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To Improve Translational Research in Subarachnoid Hemorrhage
[...]cerebrovascular anatomy and collaterals, as well as biological and secondary neuroinflammatory responses to insults, are different between species or strains, causing flawed design, unreliable outcomes, unnecessarily more costs, and experimental animals [7, 9–11]. [...]stroke patients have many...
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Published in: | Translational stroke research 2018-02, Vol.9 (1), p.1-3 |
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container_title | Translational stroke research |
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creator | Suzuki, Hidenori Nakano, Fumi |
description | [...]cerebrovascular anatomy and collaterals, as well as biological and secondary neuroinflammatory responses to insults, are different between species or strains, causing flawed design, unreliable outcomes, unnecessarily more costs, and experimental animals [7, 9–11]. [...]stroke patients have many comorbidities or vascular risk factors including hypertension, diabetes mellitus, dyslipidemia, cardiac diseases, current smoking, obesity, poor diet, inactivity, high alcohol intake, psychosocial stress and depression, social factors such as marital and residence status (i.e., living alone), and prestroke dysfunction, causing stroke severity [5, 14]. Animal models having these factors are also subjected to different stroke injuries or changes in the structure of the neurovascular unit [14]. [...]the use of young healthy animals causes a barrier for translation of findings to patients, while, in preclinical stroke studies with comorbidities, comorbidity duration and severity as well as housing conditions of the animals used, which potentially influence outcomes, should be reported in details. [...]both EBI and cerebral vasospasm occur in the time frame of 72 h in the mouse or rat model, precluding the dissociation between EBI and cerebral vasospasm-induced or other delayed brain injuries. [...]SAH researchers should understand the advantages and disadvantages of each animal model and choose a suitable model dependent on the research question. [...]we can say that the failed clinical trials could have been predicted and avoided if the review and the meta-analysis had been performed before planning the clinical trials. |
doi_str_mv | 10.1007/s12975-017-0546-2 |
format | article |
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[...]stroke patients have many comorbidities or vascular risk factors including hypertension, diabetes mellitus, dyslipidemia, cardiac diseases, current smoking, obesity, poor diet, inactivity, high alcohol intake, psychosocial stress and depression, social factors such as marital and residence status (i.e., living alone), and prestroke dysfunction, causing stroke severity [5, 14]. Animal models having these factors are also subjected to different stroke injuries or changes in the structure of the neurovascular unit [14]. [...]the use of young healthy animals causes a barrier for translation of findings to patients, while, in preclinical stroke studies with comorbidities, comorbidity duration and severity as well as housing conditions of the animals used, which potentially influence outcomes, should be reported in details. [...]both EBI and cerebral vasospasm occur in the time frame of 72 h in the mouse or rat model, precluding the dissociation between EBI and cerebral vasospasm-induced or other delayed brain injuries. [...]SAH researchers should understand the advantages and disadvantages of each animal model and choose a suitable model dependent on the research question. [...]we can say that the failed clinical trials could have been predicted and avoided if the review and the meta-analysis had been performed before planning the clinical trials.</description><identifier>ISSN: 1868-4483</identifier><identifier>EISSN: 1868-601X</identifier><identifier>DOI: 10.1007/s12975-017-0546-2</identifier><identifier>PMID: 28620886</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Bias ; Biomedical and Life Sciences ; Biomedicine ; Blood-brain barrier ; Brain research ; Cardiology ; Clinical trials ; Editorial ; Experiments ; Ischemia ; Laboratory animals ; Neurology ; Neurosciences ; Neurosurgery ; Sexes ; Stroke ; Traumatic brain injury ; Vascular Surgery</subject><ispartof>Translational stroke research, 2018-02, Vol.9 (1), p.1-3</ispartof><rights>Springer Science+Business Media, LLC 2017</rights><rights>Springer Science+Business Media, LLC 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-ac92096d02294654254586c737c439ac564f98cd2381e9abae79bfa6b83e3ad03</citedby><cites>FETCH-LOGICAL-c481t-ac92096d02294654254586c737c439ac564f98cd2381e9abae79bfa6b83e3ad03</cites><orcidid>0000-0002-8555-5448</orcidid></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/28620886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Hidenori</creatorcontrib><creatorcontrib>Nakano, Fumi</creatorcontrib><title>To Improve Translational Research in Subarachnoid Hemorrhage</title><title>Translational stroke research</title><addtitle>Transl. Stroke Res</addtitle><addtitle>Transl Stroke Res</addtitle><description>[...]cerebrovascular anatomy and collaterals, as well as biological and secondary neuroinflammatory responses to insults, are different between species or strains, causing flawed design, unreliable outcomes, unnecessarily more costs, and experimental animals [7, 9–11]. [...]stroke patients have many comorbidities or vascular risk factors including hypertension, diabetes mellitus, dyslipidemia, cardiac diseases, current smoking, obesity, poor diet, inactivity, high alcohol intake, psychosocial stress and depression, social factors such as marital and residence status (i.e., living alone), and prestroke dysfunction, causing stroke severity [5, 14]. Animal models having these factors are also subjected to different stroke injuries or changes in the structure of the neurovascular unit [14]. [...]the use of young healthy animals causes a barrier for translation of findings to patients, while, in preclinical stroke studies with comorbidities, comorbidity duration and severity as well as housing conditions of the animals used, which potentially influence outcomes, should be reported in details. [...]both EBI and cerebral vasospasm occur in the time frame of 72 h in the mouse or rat model, precluding the dissociation between EBI and cerebral vasospasm-induced or other delayed brain injuries. [...]SAH researchers should understand the advantages and disadvantages of each animal model and choose a suitable model dependent on the research question. [...]we can say that the failed clinical trials could have been predicted and avoided if the review and the meta-analysis had been performed before planning the clinical trials.</description><subject>Bias</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood-brain barrier</subject><subject>Brain research</subject><subject>Cardiology</subject><subject>Clinical trials</subject><subject>Editorial</subject><subject>Experiments</subject><subject>Ischemia</subject><subject>Laboratory animals</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Sexes</subject><subject>Stroke</subject><subject>Traumatic brain injury</subject><subject>Vascular Surgery</subject><issn>1868-4483</issn><issn>1868-601X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUhoMottQ-gBsZcONmNPcLuJGitlAQtIK7kMmk7ZSZSU06gm9vylQFwWxOIN_5c84HwDmC1whCcRMRVoLlEIkcMspzfASGSHKZc4jejg93SiUZgHGMG5gOQZRTcgoGWHIMpeRDcLvw2azZBv_hskUwbazNrvKtqbNnF50Jdp1VbfbSFSYYu259VWZT1_gQ1mblzsDJ0tTRjQ91BF4f7heTaT5_epxN7ua5pRLtcmMVhoqXEGNFOaOYUSa5FURYSpSxjNOlkrbERCKnTGGcUMXS8EISR0wJyQhc9blpzvfOxZ1uqmhdXZvW-S5qpBAUSgnIEnr5B934LqR9osZpCq4YxihRqKds8DEGt9TbUDUmfGoE9d6u7u3qZFfv7Wqcei4OyV3RuPKn49tlAnAPxPTUrlz4_fr_1C8OwYK0</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Suzuki, Hidenori</creator><creator>Nakano, Fumi</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8555-5448</orcidid></search><sort><creationdate>20180201</creationdate><title>To Improve Translational Research in Subarachnoid Hemorrhage</title><author>Suzuki, Hidenori ; Nakano, Fumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-ac92096d02294654254586c737c439ac564f98cd2381e9abae79bfa6b83e3ad03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Bias</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Blood-brain barrier</topic><topic>Brain research</topic><topic>Cardiology</topic><topic>Clinical trials</topic><topic>Editorial</topic><topic>Experiments</topic><topic>Ischemia</topic><topic>Laboratory animals</topic><topic>Neurology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Sexes</topic><topic>Stroke</topic><topic>Traumatic brain injury</topic><topic>Vascular Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Hidenori</creatorcontrib><creatorcontrib>Nakano, Fumi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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 One Psychology</collection><collection>MEDLINE - Academic</collection><jtitle>Translational stroke research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Hidenori</au><au>Nakano, Fumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>To Improve Translational Research in Subarachnoid Hemorrhage</atitle><jtitle>Translational stroke research</jtitle><stitle>Transl. Stroke Res</stitle><addtitle>Transl Stroke Res</addtitle><date>2018-02-01</date><risdate>2018</risdate><volume>9</volume><issue>1</issue><spage>1</spage><epage>3</epage><pages>1-3</pages><issn>1868-4483</issn><eissn>1868-601X</eissn><abstract>[...]cerebrovascular anatomy and collaterals, as well as biological and secondary neuroinflammatory responses to insults, are different between species or strains, causing flawed design, unreliable outcomes, unnecessarily more costs, and experimental animals [7, 9–11]. [...]stroke patients have many comorbidities or vascular risk factors including hypertension, diabetes mellitus, dyslipidemia, cardiac diseases, current smoking, obesity, poor diet, inactivity, high alcohol intake, psychosocial stress and depression, social factors such as marital and residence status (i.e., living alone), and prestroke dysfunction, causing stroke severity [5, 14]. Animal models having these factors are also subjected to different stroke injuries or changes in the structure of the neurovascular unit [14]. [...]the use of young healthy animals causes a barrier for translation of findings to patients, while, in preclinical stroke studies with comorbidities, comorbidity duration and severity as well as housing conditions of the animals used, which potentially influence outcomes, should be reported in details. [...]both EBI and cerebral vasospasm occur in the time frame of 72 h in the mouse or rat model, precluding the dissociation between EBI and cerebral vasospasm-induced or other delayed brain injuries. [...]SAH researchers should understand the advantages and disadvantages of each animal model and choose a suitable model dependent on the research question. [...]we can say that the failed clinical trials could have been predicted and avoided if the review and the meta-analysis had been performed before planning the clinical trials.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28620886</pmid><doi>10.1007/s12975-017-0546-2</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0002-8555-5448</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bias Biomedical and Life Sciences Biomedicine Blood-brain barrier Brain research Cardiology Clinical trials Editorial Experiments Ischemia Laboratory animals Neurology Neurosciences Neurosurgery Sexes Stroke Traumatic brain injury Vascular Surgery |
title | To Improve Translational Research in Subarachnoid Hemorrhage |
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