14 research outputs found

    Immune activation by casein dietary antigens in bipolar disorder

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    Objectives: Inflammation and other immune processes are increasingly linked to psychiatric diseases. Antigenic triggers specific to bipolar disorder are not yet defined. We tested whether antibodies to bovine milk caseins were associated with bipolar disorder, and whether patients recognized different epitopes of the casein protein than control individuals. Methods: Anti-bovine casein immunoglobulin G (IgG) levels were measured with solid-phase immunoassays in 75 individuals with bipolar disorder and 65 controls. Epitope recognition was evaluated in immunoassays by cross neutralization with anti-bovine casein polyclonal antibodies of defined reactivity. Group-specific reactivity and associations with symptom severity scores were detected with age-, gender-, and race-controlled regression models. Results: Individuals with bipolar disorder had significantly elevated anti-casein IgG (t-test, p = 0.001) compared to controls. Casein IgG seropositivity conferred odds ratios of 3.97 for bipolar disorder [n = 75, 95% confidence interval (CI): 1.31–12.08, p = 0.015], 5.26 for the bipolar I subtype (n = 56, 95% CI: 1.66–16.64, p = 0.005), and 3.98 for bipolar disorder with psychosis (n = 54, 95% CI: 1.32–12.00, p = 0.014). Lithium and/or antipsychotic medication did not significantly affect anti-casein IgG levels. Casein IgG measures correlated with severity of manic (R2 = 0.15, 95% CI: 0.05–0.24, p = 0.02) but not depressive symptoms. Unlike controls, sera from individuals with bipolar disorder did not inhibit binding of casein-reactive animal sera (t-test/¿2, p = 0.0001). Conclusions: Anti-casein IgG associations with bipolar I diagnoses, psychotic symptom history, and mania severity scores suggest that casein-related immune activation may relate to the psychosis and mania components of this mood disorder. Case-control differences in epitope recognition implicate disease-related alterations in how the casein molecule is digested and/or how resulting casein-derived structures are rendered immunogenic

    Subunit and whole molecule specificity of the anti-bovine casein immune response in recent onset psychosis and schizophrenia

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    Previous studies show increased antibody levels to bovine casein in some individuals with schizophrenia. The immunogenicity of specific domains of bovine casein varies among people with milk sensitivities and thus could vary among different neuropsychiatric disorders. Using ELISAs and immunoblotting, we characterized IgG class antibody specificity to whole bovine casein and to the as, ß, and ¿ subunits in individuals with recent onset psychosis (n = 95), long-term schizophrenia (n = 103), and non-psychiatric controls (n = 65). In both patient groups, we found elevated IgG to casein proteins, particularly to whole casein and the as subunit (p = 0.0001). Odds ratios of casein seroprevalence for recent onset psychosis (age-, gender-, race-, smoking-adjusted) were significant for whole casein (8.13, p = 0.0001), and the as (7.89, p = 0.0001), ß (5.23, p = 0.001) and ¿ (5.70, p = 0.0001) subunits. Odds ratios for long-term schizophrenia were significant for whole casein (7.85, p = 0.0001), and the as (4.78, p = 0.003) and ¿ (4.92, p = 0.004) subunits. Within the recent onset group, odds ratios were particularly significant for a subgroup of people with psychotic disorders that included major depressive disorders (8.22–16.48, p = 0.0001). In a different recent onset subgroup (schizophrenia-spectrum disorders), PANSS scores for negative symptoms were correlated with casein antibody levels for the as and ¿ subunits (p = 0.001–0.01). Immunoblotting patterns also exhibited group specificity, with ¿ predominant in recent onset and as in schizophrenia (Fisher's Exact Test, p = 0.001). The elevated IgG and unique patterns of antibody specificity to bovine casein among diagnostic groups provide a rationale for clinical trials to evaluate efficacies of dietary modifications in individuals with neuropsychiatric diseases

    Enxerto ósseo esponjoso autólogo em pequenos animais Autologous cancellous bone graft in small animals

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    O enxerto ósseo esponjoso autólogo é formado por osso trabecular, poroso e altamente celular. Visto ser de fundamental importância na cirurgia ortopédica de pequenos animais, o trabalho teve por objetivo discorrer sobre a função, locais de colheita, cuidados, formas de aplicação, indicações e contra-indicações desse enxerto. Ele estimula a formação óssea devido ao fornecimento de células vivas e fatores de crescimento, mas não possui suporte mecânico. A asa do ílio craniodorsal, úmero proximal, tíbia proximal e fêmur distal, são os locais de colheita mais utilizados em cães. A asa do ílio consiste no local mais satisfatório para gatos. Para maximizar a incorporação do enxerto com o tecido hospedeiro, devem ser tomados alguns cuidados entre a colheita e a transferência para a área receptora. Além disso, pode ser aplicado sem compressão dentro do local recipiente. A freqüência de complicações é considerada baixa.<br>The autologous cancellous bone is formed by trabecular bone, porous, and highly cellular. Since this graft is very important in orthopedic surgery of small animals, the purpose of this paper is to describe the function, donor sites, precautions, application methods, indications, and contraindications. It stimulates the bone formation because it provides live cells and growth factors, but it did not have mechanical support. Cranial dorsal wing of the ilium, proximal humerus, proximal tibia, and distal femur are the most common harvest sites used in dogs. The wing of the ilium is the most satisfactory harvest site in cats. To maximize the graft incorporation with the tissue it is necessary to take care during the harvest and transference to recipient site. In addition, it may be put into the recipient site with no compression. The frequency of complications is considered low
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