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									<identifier>oai:www.peertechzpublications.org:10.17352/2455-5460.000016</identifier>
									<datestamp>2017-05-26</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Bupropion Sustained released versus Placebo for seasonal affective Disorder
										</dc:title><dc:creator>Martin H Teicher</dc:creator><dc:creator> Danielle M Webster</dc:creator><dc:creator>Steven B Lowen</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Background&lt;/strong&gt;: The majority of seasonal affective disorder&amp;nbsp; (SAD) studies have evaluated&amp;nbsp; the&amp;nbsp; use of &amp;nbsp; light or selective serotonin reuptake inhibitors (SSRI). The purpose of the present study was to evaluate bupropion sustained-released (SR), a non-SSRI antidepressant, for the treatment of SAD.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Method&lt;/strong&gt;:&amp;nbsp; Forty-one adults meeting DSM IV criteria for SAD were recruited into a six-week, randomized, double-blind,&amp;nbsp; placebo-controlled trial. Participants started on bupropion&amp;nbsp; SR&amp;nbsp; 150&amp;nbsp; mg&amp;nbsp; QD&amp;nbsp; (or&amp;nbsp; equivalent placebo&amp;nbsp; pills)&amp;nbsp; and&amp;nbsp; titrated&amp;nbsp; up&amp;nbsp; to&amp;nbsp; 200&amp;nbsp; mg BID&amp;nbsp; if&amp;nbsp; tolerated&amp;nbsp; by&amp;nbsp; week 4. Participants&amp;nbsp; were&amp;nbsp; evaluated weekly with SIGH-SAD and self-reported Kellner Symptom Questionnaire (SQ). Mixed effects growth models and receiver operating characteristic (ROC) analyses were used to compare treatments.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results &lt;/strong&gt;: Analysis was done on the 36 participants who completed at least 2 weeks of treatment, as per protocol. Thirty-four participants&amp;nbsp; completed the entire&amp;nbsp; protocol; two&amp;nbsp; participants receiving placebo dropped&amp;nbsp; out&amp;nbsp; during&amp;nbsp; weeks 3 and 5. Sixteen&amp;nbsp; participants&amp;nbsp; (7 male, 9 female, 46.5&amp;nbsp; +&amp;nbsp; 9.6&amp;nbsp; years, mean+SD) received bupropion SR and 20 participants&amp;nbsp; (8 males, 12 females,&amp;nbsp; 48.2+8.8&amp;nbsp; years)&amp;nbsp; received&amp;nbsp; placebo.&amp;nbsp; Participants&amp;nbsp; receiving&amp;nbsp; bupropion&amp;nbsp; SR had a more rapid reduction&amp;nbsp; in&amp;nbsp; atypical&amp;nbsp; SIGH-SAD&amp;nbsp; depressive&amp;nbsp; symptoms and lower depression scores across time on the SQ. ROC&amp;nbsp; analyses&amp;nbsp; revealed&amp;nbsp; that&amp;nbsp; positive effects of bupropion SR on total SIGH-SAD scores were more evident in males than females. Bupropion SR was well tolerated. &lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion &lt;/strong&gt;: Bupropion SR may be beneficial for the treatment of SAD, but larger randomized placebo- controlled studies are warranted&lt;/p&gt;</dc:description>
										<dc:publisher>Archives of Depression and Anxiety - Peertechz Publications</dc:publisher>
										<dc:date>2017-05-26</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-5460.000016</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Martin H Teicher et al.</dc:rights>
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