{"id":1938,"date":"2018-05-17T10:30:28","date_gmt":"2018-05-17T15:30:28","guid":{"rendered":"https:\/\/restruct-lgmd-2021.pantheonsite.io\/?p=1938"},"modified":"2018-05-17T10:30:28","modified_gmt":"2018-05-17T15:30:28","slug":"lgmd-researcher-kathryn-wagner","status":"publish","type":"post","link":"https:\/\/www.lgmd-info.org\/de\/researcher-interview\/2018\/05\/17\/lgmd-researcher-kathryn-wagner\/","title":{"rendered":"LGMD-FORSCHER: Kathryn Wagner, MD, PhD"},"content":{"rendered":"<h2 style=\"text-align: center;\"><span style=\"color: #008000;\"><strong>LGMD \"Forschung im Blickpunkt\"<\/strong><\/span><\/h2>\n<p>&nbsp;<\/p>\n<p><strong>LGMD-FORSCHER<\/strong>: Kathryn Wagner, MD, PhD<a href=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2018\/05\/Wagner-Kathryn.png\"><img decoding=\"async\" class=\"lazyload size-medium wp-image-1941 alignright\" src=\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%27300%27%20height%3D%27225%27%20viewBox%3D%270%200%20300%20225%27%3E%3Crect%20width%3D%27300%27%20height%3D%27225%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\" data-orig-src=\"https:\/\/www.lgmd-info.org\/wp-content\/uploads\/2018\/05\/Wagner-Kathryn-300x225.png\" alt=\"\" width=\"300\" height=\"225\" \/><\/a><\/p>\n<p><strong>Zugeh\u00f6rigkeit<\/strong>:  Kennedy-Krieger-Institut<\/p>\n<p><strong>Rolle oder Position<\/strong>: Professor und Direktor des Zentrums f\u00fcr genetische Muskelst\u00f6rungen<\/p>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong>Welche Ausbildung haben Sie absolviert, um Ihre derzeitige Position zu erreichen?<\/strong><\/p>\n<p>Nach Abschluss meines MD\/PhD-Programms absolvierte ich eine Facharztausbildung in Neurologie, gefolgt von Stipendien in Neuromuskulatur und Neurogenetik.  Au\u00dferdem absolvierte ich ein Postdoktorandenstipendium in Molekularbiologie.<\/p>\n<p><strong>Was hat Sie dazu bewogen, eine Karriere in der Forschung und insbesondere in der Erforschung von Muskeldystrophie einzuschlagen?<\/strong><\/p>\n<p>Mein Vater ist ein bekannter Wissenschaftler, und ich bin immer davon ausgegangen, dass ich in die Wissenschaft gehen w\u00fcrde. Erst ziemlich sp\u00e4t auf dem College habe ich beschlossen, dass ich auch in die Medizin gehen m\u00f6chte.  Mein Interesse an Muskeldystrophie wurde geweckt, als ich in der Graduiertenschule (zuf\u00e4llig) ein Gen klonte, Dystrobrevin, das einige \u00c4hnlichkeiten mit Dystrophin hat, dem Gen, das bei Duchenne-Muskeldystrophie (DMD) fehlt.  Ich lernte alles, was ich \u00fcber Muskeldystrophie wissen konnte, und war fasziniert von den Entdeckungen, die zu dieser Zeit \u00fcber Dystrophin-assoziierte Molek\u00fcle gemacht wurden, die bei anderen Muskeldystrophien eine Rolle spielen.<\/p>\n<p><strong>Welche Themen studieren Sie?<\/strong><\/p>\n<p>Ich leite ein translationales Labor, das sich auf die Entwicklung neuer Therapeutika f\u00fcr Muskeldystrophie konzentriert.  Derzeit untersuchen wir Modelle von DMD, fazioskapulohumeraler Muskeldystrophie und LGMD.  In der Klinik untersuche ich die Auswirkungen eines von Pfizer hergestellten Anti-Myostatin-Medikaments bei LGMD2I.<\/p>\n<p><strong>Wie wird Ihre Arbeit den Patienten helfen? Ist sie eher wissenschaftlicher Natur oder k\u00f6nnte sie zu einer Behandlung f\u00fcr LGMDs oder MDs im Allgemeinen werden?<\/strong><\/p>\n<p>Unsere Laborforschung im Bereich der AAV- und Zelltherapie hat das Potenzial, zur Behandlung von LGMD und von MDs im Allgemeinen eingesetzt zu werden.  Wenn die klinische Pr\u00fcfung des Anti-Myostatin-Medikaments von Pfizer erfolgreich ist, hat dies den k\u00fcrzesten Weg zur Behandlung.<\/p>\n<p><strong>Was w\u00fcrden Sie Patienten und anderen an LGMD Interessierten gerne \u00fcber die Forschung (Ihre eigenen Projekte und \u00fcber das Gebiet im Allgemeinen) mitteilen?<\/strong><\/p>\n<p>Die Gentherapie hat in den letzten Jahren enorme Fortschritte gemacht.  Es ist realistisch anzunehmen, dass wir in naher Zukunft systemische Gentherapieversuche bei LGMD durchf\u00fchren werden.  In meiner eigenen Arbeit entwickeln wir neuartige AAV, die besser in die Muskeln und nicht in die Leber gelangen.<\/p>\n<p><strong>Was inspiriert Sie, weiterhin in diesem Bereich zu arbeiten? <\/strong><\/p>\n<p>Die Patientenpopulation ist unwiderstehlich.  Sie bem\u00fchen sich, trotz ihrer k\u00f6rperlichen Einschr\u00e4nkungen ein erf\u00fclltes und lohnendes Leben zu f\u00fchren.<\/p>\n<p><strong>Wie k\u00f6nnen Patienten Sie ermutigen und Ihre Arbeit unterst\u00fctzen?<\/strong><\/p>\n<p>Verbale Ermutigung ist wunderbar, ebenso wie finanzielle Unterst\u00fctzung f\u00fcr unsere Forschung.<\/p>\n<p>&nbsp;<\/p>\n<p>* * * Bitte LIKE, KOMMENTAR und TEILEN Sie diesen Beitrag, um das Bewusstsein f\u00fcr LGMD zu erh\u00f6hen!<\/p>\n<p>* * * Um mehr \u00fcber Gliederg\u00fcrtelmuskeldystrophie (LGMD) zu erfahren oder weitere \"Spotlight-Interviews\" zu lesen, besuchen Sie bitte unsere Website unter <u><a href=\"https:\/\/www.lgmd-info.org\/de\/\">https:\/\/lgmd-info.org<\/a>\u00a0 <\/u><\/p>","protected":false},"excerpt":{"rendered":"<p>LGMD &#8220;Spotlight on Research&#8221; &nbsp; LGMD RESEARCHER: Kathryn Wagner, MD, [&hellip;]<\/p>","protected":false},"author":1,"featured_media":1941,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[91,92],"tags":[],"class_list":["post-1938","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-researcher-interview","category-researcher"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.9 - 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