170 results on '"Salles GF"'
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2. Capítulo 3 - Avaliação Clínica e Complementar
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
- Full Text
- View/download PDF
3. Capítulo 12 - Hipertensão Arterial Secundária
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
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4. Capítulo 4 - Estratificaçã o de Risco Cardiovascular
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
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5. Capítulo 13 - Hipertensão Arterial Resistente
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
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6. Capítulo 5 - Decisão e Metas Terapêuticas
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
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7. Capítulo 1 - Conceituação, Epidemiologia e Prevenção Primária
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
- Full Text
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8. Capítulo 10 - Hipertensão na Criança e no Adolescente
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
- Full Text
- View/download PDF
9. Capítulo 14 – Crise Hipertensiva
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
- Full Text
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10. Capítulo 8 - Hipertensão e Condições Clínicas Associadas
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
- Published
- 2016
- Full Text
- View/download PDF
11. Capítulo 11 - Hipertensão Arterial no Idoso
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
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- 2016
- Full Text
- View/download PDF
12. Capítulo 6 - Tratamento não medicamentoso
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
- Published
- 2016
- Full Text
- View/download PDF
13. Capítulo 9 - Hipertensão Arterial na gestação
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
- Published
- 2016
- Full Text
- View/download PDF
14. Capítulo 7 – Tratamento Medicamentoso
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
- Published
- 2016
- Full Text
- View/download PDF
15. Capítulo 2 - Diagnóstico e Classificação
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Malachias, MVB, primary, Souza, WKSB, additional, Plavnik, FL, additional, Rodrigues, CIS, additional, Brandão, AA, additional, Neves, MFT, additional, Bortolotto, LA, additional, Franco, RJS, additional, Figueiredo, CEP, additional, Jardim, PCBV, additional, Amodeo, C, additional, Barbosa, ECD, additional, Koch, V, additional, Gomes, MAM, additional, Paula, RB, additional, Póvoa, RMS, additional, Colombo, FC, additional, Ferreira Filho, S, additional, Miranda, RD, additional, Machado, CA, additional, Nobre, F, additional, Nogueira, AR, additional, Mion Júnior, D, additional, Kaiser, S, additional, Forjaz, CLM, additional, Almeida, FA, additional, Martim, JFV, additional, Sass, N, additional, Drager, LF, additional, Muxfeldt, E, additional, Bodanese, LC, additional, Feitosa, AD, additional, Malta, D, additional, Fuchs, S, additional, Magalhães, ME, additional, Oigman, W, additional, Gomes, OM, additional, Pierin, AMG, additional, Feitosa, GS, additional, Bortolotto, MRFL, additional, Magalhães, LBNC, additional, Silva, ACS, additional, Ribeiro, JM, additional, Borelli, FAO, additional, Gus, M, additional, Passarelli Júnior, O, additional, Toledo, JY, additional, Salles, GF, additional, Martins, LC, additional, Jardim, TSV, additional, Guimarães, ICB, additional, Antonello, IC, additional, Lima Júnior, E, additional, Matsudo, V, additional, Silva, GV, additional, Costa, LS, additional, Alessi, A, additional, Scala, LCN, additional, Coelho, EB, additional, Souza, D, additional, Lopes, HF, additional, Gowdak, MMG, additional, Cordeiro Júnior, AC, additional, Torloni, MR, additional, Klein, MRST, additional, Nogueira, PK, additional, Lotaif, LAD, additional, Rosito, GBA, additional, and Moreno Júnior, H, additional
- Published
- 2016
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16. Initial and accrued damage as predictors of mortality in Brazilian patients with systemic lupus erythematosus: a cohort study
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Cardoso, CRL, primary, Signorelli, FV, additional, Papi, JAS, additional, and Salles, GF, additional
- Published
- 2008
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17. Factors associated with carotid intima-media thickness and carotid plaques in type 2 diabetic patients.
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Cardoso CR, Marques CE, Leite NC, and Salles GF
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- 2012
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18. Appropriate time interval to repeat ambulatory blood pressure monitoring in patients with white-coat resistant hypertension.
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Muxfeldt ES, Fiszman R, de Souza F, Viegas B, Oliveira FC, Salles GF, Muxfeldt, Elizabeth S, Fiszman, Roberto, de Souza, Fabio, Viegas, Bianca, Oliveira, Fernanda C, and Salles, Gil F
- Abstract
Resistant hypertension is defined as uncontrolled office blood pressure, despite the use of ≥3 antihypertensive drugs. Ambulatory blood pressure monitoring (ABPM) is mandatory to diagnose 2 different groups, those with true and white-coat resistant hypertension. Patients are found to change categories between controlled/uncontrolled ambulatory pressures without changing their office blood pressures. In this way, ABPM should be periodically repeated. The aim of this study was to evaluate the most appropriate time interval to repeat ABPM to assure sustained blood pressure control in patients with white-coat resistant hypertension. This prospective study enrolled 198 patients (69% women; mean age: 68.9±9.9 years) diagnosed as white-coat resistant hypertension on ABPM. Patients were submitted to a second confirmatory examination 3 months later and repeated twice at 6-month intervals. Statistical analyses included Bland-Altman repeatability coefficients and multivariate logistic regression. Mean office blood pressure was 163±20/84±17 mm Hg, and mean 24-hour blood pressure was 118±8/66±7 mm Hg. White-coat resistant hypertension diagnosis presented a moderate reproducibility and was confirmed in 144 patients after 3 months. In the third and fourth ABPMs, 74% and 79% of patients sustained the diagnosis. In multivariate regression, a daytime systolic blood pressure ≤115 mm Hg in the confirmatory ABPM triplicated the chance of white-coat resistant hypertension status persistence after 1 year. In conclusion, a confirmatory ABPM is necessary after 3 months of the first white-coat-resistant hypertension diagnosis, and the procedure should be repeated at 6-month intervals, except in patients with daytime systolic blood pressure ≤115 mm Hg, in whom it may be repeated annually. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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19. Prognostic significance of a reduced glomerular filtration rate and interaction with microalbuminuria in resistant hypertension: a cohort study.
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Salles GF, Cardoso CR, Pereira VS, Fiszman R, and Muxfeldt ES
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- 2011
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20. Prognostic significance of baseline and serial changes in electrocardiographic strain pattern in resistant hypertension.
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Salles GF, Cardoso CR, Fiszman R, and Muxfeldt ES
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- 2010
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21. Prognostic impact of the ambulatory arterial stiffness index in resistant hypertension.
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Muxfeldt ES, Cardoso CR, Dias VB, Nascimento AC, and Salles GF
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- 2010
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22. Prognostic value of ventricular repolarization prolongation in resistant hypertension: a prospective cohort study.
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Salles GF, Cardoso CR, and Muxfeldt ES
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- 2009
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23. Pulse pressure or dipping pattern: which one is a better cardiovascular risk marker in resistant hypertension?
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Muxfeldt ES and Salles GF
- Published
- 2008
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24. Orlistat in hypertensive overweight/obese patients: results of a randomized clinical trial.
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Bloch KV, Salles GF, Muxfeldt ES, da Rocha Nogueira A, Bloch, Katia Vergetti, Salles, Gil Fernando, Muxfeldt, Elizabeth Silaid, and Da Rocha Nogueira, Armando
- Published
- 2003
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25. QTc interval prolongation is a predictor of future strokes in patients with type 2 diabetes mellitus.
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Cardoso CR, Salles GF, Deccache W, Cardoso, Claudia R L, Salles, Gil F, and Deccache, Waldemar
- Published
- 2003
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26. Importance of the Hemoglobin Glycation Index for Risk of Cardiovascular and Microvascular Complications and Mortality in Individuals with Type 2 Diabetes.
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Humans, Male, Female, Middle Aged, Aged, Prognosis, Diabetic Angiopathies mortality, Diabetic Angiopathies etiology, Risk Factors, Follow-Up Studies, Hypoglycemia mortality, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 mortality, Diabetes Mellitus, Type 2 metabolism, Glycated Hemoglobin analysis, Cardiovascular Diseases mortality, Cardiovascular Diseases etiology
- Abstract
Backgruound: This study investigated the prognostic importance of the hemoglobin glycation index (HGI) for macrovascular and microvascular outcomes, mortality, and hypoglycemia occurrence in a type 2 diabetes cohort and compared it to glycated hemoglobin (HbA1c)., Methods: Baseline and mean first-year HGI and HbA1c, and the variability thereof, were assessed in 687 individuals with type 2 diabetes (median follow-up, 10.6 years). Multivariable Cox regression was conducted to evaluate the associations of HGI and HbA1c parameters with macrovascular (total and major cardiovascular events) and microvascular outcomes (microalbuminuria, advanced renal failure, retinopathy, and peripheral neuropathy), mortality (all-cause and cardiovascular), and moderate/severe hypoglycemia occurrence., Results: During follow-up, there were 215 total cardiovascular events (176 major) and 269 all-cause deaths (131 cardiovascular). Microalbuminuria developed in 126 patients, renal failure in 104, retinopathy in 161, and neuropathy in 177. There were 90 hypoglycemia episodes. Both HGI and HbA1c predicted all adverse outcomes, except microalbuminuria and hypoglycemia. Their adjusted risks were roughly equivalent for all outcomes. For example, the adjusted hazard ratios (HRs) with 95% confidence intervals (CIs), estimated for 1 standard deviation increments, of mean first-year HGI were 1.23 (1.05 to 1.44), 1.20 (1.03 to 1.38), 1.36 (1.11 to 1.67), 1.28 (1.09 to 1.67), and 1.29 (1.09 to 1.54), respectively, for cardiovascular events, all-cause mortality, renal failure, retinopathy, and neuropathy; whereas the respective HRs (95% CIs) of mean HbA1c were 1.31 (1.12 to 1.53), 1.28 (1.11 to 1.48), 1.36 (1.11 to 1.67), 1.33 (1.14 to 1.55), and 1.29 (1.09 to 1.53)., Conclusion: HGI was no better than HbA1c as a predictor of adverse outcomes in individuals with type 2 diabetes, and its clinical use cannot be currently advised.
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- 2024
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27. Response to Comment on: Risk of heart failure in ambulatory resistant hypertension: a meta-analysis of observational studies.
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Coccina F, Salles GF, Banegas JR, Hermida RC, Bastos JM, and Pierdomenico SD
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- Humans, Observational Studies as Topic, Heart Failure epidemiology, Hypertension
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- 2024
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28. Body weight variability and the risk of liver-related outcomes in type 2 diabetes and steatotic liver disease: a cohort study.
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Leite NC, Cardoso CRL, Villela-Nogueira CA, and Salles GF
- Subjects
- Humans, Male, Female, Middle Aged, Aged, Risk Factors, Liver Cirrhosis complications, Cohort Studies, Body Weight, Elasticity Imaging Techniques, Follow-Up Studies, Exercise, Body Mass Index, Adult, Logistic Models, Diabetes Mellitus, Type 2 complications, Liver pathology, Fatty Liver
- Abstract
Objective: The objective of this study was to evaluate the effects of body weight variability (BWV) on the occurrence of adverse liver outcomes in individuals with type 2 diabetes (T2D) and metabolic dysfunction-associated steatotic liver disease (MASLD)., Methods: A total of 549 patients with T2D and MASLD had BWV parameters assessed during the first 2 years of follow-up. The associations between increasing BWV and liver outcomes (clinical cirrhosis or a liver stiffness measurement on transient elastography > 15 kPa, performed after a median of 7 years of cohort entry) were examined by multivariable logistic regressions. Interaction/subgroup analyses were performed according to participants' physical activity during the initial 2-year period., Results: Individuals were followed up for an additional median 9.7 years, over which 34 liver outcomes occurred (14 with clinical cirrhosis and 20 with liver stiffness measurement > 15 kPa). A 1-SD increase in weight SD and average real variability was associated with 52% higher (95% CI: 4%-128%) odds of having an adverse liver outcome. Otherwise, in interaction/subgroup analyses, an increased BWV was associated with a higher likelihood of outcomes only in sedentary individuals., Conclusions: Increased BWV was associated with adverse liver outcomes in individuals with T2D and MASLD; however, in those who were physically active, it was not hazardous., (© 2024 The Obesity Society.)
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- 2024
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29. Risk of heart failure in ambulatory resistant hypertension: a meta-analysis of observational studies.
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Coccina F, Salles GF, Banegas JR, Hermida RC, Bastos JM, Cardoso CRL, Salles GC, Sánchez-Martínez M, Mojón A, Fernández JR, Costa C, Carvalho S, Faia J, and Pierdomenico SD
- Subjects
- Humans, Antihypertensive Agents therapeutic use, Blood Pressure Monitoring, Ambulatory, Observational Studies as Topic, Risk Factors, Heart Failure, Hypertension drug therapy, Hypertension complications
- Abstract
The impact of ambulatory resistant hypertension (ARH) on the occurrence of heart failure (HF) is not yet completely known. We performed for the first time a meta-analysis, by using published data or available data from published databases, on the risk of HF in ARH. Patients with ARH (24-h BP ≥ 130/80 mmHg during treatment with ≥3 drugs) were compared with those with controlled hypertension (CH, clinic BP < 140/90 mmHg and 24-h BP < 130/80 mmHg regardless of the number of drugs used), white coat uncontrolled resistant hypertension (WCURH, clinic BP ≥ 140/90 mmHg and 24-h BP < 130/80 mmHg in treated patients) and ambulatory nonresistant hypertension (ANRH, 24-h BP ≥ 130/80 mmHg during therapy with ≤2 drugs). We identified six studies/databases including 21,365 patients who experienced 692 HF events. When ARH was compared with CH, WCURH, or ANRH, the overall adjusted hazard ratio for HF was 2.32 (95% confidence interval (CI) 1.45-3.72), 1.72 (95% CI 1.36-2.17), and 2.11 (95% CI 1.40-3.17), respectively, (all P < 0.001). For some comparisons a moderate heterogeneity was found. Though we did not find variables that could explain the heterogeneity, sensitivity analyses demonstrated that none of the studies had a significant influential effect on the overall estimate. When we evaluated the potential presence of publication bias and small-study effect and adjusted for missing studies identified by Duval and Tweedie's method the estimates were slightly lower but remained significant. This meta-analysis shows that treated hypertensive patients with ARH are at approximately twice the risk of developing HF than other ambulatory BP phenotypes., (© 2024. The Author(s).)
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- 2024
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30. Impact of PNPLA3 and TM6SF2 polymorphisms on the prognosis of patients with MASLD and type 2 diabetes mellitus.
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Lavrado NC, Salles GF, Cardoso CRL, de França PHC, Melo MFDGG, Leite NC, and Villela-Nogueira CA
- Subjects
- Humans, Female, Male, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Liver Cirrhosis genetics, Fibrosis, Prognosis, Genotype, Membrane Proteins genetics, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 genetics, Fatty Liver, Non-alcoholic Fatty Liver Disease genetics
- Abstract
Background/aims: Longitudinal studies assessing the impact of genetic polymorphisms on outcomes in patients with Type 2 Diabetes Mellitus (T2DM) and Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) are scarce. This study aimed to evaluate the effect of PNPLA3 and TM6SF2 risk alleles on hepatic and extrahepatic outcomes in T2DM-MASLD individuals., Methods: Patients' polymorphisms were analysed as follows: PNPLA3 CC, CG and GG; TM6SF2 CC and CT + TT; combined comparing no mutant allele, one allele G or T or ≥2 alleles G or T. Hierarchical models were built to assess associations between polymorphisms and outcomes, independently of confounding factors. Multivariate logistic regression was used for cirrhosis and its complications and extrahepatic cancer, and Cox regression for cardiovascular events (CVEs) and all-cause mortality., Results: In total, 407 T2DM-MASLD patients (62.1 ± 10.5 years, 67.6% women) were followed for 11 (6-13) years. Having at least one G or T allele independently increased the risk of cirrhosis in the separate analysis of PNPLA3 and TM6SF2. Combined polymorphism analysis demonstrated an even higher risk of cirrhosis if two or more risk alleles were present (OR 18.48; 95% CI 6.15-55.58; p < .001). Regarding cirrhosis complications, the risk was higher in PNPLA3 GG and TM6SF2 CT + TT, also with an even higher risk when two or more risk alleles were present in the combined evaluation (OR 27.20; 95% CI 5.26-140.62; p < .001). There were no associations with CVEs or mortality outcomes., Conclusion: In T2DM, PNPLA3 and TM6SF2 polymorphisms, individually and additively, impact MASLD severity, with an increased risk of cirrhosis and its complications., (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2024
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31. Parental History of Type 2 Diabetes Mellitus and PNPLA3 Polymorphism Increase the Risk of Severe Stages of Nonalcoholic Fatty Liver Disease.
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Wajsbrot NB, Leite NC, Franca PHC, Cardoso CRL, Salles GF, and Villela-Nogueira CA
- Subjects
- Adolescent, Adult, Child, Humans, Middle Aged, Young Adult, Case-Control Studies, Fibrosis, Genetic Predisposition to Disease, Genotype, Liver pathology, Polymorphism, Single Nucleotide, Diabetes Mellitus, Type 2 epidemiology, Diabetes Mellitus, Type 2 genetics, Diabetes Mellitus, Type 2 metabolism, Non-alcoholic Fatty Liver Disease diagnostic imaging, Non-alcoholic Fatty Liver Disease epidemiology, Non-alcoholic Fatty Liver Disease genetics
- Abstract
Background & Aims: In non-alcoholic fatty liver disease (NAFLD), the influence of parental history of type 2 diabetes (T2D) allied to single nucleotide polymorphisms (SNPs) in the offspring is not known. We aimed to investigate the impact of the parental history of T2D, PNPLA3 and TM6SF2 polymorphisms in liver steatosis and fibrosis., Methods: This was a case-control study involving the offspring of T2D patients and controls without a parental history of T2D. Participants underwent clinical and laboratory evaluation, transient elastography (TE) by Fibroscan
® (Echosens, Fr) and genotyping for PNPLA3 and TM6SF2. Multivariate logistic regression evaluated the influence of parental history of T2D on liver steatosis and fibrosis, controlled for age, gender, metabolic traits and SNPs., Results: 161 T2D offspring and 78 controls, 10-46 years old, were included. The offspring of T2D had higher prevalences of obesity, T2D, arterial hypertension and sedentarism. Parental history of T2D was associated with fibrosis ≥ F2 (OR 8.89, CI 95% 1.09-72.01, p = 0.041) after adjustment for age, gender, metabolic traits and SNPs. PNPLA3 GG genotype was independently associated with steatosis ≥ S1 (OR 8.15, CI 95% 1.93-34.38, p = 0.004) and fibrosis ≥ F2 (OR 4.31, CI 95% 1.11-16.61, p = 0.034)., Conclusions: The offspring of T2D patients present a worse metabolic profile and the parental history of T2D confers an increased likelihood of hepatic fibrosis, independent of metabolic factors. PNPLA3 homozygous GG, but not TM6SF2 genotypes, also impacts on this phenotype., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)- Published
- 2024
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- View/download PDF
32. Effects of body weight variability on risks of macro- and microvascular outcomes in individuals with type 2 diabetes: The Rio de Janeiro type 2 diabetes cohort.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Humans, Risk Factors, Prognosis, Brazil epidemiology, Body Weight, Diabetes Mellitus, Type 2 complications, Peripheral Nervous System Diseases complications, Retinal Diseases, Cardiovascular Diseases etiology
- Abstract
Aims: To investigate the effects of body weight variability (BWV) on macro- and microvascular outcomes in a type 2 diabetes cohort., Methods: BWV parameters were assessed in 684 individuals. Multivariable Cox regressions examined associations between BWV parameters and cardiovascular outcomes (total cardiovascular events [CVEs], major CVEs [MACEs], cardiovascular deaths),all-cause mortality and microvascular outcomes. Interaction/subgroup analyses were performed according to being physically-active/sedentary and having/not lost ≥ 5 % of weight., Results: Median follow-up was 11 years over which 194 total CVEs (174 MACEs), and 223 all-cause deaths (110 cardiovascular), occurred. There were 215 renal, 152 retinopathy and 167 peripheral neuropathy development/worsening outcomes. In general, increased BWV was associated with higher risks of CVEs, MACEs, all-cause mortality, advanced renal failure and peripheral neuropathy outcomes, but not of microalbuminuria and retinopathy outcomes. On interaction/subgroup analyses, increased BWV was associated with higher risks of outcomes in sedentary individuals and in those who did not lose ≥ 5 % of body weight. In physically-active participants or in those who lost ≥ 5 % weight, the adjusted risks were null or protective., Conclusions: Increased BWV was associated with most adverse outcomes; however, in those who were physically-active or consistently losing weight, it was not hazardous and might be even beneficial., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)
- Published
- 2023
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33. Prognostic Impact of On-Treatment Cumulative Ambulatory Blood Pressures for Adverse Macro- and Microvascular Outcomes in Individuals With Type 2 Diabetes: The Rio de Janeiro Type 2 Diabetes Cohort.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Humans, Prognosis, Blood Pressure physiology, Blood Pressure Monitoring, Ambulatory, Prospective Studies, Brazil epidemiology, Risk Factors, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 diagnosis, Diabetes Mellitus, Type 2 epidemiology, Cardiovascular Diseases diagnosis, Cardiovascular Diseases epidemiology, Cardiovascular Diseases etiology, Renal Insufficiency, Retinal Diseases complications, Hypertension
- Abstract
Background: The prognostic value of on-treatment mean cumulative ambulatory blood pressures (BPs) in type 2 diabetes has never been investigated. We aimed to assess it in a prospective cohort of 647 individuals with type 2 diabetes., Methods: Clinic-office and ambulatory BPs were measured at baseline and serially during follow-up. Multivariable Cox analyses assessed the associations between baseline and mean cumulative BPs with the occurrence of cardiovascular events, major adverse cardiovascular events, all-cause and cardiovascular mortality, and microvascular outcomes (microalbuminuria, renal failure, retinopathy, and peripheral neuropathy). C statistics and the integrated discrimination improvement (IDI) index evaluated the improvement in risk discrimination by using cumulative ambulatory BPs instead of baseline BPs., Results: Over a median follow-up of 10.6 years, there were 202 cardiovascular events (163 major adverse cardiovascular events), 254 all-cause deaths (118 cardiovascular); 125 individuals had microalbuminuria development/progression, 104 developed advanced renal failure, 159 had retinopathy, and 174 individuals had peripheral neuropathy development/progression. The risks associated with mean cumulative ambulatory BPs were in general higher than those associated with baseline BPs, particularly for cardiovascular (HR, 1.42 versus 1.25 for increments of 1 SD in 24-hour systolic blood pressure) and mortality outcomes (1.56 versus 1.26). Compared with cumulative clinic BPs, mean cumulative ambulatory BPs improved risk discrimination for most outcomes, with IDIs from 11% to 14% for major adverse cardiovascular events and mortality up to 24% to 26% for microalbuminuria and neuropathy., Conclusions: Compared with clinic-office BPs, mean cumulative ambulatory BPs during follow-up improve risk discrimination for most complications and mortality in individuals with type 2 diabetes. Serial ambulatory BP monitoring shall be more widely used in clinical management., Competing Interests: Disclosures None.
- Published
- 2023
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34. Effects of Weight Loss and Interaction with Physical Activity on Risks of Cardiovascular Outcomes in Individuals with Type 2 Diabetes.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Humans, Risk Factors, Weight Gain, Weight Loss, Exercise, Diabetes Mellitus, Type 2 complications, Cardiovascular Diseases epidemiology, Cardiovascular Diseases etiology, Cardiovascular Diseases prevention & control
- Abstract
Backgruound: This study investigated the effects of weight loss during follow-up on cardiovascular outcomes in a type 2 diabetes cohort and tested interactions with clinical and laboratory variables, particularly physical activity, that could impact the associations., Methods: Relative weight changes were assessed in 651 individuals with type 2 diabetes and categorized as ≥5% loss, <5% loss, or gain. Associations between weight loss categories and incident cardiovascular outcomes (total cardiovascular events [CVEs], major adverse cardiovascular events [MACEs], and cardiovascular mortality) were assessed using multivariable Cox regression with interaction analyses., Results: During the initial 2 years, 125 individuals (19.2%) lost ≥5% of their weight, 180 (27.6%) lost <5%, and 346 (53.1%) gained weight. Over a median additional follow-up of 9.3 years, 188 patients had CVEs (150 MACEs) and 106 patients died from cardiovascular causes. Patients with ≥5% weight loss had a significantly lower risk of total CVEs (hazard ratio [HR], 0.52; 95% confidence interval, 0.33 to 0.89; P=0.011) than those who gained weight, but non-significant lower risks of MACEs or cardiovascular deaths. Patients with <5% weight loss had risks similar to those with weight gain. There were interactions between weight loss and physical activity. In active individuals, ≥5% weight loss was associated with significantly lower risks for total CVEs (HR, 0.20; P=0.004) and MACEs (HR, 0.21; P=0.010), whereas in sedentary individuals, no cardiovascular protective effect of weight loss was evidenced., Conclusion: Weight loss ≥5% may be beneficial for cardiovascular disease prevention, particularly when achieved with regular physical activity, even in high-risk individuals with long-standing type 2 diabetes.
- Published
- 2023
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35. Prognostic importance of obstructive sleep apnea and CPAP treatment for cardiovascular and mortality outcomes in patients with resistant hypertension: a prospective cohort study.
- Author
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Cardoso CRL and Salles GF
- Subjects
- Humans, Prospective Studies, Prognosis, Continuous Positive Airway Pressure, Sleep Apnea, Obstructive complications, Sleep Apnea, Obstructive therapy, Hypertension complications
- Abstract
The prognostic importance of obstructive sleep apnea (OSA) severity and other polysomnographic parameters in patients with resistant hypertension (RHT) has never been evaluated. We aimed to assess it in a prospective cohort of 422 individuals with RHT. OSA presence/severity was ascertained by complete polysomnography (PSG) at baseline. Multivariable Cox regressions assessed the risks associated with OSA severity and other PSG parameters (apnea-hypopnea index, sleep duration, nocturnal hypoxemia and periodic limb movements) for the primary (total cardiovascular events [CVEs] and all-cause mortality) and secondary outcomes (major CVEs). In the subgroup of patients with moderate/severe OSA, the risks associated with CPAP treatment were also estimated in relation to untreated individuals. One-hundred and eighty-six participants (44%) had no/mild OSA and 236 (56%) had moderate/severe OSA, and 67 of them were CPAP-treated. Over a mean follow-up of 5 years, there were 46 CVEs (37 major ones) and 44 all-cause deaths. Neither the presence of moderate/severe or severe OSA, nor being untreated during follow-up, was associated with significant excess risks for any outcome in relation to the subgroup with no/mild OSA. Similarly, no other PSG-derived parameter predicted any adverse outcome. Otherwise, CPAP treatment was associated with non-significant risk reductions of 37% for total CVEs, 49% for major CVEs and 63% for all-cause mortality in relation to those who remained untreated during follow-up. In conclusion, the presence/severity of OSA and its related PSG parameters were not associated with worse cardiovascular/mortality prognosis in patients with RHT. However, CPAP treatment might be protective in individuals with moderate/severe OSA., (© 2023. The Author(s), under exclusive licence to The Japanese Society of Hypertension.)
- Published
- 2023
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36. Relative prognostic importance of aortic and brachial blood pressures for cardiovascular and mortality outcomes in patients with resistant hypertension and diabetes: a two cohorts prospective study.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Humans, Arterial Pressure, Prospective Studies, Blood Pressure physiology, Prognosis, Blood Pressure Monitoring, Ambulatory, Diabetes Mellitus, Type 2 complications, Hypertension
- Abstract
Objective: The prognostic importance of derived central/aortic blood pressures (BPs) in relation to brachial office and ambulatory BPs has never been investigated in patients with resistant hypertension (RHT) or type 2 diabetes (T2D). We aimed to evaluate it in two cohorts with 532 individuals with RHT and 467 with T2D (median follow-ups 4.4 and 7.3 years, respectively)., Methods: Central/aortic pressure waveforms were estimated by radial tonometry by a type 1 device (SphygmoCor device/software), and other parameters of central hemodynamics (augmentation index and Buckberg indices) were calculated. Multivariate Cox regressions examined the associations between central and peripheral BPs with cardiovascular events incidence and mortality, and C -statistics and the integrated discrimination improvement index evaluated the improvement in risk discrimination., Results: During follow-up, there were 52 cardiovascular events and 51 all-cause deaths in the RHT and 104 and 137 in the T2D cohort. No aortic BP was better than its brachial counterpart in predicting risk or improving discrimination for any outcome in either cohort. In the RHT cohort, ambulatory BPs were superior to central and office-brachial BPs. Otherwise, the augmentation index in RHT (hazard ratios: 1.5, for 1-SD increment) and the Buckberg index in T2D (hazard ratios: 0.7-0.8) were independent predictors of cardiovascular/mortality outcomes, and improved risk discrimination (integrated discrimination improvement up to 25% in RHT and 15% in T2D)., Conclusion: Derived aortic BPs by a type 1 device did not improve cardiovascular/mortality risk prediction over brachial BPs in our cohorts of patients with RHT and T2D, but additional parameters of central hemodynamics may be useful., (Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.)
- Published
- 2023
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37. Prognostic importance of cardiovascular autonomic neuropathy on cardiovascular and mortality outcomes in individuals with type 2 diabetes: The Rio de Janeiro type 2 diabetes cohort.
- Author
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Cardoso CRL, de Oliveira VAG, Leite NC, and Salles GF
- Subjects
- Humans, Prognosis, Brazil, Autonomic Nervous System, Heart Rate physiology, Diabetes Mellitus, Type 2 complications
- Abstract
Aims: To investigate whether tests for cardiovascular autonomic neuropathy (CAN) and 24-hour heart rate variability (HRV) could improve the prediction for outcomes in type 2 diabetes., Methods: 541 type 2 diabetic individuals performed tests of CAN. A subsample (313) had 24-hour HRV (the standard deviation of all normal RR intervals [SDNN] and the standard deviation of the averaged normal RR intervals for all 5 min segments [SDANN]). Multivariate Cox regressions examined the associations between CAN/low HRV with cardiovascular events (CVEs) and all-cause mortality. The improvement in risk discrimination of adding CAN/HRV was tested by C-statistics and by the Integrated Discrimination Improvement (IDI) index., Results: 25% had CAN, and 17-18% had low HRV, respectively by SDANN-SDNN. Over a median follow-up of 12 years, there were 177 CVEs and 236 all-cause deaths in the whole cohort, and 96 CVEs and 129 all-cause deaths in the subsample. CAN was associated with 40% excess risks of CVEs/all-cause mortality, low HRV was associated with 2-fold higher risks of outcomes. HRV improved risk discrimination for CVEs/mortality with increases in C-statistics up to 0.039 and IDIs up to 25%., Conclusions: Low HRV was a better predictor of outcomes than tests of CAN, and it improved risk discrimination., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)
- Published
- 2023
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38. Non-alcoholic fatty liver disease and the impact of genetic, epigenetic and environmental factors in the offspring.
- Author
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Wajsbrot NB, Leite NC, Salles GF, and Villela-Nogueira CA
- Subjects
- Epigenesis, Genetic, Humans, Liver pathology, Non-alcoholic Fatty Liver Disease genetics, Non-alcoholic Fatty Liver Disease metabolism
- Abstract
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease worldwide and is strongly associated with metabolic deregulation. More recently, a significant impact of parental NAFLD in the offspring was demonstrated and has been widely discussed. However, pathogenetic pathways implicated in the inheritance by the offspring and relatives are still under debate. Probably, multiple mechanisms are involved as well as in NAFLD pathogenesis itself. Among the multifactorial involved mechanisms, genetic, epigenetic and environmental backgrounds are strongly related to NAFLD development in the offspring. Thus, based on recent evidence from the available literature concerning genetic, epigenetic and environmental disease modifiers, this review aimed to discuss the relationship between parental NAFLD and its impact on the offspring., Competing Interests: Conflict-of-interest statement: The authors have nothing to declare., (©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.)
- Published
- 2022
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39. Prevalence and associated factors of aspiration and severe dysphagia in asymptomatic patients in the late period after open partial laryngectomy: a videofluoroscopic evaluation.
- Author
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Freitas AS, Santos IC, Furia C, Dornelas R, Silva ACAE, Dias FL, and Salles GF
- Subjects
- Deglutition, Fluoroscopy, Humans, Laryngectomy adverse effects, Laryngectomy methods, Prevalence, Serum Albumin, Weight Loss, Deglutition Disorders diagnostic imaging, Deglutition Disorders epidemiology
- Abstract
Purpose: This study aimed to evaluate late and asymptomatic patients after open partial horizontal laryngectomy (OPHL), investigating the clinical-surgical and socio-demographic factors associated with aspiration and severe dysphagia., Methods: One-thousand videofluoroscopic swallowing studies were performed in 100 asymptomatic patients in the late period after OPHL(median 6.5 years). Aspiration and severe dysphagia were, respectively, assessed by the Penetration-Aspiration scale (PAS) and by the Dynamic Imaging Grade of Swallowing Toxicity (DIGEST) classification. Associated factors were investigated by multivariate logistic regressions., Results: 34% (95% CI 24.3-47.6%) of patients presented aspiration and 23% (95% CI 15.3-34.6%) had severe or life-threatening dysphagia (DIGEST grades 3-4). On logistic regression, the presence of aspiration was associated with lower preoperative serum albumin (odds ratio [OR]: 0.22; 95% CI 0.07-0.64; p = 0.005, for each 1 g/dL increment); a greater weight loss in early postoperative period (OR: 1.19, 95% CI 1.05-1.35; p = 0.008, for each 1 kg loss); older age at surgery (OR: 1.08; 95% CI 1.01-1.17, for each 1-year older); and with the presence of diabetes (OR: 5.16; 95% CI 1.09-27.47; p = 0.039)., Conclusion: Deglutition abnormalities are frequent in asymptomatic patients later after OPHL. Older patients, with lower preoperative serum albumin levels, with greater postoperative weight loss, and with diabetes compose the clinical profile at risk for having worse swallowing function in the late period after OPHL., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Published
- 2022
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40. Prognostic impact of changes in aortic stiffness for cardiovascular and mortality outcomes in individuals with type 2 diabetes: the Rio de Janeiro cohort study.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Brazil epidemiology, Cohort Studies, Disease Progression, Humans, Prognosis, Pulse Wave Analysis, Cardiovascular Diseases, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 diagnosis, Vascular Stiffness
- Abstract
Background: The prognostic importance of changes in aortic stiffness for the occurrence of adverse cardiovascular outcomes and mortality has never been investigated in patients with type 2 diabetes. We aimed to evaluate it in a cohort of 417 patients., Methods: Changes in aortic stiffness were assessed by 2 carotid-femoral pulse wave velocity (CF-PWV) measurements performed over a 4-year period. Multivariable Cox analysis examined the associations between changes in CF-PWV, evaluated as a continuous variable with splines and as categorical ones (quartiles and stable/reduction/increase subgroups), and the occurrence of total cardiovascular events (CVEs), major adverse CVEs (MACEs), and all-cause and cardiovascular mortality., Results: Over a median follow-up of 8.2 years after the 2nd CF-PWV measurement, there were 101 total CVEs (85 MACEs) and 135 all-cause deaths (64 cardiovascular). As a continuous variable, the lowest risk nadir was at -2.5%/year of CF-PWV change, with significantly higher risks of mortality associated with CF-PWV increases, but no excess risks at extremes of CF-PWV reduction. Otherwise, in categorical analyses, patients in the 1st quartile (greatest CF-PWV reductions) had excess risks of all-cause and cardiovascular mortality (hazard ratios [HRs]: 2.0-2.7), whereas patients in 3rd quartile had higher risks of all outcomes (HRs: 2.0-3.2), in relation to the lowest risk 2nd quartile subgroup. Patients in the 4th quartile had higher risks of all-cause mortality. Categorization as stable/reduction/increase subgroups was confirmatory, with higher risks at greater reductions (HRs: 1.7-3.3) and at greater increases in CF-PWV (HRs: 1.9-3.4), in relation to those with stable CF-PWV., Conclusions: Changes in aortic stiffness, mainly increases and possibly also extreme reductions, are predictors of adverse cardiovascular outcomes and mortality in individuals with type 2 diabetes., (© 2022. The Author(s).)
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- 2022
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41. Refractory Hypertension: a Narrative Systematic Review with Emphasis on Prognosis.
- Author
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Bacan G, Ribeiro-Silva A, Oliveira VAS, Cardoso CRL, and Salles GF
- Subjects
- Antihypertensive Agents pharmacology, Antihypertensive Agents therapeutic use, Blood Pressure physiology, Diuretics therapeutic use, Humans, Prognosis, Hypertension
- Abstract
Purpose of Review: To perform a narrative systematic review on refractory hypertension (RfHT) with particular emphasis on prognosis., Recent Findings: There were 37 articles on RfHT, 13 non-systematic reviews, and 24 original studies. RfHT, a recently described extreme phenotype of anti-hypertensive treatment failure, shall be defined as uncontrolled out-of-office blood pressure (BP) levels despite the use of at least 5 anti-hypertensive drugs, including a long-acting diuretic and a mineraloreceptor antagonist. Its prevalence ranges from 0.5 to 4.3% of general treated hypertensives and between 3.6 and 51.4% of patients with resistant hypertension (RHT). RfHT is associated with younger age, African ancestry, obesity, hypertension-mediated organ damage and clinical cardiovascular diseases, and with some comorbidities, such as diabetes and obstructive sleep apnea. Its physiopathological mechanisms probably involve sympathetic overactivity and not volume overload. Patients with RfHT have a worse prognosis than non-refractory RHT individuals, with higher risks of adverse cardiovascular and renal outcomes and of mortality. RfHT represents a rare but true extreme phenotype of anti-hypertensive treatment failure distinct from RHT and with a significantly worse prognosis. Identifying such individuals is important to tailor specific interventions., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
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- 2022
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42. Prognostic Value of Changes in Aortic Stiffness for Cardiovascular Outcomes and Mortality in Resistant Hypertension: a Cohort Study.
- Author
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Cardoso CRL and Salles GF
- Subjects
- Aged, Aged, 80 and over, Carotid-Femoral Pulse Wave Velocity, Cohort Studies, Disease Progression, Female, Heart Disease Risk Factors, Humans, Hypertension mortality, Male, Middle Aged, Prognosis, Survival Rate, Blood Pressure physiology, Hypertension physiopathology, Vascular Stiffness physiology
- Abstract
The prognostic importance of changes in aortic stiffness for the occurrence of adverse cardiovascular outcomes and mortality has never been investigated in patients with resistant hypertension. We aimed to evaluate it in a prospective cohort of 442 resistant hypertension individuals. Changes in aortic stiffness were assessed by 2 carotid-femoral pulse wave velocity (CF-PWV) measurements performed over a median time interval of 4.7 years. Multivariate Cox analysis examined the associations between changes in CF-PWV (evaluated as continuous variables and categorized into quartiles and as increased/persistently high or reduced/persistently low) and the occurrence of total cardiovascular events (CVEs), major adverse CVEs, and cardiovascular/all-cause mortalities. During a median follow-up of 4.1 years after the second CF-PWV measurement, there were 49 total CVEs (42 major adverse CVEs) and 53 all-cause deaths (32 cardiovascular). As continuous variables, increments in absolute and relative changes in CF-PWV were associated with higher risks of CVEs and major adverse CVEs occurrence, but not of mortality. Divided into quartiles of CF-PWV changes, risks increased in the third and fourth quartile subgroups in relation to the reference first quartile subgroup (those with greatest CF-PWV reductions) for all outcomes. Patients who either increased or persisted with high CF-PWV had excess risks of cardiovascular morbidity/mortality, with hazard ratios ranging from 2.7 to 3.0, in relation to those who reduced or persisted with low CF-PWV values. In conclusion, reducing or preventing progression of aortic stiffness was associated with significant cardiovascular protection in patients with resistant hypertension, suggesting that it may be an additional clinical target of antihypertensive treatment.
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- 2022
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43. Differential effects of treatment targets on risks of adverse outcomes according to diabetes duration, age and complications: Can these characteristics be used to individualize diabetes treatment? The Rio de Janeiro type 2 diabetes cohort.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Aged, Brazil epidemiology, Humans, Prognosis, Prospective Studies, Risk Factors, Cardiovascular Diseases epidemiology, Cardiovascular Diseases prevention & control, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 drug therapy
- Abstract
Aims: To investigate interactions between more/less strict treatment targets (HbA
1c , systolic blood pressure, LDL-cholesterol) and clinical characteristics (age, diabetes duration and presence of complications) for occurrence of cardiovascular/microvascular complications and mortality in type 2diabetes., Methods: 690 individuals were followed-up for 10 years (median). Interactions between treatment targets, estimated as mean values during the first 2-years, and clinical characteristics were tested in multivariable Cox regressions adjusted for other risk factors. Hazard ratios (HRs) were estimated in stratified analyses for cardiovascular/microvascular outcomes and mortality., Results: During follow-up, 214 patients had a cardiovascular event (175 MACEs); and 265 died (132 cardiovascular deaths); there were 206 renal, 161 retinopathy and 181 peripheral neuropathy events. There were interactions between treatment parameters and clinical characteristics, in most of them the HRs were higher in older individuals, in those with longer diabetes durations and with complications, particularly for the cardiovascular outcomes and mortality. For microvascular outcomes the opposite was observed. For cardiovascular mortality, the HRs of higher HbA1c were 1.31 (1.08-1.58) and 1.09 (0.88-1.34), respectively with longer/shorter diabetes duration (p-for-interaction 0.11); and 1.43 (1.14-1.79) and 1.02 (0.85-1.23) in older/younger individuals (p-for-interaction 0.019)., Conclusions: Our findings do not support less strict treatment targets for older individuals, with longer diabetes duration or with complications, particularly for cardiovascular and mortality prevention., (Copyright © 2021. Published by Elsevier Inc.)- Published
- 2022
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44. Prognostic Impact of Home Blood Pressures for Adverse Cardiovascular Outcomes and Mortality in Patients With Resistant Hypertension: A Prospective Cohort Study.
- Author
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Cardoso CRL and Salles GF
- Subjects
- Aged, Blood Pressure Monitoring, Ambulatory, Cardiovascular Diseases mortality, Female, Humans, Hypertension complications, Hypertension physiopathology, Male, Middle Aged, Prognosis, Prospective Studies, Blood Glucose Self-Monitoring adverse effects, Cardiovascular Diseases etiology, Hypertension diagnosis
- Abstract
[Figure: see text].
- Published
- 2021
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45. Effect of Continuous Positive Airway Pressure on Weight and Local Adiposity in Adults with Obstructive Sleep Apnea: A Meta-Analysis.
- Author
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Chen B, Drager LF, Peker Y, Vgontzas AN, Phillips CL, Hoyos CM, Salles GF, Guo M, and Li Y
- Subjects
- Adiposity, Adult, Body Mass Index, Humans, Obesity complications, Randomized Controlled Trials as Topic, Continuous Positive Airway Pressure, Sleep Apnea, Obstructive complications, Sleep Apnea, Obstructive therapy
- Abstract
Rationale: Evidence suggests that continuous positive airway pressure (CPAP) treatment promotes weight gain in patients with obstructive sleep apnea (OSA). It is unclear whether weight gain is influenced by CPAP adherence or comorbid disorders. Objectives: To examine the CPAP effects on body mass index (BMI) and local adiposity and the potential moderators of CPAP effects on BMI in patients with OSA. Methods: We searched PubMed/Medline, Embase, and Cochrane through December 2019. Randomized controlled trials of CPAP versus control treatment with ⩾4 weeks' treatment were included. Results: A total of 39 randomized controlled trials with 6,954 subjects were included. In intention-to-treat analysis, the BMI increased significantly after CPAP treatment compared with control treatment (weighted mean difference [WMD], 0.148 kg/m
2 ; 95% confidence interval, 0.04-0.26; P = 0.001). In studies demonstrating an increase in the BMI, waist and neck circumferences were also significantly increased. Subgroup analyses revealed that an increased BMI was attributable to CPAP use of ⩽5 h/night (WMD, 0.231) but was not attributable to CPAP use of >5 h/night (WMD, 0.001; between-group P value = 0.049). Furthermore, the BMI increased significantly in patients without cardiovascular disease (CVD; WMD, 0.200), whereas it decreased significantly in those with CVD at baseline (WMD, -0.188; between-group P value < 0.001). Moreover, the BMI increased significantly in patients with dysglycemia (WMD, 0.499) but did not increase in those without dysglycemia at baseline (WMD, 0.100; between-group P value = 0.032). Meta-regression confirmed the subgroup findings. Conclusions: The BMI increased significantly in patients with OSA after CPAP treatment, especially in those with CPAP use of ⩽5 h/night, without CVD and/or with dysglycemia at baseline. CPAP use of at least 5 h/night seems to be necessary in mitigating the risk for weight gain in patients with OSA.- Published
- 2021
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46. Prognostic impact of liver fibrosis and steatosis by transient elastography for cardiovascular and mortality outcomes in individuals with nonalcoholic fatty liver disease and type 2 diabetes: the Rio de Janeiro Cohort Study.
- Author
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Cardoso CRL, Villela-Nogueira CA, Leite NC, and Salles GF
- Subjects
- Aged, Brazil epidemiology, Cardiovascular Diseases diagnosis, Cardiovascular Diseases mortality, Diabetes Mellitus, Type 2 diagnosis, Diabetes Mellitus, Type 2 mortality, Female, Humans, Incidence, Liver Cirrhosis mortality, Longitudinal Studies, Male, Middle Aged, Non-alcoholic Fatty Liver Disease mortality, Predictive Value of Tests, Prognosis, Prospective Studies, Risk Assessment, Risk Factors, Time Factors, Cardiovascular Diseases epidemiology, Diabetes Mellitus, Type 2 epidemiology, Elasticity Imaging Techniques, Liver Cirrhosis diagnostic imaging, Non-alcoholic Fatty Liver Disease diagnostic imaging
- Abstract
Background: Liver stiffness measurement (LSM, which reflects fibrosis) and controlled attenuation parameter (CAP, which reflects steatosis), two parameters derived from hepatic transient elastography (TE), have scarcely been evaluated as predictors of cardiovascular complications and mortality in individuals with type 2 diabetes and nonalcoholic fatty liver disease (NAFLD)., Methods: Four hundred type 2 diabetic patients with NAFLD had TE examination (by Fibroscan
® ) performed at baseline. Multivariate Cox analyses evaluated the associations between TE parameters and the occurrence of cardiovascular events (CVEs) and mortality. TE parameters were assessed as continuous variables and dichotomized at low/high values reflecting advanced liver fibrosis (LSM > 9.6 kPa) and severe steatosis (CAP > 296 or > 330 dB/m). Improvements in risk discrimination were assessed by C-statistic and by the relative Integrated Discrimination Improvement (IDI) index., Results: During a median follow-up of 5.5 years, 85 patients died (40 from cardiovascular causes), and 69 had a CVE. As continuous variables, an increasing LSM was a risk marker for total CVEs (hazard ratio [HR]: 1.05; 95% CI: 1.01-1.08) and all-cause mortality (HR: 1.04; 95% CI: 1.01-1.07); whereas an increasing CAP was a protective factor for both outcomes (HR: 0.93; 95% CI: 0.89-0.98; and HR: 0.92; 95% CI: 0.88-0.97; respectively). As dichotomized variables, a high LSM remained a risk marker of adverse outcomes (with HRs ranging from 2.5 to 3.0) and a high CAP was protective (with HRs from 0.3 to 0.5). The subgroup of individuals with low-LSM/high-CAP had the lowest risks while the opposite subgroup with high-LSM/low-CAP had the highest risks. Both LSM and CAP improved risk discrimination, with increases in C-statistics up to 0.037 and IDIs up to 52%., Conclusions: Measured by hepatic TE, advanced liver fibrosis is a risk marker and severe steatosis is a protective factor for cardiovascular complications and mortality in individuals with type 2 diabetes and NAFLD., (© 2021. The Author(s).)- Published
- 2021
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47. Importance of hematological parameters for micro- and macrovascular outcomes in patients with type 2 diabetes: the Rio de Janeiro type 2 diabetes cohort study.
- Author
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Cardoso CRL, Leite NC, and Salles GF
- Subjects
- Aged, Brazil epidemiology, Cause of Death, Diabetes Mellitus, Type 2 diagnosis, Diabetes Mellitus, Type 2 mortality, Diabetic Angiopathies diagnosis, Diabetic Angiopathies mortality, Diabetic Nephropathies blood, Diabetic Nephropathies diagnosis, Diabetic Nephropathies mortality, Diabetic Neuropathies blood, Diabetic Neuropathies diagnosis, Diabetic Neuropathies mortality, Diabetic Retinopathy blood, Diabetic Retinopathy diagnosis, Diabetic Retinopathy mortality, Erythrocyte Count, Female, Humans, Lymphocyte Count, Lymphocytes, Male, Middle Aged, Platelet Count, Predictive Value of Tests, Prognosis, Prospective Studies, Risk Assessment, Risk Factors, Time Factors, Blood Platelets, Diabetes Mellitus, Type 2 blood, Diabetic Angiopathies blood, Erythrocytes, Leukocytes
- Abstract
Background: The prognostic importance of several hematological parameters has been scarcely investigated in type 2 diabetes. So, we aimed to evaluate their prognostic importance for development of complications in a cohort of type 2 diabetes., Methods: In a prospective study, 689 individuals with type 2 diabetes had blood red cell, platelet and leukocyte parameters obtained at baseline. Multivariate Cox analyses examined the associations between several hematological parameters (including neutrophyl-to-lymphocyte, lymphocyte-to-monocyte, platelet-to-lymphocyte, and monocyte-to-HDL ratios) and the occurrence of microvascular (retina, renal and peripheral neuropathy) and cardiovascular complications (total cardiovascular events [CVEs], and major adverse CVEs [MACEs]), and all-cause and cardiovascular mortality. Improvements in risk discrimination were assessed by C-statistics and Integrated Discrimination Improvement (IDI) index., Results: During a median follow-up of 10.5 years, 212 patients had a CVE (174 MACEs), 264 patients died (131 cardiovascular deaths); 206 had a renal, 161 a retinopathy and 179 patients had a neuropathy outcome. In multivariate-adjusted analyses, the lymphocytes count and lymphocyte-to-monocyte ratio were protective (hazard ratios [HRs]: 0.77 and 0.72, respectively), whereas the neutrophyl-to-lymphocyte and platelet-to-lymphocyte ratios were associated with increased risks (HRs: 1.19 and 1.17) for all-cause mortality. For cardiovascular mortality, the monocytes count, the neutrophyl-to-lymphocyte and monocyte-to-HDL ratios were associated with increased risks and the lymphocyte-to-monocyte ratio was protective. Higher lymphocyte-to-monocyte ratio was protective for renal failure outcome. However, none of them improved risk discrimination., Conclusions: Low lymphocytes count and leukocyte ratios that mainly included lymphocytes were predictors of macrovascular complications and mortality in individuals with type 2 diabetes. However, they did not improve risk prediction over traditional risk factors.
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- 2021
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48. Associations of the nocturnal blood pressure fall and morning surge with cardiovascular events and mortality in individuals with resistant hypertension.
- Author
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Cardoso CRL and Salles GF
- Subjects
- Aged, Blood Pressure, Blood Pressure Monitoring, Ambulatory, Circadian Rhythm, Humans, Prospective Studies, Cardiovascular Diseases, Hypertension
- Abstract
Objective: The prognostic importance of the nocturnal blood pressure (BP) fall and early-morning surge were scarcely investigated in patients with resistant hypertension (RHT). We investigated them in a prospective cohort of 1726 RHT individuals., Methods: The nocturnal fall and morning surge were calculated from the baseline ambulatory BP monitoring (ABPM) and also as mean cumulative values using all ABPMs performed during follow-up. Dipping patterns (normal, extreme, reduced, and reverse) were defined by classic cut-off values of the night-to-day ratio, while MS (difference between early-morning and night-time BP) was categorized into quartiles and at the extremes of its distribution (5th, 10th, 90th, and 95th percentiles). The primary outcomes were total cardiovascular events (CVEs), major adverse cardiovascular events (MACEs), all-cause and cardiovascular mortalities. Multivariate Cox analyses examined the associations between nocturnal BP fall and morning surge and outcomes., Results: Over a median follow-up of 8.3 years, 417 CVEs occurred (358 MACEs), and 391 individuals died (233 cardiovascular deaths). Reduced and reverse dipping patterns were significant predictors of CVEs and MACEs, with hazard ratios between 1.6 and 2.5, whereas extreme dipping was a protective factor in younger individuals (hazard ratios 0.3--0.4) but a hazardous factor in elderly (hazard ratios 3.7--5.0) and in individuals with previous cardiovascular diseases (hazard ratios 2.6--4.4). No morning surge parameter was predictive of any outcome in fully adjusted analyses., Conclusion: Abnormal dipping patterns but not the early-morning BP surge, were important prognostic markers for future cardiovascular morbidity in RHT patients. The prognosis of extreme dippers depended on age and the presence of cardiovascular diseases., (Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.)
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- 2021
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49. Associations Between Achieved Ambulatory Blood Pressures and Its Changes With Adverse Outcomes in Resistant Hypertension: Was There a J-Curve for Ambulatory Blood Pressures?
- Author
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Cardoso CRL and Salles GF
- Subjects
- Aged, Blood Pressure Determination, Blood Pressure Monitoring, Ambulatory, Cardiovascular Diseases mortality, Female, Follow-Up Studies, Humans, Hypertension mortality, Male, Middle Aged, Survival Rate, Blood Pressure physiology, Cardiovascular Diseases physiopathology, Hypertension physiopathology
- Abstract
[Figure: see text].
- Published
- 2021
- Full Text
- View/download PDF
50. Importance of non-invasive liver fibrosis scores for mortality and complications development in individuals with type 2 diabetes.
- Author
-
Leite NC, Cardoso CRL, and Salles GF
- Subjects
- Aged, Cohort Studies, Female, Humans, Liver Cirrhosis complications, Male, Middle Aged, Diabetes Mellitus, Type 2 complications, Diabetes Mellitus, Type 2 mortality, Liver Cirrhosis diagnosis, Non-alcoholic Fatty Liver Disease complications, Non-alcoholic Fatty Liver Disease mortality
- Abstract
Aims: To evaluate the non-alcoholic fatty liver disease (NAFLD) fibrosis score (NFS) and Fibrosis-4 score (FIB4) as predictors of complications development and mortality in a cohort of type 2 diabetes., Methods: 554 type 2 diabetic subjects had NFS and FIB4 calculated at baseline. Multivariate Cox and Poisson analyses evaluated the associations between fibrosis scores and the occurrence of microvascular and cardiovascular complications, and all-cause mortality., Results: According to recommended cut-offs of NFS, 12.8% had advanced fibrosis and 45.9% had absence of advanced fibrosis and of FIB4, 3.8% and 86.1%, respectively. During a median follow-up of 11 years, 217subjects died, 172 had cardiovascular events (CVEs), 184 had renal events, and 139 had retinopathy and 185 neuropathy events. As continuous variables, both scores predicted all-cause mortality: NFS, HR: 1.30 (p = 0.032) and FIB4, HR: 1.24 (p = 0.021); an increased NFS implied in a significant 90% excess risk of mortality, whereas a higher FIB4 in a borderline 69% higher risk. The scores were mainly predictors of mortality in women and for non-cardiovascular deaths. The NFS was a predictor of renal events, mainly for renal function deterioration., Conclusions: The NFS and FIB4 predicted all-cause mortality, particularly in women and for non-cardiovascular causes. The NFS predicted adverse renal outcomes. These liver fibrosis scores may improve stratification risk in individuals with diabetes and NAFLD., Competing Interests: Declaration of competing interest The authors declare that there is no conflict of interest., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
- Full Text
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