https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:22846 Wed 11 Apr 2018 16:46:51 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:26462 Wed 11 Apr 2018 11:12:47 AEST ]]> https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:40074 n = 1831) to evaluate if inflammation and central adiposity mediate the relationship between depression and diabetes. Methods: Depression was estimated using a behavior-based diagnostic algorithm, inflammation using venous dried blood spot (DBS) CRP, central adiposity using waist-to-height ratio (WHtR), and uncontrolled diabetes using venous DBS-glycated hemoglobin (HbA1c). Results: The association between depression and uncontrolled diabetes was partially mediated by CRP before but not after WHtR was considered. When WHtR was added to the model, it partially mediated the relationship between diabetes and depression while fully mediating the relationship between depression and CRP. Conclusions: These findings suggest that central adiposity may be a more significant mediator between diabetes and depression than inflammation and account for the relationship between these disorders and inflammation. Depression may cause an increase in central adiposity, which then may lead to diabetes, but the increase in known systemic inflammatory pathways caused by central adiposity may not be the key pathological mechanism.]]> Thu 14 Jul 2022 12:29:11 AEST ]]>