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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/18149
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dc.contributor.advisorMorrison, Katherine-
dc.contributor.authorShin, Sabina-
dc.date.accessioned2015-09-24T18:38:32Z-
dc.date.available2015-09-24T18:38:32Z-
dc.date.issued2015-11-
dc.identifier.urihttp://hdl.handle.net/11375/18149-
dc.description.abstractThere is increasing recognition of the relationship between depression and obesity in the pediatric population and recently, there has been a focus on inflammation as a potential link. Both conditions are considered to be pro-inflammatory states, and certain inflammatory markers are linked to depression in obese adults and vice versa. Leptin has also been implicated in depression as a potential mediator between inflammation and depression. Brain derived neurotrophic factor (BDNF), which is associated with depression and obesity, is influenced by inflammation and leptin in animal models as well. Few studies have examined the interactions between depression, adiposity, and biological markers in obese youth and therefore, our objective was to explore the determinants of depression in obese youth in a clinical setting. We studied 244 youth aged 8-17 years (125 girls, 119 boys) at the time of entry to a weight management program, as part of a prospective, longitudinal study. The CES-DC depression-screening tool was used to assess depressive symptoms, and a participant was classified as having high depressive symptoms if the CES-DC score ≥15 or taking antidepressants. Questionnaires assessed socio-demographic factors and puberty while adiposity was measured using dual-energy X-ray absorptiometry (DXA). Inflammatory markers (IL-6, TNFα, CRP, IL-10), leptin, and BDNF were quantified by immunoassays. Of the 244 participants, 8 were on antidepressants and 88 (36.4%) met the criteria for high depressive symptoms. We confirmed previous findings that household income and body fat were important determinants of depressive symptoms. However for the first time, it was identified that leptin levels predicted CES-DC score independent of body fat. Neither inflammatory markers nor BDNF were significantly related to depression scores. Our findings suggest that leptin may mediate the relationship of adiposity and depression but it is uncertain if this is related to direct action or to the phenomenon of leptin resistance.en_US
dc.language.isoen_USen_US
dc.subjectObesityen_US
dc.subjectPediatricsen_US
dc.subjectDepressionen_US
dc.subjectMental Healthen_US
dc.subjectchildren and adolescentsen_US
dc.subjectinflammationen_US
dc.subjectBDNFen_US
dc.subjectleptinen_US
dc.subjectbody faten_US
dc.subjectanthropometricen_US
dc.subjectsocio-demographic factorsen_US
dc.subjectHPA axisen_US
dc.subjectclinical researchen_US
dc.titleDepression and its determinants in children and adolescents with obesityen_US
dc.title.alternativeDepression and its determinants in youth with obesityen_US
dc.typeThesisen_US
dc.contributor.departmentMedical Sciencesen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Science (MSc)en_US
dc.description.layabstractObesity has a significant impact on depression in children and adolescents. Inflammation – the body’s response to injury – is measured through markers in the blood and leptin – the marker of body fat – have shown to be related to depression. Research indicates that depression influences these factors to act on obesity. However, research on the interactions of biological and socio-demographic factors with depression in youth with obesity is lacking. Therefore, our objective was to explore the impact of these factors on depression in obese youth entering into a weight management program. Using a depression-screening tool, we studied 244 youth under 18 years and confirmed that household income and body fat were important factors of depression. However for the first time, we found leptin influenced depression regardless of the amount of fat present suggesting that depression acts on obesity through leptin but it is uncertain how this occurs and further research is warranted.en_US
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