the apoE4+ group had been drinking alcohol at the time of injury (p=0.018). The mean duration of hospital stay for apoE4+ patients was significantly longer than for apoE4- patients (p<0.001). Six months after injury, 10 of 19 patients (52.6%) with apoE4 had an unfavorable outcome (dead, vegetative state, or severe disability) compared with 20 of the 81 (24.1%) patients without apoE4 (p=0.017). The apoE4+ patients had a significantly longer hospital stay and unfavorable outcomes after brain injury.
This study discloses a significant genetic association between the apoE genotypes and outcomes of traumatic brain injury. Patients with apoE4 allele are more likely to have an unfavorable clinical outcome after brain injury.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Apolipoproteins</subject><subject>Apolipoproteins E - genetics</subject><subject>Brain damage</subject><subject>Brain Injuries - genetics</subject><subject>Brain Injuries - therapy</subject><subject>Female</subject><subject>Genotype</subject><subject>Glasgow Coma Scale</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>People with disabilities</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><issn>0001-6268</issn><issn>0942-0940</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkctKxDAUhoMojo4-gBsJLnRVzbVpl8MwXmDAhboOaXoqHdqmJikyb2-GGRDcuMjJCfn-Q8KH0BUl95QQ9RBSITQjhKeVlxk_QmekFCxLhRynnqTbnOXFDJ2HsEknpgQ_RTMqJCNS8DP0tgjB2dbE1g24gvgNMGAzuq4d3ehdhHbAK_wJg4vbEbAZauymaF0P2DU4ejP1KWtx5U0i22Ez-e0FOmlMF-DysM_Rx-PqffmcrV-fXpaLdWa5zGPWSAq04FxWVV0UzJhKqVIyRaG2wioL0gpSW0pro1hloWFMQk3qJsVLwxs-R7f7uemhXxOEqPs2WOg6M4CbglZSMUm4TODdP6CQUpbFjrz5Q27c5If0C10IInIuKU0Q3UPWuxA8NHr0bW_8VlOid2L0XoxOYvROjOYpc30YPFU91L-Jgwn-A1mViXk</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Chiang, M-F</creator><creator>Chang, J-G</creator><creator>Hu, C-J</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20030801</creationdate><title>Association between apolipoprotein E genotype and outcome of traumatic brain injury</title><author>Chiang, M-F ; Chang, J-G ; Hu, C-J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-f51e18335bbd882aab7795271edc4c7ce5c40dc11da72bcef225ed0dfc359a3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Apolipoproteins</topic><topic>Apolipoproteins E - genetics</topic><topic>Brain damage</topic><topic>Brain Injuries - genetics</topic><topic>Brain Injuries - therapy</topic><topic>Female</topic><topic>Genotype</topic><topic>Glasgow Coma Scale</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>People with disabilities</topic><topic>Polymorphism, Genetic - genetics</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiang, M-F</creatorcontrib><creatorcontrib>Chang, J-G</creatorcontrib><creatorcontrib>Hu, C-J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neurochirurgica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiang, M-F</au><au>Chang, J-G</au><au>Hu, C-J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between apolipoprotein E genotype and outcome of traumatic brain injury</atitle><jtitle>Acta neurochirurgica</jtitle><addtitle>Acta Neurochir (Wien)</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>145</volume><issue>8</issue><spage>649</spage><epage>654</epage><pages>649-654</pages><issn>0001-6268</issn><eissn>0942-0940</eissn><abstract>The prognosis of traumatic brain injury is quite variable and not fully explained by the known factors. This study is to examine if the polymorphism of apolipoprotein E (apoE) influences the outcome of traumatic brain injury.
Over a period of twelve months, we prospectively studied 100 patients who sustained traumatic brain injuries and were admitted to our neurosurgical unit.
Nineteen patients were apoE4+ and 81 patients were apoE4-. There was no significant difference between apoE4+ and apoE4- groups in the cause of injury (p=0.288), type of brain injury (p=0.983) and choice of treatment (p=0.88). The proportion of patients with a lower GCS (<13), indicating a poor prognosis, was higher in the apoE4+ group (73.7%) than that in apoE4- group (61.7%), although the difference was not significant (p=0.654). Six patients (7.4%) in the apoE4- group and 5(26.3%) in the apoE4+ group had been drinking alcohol at the time of injury (p=0.018). The mean duration of hospital stay for apoE4+ patients was significantly longer than for apoE4- patients (p<0.001). Six months after injury, 10 of 19 patients (52.6%) with apoE4 had an unfavorable outcome (dead, vegetative state, or severe disability) compared with 20 of the 81 (24.1%) patients without apoE4 (p=0.017). The apoE4+ patients had a significantly longer hospital stay and unfavorable outcomes after brain injury.
This study discloses a significant genetic association between the apoE genotypes and outcomes of traumatic brain injury. Patients with apoE4 allele are more likely to have an unfavorable clinical outcome after brain injury.</abstract><cop>Austria</cop><pub>Springer Nature B.V</pub><pmid>14520543</pmid><doi>10.1007/s00701-003-0069-3</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Apolipoproteins Apolipoproteins E - genetics Brain damage Brain Injuries - genetics Brain Injuries - therapy Female Genotype Glasgow Coma Scale Humans Male Middle Aged People with disabilities Polymorphism, Genetic - genetics Predictive Value of Tests Prognosis Prospective Studies |
title | Association between apolipoprotein E genotype and outcome of traumatic brain injury |
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