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Highlights: [•] THg and Se concentrations in fish varied between estuary regions but all maintained positive Se:Hg ratios. [•] Regional negative selenium health benefit values (Se HBVs) were evident suggesting increased Hg toxicity risk. [•] Single all-encompassing Se HBV for any given species may not be appropriate when there is strong site fidelity. [•] The results highlight the importance of including Se in assessments of seafood safety. [ABSTRACT FROM AUTHOR]

Metabolic and inflammatory disorders commonly co-occur with depression and psychosis, with emerging evidence implicating immuno-metabolic dysfunction in their aetiology. Previous studies have reported metabolic dysfunction and inflammation in adults with depression and psychosis. However, longitudinal studies testing the direction of association, and the effects of different dimensions of early-life immuno-metabolic dysfunction on adult psychopathology are limited. Using data from 3258 birth cohort participants we examined longitudinal associations of three metabolic hormones (leptin, adiponectin, insulin) at age 9 with risks for depression- and psychosis-spectrum outcomes at age 24. In addition, using nine immuno-metabolic biomarkers (leptin, adiponectin, insulin, interleukin-6, C-Reactive protein, low density lipoprotein, high density lipoprotein, triglycerides, and BMI), we constructed an exploratory bifactor model showing a general immuno-metabolic factor and three specific factors (adiposity, inflammation, and insulin resistance), which were also used as exposures. Childhood leptin was associated with adult depressive episode (adjusted odds ratio (aOR)= 1.31; 95% CI, 1.02–1.71) and negative symptoms (aOR=1.15; 95% CI, 1.07–1.24), but not positive psychotic symptoms. The general immuno-metabolic factor was associated with atypical depressive symptoms (aOR=1.07; 95% CI, 1.01–1.14) and psychotic experiences (aOR=1.21; 95% CI, 1.02–1.44). The adiposity factor was associated with negative symptoms (aOR=1.07; 95% CI 1.02–1.12). Point estimates tended to be larger in women, though 95% credible intervals overlapped with those for men. In women, the inflammatory factor was associated with depressive episodes (aOR=1.27; 95% CI, 1.03–1.57). While general immuno-metabolic dysfunction in childhood may contribute to risks for both psychotic and depressive symptoms in adulthood, childhood adiposity and inflammation appear to be particularly linked to affective (depressive and negative), but not positive psychotic symptoms. • Inflammation and metabolic disorders are associated with mental health problems. • Higher leptin in childhood was linked to risk of depressive episodes. • Higher leptin in childhood was linked to more negative symptoms. • A general immuno-metabolic factor associated with depression and psychosis. • These associations were larger in women than in men. [ABSTRACT FROM AUTHOR]