{"id":1217,"date":"2018-02-14T20:20:47","date_gmt":"2018-02-14T20:20:47","guid":{"rendered":"http:\/\/www.drshevchuk.com.ua\/?p=1217"},"modified":"2018-02-14T20:20:47","modified_gmt":"2018-02-14T20:20:47","slug":"bladder-dysfunction-in-wolfram-syndrome-is-highly-prevalent-and-progresses-to-megacystis-%d0%b4%d0%b8%d1%81%d1%84%d1%83%d0%bd%d0%ba%d1%86%d1%96%d1%8f-%d1%81%d0%b5%d1%87%d0%be%d0%b2%d0%be%d0%b3%d0%be","status":"publish","type":"post","link":"http:\/\/www.drshevchuk.com.ua\/?p=1217","title":{"rendered":"Bladder dysfunction in Wolfram syndrome is highly prevalent and progresses to megacystis\/ \u0414\u0438\u0441\u0444\u0443\u043d\u043a\u0446\u0456\u044f \u0441\u0435\u0447\u043e\u0432\u043e\u0433\u043e \u043c\u0456\u0445\u0443\u0440\u0430 \u043f\u0440\u0438 \u0441\u0438\u043d\u0434\u0440\u043e\u043c\u0456 \u0412\u043e\u043b\u044c\u0444\u0440\u0430\u043c\u0430"},"content":{"rendered":"<h2>Bladder dysfunction in Wolfram syndrome is highly prevalent and progresses to megacystis<\/h2>\n<div class=\"author\">Ruth Wragg, Renuka P Dias, Timothy Barrett, Liam McCarthy<\/div>\n<div>\n<div class=\"doi\">DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.jpedsurg.2017.11.025\">https:\/\/doi.org\/10.1016\/j.jpedsurg.2017.11.025<\/a><\/div>\n<div class=\"articleSharebookmark\">\n<div class=\"addthis_toolbox addthis_default_style addthis_16x16_style\">\n<div class=\"atclear\"><\/div>\n<\/div>\n<\/div>\n<div class=\"sperator\">\u00a0<img decoding=\"async\" class=\"aligncenter colorbox-1217\" src=\"http:\/\/www.jpedsurg.org\/pb\/assets\/raw\/Health%20Advance\/journals\/yjpsu\/logo.jpg\" alt=\"Journal of Pediatric Surgery Home\" \/><\/p>\n<div class=\"abstract\">\n<h2 class=\"sectionTitle\" tabindex=\"0\">Abstract<\/h2>\n<div class=\"content\">\n<section>\n<h3 class=\"sectionTitle\" tabindex=\"0\">Aim<\/h3>\n<div class=\"content\">\n<p>Wolfram syndrome is a rare genetic defect in WFS1 or WSF2(CISD2). It includes diabetes mellitus and insipidis, sensorineural deafness, optic atrophy, but not bladder dysfunction. However, this has appeared a common finding in our national referral clinic, and we sought to quantify this problem.<\/p>\n<\/div>\n<\/section>\n<\/div>\n<div class=\"content\">\n<section>\n<h3 class=\"sectionTitle\" tabindex=\"0\">Methods<\/h3>\n<div class=\"content\">\n<p>Data were collected from a multidisciplinary team managing all Wolfram patients in the UK. The following was analyzed: age, date of non-invasive urodynamics (NIU), symptoms, bladder capacity, voided volume, post-void residual and uroflow pattern. Bladder capacity was given as percentage predicted bladder capacity (PBC). Bladders were divided into normal, overactive (OAB), and underactive (UAB). Symptoms, bladder behavior, and genotyping were correlated. Data were expressed as median (interquartile range).<\/p>\n<\/div>\n<\/section>\n<\/div>\n<div class=\"content\">\n<section>\n<h3 class=\"sectionTitle\" tabindex=\"0\">Main results<\/h3>\n<div class=\"content\">\n<p>Forty patients with Wolfram syndrome were identified, and 38 underwent NIU. This showed normal bladder function (n\u2005=\u20054), OAB (n\u2005=\u20059), UAB (n\u2005=\u200525). Symptoms were present in only 11 children. The different patterns of bladder behavior (OAB vs. normal vs. UAB) were significantly associated with different %PBC (36 (29\u201359)% vs. 105 (93\u2013233)% vs. 100 (77.5\u2013337)%; p\u2005&lt;\u20050.001), and percentage emptying (100 (80\u2013100)% vs. 100 (87\u2013100)% vs. 69 (48\u201393)%; p\u2005&lt;\u20050.05). There was no association of genotype, symptoms and bladder behavior. Patients with megacystis were older: [13.4 (9.7\u201316.1) vs. 15.4 (13.9\u201318.7) years; p\u2005&lt;\u20050.05).<\/p>\n<\/div>\n<\/section>\n<\/div>\n<div class=\"content\">\n<section>\n<h3 class=\"sectionTitle\" tabindex=\"0\">Conclusion<\/h3>\n<div class=\"content\">\n<p>Bladder dysfunction is very common in Wolfram syndrome (~90%), but most children cope (symptoms ~30%). With time there is a significant progression to megacystis, which may represent an underlying neuropathic myogenic failure and is likely to require intervention in the future.<\/p>\n<\/div>\n<\/section>\n<\/div>\n<div class=\"content\">\n<section>\n<h3 class=\"sectionTitle\" tabindex=\"0\">Level of evidence<\/h3>\n<div class=\"content\">\n<p>Level II (National cohort study of prognosis).<\/p>\n<\/div>\n<\/section>\n<\/div>\n<\/div>\n<div class=\"content\"><\/div>\n<div class=\"keywords\">\n<h4>Key words:<\/h4>\n<p><a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Wolfram%20syndrome&amp;seriesISSN=0022-3468\">Wolfram syndrome<\/a>,\u00a0<a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Bladder%20dysfunction&amp;seriesISSN=0022-3468\">Bladder dysfunction<\/a>,\u00a0<a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Urodynamics&amp;seriesISSN=0022-3468\">Urodynamics<\/a>,\u00a0<a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Diabetes%20mellitus&amp;seriesISSN=0022-3468\">Diabetes mellitus<\/a>,\u00a0<a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Diabetes%20insipidis&amp;seriesISSN=0022-3468\">Diabetes insipidis<\/a>,\u00a0<a href=\"http:\/\/www.jpedsurg.org\/action\/doSearch?searchType=quick&amp;occurrences=all&amp;ltrlSrch=true&amp;searchScope=series&amp;searchText=Megacystis&amp;seriesISSN=0022-3468\">Megacystis<\/a><\/div>\n<\/div>\n<div id=\"container\" class=\"articleInfoToggle\"><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Bladder dysfunction in Wolfram syndrome is highly prevalent and progresses to megacystis Ruth Wragg, Renuka P Dias, Timothy Barrett, Liam McCarthy DOI:\u00a0https:\/\/doi.org\/10.1016\/j.jpedsurg.2017.11.025 \u00a0 Abstract Aim Wolfram syndrome is a rare genetic defect in WFS1 or WSF2(CISD2). It includes diabetes mellitus and insipidis, sensorineural deafness, optic atrophy, but not bladder dysfunction. However, this has appeared a [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[9],"tags":[205,207,206,204,208,203],"_links":{"self":[{"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/posts\/1217"}],"collection":[{"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1217"}],"version-history":[{"count":1,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/posts\/1217\/revisions"}],"predecessor-version":[{"id":1218,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=\/wp\/v2\/posts\/1217\/revisions\/1218"}],"wp:attachment":[{"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1217"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1217"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.drshevchuk.com.ua\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1217"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}