{"id":40091,"date":"2013-09-18T16:06:52","date_gmt":"2013-09-18T20:06:52","guid":{"rendered":"http:\/\/1boringoldman.com\/?p=40091"},"modified":"2013-09-18T16:09:30","modified_gmt":"2013-09-18T20:09:30","slug":"an-open-mind","status":"publish","type":"post","link":"https:\/\/1boringoldman.com\/index.php\/2013\/09\/18\/an-open-mind\/","title":{"rendered":"an open mind&#8230;"},"content":{"rendered":"\n<p align=\"justify\">Well chasing down the leads from the last post was disappointing. <a target=\"_blank\" href=\"http:\/\/www.brainresource.com\/\">Brain Resource<\/a> [the sponsor of <a target=\"_blank\" href=\"http:\/\/www.brainresource.com\/research\/ispot\">iSPOT<\/a>] does indeed have a data sharing plan, but it&#8217;s not sharing of a particular study like <strong><font color=\"#200020\">iSPOT<\/font><\/strong>. It&#8217;s a related but separate organization called <a target=\"_blank\" href=\"http:\/\/www.brainnet.net\/about\/\">BRAINnet<\/a>. <strong><font color=\"#200020\">BRAINnet<\/font><\/strong> is a large database of neuroscientific data on both normal and a variety of patients diagnosed with various mental illnesses including neuroimaging, EEG, biochemical, and neuropsych data [from <strong><font color=\"#200020\">Brain Resource<\/font><\/strong>].&nbsp; It&#8217;s free, well sort of. You have to apply to have access, actually you have to be recommended by an existing member. It&#8217;s pretty complicated, but for our purposes, it&#8217;a a data sharing proposition [<a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/19\/personalized-medicine-brainnet\/\">personalized medicine: BRAINnet&hellip;<\/a>, <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/19\/personalized-medicine-the-brain-resources-company\/\">personalized medicine: the Brain Resources company I&hellip;<\/a>, and <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/20\/personalized-medicine-the-brain-resources-company-ii\/\">personalized medicine: the Brain Resources company II&hellip;<\/a>].<\/p>\n<div align=\"justify\">What about <strong><font color=\"#200020\">STAR*D<\/font><\/strong>? It&#8217;s something of a different story. One of its goals at inception was to gather a large dataset of information on subjects with <strong><font color=\"#200020\">Major Depressive Disorder<\/font><\/strong>. It was the largest depression study in history, costing the NIMH some $35 M [<a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/03\/a-thirty-five-million-dollar-misunderstanding\/\">a thirty-five million dollar misunderstanding&hellip;<\/a>]. <\/div>\n<blockquote>\n<div align=\"center\" class=\"big\"><a target=\"_blank\" href=\"http:\/\/ajp.psychiatryonline.org\/article.aspx?articleID=97282\">Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report.<\/a><\/div>\n<div align=\"center\" class=\"small\">by  Rush AJ, Trivedi MH,  Wisniewski SR, Nierenberg AA, Stewart  JW, Warden  D, Niederehe G, Thase  ME, Lavori PW, Lebowitz BD, McGrath  PJ, Rosenbaum  JF, Sackeim HA,  Kupfer DJ, Luther J, and Fava M.<\/p>\n<div>\n<div align=\"center\" class=\"middle\"><strong><font color=\"#004400\">American Journal of Psychiatry<\/font><\/strong>. 2006 Nov;163[11]:1905-17.<\/div>\n<p>     <\/p>\n<div align=\"justify\"><strong><u>OBJECTIVE<\/u>:<\/strong>   This   report describes the participants and compares the acute and     longer-term treatment outcomes associated with each of four successive     steps in the Sequenced Treatment Alternatives to Relieve Depression     [STAR*D] trial.<\/div>\n<div align=\"justify\"><strong><u>METHOD<\/u>:<\/strong>  A  broadly   representative adult outpatient sample with nonpsychotic  major    depressive disorder received one [N=3,671] to four [N=123]  successive    acute treatment steps. Those not achieving remission with or  unable to    tolerate a treatment step were encouraged to move to the  next step.    Those with an acceptable benefit, preferably symptom  remission, from   any  particular step could enter a 12-month naturalistic  follow-up   phase. A  score of &lt;or=5 on the Quick Inventory of  Depressive    Symptomatology-Self-Report [QIDS-SR[16]] [equivalent to  &lt;or=7 on the    17-item Hamilton Rating Scale for Depression  [HRSD[17]]] defined    remission; a QIDS-SR[16] total score of &gt;or=11  [HRSD[17]&gt;or=14]    defined relapse.<\/div>\n<div align=\"justify\"><strong><u>RESULTS<\/u>:<\/strong> <strong><font color=\"#990000\"> The   QIDS-SR[16]  remission rates were 36.8%, 30.6%, 13.7%, and 13.0%  for  the  first,  second, third, and fourth acute treatment steps,   respectively.  The  overall cumulative remission rate was 67%.<\/font><\/strong>  Overall,  those who  required  more treatment steps had higher relapse  rates  during the  naturalistic  follow-up phase. In addition, lower  relapse  rates were  found among  participants who were in remission at   follow-up entry than  for those  who were not after the first three   treatment steps.<\/div>\n<div align=\"justify\"><strong><u>CONCLUSIONS<\/u>:<\/strong>  When    more treatment steps are required, lower acute remission rates     [especially in the third and fourth treatment steps] and higher relapse     rates during the follow-up phase are to be expected. Studies  to   identify  the best multistep treatment sequences for individual    patients and the  development of more broadly effective treatments are    needed.<\/div>\n<\/p><\/div>\n<\/div>\n<\/blockquote>\n<div align=\"justify\">This blog and many others are filled with criticisms of <strong><font color=\"#200020\">STAR*D<\/font><\/strong>. I&#8217;ll just mention a few that relate to data sharing. As to the question, has this data been available? Has it ever! The authors have milked it for all it&#8217;s worth. A few years ago, I counted 123 articles [<a href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/14\/infectious-numerology\/\">infectious numerology&#8230;<\/a>]. And there were monotonous names scattered throughout the papers &#8211; just to mention the top four [the ordinate axis measures authored articles per year]:<\/div>\n<div align=\"center\"><img decoding=\"async\" width=\"350\" vspace=\"5\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/star-d-8.gif\" \/><\/div>\n<div align=\"justify\"><img decoding=\"async\" width=\"180\" vspace=\"4\" hspace=\"4\" border=\"0\" align=\"right\" src=\"http:\/\/1boringoldman.com\/images\/star-d-2.gif\" \/>In spite of milking the database, the worth certainly wasn&#8217;t in the reports on the primary outcome. The statement in red above leaves out a small detail, the patients disappeared at an impressive rate. I never could get the exact figures, but the graphic on the right is close. It was impossible to conclude how many actually remained at the end of each level. But the actual numbers didn&#8217;t come close to the numbers reported in the abstract. In addition, they changed rating scales in mid-stream. Add to that, there were multiple versions of using the rating scales that were never clarified. The Primary Outcome Variable [HAM-D] was never reported.<\/div>\n<p> <\/p>\n<div align=\"justify\"> But the peripheral papers came in a steady flow &#8211; mostly from the original authors. One investigator who vigorously pursued deconstruction of <strong><font color=\"#200020\">STAR*D <\/font><\/strong>was Dr. Ed Pigott [see <a target=\"_blank\" href=\"http:\/\/psychrights.org\/research\/Digest\/AntiDepressants\/STARDTaleandTrailofBiasPiggot2011.pdf\">STAR*D: A Tale and Trail of Bias<\/a>]. Other independent investigators have accessed the database to analyze &quot;non-ignorable drop-outs&quot; [see <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2011\/04\/15\/whats-missing\/\">what&rsquo;s missing&hellip;<\/a>]. But the main point for the moment has to do with data transparency. With all the questions about this study, was it possible for an independent source to get hold of the data and clear up some of the fog surrounding it?&nbsp; The information on how to access the database from is on the <a href=\"http:\/\/www.nimh.nih.gov\/health\/trials\/datasets\/index.shtml\" target=\"_blank\">NIMH web-site<\/a>:<\/div>\n<blockquote>\n<div align=\"justify\">The data from NIMH-supported clinical trials are an important  scientific resource. It is the view of NIMH that their full value can  only be realized if they are made available, under appropriate terms and  conditions, in a timely manner to the wider scientific community,  provided that the confidentiality and privacy of study participants are  protected. NIMH requires all investigators seeking access to data from  NIMH-supported trials held by NIMH to execute and submit as their  request the appropriate Data Use Certification pertaining to the trial.  The datasets distributed by NIMH are referred to as &quot;limited access  datasets&quot; because access is limited to qualified researchers who  complete Data Use Certifications. The current listing of these datasets  may be found on the <a href=\"http:\/\/www.nimh.nih.gov\/health\/trials\/datasets\/nimh-procedures-for-requesting-data-sets.shtml\" target=\"_blank\">Available Limited Access Datasets From NIMH Clinical Trials<\/a> page.<\/div>\n<\/blockquote>\n<div align=\"justify\">And what is a Data Use Certification? I don&#8217;t know: <\/div>\n<div align=\"justify\">\n<blockquote>\n<div align=\"justify\" class=\"big\"><a href=\"http:\/\/www.nimh.nih.gov\/health\/trials\/datasets\/nimh-procedures-for-requesting-data-sets.shtml\" target=\"_blank\">Procedures for Requesting Limited Access Datasets<\/a><\/div>\n<div>Investigators wishing to request any of the above datasets must  obtain and submit a Data Use Certificate (DUC) in order for NIMH to  release the dataset. Please note that the DUC requires the institution&#8217;s  Federal Wide Assurance (FWA) number and the signature of the  institution&#8217;s official. To request a DUC, send an email to: <a href=\"mailto:nimhdatasets@mail.nih.gov\">nimhdatasets@mail.nih.gov<\/a>. Be sure to specify the dataset that you are requesting.<\/div>\n<\/blockquote>\n<\/div>\n<div align=\"justify\">So I wrote for a Data Use Certificate [DUC] for <strong><font color=\"#200020\">STAR*D<\/font><\/strong>. My question is fairly simple. Is it possible to obtain the dataset in order the check the work of the original investigators. I understand the need for protecting subject privacy, but I wonder what else they require &#8211; what restrictions they might place on my use of the data were I to receive it? I suppose the only way to find out is apply and see what they say. Were I to receive access, I&#8217;m glad to say what I&#8217;d do with it up front. I would <em>vet<\/em> <strong><font color=\"#200020\">STAR*D<\/font><\/strong> to see if the conclusions published are supported. I don&#8217;t think it&#8217;s possible that they are, but I&#8217;d definitely keep an open mind. If they if they won&#8217;t allow me to do that, who would they allow to check the reported work on this study?&#8230;<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Well chasing down the leads from the last post was disappointing. Brain Resource [the sponsor of iSPOT] does indeed have a data sharing plan, but it&#8217;s not sharing of a particular study like iSPOT. It&#8217;s a related but separate organization called BRAINnet. BRAINnet is a large database of neuroscientific data on both normal and a [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_bbp_topic_count":0,"_bbp_reply_count":0,"_bbp_total_topic_count":0,"_bbp_total_reply_count":0,"_bbp_voice_count":0,"_bbp_anonymous_reply_count":0,"_bbp_topic_count_hidden":0,"_bbp_reply_count_hidden":0,"_bbp_forum_subforum_count":0,"footnotes":""},"categories":[2],"tags":[],"class_list":["post-40091","post","type-post","status-publish","format-standard","hentry","category-politics"],"_links":{"self":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/40091","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/comments?post=40091"}],"version-history":[{"count":16,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/40091\/revisions"}],"predecessor-version":[{"id":40115,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/40091\/revisions\/40115"}],"wp:attachment":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/media?parent=40091"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/categories?post=40091"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/tags?post=40091"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}