Autor(es):Mostrar menos -

Corbi, Samia C. T. ^{[1, 2]} ; de Vasconcellos, Jaira F. ^{[3, 4, 5]} ; Bastos, Alliny S. ^{[1, 6]} ; Bussaneli, Diego Girotto ^[2] ; da Silva, Barbara Roque ^[2] ; Santos, Raquel Alves ^[7] ; Takahashi, Catarina S. ^{[8, 9]} ; Rocha, Cristiane de S. ^[10] ; Carvalho, Benilton de Sa ^[11] ; Maurer-Morelli, V, Claudia ; Orrico, Silvana R. P. ^{[1, 6, 12]} ; Barros, Silvana P. ^[13] ; Scarel-Caminaga, Raquel M. ^[2]

Afiliação do(s) autor(es):Mostrar menos -

^[1] UNESP Sao Paulo State Univ, Sch Dent Araraquara, Dept Diag & Surg, BR-14801385 Araraquara, SP - Brazil

^[2] UNESP Sao Paulo State Univ, Sch Dent Araraquara, Dept Morphol Genet Orthodont & Pediat Dent, BR-14801385 Araraquara, SP - Brazil

^[3] NIDDK, Mol Genom & Therapeut Sect, Genet Dev & Dis Branch, NIH, 10 Ctr Dr, Bldg 10, Room 9D11, Bethesda, MD 20892 - USA

^[4] Uniformed Serv Univ Hlth Sci, Dept Surg, Bethesda, MD 20814 - USA

^[5] Henry Jackson Fdn Adv Mil Med, Bethesda, MD - USA

^[6] Orrico, Silvana R. P., Union Coll Great Lakes UNILAGO, Adv Res Ctr Med, BR-15030070 Sao Jose Do Rio Preto, SP, Brazil.Corbi, Samia C. T., UNESP Sao Paulo State Univ, Sch Dent Araraquara, Dept Diag & Surg, BR-14801385 Araraquara, SP - Brazil

^[7] Univ Franca, Postgrad Program Sci, BR-14404600 Franca, SP - Brazil

^[8] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, BR-14049900 Ribeirao Preto, SP - Brazil

^[9] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Dept Biol, BR-14049900 Ribeirao Preto, SP - Brazil

^[10] V, Univ Campinas UNICAMP, Dept Med Genet & Med Genom, BR-13083887 Campinas, SP - Brazil

^[11] Univ Estadual Campinas, Dept Stat, Inst Math Stat & Sci Comp, BR-13083859 Campinas, SP - Brazil

^[12] Union Coll Great Lakes UNILAGO, Adv Res Ctr Med, BR-15030070 Sao Jose Do Rio Preto, SP - Brazil

^[13] Univ N Carolina, Dept Periodontol, Sch Dent, Chapel Hill, NC 27515 - USA

• Tipo de documento: Artigo Científico
• Fonte: SCIENTIFIC REPORTS; v. 10, n. 1 MAY 18 2020.
• Citações Web of Science: 0

Resumo

Type 2 diabetes mellitus (T2DM), dyslipidemia and periodontitis are frequently associated pathologies; however, there are no studies showing the peripheral blood transcript profile of these combined diseases. Here we identified the differentially expressed genes (DEGs) of circulating lymphocytes and monocytes to reveal potential biomarkers that may be used as molecular targets for future diagnosis of each combination of these pathologies (compared to healthy patients) and give insights into the underlying molecular mechanisms of these diseases. Study participants (n=150) were divided into groups: (H) systemically and periodontal healthy (control group); (P) with periodontitis, but systemically healthy; (DL-P) with dyslipidemia and periodontitis; (T2DMwell-DL-P) well-controlled type 2 diabetes mellitus with dyslipidemia and periodontitis; and (T2DMpoorly-DL-P) poorly-controlled type 2 diabetes mellitus with dyslipidemia and periodontitis. We preprocessed the microarray data using the Robust Multichip Average (RMA) strategy, followed by the RankProd method to identify candidates for DEGs. Furthermore, we performed functional enrichment analysis using Ingenuity Pathway Analysis and Gene Set Enrichment Analysis. DEGs were submitted to pairwise comparisons, and selected DEGs were validated by quantitative polymerase chain reaction. Validated DEGs verified from T2DMpoorly-DL-P versus H were: TGFB1I1, VNN1, HLADRB4 and CXCL8; T2DMwell-DL-P versus H: FN1, BPTF and PDE3B; DL-P versus H: DAB2, CD47 and HLADRB4; P versus H: IGHDL-P, ITGB2 and HLADRB4. In conclusion, we identified that circulating lymphocytes and monocytes of individuals simultaneously affected by T2DM, dyslipidemia and periodontitis, showed an altered molecular profile mainly associated to inflammatory response, immune cell trafficking, and infectious disease pathways. Altogether, these results shed light on novel potential targets for future diagnosis, monitoring or development of targeted therapies for patients sharing these conditions. (AU)

• Processo FAPESP: 07/08362-8 - Avaliação da correlação entre peroxidação lipídica e o perfil de marcadores inflamatórios em pacientes portadores de diabetes mellitus tipo 2 com periodontite crônica
• Beneficiário: Silvana Regina Perez Orrico
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 14/16148-0 - Investigação do transcriptoma e do proteoma salivar e plasmático em indivíduos acometidos por diabetes mellitus tipo 2, dislipidemia e doença periodontal crônica
• Beneficiário: Sâmia Cruz Tfaile Corbi
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 10/10882-2 - Expressão gênica em indivíduos portadores de Diabetes mellitus tipo 2, dislipidemia e doença periodontal: avaliação por microarray
• Beneficiário: Raquel Mantuaneli Scarel Caminaga
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 09/16233-9 - Avaliação do efeito da descompensação do Diabetes Mellitus sobre a expressão de genes do sistema imune e sobre lesões no DNA em pacientes com periodontite crônica.
• Beneficiário: Sâmia Cruz Tfaile Corbi
• Modalidade de apoio: Bolsas no Brasil - Doutorado