{"id":10851,"date":"2018-01-26T19:59:10","date_gmt":"2018-01-26T19:59:10","guid":{"rendered":"http:\/\/drupal.test\/projects\/pegase-2-personnalisation-par-la-genomique-du-depistage-prenatal-danomalies-chromosomiques-dans-le\/"},"modified":"2022-07-26T11:07:46","modified_gmt":"2022-07-26T15:07:46","slug":"pegase-2-personnalisation-par-la-genomique-du-depistage-prenatal-danomalies-chromosomiques-dans-le","status":"publish","type":"project","link":"https:\/\/genomecanada.ca\/fr\/project\/pegase-2-personnalisation-par-la-genomique-du-depistage-prenatal-danomalies-chromosomiques-dans-le\/","title":{"rendered":"P\u00c9GASE-2 : Personnalisation par la G\u00e9nomique du d\u00e9pistage pr\u00e9natal d&rsquo;Anomalies chromosomiques dans le Sang matErnel : vers un d\u00e9pistage de premier niveau"},"content":{"rendered":"<p>La d\u00e9couverte de la pr\u00e9sence de l\u2019ADN du f\u0153tus dans le sang maternel a men\u00e9 au d\u00e9veloppement d\u2019une technique d\u2019analyse sanguine g\u00e9nomique du sang maternel baptis\u00e9e NIPS (d\u00e9pistage pr\u00e9natal par analyse non invasive), qui s\u2019est av\u00e9r\u00e9e un moyen tr\u00e8s fiable de d\u00e9pistage du syndrome de Down. En partie en raison de son co\u00fbt, la NIPS n\u2019est actuellement utilis\u00e9e qu\u2019\u00e0 titre de seconde analyse, apr\u00e8s un premier d\u00e9pistage positif de la m\u00e8re au moyen de m\u00e9thodes moins co\u00fbteuses et moins fiables, pour confirmer le r\u00e9sultat avant le recours \u00e0 l\u2019amniocent\u00e8se.<\/p>\n<p>L\u2019emploi de la NIPS comme premi\u00e8re analyse pour d\u00e9pister le syndrome de Down pourrait se r\u00e9v\u00e9ler avantageux pour les patientes en permettant une d\u00e9tection plus fiable des f\u0153tus atteints, avec un risque moindre de faux positif et en avan\u00e7ant le diagnostic de plusieurs semaines dans la grossesse. Par ailleurs, \u00e9tant donn\u00e9 que la NIPS est en mesure de d\u00e9celer d\u2019autres anomalies chromosomiques, son usage permettrait de d\u00e9pister d\u2019autres maladies. Le projet\u00a0P\u00c9GASE-2 a pour but de fournir des r\u00e9sultats probants de haute qualit\u00e9 pour justifier l\u2019utilisation de la NIPS au lieu des analyses de d\u00e9pistage classiques, en comparant son usage comme premier et deuxi\u00e8me moyen de d\u00e9pistage chez une grande cohorte de femmes enceintes. Dans le cadre de ce projet, les chercheurs se pencheront \u00e9galement sur la faisabilit\u00e9 financi\u00e8re d\u2019une extension du d\u00e9pistage \u00e0 d\u2019autres anomalies g\u00e9n\u00e9tiques et sur les implications sur le plan de l\u2019\u00e9thique, de la soci\u00e9t\u00e9 et du droit qui en d\u00e9couleraient. Ils proposeront des strat\u00e9gies pour favoriser la prise de d\u00e9cisions communes entre les couples et les professionnels de la sant\u00e9. Enfin, ils poursuivront le d\u00e9veloppement de la technologie NIPS pour r\u00e9duire son co\u00fbt de 50\u00a0% et \u00e9tendre sa capacit\u00e9 \u00e0 d\u00e9celer d\u2019autres anomalies, tout en assurant le contr\u00f4le de la qualit\u00e9 des analyses cliniques par NIPS au Canada et dans le monde.<\/p>\n<p>P\u00c9GASE-2 rendra possible l\u2019acc\u00e8s de toutes les femmes enceintes int\u00e9ress\u00e9es \u00e0 une technologie de g\u00e9nomique prometteuse financ\u00e9e par le syst\u00e8me de sant\u00e9 publique, tout en fournissant aux couples des outils en ligne pour les aider \u00e0 prendre leurs d\u00e9cisions et en assurant une formation ad\u00e9quate des professionnels de la sant\u00e9 sur la prise de d\u00e9cision concernant le d\u00e9pistage pr\u00e9natal.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La d\u00e9couverte de la pr\u00e9sence de l\u2019ADN du f\u0153tus dans le sang maternel a men\u00e9 au d\u00e9veloppement d\u2019une technique d\u2019analyse sanguine g\u00e9nomique du sang maternel baptis\u00e9e NIPS (d\u00e9pistage pr\u00e9natal par analyse non invasive), qui s\u2019est av\u00e9r\u00e9e un moyen tr\u00e8s fiable de d\u00e9pistage du syndrome de Down. En partie en raison de son co\u00fbt, la NIPS [&hellip;]<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"site-sidebar-layout":"default","site-content-layout":"default","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"default","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}}},"project-categories":[93],"genome-competitions":[213],"project-sector":[],"genome_centres":[105,104],"class_list":["post-10851","project","type-project","status-publish","hentry","project-categories-large-scale-science-fr","genome-competitions-concours-2017-projets-de-recherche-appliquee-a-grande-echelle-la-genomique-et-la-sante-de-precision","genome_centres-genome-british-columbia-fr","genome_centres-genome-quebec-fr"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>P\u00c9GASE-2 : Personnalisation par la G\u00e9nomique du d\u00e9pistage pr\u00e9natal d&#039;Anomalies chromosomiques dans le Sang matErnel : vers un d\u00e9pistage de premier niveau - GenomeCanada<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/genomecanada.ca\/fr\/project\/pegase-2-personnalisation-par-la-genomique-du-depistage-prenatal-danomalies-chromosomiques-dans-le\/\" \/>\n<meta property=\"og:locale\" content=\"fr_FR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"P\u00c9GASE-2 : Personnalisation par la G\u00e9nomique du d\u00e9pistage pr\u00e9natal d&#039;Anomalies chromosomiques dans le Sang matErnel : vers un d\u00e9pistage de premier niveau - GenomeCanada\" \/>\n<meta property=\"og:description\" content=\"La d\u00e9couverte de la pr\u00e9sence de l\u2019ADN du f\u0153tus dans le sang maternel a men\u00e9 au d\u00e9veloppement d\u2019une technique d\u2019analyse sanguine g\u00e9nomique du sang maternel baptis\u00e9e NIPS (d\u00e9pistage pr\u00e9natal par analyse non invasive), qui s\u2019est av\u00e9r\u00e9e un moyen tr\u00e8s fiable de d\u00e9pistage du syndrome de Down. 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