https://scholars.lib.ntu.edu.tw/handle/123456789/434008
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Hong T.-H. | en_US |
dc.contributor.author | Chang C.-H. | en_US |
dc.contributor.author | Ko W.-J. | en_US |
dc.contributor.author | Lin C.-F. | en_US |
dc.contributor.author | Liu H.-H. | en_US |
dc.contributor.author | LU-PING CHOW | en_US |
dc.contributor.author | CHUN-TA HUANG | en_US |
dc.contributor.author | SUNG-LIANG YU | en_US |
dc.contributor.author | YIH-SHARNG CHEN | en_US |
dc.creator | Hong T.-H.;Chang C.-H.;Ko W.-J.;Lin C.-F.;Liu H.-H.;Chow L.-P.;Huang C.-T.;Yu S.-L.;Yih-Sharng Chen | - |
dc.date.accessioned | 2019-11-27T06:54:39Z | - |
dc.date.available | 2019-11-27T06:54:39Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1479-5876 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84901626390&doi=10.1186%2f1479-5876-12-146&partnerID=40&md5=45743c9be5818697cf05d06e30a16d29 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/434008 | - |
dc.description.abstract | Background: Sepsis causes high mortality, and the mortality due to secondary infections is even higher. No studies to date have investigated the time from the primary infection to death due to a secondary infection; similarly, the factors that are significantly different in sepsis survivors relative to non-survivors or in severe sepsis patients who suffered a late death relative to those who recover have not been explored. We hypothesized that patients who survive sepsis have a weaker pro-inflammatory response than those who do not and that the mid-term survivors (which acquire secondary infections) would have a pronounced anti-inflammatory response (making them susceptible to infection); this hypothesis was verified in this study. Methods: We examined 24 patients with severe sepsis; the patients were subdivided by outcome into early death (n = 5), mid-term survival (survival through severe sepsis but death within six months or continued hospitalization for six months, n = 6), and long-term survival (recovery and survival for more than six months, n = 13) groups. The levels of CD3+, CD4+, CD8+, and CD19+ lymphocytes were analyzed by flow cytometry, and the plasma levels of carbonic anhydrase IX (CA IX), MCP-1, IL-6, IL-7, IL-8, and IL-10 were measured by ELISA on days 0, 1, 2, and 3. A statistical comparison of the variables in the groups was conducted using a mixed model. Results: The plasma levels of MCP-1, IL-6, and IL-8 in early death and survivors were significantly different, and all had p values <0.01. The plasma levels of MCP-1, IL-6, and IL-8 were also significantly different in mid-term survivors and long-term survivors, with p values of <0.01, 0.04, and <0.01, respectively. Conclusions: Our data support the hypothesis that survivors have a weaker pro-inflammatory response than non-survivors, but the mid-term survivors did not have a more pronounced anti-inflammatory response. The levels of pro-inflammatory cytokines in the mid-term and long-term survivors were significantly different. ? 2014 Hong et al.; licensee BioMed Central Ltd. | - |
dc.publisher | BioMed Central Ltd. | - |
dc.relation.ispartof | Journal of Translational Medicine | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | carbonate dehydratase IX; interleukin 10; interleukin 6; interleukin 7; interleukin 8; monocyte chemotactic protein 1; biological marker; cytokine; leukocyte antigen; adult; article; cause of death; CD19+ T lymphocyte; CD3+ T lymphocyte; CD4+ T lymphocyte; CD8+ T lymphocyte; clinical article; controlled study; disease severity; enzyme linked immunosorbent assay; female; flow cytometry; hospitalization; human; immune response; inflammation; male; protein blood level; secondary infection; sepsis; survival time; T lymphocyte; aged; blood; immunology; immunophenotyping; middle aged; sepsis; treatment outcome; Aged; Antigens, CD; Biological Markers; Cytokines; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunophenotyping; Male; Middle Aged; Sepsis; Treatment Outcome | - |
dc.title | Biomarkers of early sepsis may be correlated with outcome | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1186/1479-5876-12-146 | - |
dc.identifier.pmid | 24886652 | - |
dc.identifier.scopus | 2-s2.0-84901626390 | - |
item.fulltext | no fulltext | - |
item.grantfulltext | none | - |
dc.relation.journalvolume | 12 | - |
dc.relation.journalissue | 1 | - |
item.fulltext | no fulltext | - |
item.grantfulltext | none | - |
item.openairetype | journal article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Biochemistry and Molecular Biology | - |
crisitem.author.dept | Internal Medicine | - |
crisitem.author.dept | Internal Medicine-NTUH | - |
crisitem.author.dept | Clinical Laboratory Sciences and Medical Biotechnology | - |
crisitem.author.dept | Pathology | - |
crisitem.author.dept | Medical Device and Imaging | - |
crisitem.author.dept | Surgery-NTUH | - |
crisitem.author.dept | Surgery | - |
crisitem.author.orcid | 0000-0002-4420-211X | - |
crisitem.author.orcid | 0000-0002-5234-4986 | - |
crisitem.author.orcid | 0000-0003-4535-9036 | - |
crisitem.author.orcid | 0000-0003-3846-8162 | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
顯示於: | 醫學系 |
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