Source:http://linkedlifedata.com/resource/pubmed/id/14701701
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2004-4-20
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pubmed:abstractText |
The aim of the study was to investigate whether interleukin-10 (IL-10) genetic polymorphisms influence this cytokine production as well as the incidence and outcome of diffuse large B-cell lymphoma (DLBCL). The frequency of IL-10(-1082G) allele was found to be higher in 199 patients with DLBCL as compared with 112 control subjects (0.47 versus 0.39, P =.043). Increased serum levels of IL-10 were associated with adverse prognostic factors and poor DLBCL outcome. The frequencies of IL-10(-819T) and IL-10(-592A) alleles were lower in patients with elevated IL-10 serum levels (0.155 versus 0.32, P =.14). As compared with patients carrying the IL-10(-1082AA) genotype, patients with the IL-10(-1082G) allele (IL-10(-1082GG/GA) genotypes) had higher complete remission rate (78% [confidence interval (CI), 71%-85%] versus 65% [CI, 52%-78%], P =.07), 5-year freedom from progression (FFP) (60% [CI, 52%-68%] versus 40% [CI, 27%-53%], P =.013), and overall survival (OS) (63% [CI, 55%-71%] versus 33% [CI, 20%-45%], P =.0009). Among factors of the International Prognostic Index, IL-10(-1082G) allele remained an independent variable, predicting longer freedom from progression (FFP) (RR [relative risk] =.76, P =.00035) and OS (RR =.78, P =.0015). These results indicate that IL-10 production contributes to the clinical course of DLBCL and that this phenomenon involves a substantial genetic component.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
103
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3529-34
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:14701701-Case-Control Studies,
pubmed-meshheading:14701701-Female,
pubmed-meshheading:14701701-Gene Frequency,
pubmed-meshheading:14701701-Genotype,
pubmed-meshheading:14701701-Humans,
pubmed-meshheading:14701701-Interleukin-10,
pubmed-meshheading:14701701-Lymphoma, B-Cell,
pubmed-meshheading:14701701-Lymphoma, Large B-Cell, Diffuse,
pubmed-meshheading:14701701-Male,
pubmed-meshheading:14701701-Middle Aged,
pubmed-meshheading:14701701-Polymorphism, Genetic,
pubmed-meshheading:14701701-Prognosis,
pubmed-meshheading:14701701-Promoter Regions, Genetic,
pubmed-meshheading:14701701-Remission Induction,
pubmed-meshheading:14701701-Survival Analysis,
pubmed-meshheading:14701701-Treatment Outcome
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pubmed:year |
2004
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pubmed:articleTitle |
Interleukin-10 gene promoter polymorphisms influence the clinical outcome of diffuse large B-cell lymphoma.
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pubmed:affiliation |
Equipe d'Accueil 3737 Pathologie des Cellules Lymphoïdes, Université Claude Bernard, Lyon, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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