{"id":4276,"date":"2022-02-10T14:38:37","date_gmt":"2022-02-10T14:38:37","guid":{"rendered":"https:\/\/veritastestovi.com\/?p=4276"},"modified":"2022-02-11T08:19:22","modified_gmt":"2022-02-11T08:19:22","slug":"ajla-ridzal-magistrica-genetike-sta-je-prenatalno-testiranje-i-zasto-je-vazno","status":"publish","type":"post","link":"https:\/\/veritastestovi.com\/index.php\/2022\/02\/10\/ajla-ridzal-magistrica-genetike-sta-je-prenatalno-testiranje-i-zasto-je-vazno\/","title":{"rendered":"Ajla Rid\u017eal, magistrica genetike: \u0160ta je prenatalno testiranje i za\u0161to je va\u017eno?"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Tokom gostovanja na RTV USK <strong>na\u0161 genetski savjetnik Ajla Rid\u017eal, magistrica genetike<\/strong>, edukovala je gledaoce na temu prenatalnih testova, njihovoj va\u017enosti i benefitima. Kroz razgovor, sa stru\u010dne ta\u010dke gledi\u0161ta, odgovorila je na niz flegmi koje prate temu prenatalnog i genetskog testiranja. Saznajte koji su bili njeni odgovori na naj\u010de\u0161\u0107e postavljena pitanja i nedoumice svih novope\u010denih trudnica!<\/p>\n\n\n\n<!--more-->\n\n\n\n<h2 class=\"wp-block-heading\" id=\"sta-je-zaista-prenatalno-i-genetsko-testiranje-koliko-je-vazno\">\u0160ta je, zaista, prenatalno i genetsko testiranje? Koliko je va\u017eno?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Prenatalno testiranje<\/strong> se odnosi na skup razli\u010ditih pretraga koje se izvr\u0161avaju u toku trudno\u0107e, isklju\u010divo prije ro\u0111enja bebe. U u\u017eem smislu, odnosi se na utvr\u0111ivanje abnormalnosti koje imaju genetsku podlogu.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Rid\u017eal nagla\u0161ava: \u201cPrenatalna dijagnostika obuhvata niz razli\u010ditih metoda kojim mo\u017eemo da dobijemo informacije o zdravstvenom stanju ploda i uvidimo da li postoji neko <strong>patolo\u0161ko stanje<\/strong>.\u201d<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">U \u0161irem kontekstu, razgovarali su o <strong>genetskom testiranju<\/strong>. Dobro je poznato da su sve funkcije u na\u0161im tijelima odre\u0111ene genima, u kojima je sve zapisano o nama. Tako\u0111er, znamo da su geni dijelovi DNK sekvence.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">\u201cGenetsko testiranje se odnosi na testiranje same DNK molekule. Cilj njegove primjene u zdravstvu jeste utvr\u0111ivanje postojanja potencijalnih mutacija, promjena ili gre\u0161aka, koje se doga\u0111aju na nivou DNK molekule, uslijed kojih mo\u017ee do\u0107i do pojave razli\u010ditih klini\u010dkih slika i oboljenja\u201d, obja\u0161njava Rid\u017eal. Zatim navodi: \u201cMonogenska oboljenja se, na primjer, de\u0161avaju usljed promjene na samo jednom genu, ali je \u010de\u0161\u0107e rije\u010d o promjenama koje zahvataju veci broj gena, izazivaju\u0107i kompleksne bolesti. Promjene mogu utjecati na ve\u0107u koli\u010dinu genetskog materijala, gdje govorimo o promjenama u strukturi ili broju hromozoma, to jeste, <strong>hromozomskim aberacijama<\/strong>.\u201d<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"kakav-znacaj-za-same-roditelje-imaju-genetski-testovi\">Kakav zna\u010daj za same roditelje imaju genetski testovi?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">\u010cesto mo\u017eemo \u010duti pitanje poput: Da li beba od<strong> oba zdrava roditelja<\/strong> mo\u017ee da se rodi sa nekim <strong>oboljenjem ili sindromom<\/strong>?<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Ajla odgovara: \u201c<strong>To je \u010desta zabluda<\/strong>. Roditelji misle da ako u porodici nemaju nikoga sa, na primjer, Daunovim sindromom, ili bilo kojom drugom DNK malfunkcijom, da ne postoji nikakva mogu\u0107nost da dobiju bebu sa nekom od hromozomskih abnormalnosti. Na\u017ealost, <strong>apsolutno svi mogu<\/strong> da dobiju bebu sa nekom od hromozomskih abnormalnosti, bez obzira na porodi\u010dnu anamnezu, zdravstveno stanje, \u017eivotni stil trudnice i sli\u010dne parametre. Niko <strong>nije po\u0161te\u0111en<\/strong> takve mogucnosti.\u201d<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Sljede\u0107e naj\u010de\u0161\u0107e pitanje roditelja jeste: Koji prenatalni testovi su dostupni trudnicama <strong>kod nas<\/strong>?<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Prenatalnu dijagnostiku po pravilu dijelimo na <strong>invazivne i neinvazivne metode<\/strong>. <strong>Invazivne metode<\/strong> nose rizik komplikacija u toku trudno\u0107e i mogu dovesti do <strong>spontanog poba\u010daja<\/strong>, ali se zasnivaju na analizi DNK molekule i daju <strong>jasan i precizan rezultat<\/strong>. Sa druge strane, Ajla navodi: \u201c<strong>Neinvazivne metode<\/strong> prenatalne dijagnostike predstavile su vi\u0161e varijanti prenatalnih testova. Postoje double i triple test, kao i kombinacije testova, koji se zasnivaju na statisti\u010dkim analizama. Dok je <strong>NIPT, neinvazivni prenatalni test<\/strong>, najsavremeniji mogu\u0107i na\u010din neinvazivne prenatalne dijagnostike, jer se zasniva isklju\u010divo na podacima iz DNK molekule va\u0161e bebe.\u201d<\/p>\n\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\n<iframe title=\"NEDJELJOM ZAJEDNO RTV USK - GO\u0160\u0106A: AJLA RID\u017dAL, MAGISTRICA GENETIKE\" width=\"800\" height=\"450\" src=\"https:\/\/www.youtube.com\/embed\/eHaz05E7AWQ?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe>\n<\/div><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"sve-o-nipt-testovima-jednostavno-objasnjeno\">Sve o NIPT testovima. Jednostavno obja\u0161njeno.<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Za po\u010detak, va\u017eno je razumjeti<strong> \u0161ta je neinvazivni prenatalni test<\/strong>, ili jednostavnije re\u010deno <strong>NIPT test<\/strong>.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Magistrica genetike, Ajla obja\u0161njava: \u201cNIPT testovi su genetiski testovi koji se baziraju na analizi DNK molekule ploda, to jeste va\u0161e bebe. Ovo pravi <strong>glavnu razliku NIPT testa od drugih testova<\/strong> neinvazivne prenatalne dijagnostike, kao \u0161to su double i triple test koji se zasnivaju na testiranju biohemijskih markera iz krvi majke i na taj na\u010din procjenjuju statisti\u010dku vjerovatno\u0107u da je mo\u017eda prisutna neka hromozomska aberacija. Zaklju\u010dujemo kako rezultati ovih testova nisu jasni, dok je NIPT isklju\u010divo kreiran za va\u0161u bebu. NIPT test, ukoliko koristi <strong>najnapredniju tehnologiju sekvenciranja<\/strong>, rezultat isporu\u010duje<strong> sa precizno\u0161\u0107u od 99.9%.<\/strong>\u201d<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"a-koje-sve-informacije-mozemo-dobiti-iz-neinvazivnog-prenatalnog-testa\">A koje sve informacije mo\u017eemo dobiti iz neinvazivnog prenatalnog testa?<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Upoznati smo da svaki \u010dovjek ima 46 hromozoma, od kojih po 23 naslje\u0111uje od majke i 23 od oca. Posljednji par hromozoma jesu polni hromozomi.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Rid\u017eal savjetuje: \u201cNIPT testom, ukoliko se koriste <strong>adekvatne, moderne i savremene metode i tehnologije<\/strong> tokom sekvenciranja cjelokupnog genoma, mo\u017eemo detektovati sve hromozome u garnituri. Pojava vi\u0161ka ili nedostatka nekog hromozoma predstavlja <strong>aneuploidiju<\/strong> i povezuje se sa razli\u010ditim stepenima psihomotornih, fizi\u010dkih ili mentalnih o\u0161te\u0107enja i pote\u0161ko\u0107a. <strong>Sve strukturne i numeri\u010dke promjene hromozoma<\/strong> mogu se otkriti NIPT testom, <strong>\u010dak i one najmanje<\/strong>. Prirodno, pomo\u0107u ovog testa mo\u017eemo otkriti i <strong>pol va\u0161e bebe<\/strong>.\u201d<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"sigurno-vas-interesuje-da-li-ovaj-test-trebaju-uraditi-sve-trudnice\">Sigurno vas interesuje da li ovaj test trebaju uraditi sve trudnice?<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Ajla odgovara: \u201c<strong>Moderna medicina preporu\u010duje<\/strong> da se test uradi u svim trudno\u0107ama, kako bismo pravovremeno bili obavje\u0161teni o zdravstvenom stanju bebe. Dovoljan je samo uzorak krvi majke, <strong>ve\u0107 od 10 nedelje trudno\u0107e<\/strong>. Rezultati testiranja dozvoljavaju nam <strong>potpuni uvid u genom bebe<\/strong>, a sam NIPT test je <strong>u potpunosti siguran<\/strong> kako za majku, tako i za bebu.\u201d<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"kako-odluciti-koji-nipt-test-da-uradim\">Kako odlu\u010diti koji NIPT test da uradim?<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Na tr\u017ei\u0161tu postoji mnogo razli\u010ditih prenatalnih testova, koji <strong>imaju isti cilj<\/strong>, uvi\u0111anje hromozomskih abnormalnosti. I ako imaju svi isti cilj, ne uspijevaju svi NIPT testovi da nam jednako prika\u017eu te informacije. <strong>Razlikuju se<\/strong> u pouzdanosti, uspje\u0161nosti i preciznosti.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Magistrica genetike, Ajla Rid\u017eal odlu\u010dila je da izdvoji nekoliko kriterijuma na koje se budu\u0107i roditelji trebaju fokusirati tokom izbora NIPT testa za svoju bebu. Ona isti\u010de: \u201c<strong>Najva\u017eniji kriterijum<\/strong> pri odabiru NIPT testa jeste koja tehnologija se koristi za samo testiranje. Poznato je da je danas<strong> najsavremenija i broj 1 svjetski standard tehnologija<\/strong> koja se koristi za sekvenciranje cijelog genoma<strong> illumina platforma<\/strong>. Primarni kriterijum, odre\u0111uje ta\u010dnost va\u0161ih rezultata.<strong> Drugi va\u017ean kriterijum<\/strong> je da odabrani test <strong>ne ovisi o <a href=\"https:\/\/veritastestovi.com\/index.php\/2022\/01\/31\/sta-je-fetalna-frakcija-i-zasto-je-taj-procenat-toliko-vazan-u-prenatalnom-testiranju\/\" target=\"_blank\" rel=\"noreferrer noopener\">fetalnoj frakciji<\/a>,<\/strong> to jeste udjelu bebinog DNK u krvi majke. Sve trudnice nemaju istu fetalnu frakciju tokom trudno\u0107e i iz tog razloga, testovi koje ne koriste tako kvalitetne i savremene tehnologije mogu dati <strong>la\u017ene rezultate<\/strong>. Naposljetku, ali ne i manje va\u017ena, jeste <strong>laboratorija<\/strong> koja stoji iza samih testova. Ona mora biti transparentna, a podatci ko stoji iza nalaza jasni.\u201d<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">U na\u0161em slu\u010daju uzorci za VeritasTest se analiziraju u Veritas laboratoriji, \u0161to je svojevrsna garancija kvaliteta.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Tako\u0111e, va\u017ean kriterijum jeste da kompanija koja vam nudi neinvazivno prenatalno testiranje, pru\u017ea mogu\u0107nost genetskog savjetovanja prilikom samog odabira prenatalnog testa, kako biste bili sigurni da ste odabrali najbolju opciju za vas. Kada je u pitanju VeritasTest, za ovakve konsultacije Ajla Rid\u017eal je prava adresa.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Jo\u0161 je va\u017enija mogu\u0107nost konsultacija sa geneti\u010darima nakon dobijanja rezultata, posebno u slu\u010daju da nalaz bude pozitivan, kada oni daju preporuke za dalju dijagnostiku kako bi se potvrdila ili odbacila prona\u0111ena genetska malformacija. Ekipa VeritasTest-a u BIH u svakom trenutku ima podr\u0161ku stru\u010dnog tima iz Veritas laboratorije, koji je uvijek dostupan za dodatno tuma\u010denje nalaza i savjet o sljede\u0107im koracima.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"sta-izdvojiti-za-sam-kraj\">\u0160ta izdvojiti za sam kraj?<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">\u201c<strong>Roditeljstvo je velika odgovornost.<\/strong> Tokom planiranja potomstva se trebamo pona\u0161ati jednako odgovorno kao i kada se na\u0161e dijete rodi. Va\u017eno je iskoristiti sve metode koje nam savremena medicina omogu\u0107ava. Prenatalno testiranje, genetske konsultacije i savjetovanje jeste <strong>odgovoran i zdrav po\u010detak <\/strong>va\u0161eg roditeljskog puta\u201d, zaklju\u010duje Rid\u017eal.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Ukoliko razmi\u0161ljate da uradite neinvazivno prenatalno testiranje, ali \u017eelite znati vi\u0161e, u kompaniji BTGMED, koja je ekskluzivni i ovla\u0161teni zastupnik za VeritasTest na teritoriji Jugoisto\u010dne Evrope, mo\u017eete zakazati besplatne genetske konsultacije sa Ajlom Rid\u017eal, magistricom genetike, putem email-a <a href=\"mailto:ajla.ridzal@btgmed.com\">ajla.ridzal@btgmed.com<\/a> ili na broj telefona <a href=\"tel:0038761474813\">+ 387 61 474 813<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tokom gostovanja na RTV USK na\u0161 genetski savjetnik Ajla Rid\u017eal, magistrica genetike, edukovala je gledaoce na temu prenatalnih testova, njihovoj va\u017enosti i benefitima. Kroz razgovor, sa stru\u010dne ta\u010dke gledi\u0161ta, odgovorila je na niz flegmi koje prate temu prenatalnog i genetskog testiranja. Saznajte koji su bili njeni odgovori na naj\u010de\u0161\u0107e postavljena pitanja i nedoumice svih novope\u010denih [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":4277,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[52,53,27,28,26,29],"class_list":["post-4276","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog-bih","tag-ajla-ridzal","tag-genetsko-savjetovanje","tag-neinvazivno-prenatalno-testiranje","tag-nipt","tag-prenatalno-testiranje","tag-veritas-test"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Ajla Rid\u017eal, magistrica genetike: \u0160ta je prenatalno testiranje i za\u0161to je va\u017eno? - Veritas Genetski Testovi<\/title>\n<meta name=\"description\" content=\"\u0160ta podrazumijeva prenatalno testiranje? \u0160ta je neinvazivni prenatalni test? 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