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Association of a Large Panel of Cytokine Gene Polymorphisms with Complications and Comorbidities in Type 2 Diabetes Patients

dc.contributor.authorRodrigues, K. F.
dc.contributor.authorPietrani, N. T.
dc.contributor.authorSandrim, V. C. [UNESP]
dc.contributor.authorVieira, C. M. A. F.
dc.contributor.authorFernandes, A. P.
dc.contributor.authorBosco, A. A.
dc.contributor.authorGomes, K. B.
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSanta Casa Belo Horizonte
dc.date.accessioned2015-10-22T06:32:44Z
dc.date.available2015-10-22T06:32:44Z
dc.date.issued2015-01-01
dc.description.abstractAims. The polymorphisms of pro- and anti-inflammatory cytokines may be involved in type 2 diabetes (T2D) pathogenesis and its complications. Methods. We investigated in 102 T2D patients the association of the cytokine polymorphisms in the TNF-alpha, IL-10, IL-6, TGF-beta 1, and IFN-gamma genes with the T2D microvascular complications and comorbidities (hypertension, dyslipidemia, and obesity). Cytokine genotypes were determined by PCR using Cytokine Genotyping Tray kit. Results. Diabetic retinopathy was associated with GG genotype and G allele in TGF-beta 1 codon 25C/G polymorphism (p = 0.004 and.. = 0.018) and the nephropathy was associated the lower frequency of GG genotype in IL-10-1082G/A polymorphism (p = 0.049). Hypertension was associated with the CC genotype and C allele for IL-10 -592C/A polymorphism (p = 0.013 and p = 0.009) and higher frequencies of T (p = 0.047) and C (p = 0.033) alleles of the TGF-beta 1 codon 10T/C and IL-10-819T/C polymorphisms, respectively. The TGF-beta 1 codon 10T/C polymorphismwas associated with the BMI groups (p = 0.026): the CC genotype was more frequent in the group with BMI < 25Kg/m(2), while the TC genotype was more frequent in the group with BMI = 30 Kg/m(2). Conclusions. Our findings suggest that TGF-beta 1 and IL-10 polymorphisms are involved in complications and comorbidities in T2D patients.en
dc.description.affiliationUniv Fed Minas Gerais, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias, Botucatu, SP, Brazil
dc.description.affiliationSanta Casa Belo Horizonte, Inst Ensino &Pesquisa, Belo Horizonte, MG, Brazil
dc.description.affiliationUniv Fed Minas Gerais, Fac Farm, Dept Anal Clin &Toxicol, BR-31270901 Belo Horizonte, MG, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias, Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipPRPq/UFMG
dc.format.extent9
dc.identifierhttp://www.hindawi.com/journals/jdr/2015/605965/
dc.identifier.citationJournal Of Diabetes Research. New York: Hindawi Publishing Corporation, 9 p., 2015.
dc.identifier.doi10.1155/2015/605965
dc.identifier.issn2314-6745
dc.identifier.urihttp://hdl.handle.net/11449/129698
dc.identifier.wosWOS:000354751100001
dc.language.isoeng
dc.publisherHindawi Publishing Corporation
dc.relation.ispartofJournal Of Diabetes Research
dc.relation.ispartofjcr2.885
dc.relation.ispartofsjr1,116
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.titleAssociation of a Large Panel of Cytokine Gene Polymorphisms with Complications and Comorbidities in Type 2 Diabetes Patientsen
dc.typeArtigopt
dcterms.rightsHolderHindawi Publishing Corporation
dspace.entity.typePublication
unesp.author.orcid0000-0002-6168-7470[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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