Association of genetic polymorphisms of IL1[beta] -511 C>T, IL1RN VNTR 86 bp, IL6 -174 G>C, IL10 -819 C>T and TNF[alpha] -308 G>A, involved in symptomatic patients with dengue in Brazil

Objective In this study, single nucleotide polymorphisms (SNP) of interleukin (IL) 1[beta] -511C>T, IL1RN VNTR 86 bp, IL6 -174G>C, IL10 -819C>T and TNF[alpha] -308G>A were analyzed by PCR-RFLP with symptoms of dengue with the clinical features. Subjects 196 individuals admitted to the Sã...

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Veröffentlicht in:Inflammation research 2016-11, Vol.65 (11), p.925
Hauptverfasser: Cansanção, Isaac Farias, Do Carmo, Ana Paula, Santos, Leite, Robério Dias, Portela, Rosana Deyse, Ponte, de Sá Leitão Paiva Júnior, Sérgio, de Queiroz Balbino, Valdir, Rabenhorst, Silvia Helena, Barem
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container_end_page
container_issue 11
container_start_page 925
container_title Inflammation research
container_volume 65
creator Cansanção, Isaac Farias
Do Carmo, Ana Paula
Santos
Leite, Robério Dias
Portela, Rosana Deyse
Ponte
de Sá Leitão Paiva Júnior, Sérgio
de Queiroz Balbino, Valdir
Rabenhorst, Silvia Helena
Barem
description Objective In this study, single nucleotide polymorphisms (SNP) of interleukin (IL) 1[beta] -511C>T, IL1RN VNTR 86 bp, IL6 -174G>C, IL10 -819C>T and TNF[alpha] -308G>A were analyzed by PCR-RFLP with symptoms of dengue with the clinical features. Subjects 196 individuals admitted to the São José Infectious Diseases Hospital with suspected dengue infection. Dengue was confirmed in 111 of the patients. The control group consisted of 85 other individuals confirmed without dengue. Results It was demonstrated that the presence the T allele of IL1[beta] (P < 0.05) was associated with susceptibility to developing the disease. Other results also suggested that the polymorphism in the combinations IL6 × IL1[beta] (C and T alleles, respectively), IL1[beta] (T allele) × IL1RN (*2/*2 genotype), IL6 (C allele) × TNF[alpha] (A allele), IL10 (C/T genotype) × TNF[alpha] (A/A genotype) (P < 0.01, P = 0.01, P < 0.05 and P = 0.03, respectively) were associated with predisposition to developing the disease and its symptoms. Conclusions In summary, the findings of this study in a Brazilian population point out the importance of studies of combinations of polymorphisms in the development of dengue, which can increase the risk of dengue infection and its severity.
doi_str_mv 10.1007/s00011-016-0975-5
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Subjects 196 individuals admitted to the São José Infectious Diseases Hospital with suspected dengue infection. Dengue was confirmed in 111 of the patients. The control group consisted of 85 other individuals confirmed without dengue. Results It was demonstrated that the presence the T allele of IL1[beta] (P &lt; 0.05) was associated with susceptibility to developing the disease. Other results also suggested that the polymorphism in the combinations IL6 × IL1[beta] (C and T alleles, respectively), IL1[beta] (T allele) × IL1RN (*2/*2 genotype), IL6 (C allele) × TNF[alpha] (A allele), IL10 (C/T genotype) × TNF[alpha] (A/A genotype) (P &lt; 0.01, P = 0.01, P &lt; 0.05 and P = 0.03, respectively) were associated with predisposition to developing the disease and its symptoms. Conclusions In summary, the findings of this study in a Brazilian population point out the importance of studies of combinations of polymorphisms in the development of dengue, which can increase the risk of dengue infection and its severity.</description><identifier>ISSN: 1023-3830</identifier><identifier>EISSN: 1420-908X</identifier><identifier>DOI: 10.1007/s00011-016-0975-5</identifier><language>eng</language><publisher>New York: Springer Nature B.V</publisher><ispartof>Inflammation research, 2016-11, Vol.65 (11), p.925</ispartof><rights>Springer International Publishing 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Cansanção, Isaac Farias</creatorcontrib><creatorcontrib>Do Carmo, Ana Paula; Santos</creatorcontrib><creatorcontrib>Leite, Robério Dias</creatorcontrib><creatorcontrib>Portela, Rosana Deyse; Ponte</creatorcontrib><creatorcontrib>de Sá Leitão Paiva Júnior, Sérgio</creatorcontrib><creatorcontrib>de Queiroz Balbino, Valdir</creatorcontrib><creatorcontrib>Rabenhorst, Silvia Helena; Barem</creatorcontrib><title>Association of genetic polymorphisms of IL1[beta] -511 C&gt;T, IL1RN VNTR 86 bp, IL6 -174 G&gt;C, IL10 -819 C&gt;T and TNF[alpha] -308 G&gt;A, involved in symptomatic patients with dengue in Brazil</title><title>Inflammation research</title><description>Objective In this study, single nucleotide polymorphisms (SNP) of interleukin (IL) 1[beta] -511C&gt;T, IL1RN VNTR 86 bp, IL6 -174G&gt;C, IL10 -819C&gt;T and TNF[alpha] -308G&gt;A were analyzed by PCR-RFLP with symptoms of dengue with the clinical features. Subjects 196 individuals admitted to the São José Infectious Diseases Hospital with suspected dengue infection. Dengue was confirmed in 111 of the patients. The control group consisted of 85 other individuals confirmed without dengue. Results It was demonstrated that the presence the T allele of IL1[beta] (P &lt; 0.05) was associated with susceptibility to developing the disease. Other results also suggested that the polymorphism in the combinations IL6 × IL1[beta] (C and T alleles, respectively), IL1[beta] (T allele) × IL1RN (*2/*2 genotype), IL6 (C allele) × TNF[alpha] (A allele), IL10 (C/T genotype) × TNF[alpha] (A/A genotype) (P &lt; 0.01, P = 0.01, P &lt; 0.05 and P = 0.03, respectively) were associated with predisposition to developing the disease and its symptoms. 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Do Carmo, Ana Paula; Santos ; Leite, Robério Dias ; Portela, Rosana Deyse; Ponte ; de Sá Leitão Paiva Júnior, Sérgio ; de Queiroz Balbino, Valdir ; Rabenhorst, Silvia Helena; Barem</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_18264157873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cansanção, Isaac Farias</creatorcontrib><creatorcontrib>Do Carmo, Ana Paula; Santos</creatorcontrib><creatorcontrib>Leite, Robério Dias</creatorcontrib><creatorcontrib>Portela, Rosana Deyse; Ponte</creatorcontrib><creatorcontrib>de Sá Leitão Paiva Júnior, Sérgio</creatorcontrib><creatorcontrib>de Queiroz Balbino, Valdir</creatorcontrib><creatorcontrib>Rabenhorst, Silvia Helena; Barem</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Inflammation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cansanção, Isaac Farias</au><au>Do Carmo, Ana Paula; Santos</au><au>Leite, Robério Dias</au><au>Portela, Rosana Deyse; Ponte</au><au>de Sá Leitão Paiva Júnior, Sérgio</au><au>de Queiroz Balbino, Valdir</au><au>Rabenhorst, Silvia Helena; Barem</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of genetic polymorphisms of IL1[beta] -511 C&gt;T, IL1RN VNTR 86 bp, IL6 -174 G&gt;C, IL10 -819 C&gt;T and TNF[alpha] -308 G&gt;A, involved in symptomatic patients with dengue in Brazil</atitle><jtitle>Inflammation research</jtitle><date>2016-11-01</date><risdate>2016</risdate><volume>65</volume><issue>11</issue><spage>925</spage><pages>925-</pages><issn>1023-3830</issn><eissn>1420-908X</eissn><abstract>Objective In this study, single nucleotide polymorphisms (SNP) of interleukin (IL) 1[beta] -511C&gt;T, IL1RN VNTR 86 bp, IL6 -174G&gt;C, IL10 -819C&gt;T and TNF[alpha] -308G&gt;A were analyzed by PCR-RFLP with symptoms of dengue with the clinical features. Subjects 196 individuals admitted to the São José Infectious Diseases Hospital with suspected dengue infection. Dengue was confirmed in 111 of the patients. The control group consisted of 85 other individuals confirmed without dengue. Results It was demonstrated that the presence the T allele of IL1[beta] (P &lt; 0.05) was associated with susceptibility to developing the disease. Other results also suggested that the polymorphism in the combinations IL6 × IL1[beta] (C and T alleles, respectively), IL1[beta] (T allele) × IL1RN (*2/*2 genotype), IL6 (C allele) × TNF[alpha] (A allele), IL10 (C/T genotype) × TNF[alpha] (A/A genotype) (P &lt; 0.01, P = 0.01, P &lt; 0.05 and P = 0.03, respectively) were associated with predisposition to developing the disease and its symptoms. Conclusions In summary, the findings of this study in a Brazilian population point out the importance of studies of combinations of polymorphisms in the development of dengue, which can increase the risk of dengue infection and its severity.</abstract><cop>New York</cop><pub>Springer Nature B.V</pub><doi>10.1007/s00011-016-0975-5</doi></addata></record>
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title Association of genetic polymorphisms of IL1[beta] -511 C>T, IL1RN VNTR 86 bp, IL6 -174 G>C, IL10 -819 C>T and TNF[alpha] -308 G>A, involved in symptomatic patients with dengue in Brazil
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