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Hipertensión arterial pulmonar: un recorrido por el año 2008
Pulmonary Arterial Hypertension: a Voyage Around the Year 2008
Adolfo Baloira
Servicio de Neumología, Complexo Hospitalario de Pontevedra, Pontevedra, España
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          "palabras" => array:4 [
            0 => "Hipertensi&#243;n arterial pulmonar"
            1 => "BMPR2"
            2 => "Antiendotelina"
            3 => "Sildenafilo"
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            0 => "Pulmonary arterial hypertension"
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            2 => "Anti-endothelin"
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        "titulo" => "Resumen"
        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">La hipertensi&#243;n arterial pulmonar &#40;HAP&#41; ha tenido un espectacular desarrollo&#44; tanto en la terap&#233;utica como en el conocimiento de su patogenia&#46; Durante el a&#241;o 2008 se han publicado algunos trabajos que ha contribuido a mejorar un poco m&#225;s estos dos aspectos&#46; En lo que se refiere a la patogenia&#44; las mutaciones en BMPR2 siguen ganando puntos como actores fundamentales en el desarrollo de la enfermedad&#46; Se ha podido comprobar que los pacientes que portan alguna de ellas tienen un curso cl&#237;nico m&#225;s r&#225;pido y grave&#46; Existe una relaci&#243;n entre la v&#237;a de BMPR2 y la inflamaci&#243;n de &#225;rbol vascular pulmonar&#46; En este a&#241;o tambi&#233;n ha aparecido en escena un nuevo f&#225;rmaco antiendotelina&#58; ambrisent&#225;n&#46; Con una eficacia comparable con la de otros f&#225;rmacos de su grupo&#44; los efectos secundarios parecen ser bastante menores&#46; Un trabajo importante ha sido la demostraci&#243;n de una mejor&#237;a en diversos par&#225;metros de pacientes con HAP en clase funcional II con bosent&#225;n&#46; Tambi&#233;n se han presentado resultados de algunas nuevas combinaciones&#44; como sildenafilo y epoprostenol&#46; Un tipo frecuente de HAP es el que aparece asociado a enfermedad tromboemb&#243;lica&#46; Tanto el tratamiento con sildenafilo como&#44; en algunos casos seleccionados&#44; la angioplastia percut&#225;nea obtienen respuestas favorables&#46; Por &#250;ltimo&#44; en 2008 han visto la luz dos nuevos documentos de consenso&#44; uno espa&#241;ol y otro brit&#225;nico que&#44; sobre la base de los conocimientos actuales&#44; clarifican un poco m&#225;s el manejo de esta grave enfermedad&#46;</p>"
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      "en" => array:2 [
        "titulo" => "Abstract"
        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">There have been spectacular developments in pulmonary arterial hypertension &#40;PAH&#41;&#44; both in its treatment and knowledge of its pathogenesis&#46; Several studies have been published throughout 2008 that have contributed to improve these two aspects a little&#46; As regards the pathogenesis&#44; mutations in BMPR2 continue gaining points as fundamental factors in the development of the disease&#46; It has been shown that patients who carry any of them have a more rapid and severe clinical course&#46; There is a relationship between the BMPR2 pathway and inflammation of the pulmonary vascular tree&#46; A new anti-endothelin drug&#44; ambrisentan&#44; has also appeared on the scene this year&#46; With an efficacy comparable to other drugs of its group&#44; the secondary effects appear to be a lot less&#46; An important work has been the demonstration of an improvement in several parameters in functional class II in patients with PAH with bosentan&#46; Results using new combinations&#44; such as sildenafil and epoprostenol&#44; have also been presented&#46; A common type of PAH is that which seems to be associated with thromboembolic disease&#46; Treatment with sildenafil and in some selected cases&#44; percutaneous angioplasty&#44; has obtained favourable responses&#46; Finally&#44; in 2008&#44; two new consensus documents have emerged&#44; one Spanish and the other British&#44; which in the light of current knowledge&#44; give a clearer insight into the management of this serious disease&#46;</p>"
      ]
    ]
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                    0 => array:2 [
                      "titulo" => "Severe pulmonary arterial hypertension&#46; A forme fruste of c&#225;ncer&#63;"
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                        0 => array:2 [
                          "etal" => false
                          "autores" => array:2 [
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                      "doi" => "10.1164/rccm.200806-867ED"
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                        "tituloSerie" => "Am J Respir Crit Care Med"
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                    0 => array:2 [
                      "titulo" => "Mutaciones en el gen que codifica BMPR2 en pacientes con hipertensi&#243;n arterial pulmonar espor&#225;dica"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "A&#46; Baloira"
                            1 => "C&#46; Vilari&#241;o"
                            2 => "V&#46; Leiro"
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                        ]
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                  ]
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                    0 => array:1 [
                      "Revista" => array:6 [
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                        "volumen" => "44"
                        "paginaInicial" => "29"
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/18221724"
                            "web" => "Medline"
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                ]
              ]
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                    0 => array:2 [
                      "titulo" => "Mutations in bone morphogenetic protein type II receptor cause dysregulation of Id gene expression in pulmonary artery smooth muscle cells"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "J&#46; Yang"
                            1 => "R&#46;J&#46; Davies"
                            2 => "M&#46; Southwood"
                            3 => "L&#46; Long"
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                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:5 [
                        "tituloSerie" => "Cir Res"
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                        "volumen" => "102"
                        "paginaInicial" => "1212"
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                ]
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                    0 => array:2 [
                      "titulo" => "Genetic ablation of the BMPR2 gene in pulmonary endothelium is sufficient to predispose to pulmonary hypertension"
                      "autores" => array:1 [
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                          "etal" => true
                          "autores" => array:6 [
                            0 => "K&#46; Hong"
                            1 => "Y&#46;J&#46; Lee"
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                        ]
                      ]
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                    0 => array:2 [
                      "doi" => "10.1161/CIRCULATIONAHA.107.736801"
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                        "tituloSerie" => "Circulation"
                        "fecha" => "2008"
                        "volumen" => "118"
                        "paginaInicial" => "722"
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                        "link" => array:1 [
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/18663089"
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                      "titulo" => "Bone morphogenetic protein &#40;BMP&#41; type II receptor is required for BMP-mediated growth arrest and differentiation in pulmonary artery smooth muscle cells"
                      "autores" => array:1 [
                        0 => array:2 [
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                          "autores" => array:6 [
                            0 => "P&#46;B&#46; Yu"
                            1 => "D&#46;Y&#46; Deng"
                            2 => "H&#46; Beppu"
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                    0 => array:2 [
                      "doi" => "10.1074/jbc.M706797200"
                      "Revista" => array:6 [
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                        "fecha" => "2008"
                        "volumen" => "283"
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                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/18042551"
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                    0 => array:2 [
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                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
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                            1 => "E&#46; Waterman"
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                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.2353/ajpath.2008.070395"
                      "Revista" => array:6 [
                        "tituloSerie" => "Am J Pathol"
                        "fecha" => "2008"
                        "volumen" => "172"
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/18156213"
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                    0 => array:2 [
                      "titulo" => "Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation"
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                          "etal" => true
                          "autores" => array:6 [
                            0 => "B&#46; Sztrymf"
                            1 => "F&#46; Coulet"
                            2 => "B&#46; Girerd"
                            3 => "A&#46; Yaici"
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                      "doi" => "10.1164/rccm.200712-1807OC"
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                        "tituloSerie" => "Am J Respir Crit Care Med"
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                            "web" => "Medline"
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                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Ambrisentan for the treatment of pulmonary arterial hypertension"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "N&#46; Gali&#233;"
                            1 => "H&#46; Olschewski"
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                      "doi" => "10.1161/CIRCULATIONAHA.107.742510"
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                        "tituloSerie" => "Circulation"
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                        "volumen" => "117"
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                      "titulo" => "Pharmacokinetics and safety of ambrisentan in combination with sildenafil in healthy volunteers"
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                          "etal" => false
                          "autores" => array:4 [
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                  ]
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                      "doi" => "10.1177/0091270008324180"
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                    0 => array:2 [
                      "titulo" => "Sitaxsentan for the treatment of pulmonary arterial hypertension"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "R&#46;L&#46; Benza"
                            1 => "R&#46;J&#46; Barst"
                            2 => "N&#46; Gali&#233;"
                            3 => "A&#46; Frost"
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                            5 => "K&#46;B&#46; Highland"
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                    ]
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                    0 => array:2 [
                      "doi" => "10.1378/chest.07-0767"
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                        "tituloSerie" => "Chest"
                        "fecha" => "2008"
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                      "titulo" => "Treatment of patients with mildly symptomatic pulmonary arterial hypertension with bosentan &#40;EARLY study&#41;&#58; a double-blind&#44; randomised controlled trial"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
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                            1 => "L&#46;J&#46; Rubin"
                            2 => "M&#46;M&#46; Hoeper"
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                      "titulo" => "A randmised&#44; controlled trial of bosentan in severe COPD"
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                          "etal" => true
                          "autores" => array:6 [
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                      "autores" => array:1 [
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                        0 => array:2 [
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                  "contribucion" => array:1 [
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                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
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                            0 => "F&#46;J&#46; Garc&#237;a Hern&#225;ndez"
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Article information
ISSN: 03002896
Original language: Spanish
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