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   	<dc:title>Does inflammation explain the association between vitamin D and depression? Results of a cross-sectional study in children and adolescents</dc:title>
   	<dc:creator>Schlarbaum, Laura</dc:creator>
   	<dc:creator>Jankovic, Nicole</dc:creator>
   	<dc:creator>Bühlmeier, Judith</dc:creator>
   	<dc:creator>Engler, Harald</dc:creator>
   	<dc:creator>Hirtz, Raphael</dc:creator>
   	<dc:creator>Grasemann, Corinna</dc:creator>
   	<dc:creator>Peters, Triinu</dc:creator>
   	<dc:creator>Hinney, Anke</dc:creator>
   	<dc:creator>Antel, Jochen</dc:creator>
   	<dc:creator>Hebebrand, Johannes</dc:creator>
   	<dc:creator>Föcker, Manuel</dc:creator>
   	<dc:creator>Libuda, Lars</dc:creator>
   	<dc:description>&lt;jats:title&gt;Abstract&lt;/jats:title&gt;
                  &lt;jats:p&gt;Vitamin D has been associated with depression, potentially via anti-inflammatory mechanisms, yet data is scarce, particularly in adolescence. We investigated (1) whether lower vitamin D status is associated with greater depression severity and (2) whether this association is statistically moderated by inflammation in patients of a child and adolescent psychiatry department. At admission fasting morning venous blood was drawn. Serum vitamin D (25(OH)D) and C-reactive protein (CRP) were analyzed in all participants [n=465 (64.7%♀; 11.3-18.9 years)]. In a subsample [n=177], we additionally measured tumor necrosis factor-alpha, interferon-gamma and interleukin (IL)-1β, IL-6, IL-8, IL-10. Depression severity was assessed by the Beck Depression Inventory-II (BDI-II) [n=450], the Diagnostic System for Mental Disorders in Childhood and Adolescence via self-assessment (DISYPS Self) [n=441], and parent-assessment (DISYPS Proxy) [n=422]. Overall, 43.2% [n=201] were at risk for vitamin D deficiency (&amp;lt;30nmol/L), and 73.5%-83.2% –depending on assessment tool– showed at least mild depression. Linear regression revealed an inverse association between 25(OH)D and BDI-II in both crude and CRP-adjusted full-sample models. Logistic regressions showed a robust inverse association between 25(OH)D and DISYPS Proxy, but not for DISYPS Self. Although 25(OH)D was inversely correlated with some pro-inflammatory markers, neither their inclusion in regression models nor formal mediation analyses supported inflammation as a mediator of the vitamin D–depression association. Overall, our results suggest that vitamin D relates modestly to both depression and inflammation in adolescence. However, based on the measured parameters, we cannot confirm that anti-inflammatory effects are the link between vitamin D and depression.&lt;/jats:p&gt;</dc:description>
   	<dc:publisher>Cambridge University Press (CUP)</dc:publisher>
   	<dc:date>2026</dc:date>
   	<dc:type>info:eu-repo/semantics/article</dc:type>
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   	<dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
   	<dc:identifier>https://ris.uni-paderborn.de/record/65375</dc:identifier>
   	<dc:source>Schlarbaum L, Jankovic N, Bühlmeier J, et al. Does inflammation explain the association between vitamin D and depression? Results of a cross-sectional study in children and adolescents. &lt;i&gt;British Journal of Nutrition&lt;/i&gt;. Published online 2026:1-37. doi:&lt;a href=&quot;https://doi.org/10.1017/s0007114526106928&quot;&gt;10.1017/s0007114526106928&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
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   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/1475-2662</dc:relation>
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