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        <dc:title>Effect of vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients: results of a randomized controlled trial</dc:title>
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        <bibo:abstract>&lt;jats:title&gt;Abstract&lt;/jats:title&gt;&lt;jats:sec&gt;
&lt;jats:title&gt;Purpose&lt;/jats:title&gt;
&lt;jats:p&gt;While observational studies revealed inverse associations between serum vitamin D levels [25(OH)D] and depression, randomized controlled trials (RCT) in children and adolescents are lacking. This RCT examined the effect of an untreated vitamin D deficiency compared to an immediate vitamin D&lt;jats:sub&gt;3&lt;/jats:sub&gt; supplementation on depression scores in children and adolescents during standard day and in-patient psychiatric treatment.&lt;/jats:p&gt;
&lt;/jats:sec&gt;&lt;jats:sec&gt;
&lt;jats:title&gt;Methods&lt;/jats:title&gt;
&lt;jats:p&gt;Patients with vitamin D deficiency [25(OH)D ≤ 30 nmol/l] and at least mild depression [Beck Depression Inventory II (BDI-II) &amp;gt; 13] (&lt;jats:italic&gt;n&lt;/jats:italic&gt; = 113) were 1:1 randomized into verum (VG; 2640 IU vitamin D&lt;jats:sub&gt;3&lt;/jats:sub&gt;/d) or placebo group (PG) in a double-blind manner. During the intervention period of 28 days, both groups additionally received treatment as usual. BDI-II scores were assessed as primary outcome, DISYPS-II (Diagnostic System for Mental Disorders in Childhood and Adolescence, Self- and Parent Rating) and serum total 25(OH)D were secondary outcomes.&lt;/jats:p&gt;
&lt;/jats:sec&gt;&lt;jats:sec&gt;
&lt;jats:title&gt;Results&lt;/jats:title&gt;
&lt;jats:p&gt;At admission, 49.3% of the screened patients (&lt;jats:italic&gt;n&lt;/jats:italic&gt; = 280) had vitamin D deficiency. Although the intervention led to a higher increase of 25(OH)D levels in the VG than in the PG (treatment difference: + 14 ng/ml; 95% CI 4.86–23.77; &lt;jats:italic&gt;p&lt;/jats:italic&gt; = 0.003), the change in BDI-II scores did not differ (+ 1.3; 95% CI − 2.22 to 4.81; &lt;jats:italic&gt;p&lt;/jats:italic&gt; = 0.466). In contrast, DISYPS parental ratings revealed pronounced improvements of depressive symptoms in the VG (− 0.68; 95% CI − 1.23 to − 0.13; &lt;jats:italic&gt;p&lt;/jats:italic&gt; = 0.016).&lt;/jats:p&gt;
&lt;/jats:sec&gt;&lt;jats:sec&gt;
&lt;jats:title&gt;Conclusion&lt;/jats:title&gt;
&lt;jats:p&gt;Whereas this study failed to show a vitamin D supplementation effect on self-rated depression in adolescent in- or daycare patients, parents reported less depressive symptoms in VG at the end of our study. Future trials should consider clinician-rated depressive symptoms as primary outcome.&lt;/jats:p&gt;
&lt;/jats:sec&gt;&lt;jats:sec&gt;
&lt;jats:title&gt;Trial registration&lt;/jats:title&gt;
&lt;jats:p&gt;“German Clinical Trials Register” (&lt;jats:ext-link xmlns:xlink=&quot;http://www.w3.org/1999/xlink&quot; ext-link-type=&quot;uri&quot; xlink:href=&quot;https://www.drks.de&quot;&gt;https://www.drks.de&lt;/jats:ext-link&gt;), registration number: DRKS00009758&lt;/jats:p&gt;
&lt;/jats:sec&gt;</bibo:abstract>
        <bibo:startPage>3415-3424</bibo:startPage>
        <bibo:endPage>3415-3424</bibo:endPage>
        <bibo:doi rdf:resource="10.1007/s00394-020-02176-6" />
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