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- Due, Pernille, et al.
(författare)
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Is victimization from bullying associated with medicine use among adolescents? A nationally representative cross-sectional survey in Denmark
- 2007
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Ingår i: Pediatrics. - : American Academy of Pediatrics (AAP). - 1098-4275 .- 0031-4005. ; 120:1, s. 110-117
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Tidskriftsartikel (refereegranskat)abstract
- OBJECTIVE. The goal was to examine whether being a victim of bullying was associated with medicine use, taking into account the increased prevalence of physical and psychological symptoms. METHODS. The study population included all students in grades 5, 7, and 9 (mean ages: 11.6, 13.6, and 15.6 years, respectively) in a random sample of schools in Denmark (participation rate: 88.5%; N = 5205). The students reported health problems, medicine use, bullying, and a range of psychosocial conditions in an anonymous standardized questionnaire. The outcome measure was self-reported medicine use for headache, stomachache, difficulties in getting to sleep, and nervousness. The determinant was frequency of exposure to bullying, measured with 1 item. RESULTS. In multivariate models adjusted for age and social class, we found that adolescent victims of bullying used medicine for pains and psychological problems more often than did adolescents who were not bullied. The increased odds of using medicine were not explained by the higher prevalence of symptoms among the bullied children. CONCLUSIONS. We found victimization from bullying to be associated with medicine use, even when we controlled for the higher prevalence of symptoms among bullied victims. The medications that adolescents use can have adverse effects, in addition to the potentially health-damaging effects of bullying. Policy makers, health care professionals, and school staff should be aware that the adolescent victims of bullying are prone to excess use of medicine, and preventive actions should be taken to decrease the level of bullying as well as the use of medicine among adolescents.
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| 3. |
- Grunnet, Louise G., et al.
(författare)
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Regulation and Function of FTO mRNA Expression in Human Skeletal Muscle and Subcutaneous Adipose Tissue
- 2009
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Ingår i: Diabetes. - : American Diabetes Association. - 1939-327X .- 0012-1797. ; 58:10, s. 2402-2408
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Tidskriftsartikel (refereegranskat)abstract
- OBJECTIVE-Common variants in FTO (the fat mass- and obesity-associated gene) associate with obesity and type 2 diabetes. The regulation and biological function of FTO mRNA expression in target tissue is unknown. We investigated the genetic and nongenetic regulation of FTO mRNA in skeletal muscle and adipose tissue and their influence on in vivo glucose and fat metabolism. RESEARCH DESIGN AND METHODS-The FTO rs9939609 polymorphism was genotyped in two twin cohorts: 1) 298 elderly twins aged 62-83 years with glucose tolerance ranging from normal to type 2 diabetes and 2) 196 young (25-32 years) and elderly (58-66 years) nondiabetic twins examined by a hyperinsulinemic-euglycemic clamp including indirect calorimetry. FTO mRNA expression was determined in subcutaneous adipose tissue (n = 226) and skeletal muscle biopsies (n = 158). RESULTS-Heritability of FTO expression in both tissues was low, and FTO expression was not influenced by FTO rs9939609 genotype. FTO mRNA expression in skeletal muscle was regulated by age and sex, whereas age and BMI were predictors of adipose tissue FTO mRNA expression. FTO mRNA expression in adipose tissue was associated with an atherogenic lipid profile. In skeletal muscle, FTO mRNA expression was negatively associated to fat and positively to glucose oxidation rates as well as positively correlated with expression of genes involved in oxidative phosphorylation including PGC1 alpha. CONCLUSIONS-The heritability of FTO expression in adipose tissue and skeletal muscle is low and not influenced by obesity-associated FTO genotype. The age-dependent decline in FTO expression is associated with peripheral defects of glucose and fat metabolism. Diabetes 58:2402-2408, 2009
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| 4. |
- Ottosen, Lisbeth M., et al.
(författare)
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Electrodialytic remediation of soil slurry-removal of Cu, Cr, and As
- 2009
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Ingår i: Separation science and technology (Print). - Philadelphia, PA : Taylor & Francis. - 0149-6395 .- 1520-5754. ; 44:10, s. 2245-2268
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Severe soil contamination is often found at old wood preservation sites and a common combination of pollutants is Cu, Cr, and As. In the present work it is tested if simultaneous removal of Cu, Cr, and As can be obtained in an electrodialytic cell where the polluted soil is remediated as a stirred suspension (placed as the desalination compartment in accordance to the position of the ion exchange membranes). The soil for the experiments was sampled at an abandoned wood preservation site and contained 2170mg Cu/kg, 710mg Cr/kg and 3200mg As/kg. SEM-EDX analysis showed that Cu, Cr, As and oxygen formed particles that were cementing soil minerals together. The soil was suspended in distilled water, distilled water with I2 crystals to have an oxidizing environment, or in an acidified environment at pH about 1.0. The experiments lasted from 1 to 3 weeks. Good results were obtained in two experiments; an experiment where the soil was suspended in distilled water and the remediation lasted 3 weeks with 2.5mA and an experiment with acidification of the soil suspension with HNO3 to pH about 1.0 (2 weeks and 5mA). The best separation of pollutants and soil was obtained in the experiment with suspension in distilled water. Based on soil concentrations, good Cu removal (95%) was obtained in both experiments. Removal of Cr was most efficient from the acidified soil suspension (74%). Both Cu and Cr concentrations were below the limiting values after the remediation. The As concentration, however, was not even although 61% was removed. In the soil remained about 1070mg As/kg soil and since the limiting value is 40mg As/kg, the removal was not efficient enough. So simultaneous removal was possible, but the target values were only met in the case of Cu and Cr, and more research is needed to remove As to a sufficiently low concentration, as well.
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| 5. |
- Rung, Johan, et al.
(författare)
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Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia
- 2009
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Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 41:10, s. 89-1110
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Tidskriftsartikel (refereegranskat)abstract
- Genome-wide association studies have identified common variants that only partially explain the genetic risk for type 2 diabetes (T2D). Using genome-wide association data from 1,376 French individuals, we identified 16,360 SNPs nominally associated with T2D and studied these SNPs in an independent sample of 4,977 French individuals. We then selected the 28 best hits for replication in 7,698 Danish subjects and identified 4 SNPs showing strong association with T2D, one of which (rs2943641, P = 9.3 x 10(-12), OR = 1.19) was located adjacent to the insulin receptor substrate 1 gene (IRS1). Unlike previously reported T2D risk loci, which predominantly associate with impaired beta cell function, the C allele of rs2943641 was associated with insulin resistance and hyperinsulinemia in 14,358 French, Danish and Finnish participants from population-based cohorts; this allele was also associated with reduced basal levels of IRS1 protein and decreased insulin induction of IRS1-associated phosphatidylinositol-3-OH kinase activity in human skeletal muscle biopsies.
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